9H-Fluoren-9-one (9-Fluorenone) [C13H8O]

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Reaxys ID 1636531 View in Reaxys

1/1 CAS Registry Number: 486-25-9 Chemical Name: 9-fluorenone; fluorenone Linear Structure Formula: OCC12H8 Molecular Formula: C13H8O Molecular Weight: 180.206 Type of Substance: isocyclic InChI Key: YLQWCDOCJODRMT-UHFFFAOYSA-N Note:

O

Substance Label (230) Label References I

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2c

Al-Thebeiti, Marzoog S.; El-Zohry, Maher F.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 37; nb. 8; (1998); p. 804 - 809, View in Reaxys; Al-Thebeiti, Marzoog S.; Heterocycles; vol.

53; nb. 3; (2000); p. 621 - 628, View in Reaxys; Abdel-Hafez, Ali A.; El-Zohry, Maher F.; Heterocyclic Communications; vol. 7; nb. 6; (2001); p. 583 - 588, View in Reaxys; El-Zohry, Maher F.; Al-Ahmadi, Abdullah A.; Aquily, Fatimah A.; Heterocyclic Communications; vol. 8; nb. 2; (2002); p. 187 - 194, View in Reaxys; Lykakis, Ioannis N.; Orfanopoulos, Michael; Tetrahedron Letters; vol. 46; nb. 45; (2005); p. 7835 - 7839, View in Reaxys; Xu, Yuan; Yang, Zhenping; Hu, Jiantao; Yan, Jie; Synthesis (Germany); vol. 45; nb. 3; (2013); p. 370 - 374; Art.No: SS-2012-F0873OP, View in Reaxys

6a

Oota, Atsushi; Imai, Toshinobu; Yamazaki, Ayumi; Oba, Toru; Karikomi, Michinori; Minabe, Masahiro; Bulletin of the Chemical Society of Japan; vol. 79; nb. 2; (2006); p. 333 - 335, View in Reaxys; Khurana, Jitender M.; Chaudhary, Ankita; Kumar, Sanjay; Organic Preparations and Procedures International; vol. 45; nb. 3; (2013); p. 241 - 245, View in Reaxys; Puenner, Florian; Schieven, Justin; Hilt, Gerhard; Organic Letters; vol. 15; nb. 18; (2013); p.

4888 - 4891, View in Reaxys

2h

Cui, Yi; Yamashita, Yasuhiro; Kobayashi, Shu; Chemical Communications; vol. 48; nb. 83; (2012); p. 10319 - 10321, View in Reaxys; Chen, Shufeng; Yuan, Fang; Zhao, Haiying; Li, Baoguo; Research on Chemical Intermediates; vol.

39; nb. 6; (2013); p. 2391 - 2399, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

8/144

2018-06-21 20:37:19

compound F10

Patent; CANON KABUSHIKI KAISHA; Nishide, Yosuke; Watanabe, Taiki; Kosuge, Tetsuya; Yamada, Naoki; Saitoh, Akihito; US2013/49581; (2013); (A1) English, View in Reaxys

10a

Coelho, Jaime A. S.; Trindade, Alexandre F.; Wanke, Riccardo; Rocha, Bruno G. M.; Veiros, Luis F.; Gois, Pedro M. P.; Pombeiro, Armando J. L.; Afonso, Carlos A. M.; European Journal of Organic Chemistry; nb. 8; (2013); p.

1471 - 1478, View in Reaxys

VPC-3002

Li, Huifang; Hassona, Mohamed D.H.; Lack, Nathan A.; Axerio-Cilies, Peter; Leblanc, Eric; Tavassoli, Peyman; Kanaan, Natalia; Frewin, Kate; Singh, Kriti; Adomat, Hans; Boehm, Konrad J.; Prinz, Helge; Guns, Emma Tomlinson; Rennie, Paul S.; Cherkasov, Artem; Molecular Cancer Therapeutics; vol. 12; nb. 11; (2013); p. 2425 2435, View in Reaxys

XV

Andrievskii; Gorelik; Linko; Grachev; Russian Journal of Organic Chemistry; vol. 49; nb. 10; (2013); p. 1474 - 1481; Zhurnal Organicheskoi Khimii; vol. 49; nb. 10; (2013); p. 1496 - 1502,7, View in Reaxys

5b

Hou; Koizumi; Fujita; Yamazaki; Wakatsuki; Journal of the American Chemical Society; vol. 123; nb. 24; (2001); p.

5812 - 5813, View in Reaxys; Hesse, Nadine; Froehlich, Roland; Wibbeling, Birgit; Wuerthwein, Ernst-Ulrich; European Journal of Organic Chemistry; nb. 17; (2006); p. 3923 - 3937, View in Reaxys; Wiedemann, Sean H.; Bio, Matthew M.; Brown, Liane M.; Hansen, Karl B.; Langille, Neil F.; Synlett; vol. 23; nb. 15; (2012); p. 2231 - 2236, View in Reaxys

1d

Gholap, Atul R.; Paul, Vincent; Srinivasan, Kumar V.; Synthetic Communications; vol. 38; nb. 17; (2008); p. 2967 2982, View in Reaxys; Cui, Hua; Li, Ying; Zhang, Songlin; Organic and Biomolecular Chemistry; vol. 10; nb. 14; (2012); p. 2862 - 2869, View in Reaxys

43

Balkrishna, Shah Jaimin; Prasad, Ch Durga; Panini, Piyush; Chopra, Deepak; Kumar, Sangit; Detty, Michael R.; Journal of Organic Chemistry; vol. 77; nb. 21; (2012); p. 9541 - 9552,12, View in Reaxys

f'

Tandon, Praveen K.; Singh, Santosh B.; Singh, Satpal; Kesarwani, Bhawana; Journal of the Indian Chemical Society; vol. 89; nb. 10; (2012); p. 1363 - 1367, View in Reaxys

13a

Lim, Chae Mi; Ha, Su Jeong; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 12; (2012); p.

4258 - 4260, View in Reaxys

E4; D12

Patent; CANON KABUSHIKI KAISHA; NISHIDE, Yosuke; MIYASHITA, Hirokazu; KAMATANI, Jun; SAITOH, Akihito; WO2011/96272; (2011); (A1) English, View in Reaxys

Flu

Ohura, Takeshi; Amagai, Takashi; Makino, Masakazu; Chemosphere; vol. 70; nb. 11; (2008); p. 2110 - 2117, View in Reaxys

28

Schank, Kurt; Beck, Horst; Buschlinger, Michael; Eder, Joerg; Heisel, Thomas; Pistorius, Susanne; Wagner, Christiane; Helvetica Chimica Acta; vol. 83; nb. 4; (2000); p. 801 - 826, View in Reaxys; Kommreddy, Amitha; Bowsher, Michael S.; Gunna, Meena R.; Botha, Kirankumar; Vinod, Thottumkara K.; Tetrahedron Letters; vol.

49; nb. 28; (2008); p. 4378 - 4382, View in Reaxys

12a

Zarudnitskii, Evgenij V.; Pervak, Igor I.; Merkulov, Anatolij S.; Yurchenko, Aleksandr A.; Tolmachev, Andrej A.; Tetrahedron; vol. 64; nb. 45; (2008); p. 10431 - 10442, View in Reaxys

16

Xiao, Xiangshu; Antony, Smitha; Kohlhagen, Glenda; Pommier, Yves; Cushman, Mark; Journal of Organic Chemistry; vol. 69; nb. 22; (2004); p. 7495 - 7501, View in Reaxys; Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys

educt to L

Zhou, Hong-ping; Li, Dong-mei; Wang, Peng; Cheng, Le-hua; Gao, Yuan-hao; Zhu, Yong-min; Wu, Jie-ying; Tian, Yu-peng; Tao, Xu-tang; Jiang, Min-hua; Fun, Hoong-Kun; Journal of Molecular Structure; vol. 826; nb. 2-3; (2007); p. 205 - 210, View in Reaxys

starting to 7

Hua, Guoxiong; Li, Yang; Slawin, Alexandra M. Z.; Woollins, J. Derek; Dalton Transactions; nb. 15; (2007); p. 1477 - 1480, View in Reaxys

9-FLUO; (3)

Hashimoto, Shinya; Ueda, Yasuhiro; Kurihara, Ryo; Shiraishi, Fujio; Environmental Toxicology and Chemistry; vol. 26; nb. 2; (2007); p. 279 - 286, View in Reaxys

1l

Albrecht, Uwe; Langer, Peter; Tetrahedron; vol. 63; nb. 22; (2007); p. 4648 - 4654, View in Reaxys

educt tab. 3, entr.18

Yu; Zeng; Sun; Deng; Dong; Chen; Wang; Pei; Journal of Organometallic Chemistry; vol. 692; nb. 11; (2007); p.

2306 - 2313, View in Reaxys

table 1, entry 10

Sadeghi; Mohammadpoor-Baltork; Azarm; Mazidi; Synthetic Communications; vol. 31; nb. 3; (2001); p. 435 - 438, View in Reaxys; Shaabani, Ahmad; Rahmati, Abbas; Sharifi, Masoumeh; Rad, Jafar Mogimi; Aghaaliakbari, Behnaz; Farhangi, Elham; Lee, Donald G.; Monatshefte fur Chemie; vol. 138; nb. 7; (2007); p. 649 - 651, View in Reaxys

9Fl

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol.

67; nb. 2; (2007); p. 316 - 320, View in Reaxys; Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 444 - 449, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

9/144

2018-06-21 20:37:19

FLO

Misaki, Kentaro; Kawami, Hirofumi; Tanaka, Tota; Handa, Yoji; Nakamura, Masafumi; Matsui, Saburo; Matsuda, Tomonari; Environmental Toxicology and Chemistry; vol. 26; nb. 7; (2007); p. 1370 - 1379, View in Reaxys

starting to 1

Hubert, Cecile; Tran, Khoa; Hauquier, Fanny; Cougnon, Charles; Pilard, Jean-Francois; Gosselin, Pascal; RaultBerthelot, Joelle; Raoult, Eugene; New Journal of Chemistry; vol. 31; nb. 10; (2007); p. 1730 - 1737, View in Reaxys

educt to 7b

Mlostoń, Grzegorz; Heimgartner, Heinz; Helvetica Chimica Acta; vol. 90; nb. 9; (2007); p. 1758 - 1764, View in Reaxys

1e; 1f

Hatano, Manabu; Takagi, Eri; Ishihara, Kazuaki; Organic Letters; vol. 9; nb. 22; (2007); p. 4527 - 4530, View in Reaxys

Tab.1.run3

Sano, Yuki; Tanaka, Takanori; Hayashi, Masahiko; Chemistry Letters; vol. 36; nb. 12; (2007); p. 1414 - 1415, View in Reaxys

Table 1; Entry 5

Nakanishi, Masafumi; Bolm, Carsten; Advanced Synthesis and Catalysis; vol. 349; nb. 6; (2007); p. 861 - 864, View in Reaxys

IVa

Chaikovskii; Filimonov; Skorokhodov; Ogorodnikov; Russian Journal of Organic Chemistry; vol. 43; nb. 9; (2007); p. 1278 - 1281, View in Reaxys

3a-Fl

Moorthy, Jarugu Narasimha; Samanta, Subhas; Journal of Organic Chemistry; vol. 72; nb. 25; (2007); p. 9786 9789, View in Reaxys

31

Blagoev, Milen; Linden, Anthony; Heimgartner, Heinz; Helvetica Chimica Acta; vol. 82; nb. 12; (1999); p. 2316 2335, View in Reaxys; Shing, Tony K. M.; Yeung, Ying-Yeung; Su, Pak L.; Organic Letters; vol. 8; nb. 14; (2006); p.

3149 - 3151, View in Reaxys

starting to 9b

Mloston, Grzegorz; Celeda, Malgorzata; Linden, Anthony; Heimgartner, Heinz; Heterocycles; vol. 68; nb. 1; (2006); p. 33 - 45, View in Reaxys

T.I, Entry 11, Product

Badri, Rashid; Mostoufi, Azar; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 181; nb. 7; (2006); p.

1513 - 1519, View in Reaxys

educt to 6a

Jones, David J.; Gibson, Vernon C.; Heterocycles; vol. 68; nb. 6; (2006); p. 1121 - 1138, View in Reaxys

product, tab 1/24

Hajipour; Bagheri; Ruoho; Russian Journal of Organic Chemistry; vol. 42; nb. 6; (2006); p. 844 - 848, View in Reaxys

8IIg

Pesquet, Anthony; Daich, Adam; Van Hijfte, Luc; Journal of Organic Chemistry; vol. 71; nb. 14; (2006); p. 5303 5311, View in Reaxys

product, tab 3/37

Farhadi, Saeid; Zabardasti, Abedien; Babazadeh, Zaynab; Tetrahedron Letters; vol. 47; nb. 50; (2006); p. 8953 8957, View in Reaxys

20

Li; Zhang; Petersen; Wang; Journal of Organic Chemistry; vol. 66; nb. 20; (2001); p. 6662 - 6668, View in Reaxys; Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol. 45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys

product T. 1, E. 22

Hajipour, Abdol R.; Guo, Lian-Wang; Ruoho, Arnold E.; Molecular Crystals and Liquid Crystals; vol. 456; nb. 1; (2006); p. 85 - 93, View in Reaxys

30

Lathioor, Edward C.; Leigh, William J.; Photochemistry and Photobiology; vol. 82; nb. 1; (2006); p. 291 - 300, View in Reaxys

prod., Tab. 2, entry 1

Park, Kwanghee Koh; Tsou, Lun K.; Hamilton, Andrew D.; Synthesis; nb. 21; (2006); p. 3617 - 3620, View in Reaxys

subst., Tab.3, entry 10

Setamdideh, Davood; Zeynizadeh, Behzad; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 61; nb. 10; (2006); p. 1275 - 1281, View in Reaxys

19

Kolano, Christoph; Bucher, Goetz; Schade, Olaf; Grote, Dirk; Sander, Wolfram; Journal of Organic Chemistry; vol.

70; nb. 17; (2005); p. 6609 - 6615, View in Reaxys; Chen, Xudong; Lemal, David M.; Journal of Fluorine Chemistry; vol. 127; nb. 9; (2006); p. 1158 - 1167, View in Reaxys

3h

Hatano, Bunpei; Kubo, Daisuke; Tagaya, Hideyuki; Chemical and Pharmaceutical Bulletin; vol. 54; nb. 9; (2006); p.

1304 - 1307, View in Reaxys

II

Kolyadina; Soldatenkov; Gridunova; Prostakov; Chemistry of Heterocyclic Compounds; vol. 34; nb. 7; (1998); p.

833 - 836, View in Reaxys; Ohura, Takeshi; Kitazawa, Atsushi; Amagai, Takashi; Makino, Masakazu; Environmental Science and Technology; vol. 39; nb. 1; (2005); p. 85 - 91, View in Reaxys

5e

Olah, George A.; Mathew, Thomas; Farnia, Morteza; Prakash, G. K. Surya; Katherine; Donald; Synlett; nb. 7; (1999); p. 1067 - 1068, View in Reaxys; Ali, Mohammed Hashmat; Gomes, Maria Goretti; Synthesis; nb. 8; (2005); p. 1326 - 1332; Art.No: M05004SS, View in Reaxys

tab1, col2, entry4

Hunsen, Mo; Tetrahedron Letters; vol. 46; nb. 10; (2005); p. 1651 - 1653, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

10/144

2018-06-21 20:37:19

educt of tab.2, entr.21

Firouzabadi, Habib; Iranpoor, Nasser; Jafari, Abbas Ali; Journal of Organometallic Chemistry; vol. 690; nb. 6; (2005); p. 1556 - 1559, View in Reaxys

21b

Nair, Vijay; Suja; Mohanan, Kishor; Tetrahedron Letters; vol. 46; nb. 18; (2005); p. 3217 - 3219, View in Reaxys

7-1d0

Tilly, David; Samanta, Subhendu S.; De, Asish; Castanet, Anne-Sophie; Mortier, Jacques; Organic Letters; vol. 7; nb. 5; (2005); p. 827 - 830, View in Reaxys

Tab 2/1 Substrate

Zaccheria, Federica; Ravasio, Nicoletta; Ercoli, Mauro; Allegrini, Pietro; Tetrahedron Letters; vol. 46; nb. 45; (2005); p. 7743 - 7745, View in Reaxys

tab.4, entry 5, prod.

Wang, Jia-Rui; Liu, Lei; Wang, Ye-Feng; Zhang, Ying; Deng, Wei; Guo, Qing-Xiang; Tetrahedron Letters; vol. 46; nb. 27; (2005); p. 4647 - 4651, View in Reaxys

VIII

Krasnokutskaya; Trusova; Filimonov; Russian Journal of Organic Chemistry; vol. 41; nb. 12; (2005); p. 1750 - 1751, View in Reaxys

educt to 18b

Yamaguchi, Shigehiro; Xu, Caihong; Yamada, Hiroshi; Wakamiya, Atsushi; Journal of Organometallic Chemistry; vol. 690; nb. 23; (2005); p. 5365 - 5377, View in Reaxys

3o

Qian, Weixing; Jin, Erlei; Bao, Weiliang; Zhang, Yongmin; Angewandte Chemie - International Edition; vol. 44; nb.

6; (2005); p. 952 - 955, View in Reaxys

Tab. 1, entry 3, prod.

Hunsen, Mo; Journal of Fluorine Chemistry; vol. 126; nb. 9-10; (2005); p. 1356 - 1360, View in Reaxys

product tab. 3, entry Li, Shi-Jun; Wang, Yan-Guang; Tetrahedron Letters; vol. 46; nb. 46; (2005); p. 8013 - 8015, View in Reaxys 7 subst., Tab.2, entry 7

Zeynizadeh, Behzad; Behyar, Tarifen; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol.

60; nb. 4; (2005); p. 453 - 457, View in Reaxys

unsubst. fluorenone Kirichenko; Meshkova; Topilova; Kiriyak; Lyapunov; Kulygina; Luk'yanenko; Russian Journal of General Chemistry; vol. 75; nb. 2; (2005); p. 272 - 277, View in Reaxys A

Patent; Cephalon, Inc.; US2005/234040; (2005); (A1) English, View in Reaxys

Table 1., substrate 5.

Aceves; Arroyo; Vargas; Miranda; Cabrera; Delgado; Heteroatom Chemistry; vol. 15; nb. 1; (2004); p. 71 - 76, View in Reaxys

2l'

Mohammadpoor-Baltork, Iraj; Memarian, Hamid Reza; Bahrami, Kiumars; Monatshefte fur Chemie; vol. 135; nb.

4; (2004); p. 411 - 418, View in Reaxys

42

Nicolaou; Mathison, Casey J. N.; Montagnon, Tamsyn; Journal of the American Chemical Society; vol. 126; nb. 16; (2004); p. 5192 - 5201, View in Reaxys

Table 1, entry 10

Kim, Sung Soo; Rajagopal, Gurusamy; Synthetic Communications; vol. 34; nb. 12; (2004); p. 2237 - 2243, View in Reaxys

6 (R1 = R2 = H)

Epperson, James R.; Bruce, Marc A.; Catt, John D.; Deskus, Jeffrey A.; Hodges, Donald B.; Karageorge, George N.; Keavy, Daniel J.; Mahle, Cathy D.; Mattson, Ronald J.; Ortiz, Astrid A.; Parker, Michael F.; Takaki, Katherine S.; Watson, Brett T.; Yevich, Joseph P.; Bioorganic and Medicinal Chemistry; vol. 12; nb. 17; (2004); p. 4601 4611, View in Reaxys

11b

Bei, Xiaohong; Hagemeyer, Alfred; Volpe, Anthony; Saxton, Robert; Turner, Howard; Guram, Anil S.; Journal of Organic Chemistry; vol. 69; nb. 25; (2004); p. 8626 - 8633, View in Reaxys

C6H4COC6H4

Zheng, Guorong; Li, Wei; Wang, Zixing; Lu, Ping; Australian Journal of Chemistry; vol. 57; nb. 8; (2004); p. 811 814, View in Reaxys

6h; 9b

Tanaka, Hirotaka; Hashimoto, Kentaro; Suzuki, Kyosuke; Kitaichi, Yasunori; Sato, Mitsuo; Ikeno, Taketo; Yamada, Tohru; Bulletin of the Chemical Society of Japan; vol. 77; nb. 10; (2004); p. 1905 - 1914, View in Reaxys

subs., Tab. 2, entry 4

Zeynizadeh, Behzad; Yahyaei, Saiedeh; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol.

59; nb. 6; (2004); p. 704 - 710, View in Reaxys

Product, Tab.2, run 5

Moorthy, Jarugu Narasimha; Singhal, Nidhi; Venkatakrishnan; Tetrahedron Letters; vol. 45; nb. 28; (2004); p. 5419 - 5424, View in Reaxys

9-fluorenyl-C=O

Blake, Jessie A.; Ingold, Keith U.; Lin, Shuqiong; Mulder, Peter; Pratt, Derek A.; Sheeller, Brad; Walton, John C.; Organic and Biomolecular Chemistry; vol. 2; nb. 3; (2004); p. 415 - 420, View in Reaxys

Tab. 1, entry 1

Guram, Anil; Hagemeyer, Alfred; Lugmair, Claus G.; Turner, Howard W.; Volpe Jr., Anthony F.; Weinberg, W. Henry; Yaccato, Karin; Advanced Synthesis and Catalysis; vol. 346; nb. 2-3; (2004); p. 215 - 230, View in Reaxys

Tab.1. product

Kawabata, Hirotoshi; Hayashi, Masahiko; Tetrahedron Letters; vol. 45; nb. 28; (2004); p. 5457 - 5459, View in Reaxys

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

11/144

2018-06-21 20:37:19

3l

Hajipour, Abdol R.; Mallakpour, Shadpour E.; Mohammadpoor-Baltork, Iraj; Adibi, Hadi; Monatshefte fur Chemie; vol. 134; nb. 1; (2003); p. 45 - 49, View in Reaxys

Product, Tab.1, run 37

Mohammadpoor-Baltork, Iraj; Khodaei, Mohammad Mehdi; Nikoofar, Kobra; Tetrahedron Letters; vol. 44; nb. 3; (2003); p. 591 - 594, View in Reaxys

product, tab 2, e 4

Das, Sasmita; Panigrahi; Maikap, Golak C.; Tetrahedron Letters; vol. 44; nb. 7; (2003); p. 1375 - 1377, View in Reaxys

9-F

Yamaji, Minoru; Wakabayashi, Sayaka; Ueda, Shin-Ichi; Shizuka, Haruo; Tobita, Seiji; Chemical Physics Letters; vol. 368; nb. 1-2; (2003); p. 41 - 48, View in Reaxys

Tab2.run3

Jablonski, Lukas; Billard, Thierry; Langlois, Bernard R.; Tetrahedron Letters; vol. 44; nb. 5; (2003); p. 1055 - 1057, View in Reaxys

FLU

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

4u

Pierres, Camille; George, Pascal; Van Hijfte, Luc; Ducep, Jean-Bernard; Hibert, Marcel; Mann, Andre; Tetrahedron Letters; vol. 44; nb. 18; (2003); p. 3645 - 3647, View in Reaxys

T. 2., prod. 7

Fernandes, Rodney A.; Kumar, Pradeep; Tetrahedron Letters; vol. 44; nb. 6; (2003); p. 1275 - 1278, View in Reaxys

36

Nair, Vijay; Bindu; Sreekumar; Balagopal, Lakshmi; Synthesis; nb. 9; (2003); p. 1446 - 1456, View in Reaxys

Tab.2, prod., entry 7

Kim, Sung Soo; Kim, Dong Won; Synlett; nb. 10; (2003); p. 1391 - 1394, View in Reaxys

Product, Tab.2, run 4

Jurado-Gonzalez, Magdalena; Sullivan, Alice C.; Wilson, John R. H.; Tetrahedron Letters; vol. 44; nb. 22; (2003); p.

4283 - 4286, View in Reaxys

5p

Zhang, Baolian; Zhu, Xiao-Qing; Lu, Jin-Yong; He, Jiaqi; Wang, Peng G.; Cheng, Jin-Pei; Journal of Organic Chemistry; vol. 68; nb. 8; (2003); p. 3295 - 3298, View in Reaxys

FL

Jacques; Allonas; Sarbach; Haselbach; Vauthey; Chemical Physics Letters; vol. 378; nb. 1-2; (2003); p. 185 - 191, View in Reaxys; Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys

T. 2-10, product

Kim, Sung Soo; Borisova, Galina; Synthetic Communications; vol. 33; nb. 22; (2003); p. 3961 - 3967, View in Reaxys

1g

Korotchenko; Shastin; Nenaidenko; Balenkova; Russian Chemical Bulletin; vol. 52; nb. 2; (2003); p. 492 - 497, View in Reaxys

1e

Bertini, Vincenzo; Lucchesini, Francesco; Pocci, Marco; Alfei, Silvana; De Munno, Angela; Synlett; nb. 8; (2003); p. 1201 - 1203, View in Reaxys

subst., Tab.2, entry 4

Zeynizadeh, Behzad; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 58; nb. 12; (2003); p. 1220 - 1226, View in Reaxys

25c

Kauffman, Joel M.; Moyna, Guillermo; Journal of Organic Chemistry; vol. 68; nb. 3; (2003); p. 839 - 853, View in Reaxys

8

Hanson, Peter; Rowell, Simon C.; Taylor, Alec B.; Walton, Paul H.; Timms, Allan W.; Journal of the Chemical Society. Perkin Transactions 2; nb. 6; (2002); p. 1126 - 1134, View in Reaxys; Yang, Yonghong; Petersen, Jeffrey L.; Wang, Kung K.; Journal of Organic Chemistry; vol. 68; nb. 22; (2003); p. 8545 - 8549, View in Reaxys

FLUO

Lund, Torben; Christensen, Peter; Wilbrandt, Robert; Organic and Biomolecular Chemistry; vol. 1; nb. 6; (2003); p.

1020 - 1025, View in Reaxys

educt to 5b-5d

Vougioukalakis, Georgios C.; Orfanopoulos, Michael; Tetrahedron Letters; vol. 44; nb. 48; (2003); p. 8649 - 8652, View in Reaxys

5g

Hajipour; Mallakpour; Mohammadpoor-Baltork; Khoee; Synthetic Communications; vol. 31; nb. 8; (2001); p. 1187 - 1194, View in Reaxys; Hajipour; Mallakpour; Khoee; Synthetic Communications; vol. 32; nb. 1; (2002); p. 9 - 15, View in Reaxys

t.2, ketone, entry 7

Tangestaninejad; Habibi; Mirkhani; Moghadam; Molecules; vol. 7; nb. 2; (2002); p. 264 - 270, View in Reaxys

Table 2, E1, Product

Hashimoto, Kentaro; Tanaka, Hirotaka; Ikeno, Taketo; Yamada, Tohru; Chemistry Letters; nb. 6; (2002); p. 582 583, View in Reaxys

prod., Table 2./2

Matsuo, Jun-ichi; Kawana, Asahi; Pudhom, Khanitha; Mukaiyama, Teruaki; Chemistry Letters; nb. 2; (2002); p.

250 - 251, View in Reaxys

13d

Giurg; Wojtowicz; Mlochowski; Polish Journal of Chemistry; vol. 76; nb. 4; (2002); p. 537 - 542, View in Reaxys

11

Prashad, Mahavir; Liu, Yugang; Mak, Xiao Yin; Har, Denis; Repic, Oljan; Blacklock, Thomas J.; Tetrahedron Letters; vol. 43; nb. 47; (2002); p. 8559 - 8562, View in Reaxys

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tab. 1, entry 18, prod.

Bisai, Alakesh; Chandrasekhar; Singh, Vinod K.; Tetrahedron Letters; vol. 43; nb. 46; (2002); p. 8355 - 8357, View in Reaxys

Product, Tab.2, run 20

Ganchegui, Benjamin; Bouquillon, Sandrine; Henin, Francoise; Muzart, Jacques; Tetrahedron Letters; vol. 43; nb.

37; (2002); p. 6641 - 6644, View in Reaxys

product, T1, E12

Shaabani, Ahmad; Bazgir, Ayoob; Teimouri, Fatemeh; Lee, Donald G; Tetrahedron Letters; vol. 43; nb. 29; (2002); p. 5165 - 5167, View in Reaxys

16a

Weber, Edwin; Nitsche, Silke; Wierig, Andreas; Csoeregh, Ingeborg; European Journal of Organic Chemistry; nb. 5; (2002); p. 856 - 872, View in Reaxys

1w

Clerici, Angelo; Pastori, Nadia; Porta, Ombretta; European Journal of Organic Chemistry; nb. 19; (2002); p. 3326 3335, View in Reaxys

11a

De Lijser, H. J. Peter; Fardoun, Fadia H.; Sawyer, Jody R.; Quant, Michelle; Organic Letters; vol. 4; nb. 14; (2002); p. 2325 - 2328, View in Reaxys

Fl=O

Larsen, Anna S.; Wang, Kun; Lockwood, Mark A.; Rice, Gordon L.; Won, Tae-Jin; Lovell, Scott; Sadilek, Martin; Turecek, Frantisek; Mayer, James M.; Journal of the American Chemical Society; vol. 124; nb. 34; (2002); p.

10112 - 10123, View in Reaxys

(E)

Patent; Symyx Technologies, Inc.; US6350916; (2002); (B1) English, View in Reaxys

4f

Miyashita, Kazuyuki; Minagawa, Masatoshi; Ueda, Yohko; Tada, Yukie; Hoshino, Nobuhiro; Imanishi, Takeshi; Tetrahedron; vol. 57; nb. 16; (2001); p. 3361 - 3367, View in Reaxys

educt of 2b

Billard, Thierry; Langlois, Bernard R.; Blond, Gaelle; European Journal of Organic Chemistry; nb. 8; (2001); p.

1467 - 1471, View in Reaxys

FLone

Sabate; Bayona; Solanas; Chemosphere; vol. 44; nb. 2; (2001); p. 119 - 124, View in Reaxys

product, Tab 2, entry 7

Hashimoto, Kentaro; Kitaichi, Yasunori; Tanaka, Hirotaka; Ikeno, Taketo; Yamada, Tohru; Chemistry Letters; nb.

9; (2001); p. 922 - 923, View in Reaxys

T.1. ketone 19

Kamble, Rajesh M; Singh, Vinod K; Tetrahedron Letters; vol. 42; nb. 42; (2001); p. 7525 - 7526, View in Reaxys

9c (tab VI)

Hajipour; Mallakpour; Molecular Crystals and Liquid Crystals Science and Technology, Section A: Molecular Crystals and Liquid Crystals; vol. 356; (2001); p. 371 - 387, View in Reaxys

55

Robarge; Husbands; Kieltyka; Brodbeck; Thurkauf; Newman; Journal of Medicinal Chemistry; vol. 44; nb. 19; (2001); p. 3175 - 3186, View in Reaxys

9-Fl-one

Garon; Krivobok; Seigle-Murandi; Chemosphere; vol. 40; nb. 1; (2000); p. 91 - 97, View in Reaxys

run 5, electrophile

O'Neil, Ian A.; Wynn, Duncan; Lai, Justine Y. Q.; Tetrahedron Letters; vol. 41; nb. 2; (2000); p. 271 - 274, View in Reaxys

educt comp. to 11

Liu, Kwang-Ting; Chang, Chih-Wei; Chen, Hung-I.; Chin, Chien-Pu; Duann, Yen-Fang; Journal of Physical Organic Chemistry; vol. 13; nb. 4; (2000); p. 203 - 207, View in Reaxys

9FL

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 - 150, View in Reaxys

Tab.1. col. 1. run 1

Hicks; Han; Fry; Tetrahedron Letters; vol. 41; nb. 41; (2000); p. 7817 - 7820, View in Reaxys

1k

Chaikovski; Filimonov; Yagovkin; Kharlova; Tetrahedron Letters; vol. 41; nb. 47; (2000); p. 9101 - 9104, View in Reaxys

product 1 (fig. 7.)

Nuechter, Matthias; Ondruschka, Bernd; Jungnickel, Anja; Mueller, Ute; Journal of Physical Organic Chemistry; vol. 13; nb. 10; (2000); p. 579 - 586, View in Reaxys

8d

Large; Roques; Langlois; Journal of Organic Chemistry; vol. 65; nb. 26; (2000); p. 8848 - 8856, View in Reaxys

substrate for 4b

Billard; Bruns; Langlois; Organic Letters; vol. 2; nb. 14; (2000); p. 2101 - 2103, View in Reaxys

Table 2 Entry 4 Prod.

Matsunaka, Katsuhisa; Iwahama, Takahiro; Sakaguchi, Satoshi; Ishii, Yasutaka; Tetrahedron Letters; vol. 40; nb.

11; (1999); p. 2165 - 2168, View in Reaxys

precursor of 2i

Mloston, Grzegorz; Romanski, Jaroslaw; Swiatek, Anna; Heimgartner, Heinz; Helvetica Chimica Acta; vol. 82; nb.

6; (1999); p. 946 - 956, View in Reaxys

3c (Tab. 2)

Hajipour, Abdol Reza; Mohammadpoor-Baltork, Iraj; Niknam, Kurosh; Organic Preparations and Procedures International; vol. 31; nb. 3; (1999); p. 335 - 341, View in Reaxys

Table 3, entry 6

Yamazaki, Shigekazu; Organic Letters; vol. 1; nb. 13; (1999); p. 2129 - 2132, View in Reaxys

Table 3, Entry 10

Mohammadpoor-Baltork, Iraj; Hajipour, Abdol Reza; Mohammadi, Hasan; Bulletin of the Chemical Society of Japan; vol. 71; nb. 7; (1998); p. 1649 - 1653, View in Reaxys

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starting to int. to 1

Henkel, Bernd; Bayer, Ernst; Tetrahedron Letters; vol. 39; nb. 51; (1998); p. 9401 - 9402, View in Reaxys

3j

Hajipour, Abdol Reza; Baltork, Iraj Mohammadpoor; Kianfar, Godaraz; Bulletin of the Chemical Society of Japan; vol. 71; nb. 11; (1998); p. 2655 - 2659, View in Reaxys

12

Banciu, Mircea D.; Draghici, Constantin; Popescu, Angela; Banciu, Anca; Simion, Alina; Revue Roumaine de Chimie; vol. 43; nb. 7; (1998); p. 649 - 660, View in Reaxys

entry 31, prod.

Baltork, I. Mohammadpoor; Sadeghi, M. M.; Mahmoodi, N.; Kharamesh, B.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 36; nb. 5; (1997); p. 438 - 441, View in Reaxys

IIIa

Soldatenkov; Kolyadina; Kuleshova; Khrustalev; Chemistry of Heterocyclic Compounds; vol. 32; nb. 7; (1996); p.

817 - 821, View in Reaxys

124

Paxeus, Nicklas; Water Research; vol. 30; nb. 5; (1996); p. 1115 - 1122, View in Reaxys

Table 4; 37

Fobe, Bart O.; Vleugels, Greta J.; Roekens, Eddy J.; Grieken, Rene E. Van; Hermosin, Bernardo; et al.; Environmental Science & Technology; vol. 29; nb. 6; (1995); p. 1691 - 1701, View in Reaxys

Patent-Specific Data (9) Prophetic ComLocation in Patent pound

References Patent; NAGOYA INSTITUTE OF TECHNOLOGY; TOSOH F-TECH INCORPORATED; SHIBATA, NORIO; OKUSU, SATOSHI; KAGAWA, TAKUMI; (15 pag.); JP2016/204276; (2016); (A) Japanese, View in Reaxys Patent; TAOKA CHEMICAL COMPANY LIMITED; MATSUBARA, MASAAKI; KAWAMURA, YOSHINORI; FUJII, KATSUHIRO; (14 pag.); JP2016/3220; (2016); (A) Japanese, View in Reaxys Patent; Osaka Gas Chemical Co., Ltd.; Nishiyama, Yutaro; Kuratani, Yuji; Miyauchi, Shinsuke; (9 pag.); JP2016/196445; (2016); (A) Japanese, View in Reaxys

Page/Page column

Patent; Dickmeis, Marcus; Cinar, Hakan; Ritter, Helmut; US2013/18140; (2013); (A1) English, View in Reaxys; Patent; Martineau, Louis C.; US2014/135359; (2014); (A1) English, View in Reaxys; Patent; SOLVAY (SOCIETE ANONYME); Bascour, Dominique; Catinat, Jean-Pierre; US9076971; (2015); (B2) English, View in Reaxys Patent; CIBA HOLDING INC.; WO2009/47151; (2009); (A1) English, View in Reaxys Patent; Symyx Technologies, Inc.; US6350916; (2002); (B1) English, View in Reaxys Patent; Board of Regents, The University of Texas System; US6362200; (2002); (B1) English, View in Reaxys

prophetic product

Claim

prophetic product

Patent; Rhone-Poulenc Chimie; US5414153; (1995); (A) English, View in Reaxys; Patent; Rhone-Poulenc Chimie; US5434317; (1995); (A) English, View in Reaxys Patent; Hitachi Chemical Company, Ltd.; US5352834; (1994); (A) English, View in Reaxys

Druglikeness (1) 1 of 1

LogP

3.494

H Bond Donors

0

H Bond Acceptors

1

Rotatable Bonds

0

TPSA

17.07

Lipinski Number

4

Veber Number

2

Related Structure (1) Related Structure References Die frueher von Hey et al.; Journal of the Chemical Society; (1962); p. 4579,4581, View in Reaxys Finzi, Bellavita (s.

E III 2331) unter dieser Konstitution beschriebene Verbindung ist als Benzo<#c!>chromen-6on zu formulieren.

Derivative (71)

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Comment (Derivative)

Derivative

References

fluorenone-2,4-dinitrophenylhydrazone

Kuselan, P.; Venkatasubramanian, N.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 21; nb. 12; (1982); p. 1095 - 1097, View in Reaxys; Banerjee, Amalendu; Mandal, Dinabandhu; Ray, Arindam; Banerjee, Pulak; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 72; nb. 3; (1995); p. 205 - 208, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 84.5grad

Olah et al.; Synthesis; (1979); p. 274, View in Reaxys

BCl3-Komplex: Abs.-Sp. (Fig. 3); Fluoreszenz (Fig. 4)

Snyder; Testa; Journal of Physical Chemistry; vol. 83; (1979); p. 3041, View in Reaxys

2,4-Dinitrophenylhydrazon; mp: 240grad

Olah,G.A.; Welch,J.; Journal of the American Chemical Society; vol. 100; (1978); p. 5396 5402, View in Reaxys

2,4-Dinitrophenylhydrazin: F: 285-287grad

Wittig; Schoch-Gruebler; Justus Liebigs Annalen der Chemie; (1978); p. 362,364,365,368, View in Reaxys

Hydrazon: Kinetik d. Wolff-KishnerReaktion, ΔH(excit.), ΔS(excit.)

Szmant; Alciaturi; Journal of Organic Chemistry; vol. 42; (1977); p. 1081, View in Reaxys

2,4-Dinitrophenylhydrazon: F:276-278grad(Zers .)

Eckell,A.; Huisgen,R.; Chemische Berichte; vol. 110; (1977); p. 559 - 570, View in Reaxys

2,4-Dinitrophenylhydrazon: F:281-283grad(Zers .); F:291grad(Zers.)

Huisgen et al.; Chemische Berichte; vol. 110; (1977); p. 514,518, View in Reaxys

Oxim (Tab. 1)

Terent'eva; Petrenko; J. Anal. Chem. USSR (Engl. Transl.); vol. 31; (1976); p. 2452,1805, View in Reaxys

Komplex mi Phenol: Gleichgew.konst., IR (HBruecken)

Bostwick et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 1505,1506, 1508, View in Reaxys

39K-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

23Na-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

85Rb-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

87Rb-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

133Cs-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

Prot. Form: Abs. Sp. (Fig. 1); SCFCl-Lad.-Dichte (Fig. 3)

Filipescu et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 2276, View in Reaxys

Lu-Komplexes: NMR

Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys

Eu-FluorenonKomplex: NMR

Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys

Yb-FluorenonKomplex: NMR

Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys

Oxim: F: 194-195grad (Bzl.)

Troszkiewicz et al.; Roczniki Chemii; vol. 46; (1972); p. 399,403, 404, View in Reaxys

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2,4-Dinitrophenylhydrazon: F.: 284grad

Saxena; Kulshreshtha; Journal of the Indian Chemical Society; vol. 48; (1971); p. 137, View in Reaxys

Thiosemicarbazon, F: 172grad, aus Alkohol

Taha; Hassan; Journal of Chemistry of the United Arab Republic; vol. 14; (1971); p. 531, View in Reaxys

bei der Bildung entsteht bei laengerer Reaktionszeit ein DMSO-Addukt (X)

Rawson; Wynberg; Recueil des Travaux Chimiques des Pays-Bas; vol. 90; (1971); p. 39,43, 44, View in Reaxys

Na2(Fl)2

Norris; Weissman; Journal of Physical Chemistry; vol. 73; (1969); p. 3119, View in Reaxys

Na+ <C13H7O>- : 23Na-NMR

Canters et al.; Chemical Physics Letters; vol. 1; (1968); p. 627, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 282-284grad

Peddle; Ward; Journal of Organometallic Chemistry; vol. 14; (1968); p. 131,136, View in Reaxys

2,4-Dinitro-phenylhydrazon: F: 305grad

Rappoport,Z.; Sheradsky,T.; Journal of the Chemical Society [Section] B: Physical Organic; (1967); p. 898 - 903, View in Reaxys

Fluorenonkalium: Temp.-Abhaengigk. der 13C-Aufspalt. des ESR-Spektrums

Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys

Fluorenonlithium: Temp.-Abhaengigk. der Li- u. 13C-Aufspalt. des ESRSpektrums

Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys

Fluorenoncaesium: Temp.-Abhaengigk. der Cs- u. der 13CAufspalt. des ESRSpektrums

Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys

K-Ketyl: Temp.-abhaengigkeit der 13C-Aufspaltung (der Carbonylgruppe) in 1,2-Dimethoxy-ethan, -70 - +60grad

Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys

Li-Ketyl: Temp.abhaengigkeit der 13C-Aufspaltung (der Carbonylgruppe) in 1,2-Dimethoxy-ethan, -60 - +30grad

Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys

Fluorenonnatrium: ESR-Spektrum in 1,2-Dimethoxyethan u. in DMF (Temp.-Abhaengigk. der Na- u.

13C-Aufspalt.)

Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys

Cs-Ketyl: Temp.abhaengigkeit der 13C-Aufspaltung (der Carbonylgruppe) in THF, -60 - +50grad, in 1,2-

Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys

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Dimethoxy-ethan, -90 - +50grad Na-Ketyl: Temp.abhaengigkeit der 13C-Aufspaltung (der Carbonylgruppe) in 1,2-Dimethoxy-ethan, -90 - +30grad, in THF, -60 - +20grad, in DMF -15 - +75grad

Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 282-283grad, orange

Chiba; Kogyo Kagaku Zasshi; vol. 69; (1966); p. 1289,1292, View in Reaxys

Ketylradikal: B: elektrochem. Red. (nult-ionischer, semi-ionischer u. ionischer Rk.mechanismus), 38percentig. wss.

A., 23grad; Dimerisierungskonst.; 929

Kalinowski; Grabowski; Transactions of the Faraday Society; vol. 62; (1966); p. 926,931, View in Reaxys

Ketylradikal: B: elektrochem. Red. (nult-ionischer, semi-ionischer u. ionischer Rk.mechanismus), 38percentig. wss.

A., 23grad; Geschwindigkeitskonst., Disproportionierung

Kalinowski; Grabowski; Transactions of the Faraday Society; vol. 62; (1966); p. 926,931, View in Reaxys

Oxidations sowie Redox-Potential des bei der elektrochem. Red. gebildeten Ketylradikals (920): Geschwindigkeitskonst. der Dimerisierung des Ketyl-Radikals (921); Dissoziationsexponent pK (922)

Kalinowski et al.; Transactions of the Faraday Society; vol. 62; (1966); p. 918, View in Reaxys

Ba-Verb.: Abs.Max. (in THF)

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Ca-Verb.: Abs.Max. (in THF); S.2539

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Mg-Verb.: Abs.Max. (in THF); S.2539

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Phenylhydrazon: F: 146 - 149grad

Nickon,A.; Hill,A.S.; Journal of the American Chemical Society; vol. 86; (1964); p. 1152 - 1159, View in Reaxys

Fluorenonketyle s.

Syst. Nr. 540

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Radikalanion: ESRSpektrum des Radikal-Anions in Mischungen von Me. u.

Luckhurst; Orgel; Molecular Physics; vol. 8; (1964); p. 117,118, View in Reaxys

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N,N-Dimethyl-formamid Na-Verb.: Abs.Max. (in THF); Abs.-Sp. (in Me/ THF, THF, DME, bzw. Toluol) (S.2540, 2541); ESR-Sp. (in Me/ THF) (S.2541)

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Radikal-Anion: ESR-Spektrum u.

Daten

Dehl; Fraenkel; Journal of Chemical Physics; vol. 39; (1963); p. 1793, View in Reaxys

CT-Komlex m. 1 Ba: Abs.-Max. i.

Lsg. (Dioxan)

Mathias; Warhurst; Transactions of the Faraday Society; vol. 58; (1962); p. 948,949, View in Reaxys

CT-Komlex m. 1/2 Ba: Abs.-Max. i.

Lsg. (Dioxan)

Mathias; Warhurst; Transactions of the Faraday Society; vol. 58; (1962); p. 948,949, View in Reaxys

Kalium-Verb.

C13H8*K: Elektronen paramangn.

Resonaz. in THF

Kasakowa; Syrkin; Journal of Structural Chemistry; vol. 3; (1962); p. 518; Zhurnal Strukturnoi Khimii; vol. 3; (1962); p. 536, View in Reaxys

Zur RadikalanionB. i. Ggw. v. Fluorenol-(9) (1:), Ktert-butylat in tertButanol, Dimethylsulfoxid

Russel et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 4155,4156, View in Reaxys

Kalium-Verb.: Spin-Spin-Aufspaltung d. paramagnet.

Elektronenresonanz; B. v. Dimeren in 2-Methyl-tetrahydrofuran

Hirota; Weissman; Molecular Physics; vol. 5; (1962); p. 537, View in Reaxys

Lithium-Verb.: ESR-p. (2-Methyltetrahydrofuran bei 77K); Spin-SpinAufspaltung d. paramagnet. Elektronenresonanz; B. v.

Dimeren (in 2Methyl-tetrahydrofuran)

Hirota; Weissman; Molecular Physics; vol. 5; (1962); p. 537, View in Reaxys

Natrium-Verb.: Abs.max. (2-Methyl-tetrahydrofuran bei 300K): 5200 A; Spin-Spin-Aufspaltung d. paramagnet.

Elektronenresonanz; B. eines Dimeren (Abs.Max.: 4550 A)

Hirota; Weissman; Molecular Physics; vol. 5; (1962); p. 537, View in Reaxys

Phenylhydrazon: C20H14N2O4

Kuhn et al.; Chemische Berichte; vol. 94; (1961); p. 2252,2257, View in Reaxys

Komplex m. 1 K (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. 2 K (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

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Komplex m. 1 Li (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. 1 Na (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. 2 Li (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. 2 Na (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. Na (Dioxan): Kinetik der Rk. m. Methyliodid, 12 - 40grad

Mathias; Warhurst; Transactions of the Faraday Society; vol. 56; (1960); p. 348, View in Reaxys

Komplex m. Na (in Dioxan): Kinetik der Rk. m. Methyliodid; Kinetik der Rk. m. Propylbromid

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 343,345, View in Reaxys

2-diphenylacetyl-3oxo-indan-1-ylidenehydrazone (mp: 282-283 degree )

Braun; Mosher; Journal of the American Chemical Society; vol. 80; (1958); p. 3048, View in Reaxys

4-nitro-phenylhydrazone (mp: 143-144 degree )

de Toma; Gazzetta Chimica Italiana; vol. 82; (1952); p. 40,44, View in Reaxys

2.4-dinitro-phenylhydrazone (mp: 302 degree )

Cavill; Robertson; Whalley; Journal of the Chemical Society; (1949); p. 1567,1570, View in Reaxys

2.4-dinitro-phenylhydrazone (mp: 299-301 degree )

Campbell; Wang; Journal of the Chemical Society; (1949); p. 2186, View in Reaxys

phenylhydrazone (mp: 151-152 degree )

Oliveri-Mandala; Deleo; Gazzetta Chimica Italiana; vol. 70; (1940); p. 186,189, View in Reaxys; Wislicenus; Densch; Chemische Berichte; vol. 35; (1902); p. 761, View in Reaxys; Wislicenus; Russ; Chemische Berichte; vol. 43; (1910); p. 2729, View in Reaxys

p-nitro-phenylhydrazone (mp: 269 degree )

Schmidt,J.; Wagner; Chemische Berichte; vol. 43; (1910); p. 1800; Justus Liebigs Annalen der Chemie; vol. 387; (1912); p. 159, View in Reaxys

compound of fluorenone with 9oxy-9-p-diphenylyl-fluorene (mp: 123 degree , light yellow octahedrons); Further Data see Handbook (Preparation)

Schlenk; Herzenstein; Justus Liebigs Annalen der Chemie; vol. 372; (1910); p. 30, View in Reaxys

phenylhydrazone (mp: 151-151,5 degree )

Goldschmiedt; Schranzhofer; Monatshefte fuer Chemie; vol. 16; (1895); p. 812, View in Reaxys

Melting Point (96) 1 of 96

Melting Point [°C]

83 - 84

Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys; Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys; Huang, Tianzeng; Chen, Tieqiao; Han, Li-Biao; Journal of Organic Chemistry; vol. 83; nb. 5; (2018); p. 2959 - 2965, View in Reaxys 2 of 96

Melting Point [°C]

80 - 82

Location

supporting information

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Maji, Arun; Rana, Sujoy; Akanksha; Maiti, Debabrata; Angewandte Chemie - International Edition; vol. 53; nb. 9; (2014); p. 2428 - 2432; Angew. Chem.; vol. 126; nb. 9; (2014); p. 2460 - 2464,5, View in Reaxys; Gao, Qian; Xu, Senmiao; Organic and Biomolecular Chemistry; vol. 16; nb. 2; (2018); p. 208 - 212, View in Reaxys 3 of 96

Melting Point [°C]

81

Location

supporting information

Laudadio, Gabriele; Govaerts, Sebastian; Wang, Ying; Ravelli, Davide; Koolman, Hannes F.; Fagnoni, Maurizio; Djuric, Stevan W.; Noël, Timothy; Angewandte Chemie - International Edition; vol. 57; nb. 15; (2018); p. 4078 - 4082; Angew. Chem.; vol. 130; nb. 15; (2018); p. 4142 - 4146,5, View in Reaxys 4 of 96

Melting Point [°C]

80

Location

supporting information

Finney, Laura C.; Mitchell, Lorna J.; Moody, Christopher J.; Green Chemistry; vol. 20; nb. 10; (2018); p. 2242 - 2249, View in Reaxys 5 of 96

Melting Point [°C]

85 - 87

Location

Paragraph 0064; 0068; 0072

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys 6 of 96

Melting Point [°C]

79 - 80

Location

supporting information

Guo, Shu; Zeng, Renyou; Li, Caiye; Synthetic Communications; vol. 46; nb. 17; (2016); p. 1446 - 1453, View in Reaxys; Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys 7 of 96

Melting Point [°C]

81 - 83

Location

supporting information

Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys 8 of 96

Melting Point [°C]

82 - 83

Ruzi, Rehanguli; Zhang, Muliang; Ablajan, Keyume; Zhu, Chengjian; Journal of Organic Chemistry; vol. 82; nb. 23; (2017); p. 12834 - 12839, View in Reaxys 9 of 96

Melting Point [°C]

83 - 85

Location

supporting information

Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong; Chemical Communications; vol. 52; nb. 18; (2016); p.

3635 - 3638, View in Reaxys 10 of 96

Melting Point [°C]

80 - 81

Location

supporting information

Bhardwaj, Madhvi; Sharma, Harsha; Paul, Satya; Clark, James H.; New Journal of Chemistry; vol. 40; nb. 6; (2016); p.

4952 - 4961, View in Reaxys 11 of 96

Melting Point [°C]

60

Mishra, Kalpana; Pandey, Ashok Kumar; Singh, Jay Bahadur; Singh, Radhey M.; Organic and Biomolecular Chemistry; vol. 14; nb. 26; (2016); p. 6328 - 6336, View in Reaxys 12 of 96

Melting Point [°C]

79 - 81

Shaabani, Ahmad; Shaabani, Shabnam; Afaridoun, Hadi; RSC Advances; vol. 6; nb. 54; (2016); p. 48396 - 48404, View in Reaxys 13 of 96

Melting Point [°C]

84 - 85

Location

supporting information

Gülcemal, Süleyman; Gülcemal, Derya; Whitehead, George F. S.; Xiao, Jianliang; Chemistry - A European Journal; vol.

22; nb. 30; (2016); p. 10513 - 10522, View in Reaxys 14 of 96

Melting Point [°C]

80 - 83

Location

supporting information

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2018-06-21 20:37:19

Wang, Huiqiao; Wang, Zhong; Huang, Hongchun; Tan, Jiajing; Xu, Kun; Organic Letters; vol. 18; nb. 21; (2016); p. 5680 5683, View in Reaxys 15 of 96

Melting Point [°C]

83 - 84

Location

Paragraph 0037; 0039; 0041; 0043

Patent; Zhongwei Lianjiao Technology National Engineering Research Center Co.,Ltd; Wang, Guang Xing; Wang, Shou Kai; Li, Qiang; CAI, Hong Tao; Jin, Dan; Wang, LiLi; (6 pag.); CN104230690; (2016); (B) Chinese, View in Reaxys 16 of 96

Melting Point [°C]

82 - 84

Location

Paragraph 0045; 0047

Patent; Zhongwei Lianjiao Technology National Engineering Research Center Co.,Ltd; Wang, Guang Xing; Wang, Shou Kai; Li, Qiang; CAI, Hong Tao; Jin, Dan; Wang, LiLi; (6 pag.); CN104230690; (2016); (B) Chinese, View in Reaxys 17 of 96

Melting Point [°C]

83

Tandon, Praveen K.; Singh, Santosh B.; Singh, Satpal; Kesarwani, Bhawana; Journal of the Indian Chemical Society; vol.

89; nb. 10; (2012); p. 1363 - 1367, View in Reaxys; Diehl, Fabrice; Barbier, Jacques; Duprez, Daniel; Guibard, Isabelle; Mabilon, Gil; Applied Catalysis A: General; vol. 504; (2015); p. 37 - 43, View in Reaxys 18 of 96

Melting Point [°C]

82 - 83

Location

supporting information

Wei, Peng; Zhang, Datong; Gao, Zhigang; Cai, Wenqing; Xu, Weiren; Tang, Lida; Zhao, Guilong; Synthetic Communications; vol. 45; nb. 12; (2015); p. 1457 - 1470, View in Reaxys 19 of 96

Melting Point [°C]

83 - 84

Ma, Jiaqi; Hu, Zhiming; Li, Meichao; Zhao, Weijuan; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Shen, Zhenlu; Tetrahedron; vol. 71; nb. 38; (2015); p. 6733 - 6739, View in Reaxys 20 of 96

Melting Point [°C]

82 - 84

Location

supporting information

Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys; Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys 21 of 96

Melting Point [°C]

80 - 82

Saluja, Pooja; Magoo, Devanshi; Khurana, Jitender M.; Synthetic Communications; vol. 44; nb. 6; (2014); p. 800 - 806, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys 22 of 96

Melting Point [°C]

81 - 83

Location

supporting information

Fukuyama, Takahide; Maetani, Shinji; Miyagawa, Kazusa; Ryu, Ilhyong; Organic Letters; vol. 16; nb. 12; (2014); p. 3216 3219, View in Reaxys 23 of 96

Melting Point [°C]

81 - 83

Wang, Guang-Zu; Li, Xing-Long; Dai, Jian-Jun; Xu, Hua-Jian; Journal of Organic Chemistry; vol. 79; nb. 15; (2014); p.

7220 - 7225, View in Reaxys 24 of 96

Melting Point [°C]

80 - 83

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys 25 of 96

Melting Point [°C]

81 - 82

Location

supporting information

Baars, Hannah; Unoh, Yuto; Okada, Takeshi; Hirano, Koji; Satoh, Tetsuya; Tanaka, Ken; Bolm, Carsten; Miura, Masahiro; Chemistry Letters; vol. 43; nb. 11; (2014); p. 1782 - 1784, View in Reaxys 26 of 96

Melting Point [°C]

84 - 86

Xu, Yuan; Yang, Zhenping; Hu, Jiantao; Yan, Jie; Synthesis (Germany); vol. 45; nb. 3; (2013); p. 370 - 374; Art.No: SS-2012-F0873-OP, View in Reaxys 27 of 96

Melting Point [°C]

79 - 80

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys

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28 of 96

Melting Point [°C]

82 - 84

Khurana, Jitender M.; Chaudhary, Ankita; Kumar, Sanjay; Organic Preparations and Procedures International; vol. 45; nb.

3; (2013); p. 241 - 245, View in Reaxys 29 of 96

Melting Point [°C]

72

Location

supporting information

Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 2745, View in Reaxys 30 of 96

Melting Point [°C]

82 - 84

Location

supporting information

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys 31 of 96

Melting Point [°C]

83 - 85

Li, Dan-Dan; Yuan, Ting-Ting; Wang, Guan-Wu; Journal of Organic Chemistry; vol. 77; nb. 7; (2012); p. 3341 - 3347, View in Reaxys 32 of 96

Melting Point [°C]

83 - 84

Bahrami, Kiumars; Khodaei, Mohammad M.; Shakibaian, Vida; Khaledian, Donya; Yousefi, Behrooz H.; Journal of Sulfur Chemistry; vol. 33; nb. 2; (2012); p. 155 - 163, View in Reaxys 33 of 96

Melting Point [°C]

79 - 80

Location

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 34 of 96

Melting Point [°C]

82 - 83

Location

supporting information

Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys 35 of 96

Melting Point [°C]

75 - 77

Location

supporting information

Dohi, Toshifumi; Takenaga, Naoko; Goto, Akihiro; Fujioka, Hiromichi; Kita, Yasuyuki; Journal of Organic Chemistry; vol.

73; nb. 18; (2008); p. 7365 - 7368, View in Reaxys; Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys 36 of 96

Melting Point [°C]

84 - 86

Cui, Li-Qian; Liu, Kai; Zhang, Chi; Organic and Biomolecular Chemistry; vol. 9; nb. 7; (2011); p. 2258 - 2265, View in Reaxys 37 of 96

Melting Point [°C]

78 - 80

Location

supporting information

Cosner, Casey C.; Cabrera, Pablo J.; Byrd, Katherine M.; Adams Thomas, Asia M.; Helquist, Paul; Organic Letters; vol.

13; nb. 8; (2011); p. 2071 - 2073, View in Reaxys 38 of 96

Melting Point [°C]

74.5 - 76.3

Location

supporting information

Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys 39 of 96

Melting Point [°C]

83 - 85

Solvent (Melting Point)

ethanol

Zhang, Xin; Ji, Xuan; Jiang, Shanshan; Liu, Lili; Weeks, Brandon L.; Zhang, Zhao; Green Chemistry; vol. 13; nb. 7; (2011); p. 1891 - 1896, View in Reaxys 40 of 96

Melting Point [°C]

75 - 77

Lv, Xiao-Ming; Kong, Ling-Jie; Lin, Qi; Liu, Xiao-Feng; Zhou, Ya-Ming; Jia, Yu; Synthetic Communications; vol. 41; nb.

21; (2011); p. 3215 - 3222, View in Reaxys

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41 of 96

Melting Point [°C]

80 - 82

Location

supporting information

Tilly, David; Fu, Jian-Min; Zhao, Bao-Ping; Alessi, Manlio; Castanet, Anne-Sophie; Snieckus, Victor; Mortier, Jacques; Organic Letters; vol. 12; nb. 1; (2010); p. 68 - 71, View in Reaxys 42 of 96

Melting Point [°C]

81 - 82

Solvent (Melting Point)

dichloromethane; hexane

Catir, Mustafa; Kilic, Hamdullah; Synlett; nb. 9; (2010); p. 1319 - 1322, View in Reaxys 43 of 96

Melting Point [°C]

83 - 84

Location

supporting information

Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys 44 of 96

Melting Point [°C]

80

Bahrami, Kiumars; Khodaei, Mohammad M.; Farrokhi, Azita; Tetrahedron; vol. 65; nb. 36; (2009); p. 7658 - 7661, View in Reaxys; Bahrami, Kiumars; Khodaei, Mohammad Mehdi; Tajik, Maryam; Synthesis; nb. 24; (2010); p. 4282 4286; Art.No: Z21310SS, View in Reaxys 45 of 96

Melting Point [°C]

82 - 83

Fang, Xin-Qiang; Xu, Hua-Jian; Jiang, Hong; Liu, You-Cheng; Fu, Yao; Wu, Yun-Dong; Tetrahedron Letters; vol. 50; nb.

3; (2009); p. 312 - 315, View in Reaxys 46 of 96

Melting Point [°C]

81 - 83

Hajipour, Abdol R.; Safaei, Somayeh; Ruoho, Arnold E.; Synthetic Communications; vol. 39; nb. 20; (2009); p. 3687 - 3692, View in Reaxys 47 of 96

Melting Point [°C]

82

Habibzadeh, Setareh; Tajbakhsh, Mahmood; Journal of Chemical Research; nb. 11; (2009); p. 696 - 698, View in Reaxys 48 of 96

Melting Point [°C]

80 - 81

Shaabani, Ahmad; Farhangi, Elham; Rahmati, Abbas; Monatshefte fur Chemie; vol. 139; nb. 8; (2008); p. 905 - 908, View in Reaxys 49 of 96

Melting Point [°C]

82

Batterbee; Bailey; Journal of Organic Chemistry; vol. 32; (1967); p. 3899,3902, View in Reaxys; Davies; Waring; Journal of the Chemical Society [Section] C: Organic; (1968); p. 2332, View in Reaxys; Oae, Shigeru; Inubushi, Yoichi; Yoshihara, Masakuni; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 103; nb. 1-4; (1995); p. 101 - 110, View in Reaxys; Qian, Weixing; Jin, Erlei; Bao, Weiliang; Zhang, Yongmin; Angewandte Chemie - International Edition; vol. 44; nb. 6; (2005); p.

952 - 955, View in Reaxys 50 of 96

Melting Point [°C]

82 - 83

Campo; Larock; Organic letters; vol. 2; nb. 23; (2000); p. 3675 - 3677, View in Reaxys; Campo, Marino A.; Larock, Richard C.; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5616 - 5620, View in Reaxys 51 of 96

Melting Point [°C]

82 - 84

Solvent (Melting Point)

methanol

Patent; Humanetics Corporation; US6384251; (2002); (B1) English, View in Reaxys 52 of 96

Melting Point [°C]

83

Solvent (Melting Point)

ethanol

Carnelley; Dunn; Chemische Berichte; vol. 21; (1888); p. 2005, View in Reaxys; Schank, Kurt; Beck, Horst; Buschlinger, Michael; Eder, Joerg; Heisel, Thomas; Pistorius, Susanne; Wagner, Christiane; Helvetica Chimica Acta; vol. 83; nb. 4; (2000); p. 801 - 826, View in Reaxys 53 of 96

Melting Point [°C]

82 - 84

Solvent (Melting Point)

hexane

Mirafzal, Gholam A.; Lozeva, Albena M.; Tetrahedron Letters; vol. 39; nb. 40; (1998); p. 7263 - 7266, View in Reaxys 54 of 96

Melting Point [°C]

83 - 85

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2018-06-21 20:37:19

Abramovitch; Robson; Journal of the Chemical Society [Section] C: Organic; (1967); p. 1101, View in Reaxys; Nicolaides, Demetrios N.; Awad, R. Wajih; Papageorgiou, Georgios K.; Kojanni, Efthalia; Tsoleridis, Constantinos A.; Journal of Heterocyclic Chemistry; vol. 34; nb. 6; (1997); p. 1651 - 1656, View in Reaxys 55 of 96

Melting Point [°C]

78 - 79

Sanabria, R.; Castaneda, P.; Miranda, R.; Tobon, A.; Delgado, F.; Velasco, L.; Organic Preparations and Procedures International; vol. 27; nb. 4; (1995); p. 480 - 482, View in Reaxys 56 of 96

Melting Point [°C]

76 - 80

Braven, J.; Hanson, R. W.; Smith, N. G.; Journal of Heterocyclic Chemistry; vol. 32; nb. 3; (1995); p. 1051 - 1056, View in Reaxys 57 of 96

Melting Point [°C]

81

Comment (Melting Point)

Method: distilled sample

Banerjee, Amalendu; Mandal, Dinabandhu; Ray, Arindam; Banerjee, Pulak; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 72; nb. 3; (1995); p. 205 - 208, View in Reaxys 58 of 96

Melting Point [°C]

81

Abdou, Wafaa M.; Elkhoshnieh, Yehia O.; Sidky, Mahmoud M.; Tetrahedron; vol. 50; nb. 11; (1994); p. 3595 - 3602, View in Reaxys 59 of 96

Melting Point [°C]

83.5 - 84

Solvent (Melting Point)

cyclohexane

Brown, Eric; Leze, Antoine; Touet, Joel; Tetrahedron Letters; vol. 32; nb. 34; (1991); p. 4309 - 4310, View in Reaxys 60 of 96

Melting Point [°C]

83 - 84

Akiba,K.-Y. et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 2674 - 2683, View in Reaxys; Brown,P.M. et al.; Journal of the Chemical Society [Section] C: Organic; (1968); p. 842 - 848, View in Reaxys; Battaglia,A. et al.; Synthesis; (1971); p. 378 - 379, View in Reaxys; Fridman,A.L. et al.; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 1126 - 1128,1154 1156, View in Reaxys; Fridman,A.L. et al.; Zhurnal Organicheskoi Khimii; vol. 8; nb. 12; (1972); p. 2457 - 2462,2505 - 2509, View in Reaxys; Stobbe; Chemische Berichte; vol. 44; (1911); p. 1481, View in Reaxys; Soboleva et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1787,1799,1800,1801, View in Reaxys; Futami; Hishino; Kurosawa; Bulletin of the Chemical Society of Japan; vol. 62; nb. 11; (1989); p. 3567 - 3571, View in Reaxys 61 of 96

Melting Point [°C]

77 - 79

Suzuki,K. et al.; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 2217 - 2222, View in Reaxys; Hendrickson, James B.; Hussoin, Md. Sajjat; Journal of Organic Chemistry; vol. 54; nb. 5; (1989); p. 1144 - 1149, View in Reaxys 62 of 96

Melting Point [°C]

78 - 82

Solvent (Melting Point)

hexane; toluene

Rich, Jonathan D.; Journal of the American Chemical Society; vol. 111; nb. 15; (1989); p. 5886 - 5893, View in Reaxys 63 of 96

Melting Point [°C]

80 - 81

Minabe,M. et al.; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 1614 - 1619, View in Reaxys; DiBiase,S.A. et al.; Journal of Organic Chemistry; vol. 44; nb. 25; (1979); p. 4640 - 4649, View in Reaxys; Otsuka et al.; Justus Liebigs Annalen der Chemie; (1975); p. 626,635, View in Reaxys; Anjaneyulu, P. S. R.; Lala, Anil K.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 23; nb. 9; (1984); p. 802 - 807, View in Reaxys; Chidambaram, Nallaperumal; Chandrasekaran, Srinivasan; Journal of Organic Chemistry; vol. 52; nb. 22; (1987); p. 5048 - 5051, View in Reaxys 64 of 96

Melting Point [°C]

81 - 83

Ratusky; Collection of Czechoslovak Chemical Communications; vol. 37; (1972); p. 2436,2448, View in Reaxys; Tamarkin, Dov; Rabinovitz, Mordecai; Journal of Organic Chemistry; vol. 52; nb. 15; (1987); p. 3472 - 3474, View in Reaxys 65 of 96

Melting Point [°C]

75 - 80

Solvent (Melting Point)

petroleum ether; CH2Cl2

Lianis, Pygmalion S.; Rodios, Nestor A.; Alexandrou, Nicholas E.; Liebigs Annalen der Chemie; (1987); p. 537 - 540, View in Reaxys 66 of 96

Melting Point [°C]

83

Kappe et al.; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 34; (1979); p. 716, View in Reaxys; Cardillo et al.; Synthesis; (1976); p. 394, View in Reaxys; Parsons; Cohen; Journal of the American Chemical Society; vol. 96; (1974); p. 2948,2950,2951, View in Reaxys; Ogata et al.; Journal of Organic Chemistry; vol. 40; (1975); p.

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615,618, View in Reaxys; Kajigaeshi; Nippon Kagaku Zasshi; vol. 83; (1962); p. 228; Chem.Abstr.; vol. 59; nb. 522; (1963), View in Reaxys; Patent; Simikow et al.; SU449029; (1975); Ref. Zh., Khim.; vol. 7; nb. N354P; (1976), View in Reaxys; Cohen; Parsons; Journal of the American Chemical Society; vol. 92; (1970); p. 7603, View in Reaxys; Sellers; Suschitzky; Journal of the Chemical Society [Section] C: Organic; (1969); p. 2139,2140, 2142, View in Reaxys; Yonemura, Hiroshi; Nishino, Hiroshi; Kurosawa, Kazu; Bulletin of the Chemical Society of Japan; vol. 59; (1986); p. 3153 - 3160, View in Reaxys 67 of 96

Melting Point [°C]

85 - 86

Solvent (Melting Point)

light petroleum

Grant, Richard D.; Pinhey, John T.; Rizzardo, Ezio; Smith, Geoffrey C.; Australian Journal of Chemistry; vol. 38; nb. 10; (1985); p. 1505 - 1519, View in Reaxys 68 of 96

Melting Point [°C]

83 - 84

Solvent (Melting Point)

petroleum ether

Stone, Paul G.; Cohen, Saul G.; Journal of the American Chemical Society; vol. 104; nb. 12; (1982); p. 3435 - 3440, View in Reaxys 69 of 96

Melting Point [°C]

84

Schoenberg,A.; Praefcke,K.; Chemische Berichte; vol. 99; (1966); p. 205 - 212, View in Reaxys; Fetizon,M. et al.; Tetrahedron; vol. 31; (1975); p. 165 - 170, View in Reaxys; Staudinger; Kon; Justus Liebigs Annalen der Chemie; vol. 384; (1911); p.

88, View in Reaxys; Cohen; Recueil des Travaux Chimiques des Pays-Bas; vol. 38; (1919); p. 121, View in Reaxys; Saxena; Kulshreshtha; Journal of the Indian Chemical Society; vol. 48; (1971); p. 137, View in Reaxys; Pruefcke et al.; Chemische Berichte; vol. 107; (1974); p. 2931,2936, View in Reaxys; Kashin, A. N.; Bumagin, N. A.; Beletskaya, I. P.; Reutov, O. A.; Journal of Organic Chemistry USSR (English Translation); vol. 16; nb. 12; (1980); p. 2190 - 2195; Zhurnal Organicheskoi Khimii; vol. 16; nb. 12; (1980); p. 2561 - 2566, View in Reaxys; Kashin, A. N.; Bumagin, N. A.; Bessonova, M. P.; Beletskaya, I. P.; Reutov, O. A.; Journal of Organic Chemistry USSR (English Translation); vol. 16; nb. 7; (1980); p. 1153 - 1159; Zhurnal Organicheskoi Khimii; vol. 16; nb. 7; (1980); p. 1345 - 1352, View in Reaxys 70 of 96

Melting Point [°C]

80 - 82

Bonini,B.F. et al.; Gazzetta Chimica Italiana; vol. 107; (1977); p. 283 - 288, View in Reaxys; Scretlas; Cazianis; Tetrahedron; vol. 34; (1978); p. 933,935,939, View in Reaxys; Minabe; Suzuki; Journal of Organic Chemistry; vol. 40; (1975); p. 1298,1302, View in Reaxys; Nesmeyanov et al.; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 550,556,557-559, View in Reaxys; Trost; Kinson; Journal of Organic Chemistry; vol. 37; (1972); p. 1273, View in Reaxys; Patrick, Timothy B.; Cantrell, Gary L.; Inga, Sandra M.; Journal of Organic Chemistry; vol. 45; nb. 8; (1980); p. 1409 - 1413, View in Reaxys 71 of 96

Melting Point [°C]

84

Solvent (Melting Point)

ethanol

Miura, Masahiro; Nojima, Masamoto; Kusabayashi, Shigekazu; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1980); p. 1950 - 1954, View in Reaxys 72 of 96

Melting Point [°C]

82 - 85

Beelitz et al.; Chemiker-Zeitung; vol. 103; (1979); p. 179, View in Reaxys 73 of 96

Melting Point [°C]

81 - 82

Kuo,Y.-N.; Nye,M.J.; Canadian Journal of Chemistry; vol. 51; (1973); p. 1995 - 2000, View in Reaxys; Lynch,E.R.; Journal of the Chemical Society; (1962); p. 3729 - 3733, View in Reaxys; Patent; Schering AG; DE2418503; (1975); Chem.Abstr.; vol.

84; nb. 30929, View in Reaxys; Akermark et al.; Journal of Organic Chemistry; vol. 40; (1975); p. 1365, View in Reaxys; Gait et al.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1974); p.

1248,1257, View in Reaxys; Wade et al.; Journal of Organic Chemistry; vol. 44; (1979); p. 3724, View in Reaxys 74 of 96

Melting Point [°C]

85 - 86

Sieglitz; Chemische Berichte; vol. 57; (1924); p. 317, View in Reaxys; Gukasyan; Shakhnazaryan; Armyanskii Khimicheskii Zhurnal; vol. 31; (1978); p. 711,712; Chem.Abstr.; vol. 90; nb. 87116x, View in Reaxys 75 of 96

Melting Point [°C]

80 - 80.5

Gorman et al.; Journal of Photochemistry; vol. 9; (1978); p. 11,14, View in Reaxys 76 of 96

Melting Point [°C]

82 - 84

Minabe,M. et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 3373 - 3376, View in Reaxys; Goerner,R.N. et al.; Journal of Organic Chemistry; vol. 42; nb. 1; (1977); p. 19 - 28, View in Reaxys 77 of 96

Melting Point [°C]

78 - 80

Eckell,A.; Huisgen,R.; Chemische Berichte; vol. 110; (1977); p. 571 - 577, View in Reaxys 78 of 96

Melting Point [°C]

72 - 73

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Huisgen et al.; Chemische Berichte; vol. 110; (1977); p. 514,518, View in Reaxys 79 of 96

Melting Point [°C]

75 - 78

Eckell,A.; Huisgen,R.; Chemische Berichte; vol. 110; (1977); p. 559 - 570, View in Reaxys 80 of 96

Melting Point [°C]

82 - 83

Horner,L.; Fernekess,H.; Chemische Berichte; vol. 94; (1961); p. 712 - 724, View in Reaxys; Pagano,A.H.; Shechter,H.; Journal of Organic Chemistry; vol. 35; (1970); p. 295 - 303, View in Reaxys; Wislicenus; Waldmueller; Chemische Berichte; vol.

41; (1908); p. 3338, View in Reaxys; Gokel; Durst; Synthesis; (1976); p. 168,180, View in Reaxys; Rosini et al.; Journal of Organic Chemistry; vol. 39; (1974); p. 3504, View in Reaxys; Huurdeman et al.; Tetrahedron Letters; (1971); p. 3449, View in Reaxys 81 of 96

Melting Point [°C]

79

Cirigottis,K.A. et al.; Australian Journal of Chemistry; vol. 27; (1974); p. 2209 - 2228, View in Reaxys 82 of 96

Melting Point [°C]

83.2

Tanaka et al.; Nippon Kagaku Kaishi; (1973); p. 126,127-130, View in Reaxys 83 of 96

Melting Point [°C]

82.5

Metz; Synthesis; (1972); p. 612, View in Reaxys 84 of 96

Melting Point [°C]

84 - 85

Rawson; Wynberg; Recueil des Travaux Chimiques des Pays-Bas; vol. 90; (1971); p. 39,43, 44, View in Reaxys 85 of 96

Melting Point [°C]

81.5 - 82.5

Solvent (Melting Point)

benzene; petroleum ether

Yamase et al.; Kogyo Kagaku Zasshi; vol. 72; (1969); p. 162,163, 164; Chem.Abstr.; vol. 70; nb. 95983; (1969), View in Reaxys 86 of 96

Melting Point [°C]

84

Solvent (Melting Point)

acetic acid

Schoenberg,A.; Praefcke,K.; Chemische Berichte; vol. 99; (1966); p. 205 - 212, View in Reaxys 87 of 96

Melting Point [°C]

82 - 83.5

Chiba; Kogyo Kagaku Zasshi; vol. 69; (1966); p. 1289,1292, View in Reaxys 88 of 96

Melting Point [°C]

84 - 85

Solvent (Melting Point)

hexane

Godfroid,J.-J.; Bulletin de la Societe Chimique de France; (1964); p. 2929 - 2943, View in Reaxys 89 of 96

Melting Point [°C]

83.5 - 84.5

Wiemann; Godefroid; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 255; (1962); p. 2608, View in Reaxys 90 of 96

Melting Point [°C]

81.5

Colonge,J.; Daunis,H.; Bulletin de la Societe Chimique de France; (1961); p. 2238 - 2241, View in Reaxys 91 of 96

Melting Point [°C]

84

Solvent (Melting Point)

aq. ethanol

Davies; Ennis; Journal of the Chemical Society; (1960); p. 1488,1490, View in Reaxys 92 of 96

Melting Point [°C]

54

Copeland et al.; Journal of the Chemical Society; (1960); p. 3230,3233, View in Reaxys 93 of 96

Melting Point [°C]

85

Solvent (Melting Point)

aq. methanol

Jeanes; Adams; Journal of the American Chemical Society; vol. 59; (1937); p. 2608,2619, View in Reaxys 94 of 96

Melting Point [°C]

84 - 86

Schmidt,J.; Wagner; Chemische Berichte; vol. 43; (1910); p. 1800; Justus Liebigs Annalen der Chemie; vol. 387; (1912); p.

159, View in Reaxys

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95 of 96

Solvent (Melting Point)

ethanol

P.Groth, Chemische Krystallographie 5.Teil <Leipzig 1919> S. 429, View in Reaxys; v. Reusch; Justus Liebigs Annalen der Chemie; vol. 193; (1878); p. 118, View in Reaxys; Friedlaender; Zeitschrift fuer Kristallographie, Kristallgeometrie, Kristallphysik, Kristallchemie; vol. 1; (1877); p. 623; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1877); p. 742, View in Reaxys 96 of 96

Melting Point [°C]

83.5 - 84

Fittig; Ostermayer; Justus Liebigs Annalen der Chemie; vol. 166; (1873); p. 363, View in Reaxys Boiling Point (9) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

342

References Diehl, Fabrice; Barbier, Jacques; Duprez, Daniel; Guibard, Isabelle; Mabilon, Gil; Applied Catalysis A: General; vol. 504; (2015); p. 37 - 43, View in Reaxys

177

760

Hajipour; Mallakpour; Molecular Crystals and Liquid Crystals Science and Technology, Section A: Molecular Crystals and Liquid Crystals; vol. 356; (2001); p. 371 - 387, View in Reaxys

179

760

Hajipour; Mohammadpoor-Baltork; Kianfar; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 38; nb. 2; (1999); p. 221 - 224, View in Reaxys

177

Hajipour, Abdol Reza; Mohammadpoor-Baltork, Iraj; Niknam, Kurosh; Organic Preparations and Procedures International; vol. 31; nb. 3; (1999); p. 335 - 341, View in Reaxys

120

12

Dutt, Sachchidananda; Banerjee, Santanu; Hazra, Banasri; Banerjee, Amalendu; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 64; (1987); p. 704 - 705, View in Reaxys

160 - 165

6-7

Dutta, Hasi; Hazra, Banasri; Banerjee, Amalendu; Banerjee, Santanu; Journal of the Indian Chemical Society; vol. 64; (1987); p. 706 - 707, View in Reaxys

341.5

760

Goerner,R.N. et al.; Journal of Organic Chemistry; vol. 42; nb. 1; (1977); p. 19 - 28, View in Reaxys; Graebe; Rateanu; Justus Liebigs Annalen der Chemie; vol. 279; (1894); p. 266 Anm., View in Reaxys

341.5

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p.

2720,2724, View in Reaxys

235 - 250

Carnelley; Dunn; Chemische Berichte; vol. 21; (1888); p. 2005, View in Reaxys

Sublimation (1) Sublimation [°C] 100

Pressure (Sublimation) [Torr]

References

0.5

Badger; Journal of the Chemical Society; (1941); p. 535,537, View in Reaxys

Refractive Index (2) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C]

References

1.6272

656.3

99.4

v. Auwers; Fruehling; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 224, View in Reaxys

1.6369

589

99.4

v. Auwers; Fruehling; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 224, View in Reaxys

Density (4) 1 of 4

Measurement Temperature 21.24 [°C] Type (Density)

crystallographic

Location

supporting information

Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys 2 of 4

Density [g·cm-3]

1.254

Krishnan; Banerjee; Philosophical Transactions of the Royal Society of London; vol. <A> 234; (1935); p. 265,280, View in Reaxys 3 of 4

Density [g·cm-3]

1.228

Mukherjee; Indian Journal of Physics (1926-1976); vol. 8; (1933); p. 147,149, View in Reaxys

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4 of 4

Density [g·cm-3]

1.13

Reference Temperature [°C]

4

Measurement Temperature 99.4 [°C] v. Auwers; Fruehling; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 224, View in Reaxys Adsorption (MCS) (2) 1 of 2

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

zeolite L

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 2408, View in Reaxys 2 of 2

Description (Adsorption (MCS))

Desorption

Partner (Adsorption (MCS))

methylsilicone stationary phase

Krieger; Hites; Environmental Science and Technology; vol. 28; nb. 6; (1994); p. 1129 - 1133, View in Reaxys Association (MCS) (15) 1 of 15

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

methanol; water

Partner (Association (MCS))

cucurbit[7]uril

Ghosh, Indrajit; Mukhopadhyay, Arindam; Koner, Apurba Lal; Samanta, Subhas; Nau, Werner M.; Moorthy, Jarugu Narasimha; Physical Chemistry Chemical Physics; vol. 16; nb. 31; (2014); p. 16436 - 16445, View in Reaxys 2 of 15

Description (Association (MCS))

IR spectrum of the complex

Temperature (Association (MCS)) [°C]

20

Partner (Association (MCS))

octanol

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb.

1-3; (2007); p. 44 - 48, View in Reaxys 3 of 15

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

heptane

Partner (Association (MCS))

1,2,3,4-tetrahydroisoquinoline

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 - 150, View in Reaxys 4 of 15

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

H2O

Comment (Association (MCS))

ambient temperature. Object(s) of Study: concentration dependence

Partner (Association (MCS))

alpha cyclodextrin

Murphy; Barros; Barnes; Mayer; Marconi; Bohne; Journal of Physical Chemistry A; vol. 103; nb. 1; (1999); p. 137 - 146, View in Reaxys

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5 of 15

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Comment (Association (MCS))

concentration dependence

Partner (Association (MCS))

alpha cyclodextrin

Murphy; Barros; Barnes; Mayer; Marconi; Bohne; Journal of Physical Chemistry A; vol. 103; nb. 1; (1999); p. 137 - 146, View in Reaxys 6 of 15

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Partner (Association (MCS))

β-cyclodextrin

Murphy; Barros; Barnes; Mayer; Marconi; Bohne; Journal of Physical Chemistry A; vol. 103; nb. 1; (1999); p. 137 - 146, View in Reaxys 7 of 15

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

acetonitrile

Partner (Association (MCS))

ethanol

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb.

7; (1996); p. 1833 - 1839, View in Reaxys 8 of 15

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

cyclohexane

Partner (Association (MCS))

ethanol

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb.

7; (1996); p. 1833 - 1839, View in Reaxys 9 of 15

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

acetonitrile

Partner (Association (MCS))

ethanol

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb.

7; (1996); p. 1833 - 1839, View in Reaxys 10 of 15

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

dimethylsulfoxide

Partner (Association (MCS))

hydroxylamine, sodium methoxide, methanol

Tachibana, Masaki; Furusawa, Motohisa; Bulletin of the Chemical Society of Japan; vol. 61; nb. 7; (1988); p. 2353 - 2358, View in Reaxys 11 of 15

Description (Association (MCS))

UV/VIS spectrum of the complex

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Solvent (Association (MCS))

propan-2-ol

Partner (Association (MCS))

1,4-diaza-bicyclo[2.2.2]octane

Peters, K. S.; Freilich, S. C.; Schaeffer, C. G.; Journal of the American Chemical Society; vol. 102; nb. 17; (1980); p. 5701 5702, View in Reaxys 12 of 15

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

tetrahydrofuran

Partner (Association (MCS))

Sr/Hg

Konishi, S.; Morioka, Y.; Nakagawa, I.; Journal of Molecular Structure; vol. 64; (1980); p. 157 - 162, View in Reaxys 13 of 15

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

tetrahydrofuran

Partner (Association (MCS))

Ba/Hg

Konishi, S.; Morioka, Y.; Nakagawa, I.; Journal of Molecular Structure; vol. 64; (1980); p. 157 - 162, View in Reaxys 14 of 15

Description (Association (MCS))

Stability constant of the complex with ...

Dunken; Fritzsche; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 249, View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys 15 of 15

Description (Association (MCS))

Enthalpy of association

Dunken; Fritzsche; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 249, View in Reaxys Chromatographic Data (6) Chromatographic Location data HPLC (High performance liquid chromatography)

References

supporting informa- Konishi, Hideyuki; Futamata, Suguru; Wang, Xi; Manabe, Kei; Advanced Synthesis and Cattion alysis; vol. 360; nb. 9; (2018); p. 1805 - 1809, View in Reaxys

HPLC (High performance liquid chromatography)

Serra, Stefano; European Journal of Organic Chemistry; vol. 2015; nb. 29; (2015); p. 6472 6478, View in Reaxys; Hall, Emma A.; Sarkar, Md Raihan; Bell, Stephen G.; Catalysis Science and Technology; vol. 7; nb. 7; (2017); p. 1537 - 1548, View in Reaxys

TLC (Thin layer chromatography)

Parida, Keshaba Nanda; Jhulki, Samik; Mandal, Susovan; Moorthy, Jarugu Narasimha; Tetrahedron; vol. 68; nb. 47; (2012); p. 9763 - 9768, View in Reaxys; Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys; Mendkovich, Andrey S.; Syroeshkin, Mikhail A.; Nasybullina, Darya V.; Mikhailov, Mikhail N.; Gultyai, Vadim P.; Elinson, Mikhail N.; Rusakov, Alexander I.; Electrochimica Acta; vol. 191; (2016); p. 962 - 973, View in Reaxys

GC (Gas chromatography)

supporting informa- Nagaki, Aiichiro; Ichinari, Daisuke; Yoshida, Jun-Ichi; Journal of the American Chemical Sotion ciety; vol. 136; nb. 35; (2014); p. 12245 - 12248, View in Reaxys; Hossain, Md. Munkir; Shyu, Shin-Guang; Tetrahedron; vol. 72; nb. 29; (2016); p. 4252 - 4257, View in Reaxys

GC (Gas chromatography)

Sigrist, Rolf; Hansen, Hans-Juergen; Helvetica Chimica Acta; vol. 97; nb. 8; (2014); p. 1165 1175, View in Reaxys; Cao, Gang; Xu, Zhiwei; Wu, Xin; Li, Qingli; Chen, Xiaocheng; Natural Product Research; vol. 28; nb. 19; (2014); p. 1607 - 1612, View in Reaxys; Sharma, Anubhuti; Sood, Salej; Agrawal; Kant; Bhatt; Pattanayak; Asian Journal of Chemistry; vol. 28; nb. 7; (2016); p. 1633 - 1637, View in Reaxys

TLC (Thin layer chromatography)

supporting informa- Furusawa, Takuma; Morimoto, Tsumoru; Oka, Nagato; Tanimoto, Hiroki; Nishiyama, Yation suhiro; Kakiuchi, Kiyomi; Chemistry Letters; vol. 45; nb. 4; (2016); p. 406 - 408, View in Reaxys; Furusawa, Takuma; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Tanimoto, Hiroki; Kakiuchi, Kiyomi; Chemistry - An Asian Journal; vol. 11; nb. 16; (2016); p. 2312 - 2315, View in Reaxys

Circular Dichroism (1)

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Solvent (Circular Dichroism)

Comment (Circular Dichroism)

References

various solvent(s)

300 - 400 nm

Schipper, Pieter E.; O'Brien, Joanne M.; Ridley, Damon D.; Journal of Physical Chemistry; vol. 89; (1985); p. 5805 - 5810, View in Reaxys

Crystal Phase (4) Description (Crystal Phase)

Comment (Crystal Phase)

References

Rate of transition

Biczok, Laszlo; Berces, Tibor; Journal of Physical Chemistry; vol. 92; nb. 13; (1988); p. 3842 3845, View in Reaxys

Crystal structure determination

Iball; Zeitschrift fuer Kristallographie, Kristallgeometrie, Kristallphysik, Kristallchemie; vol. 94; (1936); p. 397,404, View in Reaxys; Garten; Head; Nature (London, United Kingdom); vol. 205; (1965); p. 160, View in Reaxys; Zwarich et al.; Journal of Molecular Spectroscopy; vol. 51; (1974); p. 38,42-47, View in Reaxys; Luss; Smith; Acta Crystallographica, Section B: Structural Crystallography and Crystal Chemistry; vol. 28; (1972); p. 884, View in Reaxys

Polymorphism

Ueber die Existenz Kofler; Mikrochemie; vol. 34; (1948); p. 20,21; Chem.Abstr.; (1948); p. 8713, View in Reaxys instabiler Modifikationen vom F: 72grad, F: 54grad und F: 52grad.

Crystal structure determination

a=16 Angstroem, b=12.5 Angstroem, c=18.63 Angstroem, n=16.; aus dem Roentgendiagramm ermittelt.

Crystal Property Description (16) Colour & Other Location Properties yellow

Iball; Zeitschrift fuer Kristallographie, Kristallgeometrie, Kristallphysik, Kristallchemie; vol. 94; (1936); p. 397,404, View in Reaxys

References

supporting informa- Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte tion Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9926 - 9930, View in Reaxys; Li, Hu; Zhu, Ru-Yi; Shi, Wen-Juan; He, Ke-Han; Shi, Zhang-Jie; Organic Letters; vol. 14; nb. 18; (2012); p. 4850 - 4853,4, View in Reaxys; Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 - 2745, View in Reaxys; Puenner, Florian; Schieven, Justin; Hilt, Gerhard; Organic Letters; vol. 15; nb. 18; (2013); p.

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gelbe Nadeln

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weisse Nadeln oder Platten

Carnelley; Dunn; Chemische Berichte; vol. 21; (1888); p. 2005, View in Reaxys

gelb

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p. 623; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1877); p. 742, View in Reaxys Crystal System (1) Crystal System Location Rhombic

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Dielectric Constant (1) References Nagai et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1022, View in Reaxys; Zeil et al.; Zeitschrift fuer Elektrochemie; vol. 63; (1959); p. 1110,1111-1120; Chem.Abstr.; nb. 5194; (1960), View in Reaxys Dissociation Exponent (5) 1 of 5

Comment (Dissociation Exponent)

(pk')Radikal: pK(a)

Rao; Hayon; Analytical Chemistry; vol. 48; (1976); p. 564,565, View in Reaxys 2 of 5

Comment (Dissociation Exponent)

(pk')e-(aq)-Addukt (Ketyl): pk (Tab.II)

Hayon et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 2072, View in Reaxys 3 of 5

Comment (Dissociation Exponent)

(k')S445

Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 33; (1971); p. 419,421, View in Reaxys 4 of 5

Comment (Dissociation Exponent)

(pk')pK(a)-Best. (UV-spektrometrisch) in wssr. H2SO4

Greig; Johnson; Journal of the American Chemical Society; vol. 90; (1968); p. 6453, View in Reaxys 5 of 5

Comment (Dissociation Exponent)

(pk')pK(BH+): -6.65

Stewart et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 1065,1066, View in Reaxys Electrical Data (4) 1 of 4

Description (Electrical Da- Dielectric relaxation time ta) Nagai et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1022, View in Reaxys; Zeil et al.; Zeitschrift fuer Elektrochemie; vol. 63; (1959); p. 1110,1111-1120; Chem.Abstr.; nb. 5194; (1960), View in Reaxys

2 of 4

Description (Electrical Da- Electrical properties ta) Davies; Swain; Chemical Physics Letters; vol. 2; (1968); p. 42, View in Reaxys

3 of 4

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von Loesungen in Benzol, CCl4 und Heptan bei 20-60grad/1000-9700 MHz bzw. 1.25-50 cm.

Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys; Zeil et al.; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 63; (1959); p. 1110,1116, View in Reaxys

4 of 4

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von in Benzol, CCl4 und Heptan geloestem Fluoren-9-on bei 20-60grad.

Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys; Zeil et al.; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 63; (1959); p. 1110,1116, View in Reaxys

Electrical Moment (10) 1 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.7

Method (Electrical Moment)

Microwave absorption

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Solvent (Electrical Moment)

benzene

Fessenden, Richard W.; Carton, Paul M.; Shimamori, H.; Scalano, Juan C.; Journal of Physical Chemistry; vol. 86; (1982); p. 3803 - 3811, View in Reaxys 2 of 10

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in o-Terphenyl

Crossley et al.; Journal of Chemical Physics; vol. 69; (1978); p. 1980, View in Reaxys 3 of 10

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ (tabelliert)

Nagai et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1022, View in Reaxys 4 of 10

Description (Electrical Moment)

Dipole moment

Davies; Swain; Transactions of the Faraday Society; vol. 67; (1971); p. 1637,1647,1648, View in Reaxys 5 of 10

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ

Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p.

377,393, View in Reaxys 6 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.34

Temperature (Electrical Moment) [°C]

60

Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys 7 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.38

Temperature (Electrical Moment) [°C]

20

Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys 8 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.38

Temperature (Electrical Moment) [°C]

40

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Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys 9 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.35

Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Hughes; Le Fevre; Le Fevre; Journal of the Chemical Society; (1937); p. 202,206, View in Reaxys 10 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.29

Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Bergmann; Engel; Hoffmann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 17; (1932); p. 92,97, View in Reaxys; Bergmann; Engel; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 37; (1931); p. 563,566, View in Reaxys Electrochemical Behaviour (5) Description (Elec- Comment (Electrotrochemical Behav- chemical Behaviour) iour)

References

Polarography

House,H.O.; Umen,M.J.; Journal of the American Chemical Society; vol. 94; (1972); p. 5495 5497, View in Reaxys; Kalinowski et al.; Transactions of the Faraday Society; vol. 62; (1966); p.

918, View in Reaxys; Kalinowski; Grabowski; Transactions of the Faraday Society; vol. 62; (1966); p. 926,931, View in Reaxys; Karpinets; Bezuglyi; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 2116,1857,1859, View in Reaxys; Tsebrii et al.; Sov. Prog. Chem. (Engl.

Transl.); vol. 41; nb. 7; (1975); p. 702,27, View in Reaxys; Kemula et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 6863, View in Reaxys; Kalinowski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 18; (1970); p. 685, View in Reaxys; Molnar et al.; Chemicke Zvesti; vol. 14; (1960); p. 783,786,787; Chem.Abstr.; vol. 55; nb. 16221; (1961), View in Reaxys; Berg; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 229; (1965); p. 138,141, View in Reaxys

Electrochemical properties

Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 33; (1971); p. 419,421, View in Reaxys; Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 73; (1976); p. 163,168, View in Reaxys; Saveant; Binh; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 88; (1978); p. 27,30, View in Reaxys; Lunazzi et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 162,163, View in Reaxys; Vykhodtseva; Nekrasov; Doklady Physical Chemistry; vol.

220-225; (1975); p. 861, View in Reaxys; Kalinowski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 18; (1970); p. 685, View in Reaxys

Basicity

Paspaleev; Kojucharova; Monatshefte fuer Chemie; vol. 100; (1969); p. 1213,1216, View in Reaxys

Thermodynamic parameters for autoprotolysis

mit Diphenylamin.

Pusin; Rikovski; Milutinovic; Glasnik Hemijskog Drustva Beograd; vol. 14; (1949); p. 173,177; Chem.Abstr.; (1952); p. 4344, View in Reaxys

Basicity

gegen starke Saeuren.

Stobbe; Seydel; Justus Liebigs Annalen der Chemie; vol. 370; (1909); p. 141, View in Reaxys

Electrochemical Characteristics (39)

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1 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

dichloromethane

Location

supporting information

Comment (Electrochemical Characteristics)

Other electrode; potential diagram; 0.1 M tetrabutylammonium hexafluorophosphate

Li, Shuangjiang; Aljhdli, Merfat; Thakellapalli, Haresh; Farajidizaji, Behzad; Zhang, Yu; Akhmedov, Novruz G.; Milsmann, Carsten; Popp, Brian V.; Wang, Kung K.; Organic Letters; vol. 19; nb. 15; (2017); p. 4078 - 4081, View in Reaxys 2 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide

Comment (Electrochemical Characteristics)

transmitted electrons -1; Cathodic peak potential; -1.23 V; Saturated calomel electrode (SCE); potential diagram; 0.1 M tetrabutylammonium perchlorate

Product

radical anion of fluorene-9-one

Mendkovich, Andrey S.; Syroeshkin, Mikhail A.; Nasybullina, Darya V.; Mikhailov, Mikhail N.; Gultyai, Vadim P.; Elinson, Mikhail N.; Rusakov, Alexander I.; Electrochimica Acta; vol. 191; (2016); p. 962 - 973, View in Reaxys 3 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide

Temperature (Electrochemical Characteristics) [°C]

25

Location

supporting information

Comment (Electrochemical Characteristics)

Saturated calomel electrode (SCE); potential diagram; 0.03 M Bu4NClO4

Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko; Journal of Organic Chemistry; vol. 81; nb. 22; (2016); p. 11043 - 11056, View in Reaxys 4 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide

Comment (Electrochemical Characteristics)

Saturated calomel electrode (SCE); potential diagram; 0.1 M N-tetrabutylammonium tetrafluoroborate

Reche, Irene; Gallardo, Iluminada; Guirado, Gonzalo; New Journal of Chemistry; vol. 38; nb. 10; (2014); p. 5030 - 5036, View in Reaxys 5 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

dichloromethane

Comment (Electrochemical Characteristics)

Saturated silver chloride electrode; potential diagram; 0.1M tetrabutylammonium hexafluorophosphate

Guenes, Arzu; Cihaner, Atilla; Oenal, Ahmet M.; Electrochimica Acta; vol. 89; (2013); p. 339 - 345, View in Reaxys 6 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

dichloromethane

Location

supporting information

Comment (Electrochemical Characteristics)

Other electrode; potential diagram; 0.1 mol L−1 tetrabutylammonium hexafluorophosphate

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Eakins, Galen L.; Cooper, Matthew W.; Gerasimchuk, Nikolay N.; Phillips, Terry J.; Breyfogle, Bryan E.; Stearman, Chad J.; Canadian Journal of Chemistry; vol. 91; nb. 11; (2013); p. 1059 - 1071, View in Reaxys 7 of 39

Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide; water

Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochemical Characteristics)

transmitted electrons -1; Cathodic peak potential; -1.79 V; Ferrocene/ferrocenium; potential diagram; 0.1 M Bu4NClO4

Product

C13H8O(1+)

Mendkovich; Syroeshkin; Mikhailov; Ranchina; Rusakov; Russian Chemical Bulletin; vol. 62; nb. 7; (2013); p. 1668 - 1670; Izv. Akad. Nauk, Ser. Khim.; nb. 7; (2013); p. 1668 - 1670,3, View in Reaxys 8 of 39

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Location

supporting information

Cocherel, Nicolas; Poriel, Cyril; Rault-Berthelot, Joelle; Barriere, Frederic; Audebrand, Nathalie; Slawin, Alexandra M. Z.; Vignau, Laurence; Chemistry - A European Journal; vol. 14; nb. 36; (2008); p. 11328 - 11342, View in Reaxys; Amaya, Toru; Hifumi, Maiko; Okada, Michiaki; Shimizu, Yasutomo; Moriuchi, Toshiyuki; Segawa, Kouji; Ando, Yoichi; Hirao, Toshikazu; Journal of Organic Chemistry; vol. 76; nb. 19; (2011); p. 8049 - 8052, View in Reaxys; Eakins, Galen L.; Alford, Joshua S.; Tiegs, Brandon J.; Breyfogle, Bryan E.; Stearman, Chad J.; Journal of Physical Organic Chemistry; vol. 24; nb.

11; (2011); p. 1119 - 1128, View in Reaxys 9 of 39

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Dufresne, Stephane; Skalski, Thomas; Skene; Canadian Journal of Chemistry; vol. 89; nb. 2; (2011); p. 173 - 180, View in Reaxys; Carbas, Buket Bezgin; Kivrak, Arif; Oenal, Ahmet M.; Electrochimica Acta; vol. 58; nb. 1; (2011); p. 223 230, View in Reaxys 10 of 39

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

acetonitrile

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 - 150, View in Reaxys; Zhang, Kai; Chen, Zhao; Yang, Chuluo; Tao, Youtian; Zou, Yang; Qin, Jingui; Cao, Yong; Journal of Materials Chemistry; vol. 18; nb. 3; (2008); p. 291 - 298, View in Reaxys 11 of 39

Description (Electrochemical Characteristics)

cyclic voltammetry

Solvent (Electrochemical Characteristics)

dimethylformamide

Rejnak, Michal; Klima, Jiri; Svoboda, Jiri; Ludvik, Jiri; Collection of Czechoslovak Chemical Communications; vol. 69; nb.

1; (2004); p. 242 - 260, View in Reaxys; Wang, Changsheng; Batsanov, Andrei S.; Bryce, Martin R.; Sage, Ian; Organic Letters; vol. 6; nb. 13; (2004); p. 2181 - 2184, View in Reaxys 12 of 39

Description (Electrochemical Characteristics)

oxidation potential

Solvent (Electrochemical Characteristics)

acetonitrile; various solvent(s)

Jacques; Allonas; Sarbach; Haselbach; Vauthey; Chemical Physics Letters; vol. 378; nb. 1-2; (2003); p. 185 - 191, View in Reaxys 13 of 39

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

20

Enemaerke, Rasmus J.; Christensen, Torben B.; Jensen, Henrik; Daasbjerg, Kim; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (2001); p. 1620 - 1630, View in Reaxys

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14 of 39

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

tetrahydrofuran

Temperature (Electrochemical Characteristics) [°C]

20

Enemaerke, Rasmus J.; Hertz, Trille; Skrydstrup, Troels; Daasbjerg, Kim; Chemistry - A European Journal; vol. 6; nb. 20; (2000); p. 3747 - 3754, View in Reaxys 15 of 39

Description (Electrochemical Characteristics)

cyclic voltammetry

Solvent (Electrochemical Characteristics)

tetrahydrofuran

Temperature (Electrochemical Characteristics) [°C]

24.85

Behrendt, Andreas; Screttas, Constantinos G.; Bethell, Donald; Schiemann, Olav; Steele, Barry R.; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (1998); p. 2039 - 2045, View in Reaxys 16 of 39

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

23

Svyatkina; Dmitrieva; Kurov; Russian Journal of General Chemistry; vol. 66; nb. 2; (1996); p. 303 - 305, View in Reaxys 17 of 39

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

20

Comment (Electrochemical Characteristics)

-1.25 V; Product: /BRN= 4046027/. No. of transm. electrons: 1. Method: potentiometry

Product

fluorenone radical anion potassium contact ion pair

Umemoto, Kisaburo; Nagase, Yutaka; Sasaki, Yukio; Bulletin of the Chemical Society of Japan; vol. 67; nb. 12; (1994); p.

3245 - 3248, View in Reaxys 18 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.21 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 19 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

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Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.25 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 20 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

N,N-dimethyl-acetamide

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.27 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 21 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.21 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 22 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

hexamethylphosphoric acid triamide

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.45 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 23 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

various solvent(s)

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Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.15 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 24 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

various solvent(s)

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.29 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 25 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

House,H.O. et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 8471 - 8475, View in Reaxys; Pragst et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 257; (1976); p. 465,471, View in Reaxys; Wilkinson; Garner; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 73; (1977); p. 222,224, View in Reaxys; Rashkov et al.; Monatshefte fuer Chemie; vol. 101; (1970); p. 1797,1801, View in Reaxys; Loutfy; Loutfy; Canadian Journal of Chemistry; vol. 50; (1972); p. 4052,4054, View in Reaxys; Kalinowski; Chemical Physics Letters; vol. 7; (1970); p. 55, View in Reaxys; Karpinets; Bezuglyi; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 2116,1857,1859, View in Reaxys; Kalinowski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 18; (1970); p.

685, View in Reaxys; Fournier, Francoise; Berthelot, Jacques; Pascal, Yves-Louis; Canadian Journal of Chemistry; vol. 61; (1983); p. 2121 - 2125, View in Reaxys; Loutfy; Hsiao; Ong; Keoshkerian; Canadian Journal of Chemistry; vol. 62; nb. 10; (1984); p. 1877 - 1885, View in Reaxys; Nagaoka, Tsutomu; Fukunaga, Toshikazu; Yoshino, Takashi; Watanabe, Iwao; Nakayama, Toshiro; Okazaki, Satoshi; Analytical Chemistry; vol. 60; nb. 24; (1988); p. 2766 - 2769, View in Reaxys; Karpinets, A. P.; Benzuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 6; (1980); p. 1376 - 1379,1119 - 1122, View in Reaxys; Wagner, Elzbieta; Kalinowski, Marek K.; Monatshefte fuer Chemie; vol. 116; (1985); p. 1413 - 1418, View in Reaxys 26 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

1.28 V; Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: 0.1M tetrabutylammonium perchlorate, saturated calomel electrode

Product

fluorenone ketyl radical anion

Empis, Jose M. A.; Herold, Bernardo J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1986); p. 425 - 430, View in Reaxys 27 of 39

Description (Electrochemical Characteristics)

redox potential

Comment (Electrochemical Characteristics)

-1.28 V; Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: not given. Description: mercury drop electrode, comparison electrode - saturated calomel electrode

Product

fluorenone ketyl radical anion

Pragst, Fritz; Stoesser, Reinhard; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 25; nb. 6; (1985); p. 222, View in Reaxys 28 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

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Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

24.9

Comment (Electrochemical Characteristics)

1.71 V; Product: /BRN= 3550463/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: glassy carbon, Pt or Au electrodes

Product

9,10-anthraquinone radical anion

Nagaoka, Tsutomu; Okazaki, Satoshi; Journal of Physical Chemistry; vol. 89; nb. 11; (1985); p. 2340 - 2344, View in Reaxys 29 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide; H2O

Comment (Electrochemical Characteristics)

1.24 V; Product: /BRN= 3873884/. No. of transm. electrons: 1. Method: polarography. Description: calomel/sat. KCl; TBABr. Byprod.: alcohol (INO 380)

Product

difluorenyl-1,1'diol-1,1' * fluorenol

Fournier, F.; Berthelot, J.; Pascal, Y. L.; Tetrahedron; vol. 40; nb. 2; (1984); p. 339 - 347, View in Reaxys 30 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide; H2O

Comment (Electrochemical Characteristics)

1.91 V; Product: /BRN= 3873884/. Method: polarography. Description: calomel/sat. KCl; TBABr. Byprod.:INO 380

Product

difluorenyl-1,1'diol-1,1' * fluorenol

Fournier, F.; Berthelot, J.; Pascal, Y. L.; Tetrahedron; vol. 40; nb. 2; (1984); p. 339 - 347, View in Reaxys 31 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

Type: Reversible half-wave potential

Svaan, Morten; Parker, Vernon D.; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 38; nb.

9; (1984); p. 759 - 766, View in Reaxys 32 of 39

Description (Electrochemical Characteristics)

redox potential

Gorman et al.; Journal of Photochemistry; vol. 9; (1978); p. 11,14, View in Reaxys; Pons, Jean-Marc; Santelli, Maurice; Tetrahedron Letters; vol. 23; nb. 47; (1982); p. 4937 - 4940, View in Reaxys; Cerfontain, Hans; Geenevasen, Jan A. J.; Noort, Paul C. M. van; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p.

1057 - 1062, View in Reaxys 33 of 39

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

0.1

Comment (Electrochemical Characteristics)

-1.53 V; Product: /BRN= 3546256/. No. of transm. electrons: 1. Method: voltammetry. Description: reversible potential, a mercury electrode vs. Ag/Ag+

Product

radical anion of fluorene-9-one

Svaan, Morten; Parker, Vernon D.; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 36; nb.

6; (1982); p. 365 - 370, View in Reaxys 34 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

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Solvent (Electrochemical Characteristics)

acetonitrile

Comment (Electrochemical Characteristics)

-1.26 V; Product: /BRN= 3546256/. No. of transm. electrons: 1. Method: not given. Description: vs.

SCE, (n-Bu)4NClO4, supp. electrolite

Product

radical anion of fluorene-9-one

Miyashita, Tokuji; Matsuda, Minoru; Bulletin of the Chemical Society of Japan; vol. 54; nb. 6; (1981); p. 1740 - 1742, View in Reaxys 35 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

in Formamid-Acetamid-Gemischen.

Hook et al.; Journal of Physical Chemistry; vol. 58; (1954); p. 81, View in Reaxys 36 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

in Formamid.

Letaw; Gropp; Journal of Physical Chemistry; vol. 57; (1953); p. 964, View in Reaxys 37 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

in wss.-aethanol. Loesungen vom pH 1,2-12,2.

Day et al.; Journal of the American Chemical Society; vol. 74; (1952); p. 2741,2742, View in Reaxys; Day; Kirkland; Journal of the American Chemical Society; vol. 72; (1950); p. 2766, View in Reaxys 38 of 39

Description (Electrochemical Characteristics)

oxidation potential

Adkins et al.; Journal of the American Chemical Society; vol. 71; (1949); p. 3622,3623, View in Reaxys; Baker; Adkins; Journal of the American Chemical Society; vol. 62; (1940); p. 3305,3306, View in Reaxys 39 of 39

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Ashworth; Collection of Czechoslovak Chemical Communications; vol. 13; (1948); p. 229,237-243, View in Reaxys Electron Binding (2) Description (Elec- References tron Binding) Electronic states

Eakins, Galen L.; Cooper, Matthew W.; Gerasimchuk, Nikolay N.; Phillips, Terry J.; Breyfogle, Bryan E.; Stearman, Chad J.; Canadian Journal of Chemistry; vol. 91; nb. 11; (2013); p. 1059 - 1071, View in Reaxys; Soep, Benoît; Mestdagh, Jean-Michel; Briant, Marc; Gaveau, Marc-André; Poisson, Lionel; Physical Chemistry Chemical Physics; vol. 18; nb. 33; (2016); p. 22914 - 22920, View in Reaxys

Electron affinity

Chen; Wentworth; Journal of Chemical Physics; vol. 63; (1975); p. 3183,3189, View in Reaxys

Energy Barriers (1) References Herkstroeter et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 4537,4539, View in Reaxys Energy Data (MCS) (1) 1 of 1

Description (Energy Data (MCS))

Entropy of mixtures

Dunken; Fritzsche; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 249, View in Reaxys Enthalpy of Combustion (1) Comment (Enthal- References py of Combustion) Enthalpy of combustion given

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb.

9; (2012); p. 2486 - 2496,11, View in Reaxys

Enthalpy of Formation (2)

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Comment (Enthalpy of Formation)

References

Enthalpy of formation given

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb.

9; (2012); p. 2486 - 2496,11, View in Reaxys Karpinets; Bezuglyi; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 2116,1857,1859, View in Reaxys

Further Information (68) Description (FurReferences ther Information) Further information Beitz; Miller; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1979); p. 4579, View in Reaxys Further information Greene et al.; Journal of Chemical Physics; vol. 70; (1979); p. 1247, View in Reaxys Further information Borisevich; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 42; nb. 2; (1978); p. 1; ; p. 226, View in Reaxys Further information Barwise et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 1814,1817, View in Reaxys Further information Szabo et al.; Justus Liebigs Annalen der Chemie; (1977); p. 747,758, View in Reaxys Further information Khel'mer et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 40; nb. 2; (1976); p. 111; ; p. 348, View in Reaxys Further information Gaines et al.; Analytical Chemistry; vol. 47; (1975); p. 1373, View in Reaxys Further information Nakamura et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1593, View in Reaxys Further information Parsons et al.; Journal of the American Chemical Society; vol. 96; (1974); p. 6643,6645, View in Reaxys Further information Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys Further information Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys Further information Shears; Williams; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 69; (1973); p. 608, View in Reaxys Further information Potapov et al.; High Energy Chemistry; vol. 6; (1972); p. 347; ; p. 392, View in Reaxys Further information Davies; Swain; Transactions of the Faraday Society; vol. 67; (1971); p. 1637,1647,1648, View in Reaxys Further information Chapman et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 2918,2924, View in Reaxys Further information Potapov; Sorokin; High Energy Chemistry; vol. 5; (1971); p. 435; ; p. 487, View in Reaxys Further information Ioune; Tanizaki; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 73; (1970); p. 48,57, View in Reaxys Further information Axelrod et al.; Tetrahedron Letters; (1969); p. 5031, View in Reaxys Further information Gautier; Miocque; Moskowitz; Blanc-Guenee; Annales pharmaceutiques francaises; vol. 27; nb. 4; (1969); p. 303 308, View in Reaxys Further information Mullen Orloff; Journal of Molecular Spectroscopy; vol. 30; (1969); p. 140, View in Reaxys Further information Gocmen; Coudane; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 269; (1969); p. 467, View in Reaxys Further information Norris; Weissman; Journal of Physical Chemistry; vol. 73; (1969); p. 3119, View in Reaxys Further information Liu; Edman; Journal of the American Chemical Society; vol. 91; (1969); p. 1492, View in Reaxys Further information Caldwell; Journal of Organic Chemistry; vol. 34; (1969); p. 1886, View in Reaxys Further information Deboer; Journal of the American Chemical Society; vol. 91; (1969); p. 1855, View in Reaxys Further information Pacifici; Irick Jun.; Tetrahedron Letters; (1969); p. 2207, View in Reaxys Further information Wohl; Tetrahedron; vol. 24; (1968); p. 6889, View in Reaxys Further information Canters et al.; Chemical Physics Letters; vol. 1; (1968); p. 627, View in Reaxys Further information Sauers; Shurpik; Journal of Organic Chemistry; vol. 33; (1968); p. 799, View in Reaxys Further information Liu; Gale; Journal of the American Chemical Society; vol. 90; (1968); p. 1897, View in Reaxys Further information Saltiel; Journal of the American Chemical Society; vol. 90; (1968); p. 6394,6395, View in Reaxys

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Further information Rudzit et al.; Pharmaceutical Chemistry Journal; nb. 5; (1967); p. 245; Khimiko-Farmatsevticheskii Zhurnal; nb. 5; (1967); p. 14, View in Reaxys Further information Cantrell; Shechter; Journal of the American Chemical Society; vol. 89; (1967); p. 5877,5884, View in Reaxys Further information Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys Further information Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys Further information Ramirez,F. et al.; Journal of the American Chemical Society; vol. 89; (1967); p. 6283 - 6288, View in Reaxys Further information Normant; Bulletin de la Societe Chimique de France; (1966); p. 3601,3606, View in Reaxys Further information Kalinowski; Grabowski; Transactions of the Faraday Society; vol. 62; (1966); p. 926,931, View in Reaxys Further information Nelsen; Bartlett; Journal of the American Chemical Society; vol. 88; (1966); p. 143,148, View in Reaxys Further information Michl et al.; Journal of Physical Chemistry; vol. 70; (1966); p. 1732,1734,1735, View in Reaxys Further information Astakhova; Khidekel'; Doklady Chemistry; vol. 162; (1965); p. 558; Doklady Akademii Nauk SSSR; vol. 162; (1965); p. 1057, View in Reaxys Further information Shuman; Amstutz; Recueil des Travaux Chimiques des Pays-Bas; vol. 84; (1965); p. 441,445, View in Reaxys Further information Eland; Danby; Journal of the Chemical Society; (1965); p. 5935,5936, View in Reaxys Further information Faust et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 20; (1965); p.

1128,1133, View in Reaxys Further information Heller; Wasserman; Journal of Chemical Physics; vol. 42; (1965); p. 949,952, View in Reaxys Further information Shigorin; Potapov; Doklady Physical Chemistry; vol. 161; (1965); p. 237,238; ; p. 406, View in Reaxys Further information Doerr; Dehler; Tetrahedron Letters; (1965); p. 189,191, View in Reaxys Further information Fritzsche; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 459, View in Reaxys Further information Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys Further information Demmering; Doerr; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 19; (1964); p. 365, View in Reaxys Further information Berg; Kramarczyk; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 296, View in Reaxys Further information Martin et al.; Tetrahedron; vol. 20; (1964); p. 1505,1513, 1514, View in Reaxys Further information Luckhurst; Orgel; Molecular Physics; vol. 8; (1964); p. 117,118, View in Reaxys Further information Cookson; Wallis; Proceedings of the Chemical Society, London; (1963); p. 58, View in Reaxys Further information Nelles; Streicher; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 3; (1963); p. 188, View in Reaxys Further information Haase; Zeil; Zeitschrift fuer Naturforschung; vol. 18a; (1963); p. 828, View in Reaxys Further information Dehl; Fraenkel; Journal of Chemical Physics; vol. 39; (1963); p. 1793, View in Reaxys Further information Russel et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 4155,4156, View in Reaxys Further information Kasakowa; Syrkin; Journal of Structural Chemistry; vol. 3; (1962); p. 518; Zhurnal Strukturnoi Khimii; vol. 3; (1962); p. 536, View in Reaxys Further information Hirota; Weissman; Molecular Physics; vol. 5; (1962); p. 537, View in Reaxys Further information Mathias; Warhurst; Transactions of the Faraday Society; vol. 58; (1962); p. 948,949, View in Reaxys Further information Copeland et al.; Chemistry and Industry (London, United Kingdom); (1960); p. 98, View in Reaxys Further information Kemula; Naturwissenschaften; vol. 47; (1960); p. 514, View in Reaxys Further information Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 343,345, View in Reaxys Further information Beynon; Williams; Applied Spectroscopy; vol. 14; (1960); p. 156,158, View in Reaxys Further information Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys Further information Mathias; Warhurst; Transactions of the Faraday Society; vol. 56; (1960); p. 348, View in Reaxys Further information Beynon; Advances in Mass Spectrometry; (1959); p. 328,348, View in Reaxys Interatomic Distances and Angles (1) Description References

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Electron distribution

Mc Clelland; Transactions of the Faraday Society; vol. 57; (1961); p. 2073, View in Reaxys

Ionization Potential (2) Ionization Potential Method (Ionization [eV] Potential) 8.37

Photoelectron Spectroscopy

References Soep, Benoît; Mestdagh, Jean-Michel; Briant, Marc; Gaveau, Marc-André; Poisson, Lionel; Physical Chemistry Chemical Physics; vol. 18; nb. 33; (2016); p. 22914 - 22920, View in Reaxys Potapov et al.; High Energy Chemistry; vol. 6; (1972); p. 347; ; p. 392, View in Reaxys; Aussems et al.; Bulletin des Societes Chimiques Belges; vol. 78; (1969); p. 487, View in Reaxys; Centineo et al.; Journal of Molecular Structure; vol. 44; (1978); p. 203,204, View in Reaxys; Potapov; Sorokin; High Energy Chemistry; vol. 5; (1971); p. 435; ; p. 487, View in Reaxys; Shigorin; Potapov; Doklady Physical Chemistry; vol. 161; (1965); p. 237,238; ; p. 406, View in Reaxys

Liquid/Liquid Systems (MCS) (1) 1 of 1

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

chloroform

Abraham, Michael H.; Platts, James A.; Hersey, Anne; Leo, Albert J.; Taft, Robert W.; Journal of Pharmaceutical Sciences; vol. 88; nb. 7; (1999); p. 670 - 679, View in Reaxys Liquid/Solid Systems (MCS) (6) 1 of 6

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Temperature (Liquid/Solid Systems (MCS)) [°C]

29.99

Partner (Liquid/Solid Systems (MCS))

dibenzofuran; ethanol

Wei, Yufeng; Dang, Leping; Zhang, Xiangyang; Cui, Weimin; Wei, Hongyuan; Journal of Chemical and Engineering Data; vol. 57; nb. 4; (2012); p. 1279 - 1287, View in Reaxys 2 of 6

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Temperature (Liquid/Solid Systems (MCS)) [°C]

29.99

Partner (Liquid/Solid Systems (MCS))

9H-fluorene; ethanol

Wei, Yufeng; Dang, Leping; Zhang, Xiangyang; Cui, Weimin; Wei, Hongyuan; Journal of Chemical and Engineering Data; vol. 57; nb. 4; (2012); p. 1279 - 1287, View in Reaxys 3 of 6

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Temperature (Liquid/Solid Systems (MCS)) [°C]

29.99

Partner (Liquid/Solid Systems (MCS))

acenaphthene; ethanol

Wei, Yufeng; Dang, Leping; Zhang, Xiangyang; Cui, Weimin; Wei, Hongyuan; Journal of Chemical and Engineering Data; vol. 57; nb. 4; (2012); p. 1279 - 1287, View in Reaxys 4 of 6

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Partner (Liquid/Solid Systems (MCS))

o-terphenyl

Murthy, S. S. N.; Kumar, Deepak; Journal of the Chemical Society, Faraday Transactions; vol. 89; nb. 14; (1993); p. 2423 2428, View in Reaxys 5 of 6

Description (Liquid/Solid Systems (MCS))

Eutectic

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Temperature (Liquid/Solid Systems (MCS)) [°C]

51.2

Comment (Liquid/Solid Systems (MCS))

thermische Analyse.

Partner (Liquid/Solid Systems (MCS))

acenaphthene

Pfeiffer; Justus Liebigs Annalen der Chemie; vol. 440; (1924); p. 247,248, 259, 261, 285, 286, 289, View in Reaxys 6 of 6

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

59

Comment (Liquid/Solid Systems (MCS))

thermische Analyse.

Partner (Liquid/Solid Systems (MCS))

naphthalen-2-ylamine

Pfeiffer; Justus Liebigs Annalen der Chemie; vol. 440; (1924); p. 247,248, 259, 261, 285, 286, 289, View in Reaxys Magnetic Data (1) Description (Magnetic Data)

References

Anisotropy of mag- Bergmann et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 49; (1952); p. 474,476, netic susceptibility View in Reaxys Magnetic Susceptibility (3) Magnetic Suscepti- Comment (Magnet- References bility ic Susceptibility) [10-6cm3mol-1] -99.4

Matsunaga; Bulletin of the Chemical Society of Japan; vol. 31; (1958); p. 774, View in Reaxys

-101.4

Bergmann et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 49; (1952); p. 474,476, View in Reaxys paramagnetic.

Krishnan; Banerjee; Philosophical Transactions of the Royal Society of London; vol. <A> 234; (1935); p. 265,280, View in Reaxys; Bose; Phil. Mag.; vol. <7> 21; (1936); p. 1119,1124, View in Reaxys; Mueller; Janke; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 45; (1939); p. 380,392, View in Reaxys

Molecular Deformation (2) Description (MoReferences lecular Deformation) Force constants

Sahini; Ciurea; Revue Roumaine de Chimie; vol. 17; (1972); p. 273,276-279,282, View in Reaxys; Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Fundamental vibra- Kolev, Tsonko; Journal of Molecular Structure; vol. 349; (1995); p. 381 - 384, View in Reaxys tions Other Thermochemical Data (2) Description (Other References Thermochemical Data) Thermodynamic properties

Engel et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 7009,7010, View in Reaxys; Liberman; Batra; Journal of Chemical Physics; vol. 59; (1973); p. 3723,3727, View in Reaxys; Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys

Enthalpy

Valentine; Hammond; Journal of the American Chemical Society; vol. 94; (1972); p. 3449,3452, View in Reaxys

Solubility (MCS) (5) 1 of 5

Saturation

in solution

Alsten, John G. Van; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 38; nb. 4; (1993); p. 605 - 610, View in Reaxys 2 of 5

Temperature (Solubility (MCS)) [°C]

23

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Solvent (Solubility (MCS))

ethanol

Comment (Solubility (MCS))

100 g solvent dissolves. 7.5 g Substance.

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys 3 of 5

Temperature (Solubility (MCS)) [°C]

23

Solvent (Solubility (MCS))

diethyl ether

Comment (Solubility (MCS))

100 g solvent dissolves. 31 g Substance.

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys 4 of 5

Temperature (Solubility (MCS)) [°C]

23

Solvent (Solubility (MCS))

CCl4

Comment (Solubility (MCS))

100 g solvent dissolves. 19 g Substance.

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys 5 of 5

Temperature (Solubility (MCS)) [°C]

23

Solvent (Solubility (MCS))

benzene

Comment (Solubility (MCS))

100 g solvent dissolves. 68 g Substance.

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys Solution Behaviour (MCS) (1) 1 of 1

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 23 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

maleic anhydride-hexyl vinyl copolymer

Zdanowicz, Vincent S.; Strauss, Ulrich P.; Journal of Physical Chemistry B; vol. 102; nb. 1; (1998); p. 40 - 43, View in Reaxys Space Group (2) Space Group 61

Location

Comment (Space Group)

References

supporting informa- a = 16.0871 Å; b = Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Contion 12.5495 Å; c = gde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 18.6772 Å; Z = 16; 1592, View in Reaxys T = 294.4 K; Method = X-ray diffraction; atomic positions available

61

Iball; Zeitschrift fuer Kristallographie, Kristallgeometrie, Kristallphysik, Kristallchemie; vol. 94; (1936); p. 397,404, View in Reaxys

Transport Phenomena (MCS) (2) 1 of 2

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

dimethylformamide

Temperature (Transport Phenomena (MCS)) [°C]

24.9

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Partner (Transport Phenomena (MCS))

tetrabutylammonium perchlorate

Nagaoka, Tsutomu; Okazaki, Satoshi; Journal of Physical Chemistry; vol. 89; nb. 11; (1985); p. 2340 - 2344, View in Reaxys 2 of 2

Description (Transport Phenomena (MCS))

Diffusion

Guttenplan; Cohen; Tetrahedron Letters; (1972); p. 2163, View in Reaxys Vapour Pressure (89) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]

Comment (Vapour Pressure)

References

0.000667567

39.03

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.000862586

41.05

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00107261

42.95

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00135014

45.02

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00168767

47.04

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0020477

48.95

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00258026

51.03

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00322532

53.03

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00337534

53.72

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0039604

54.95

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0039754

55.16

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00457546

56.67

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00478548

57.02

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

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Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.00540054

58.14

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0059706

59.02

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0060006

54.69

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00637564

59.65

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00712571

56.66

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00732823

60.94

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00735074

61.13

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00840084

58.63

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.00847585

62.62

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.009976

60.64

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.009976

64.09

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0114761

65.59

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0119262

62.62

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0132763

67.05

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0138764

64.58

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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68.53

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0162766

66.56

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0176268

70.03

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0193519

68.6

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.020402

71.52

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0224272

70.56

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0233273

73.04

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0261026

72.5

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0266277

74.52

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0306781

74.52

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0306781

76.01

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0350285

77.49

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0351035

76.5

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0408041

78.98

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0408791

78.47

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.0472547

80.47

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0548305

82.42

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0630063

84.43

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0735824

86.66

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0830333

88.43

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0834083

88.41

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.0963846

90.63

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.108461

92.36

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.124587

94.58

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.141539

96.37

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.161941

98.56

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.182643

100.37

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.207621

102.51

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.234623

104.31

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.264701

106.49

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.296655

108.24

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.333858

110.44

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.376613

112.31

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.423417

114.4

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.531203

118.35

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.581683

120.25

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.657216

122.25

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.725698

124.2

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.816832

126.19

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

0.90159

128.16

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

1.0066

130.14

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

1.16862

133.09

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

1.23462

134.1

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

1.35614

136.02

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

1.51065

138.05

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 1.65467

140.01

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

1.83018

142.01

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

2.00945

143.95

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

2.21122

145.97

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

2.43174

147.9

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

2.66277

149.88

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

2.90504

151.84

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

3.21632

153.86

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

3.50285

155.79

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

3.83288

157.61

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

4.18092

159.76

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

4.53045

161.74

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

4.952

163.7

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

5.40354

165.71

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

5.88359

167.69

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.000124 - 0.018

298.2 - 343.2

Table exists

Hansen, Philip C.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 31; nb. 1; (1986); p. 1 - 3, View in Reaxys

NMR Spectroscopy (155) 1 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Dohi, Toshifumi; Takenaga, Naoko; Goto, Akihiro; Fujioka, Hiromichi; Kita, Yasuyuki; Journal of Organic Chemistry; vol.

73; nb. 18; (2008); p. 7365 - 7368, View in Reaxys; Finney, Laura C.; Mitchell, Lorna J.; Moody, Christopher J.; Green Chemistry; vol. 20; nb. 10; (2018); p. 2242 - 2249, View in Reaxys 2 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Urgoitia, Garazi; Sanmartin, Raul; Herrero, Maria Teresa; Dominguez, Esther; Green Chemistry; vol. 13; nb. 8; (2011); p.

2161 - 2166, View in Reaxys; Finney, Laura C.; Mitchell, Lorna J.; Moody, Christopher J.; Green Chemistry; vol. 20; nb.

10; (2018); p. 2242 - 2249, View in Reaxys 3 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Seo, Sangwon; Slater, Mark; Greaney, Michael F.; Organic Letters; vol. 14; nb. 10; (2012); p. 2650 - 2653, View in Reaxys; Ma, Jiaqi; Hu, Zhiming; Li, Meichao; Zhao, Weijuan; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Shen, Zhenlu; Tetrahedron; vol. 71; nb. 38; (2015); p. 6733 - 6739, View in Reaxys; Chebolu, Rajesh; Bahuguna, Ashish; Sharma, Reena; Mishra, Vivek Kumar; Ravikumar; Chemical Communications; vol. 51; nb. 84; (2015); p. 15438 - 15441, View in Reaxys; Komagawa, Hiromi; Maejima, Yukako; Nagano, Takashi; Synlett; vol. 27; nb. 5; (2016); p. 789 - 793, View in Reaxys; Furusawa, Takuma; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Tanimoto, Hiroki; Kakiuchi, Kiyomi; Chemistry - An Asian Journal; vol. 11; nb. 16; (2016); p. 2312 - 2315, View in Reaxys; Konishi, Hideyuki; Futamata, Suguru; Wang, Xi; Manabe, Kei; Advanced Synthesis and Catalysis; vol. 360; nb. 9; (2018); p. 1805 - 1809, View in Reaxys 4 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

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Location

supporting information

Maji, Arun; Rana, Sujoy; Akanksha; Maiti, Debabrata; Angewandte Chemie - International Edition; vol. 53; nb. 9; (2014); p. 2428 - 2432; Angew. Chem.; vol. 126; nb. 9; (2014); p. 2460 - 2464,5, View in Reaxys; Fukuyama, Takahide; Maetani, Shinji; Miyagawa, Kazusa; Ryu, Ilhyong; Organic Letters; vol. 16; nb. 12; (2014); p. 3216 - 3219, View in Reaxys; Wang, Guang-Zu; Li, Xing-Long; Dai, Jian-Jun; Xu, Hua-Jian; Journal of Organic Chemistry; vol. 79; nb. 15; (2014); p. 7220 7225, View in Reaxys; Baars, Hannah; Unoh, Yuto; Okada, Takeshi; Hirano, Koji; Satoh, Tetsuya; Tanaka, Ken; Bolm, Carsten; Miura, Masahiro; Chemistry Letters; vol. 43; nb. 11; (2014); p. 1782 - 1784, View in Reaxys; Song, Juan; Wei, Fuliang; Sun, Wei; Li, Ke; Tian, Yanan; Liu, Chao; Li, Yali; Xie, Linghai; Organic Letters; vol. 17; nb. 9; (2015); p. 2106 2109, View in Reaxys; Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong; Chemical Communications; vol.

52; nb. 18; (2016); p. 3635 - 3638, View in Reaxys; Devari, Shekaraiah; Rizvi, Masood Ahmad; Shah, Bhahwal Ali; Tetrahedron Letters; vol. 57; nb. 30; (2016); p. 3294 - 3297, View in Reaxys; Gülcemal, Süleyman; Gülcemal, Derya; Whitehead, George F. S.; Xiao, Jianliang; Chemistry - A European Journal; vol. 22; nb. 30; (2016); p. 10513 - 10522, View in Reaxys; Wu, Jianglong; Liu, Yan; Ma, Xiaowei; Liu, Ping; Gu, Chengzhi; Dai, Bin; Synthetic Communications; vol. 46; nb. 21; (2016); p.

1747 - 1758, View in Reaxys; Yang, Yiwen; Ma, Hongxia; Tetrahedron Letters; vol. 57; nb. 47; (2016); p. 5278 - 5280, View in Reaxys; Laha, Joydev K.; Patel, Ketul V.; Dubey, Gurudutt; Jethava, Krupal P.; Organic and Biomolecular Chemistry; vol. 15; nb. 10; (2017); p. 2199 - 2210, View in Reaxys; Wu, Jianglong; Liu, Yan; Liu, Ping; Gu, Chengzhi; Letters in Organic Chemistry; vol. 14; nb. 4; (2017); p. 254 - 260, View in Reaxys; Malekafzali; Malinovska; Patureau; New Journal of Chemistry; vol. 41; nb. 15; (2017); p. 6981 - 6985, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys; Wu, Jianglong; Liu, Yan; Ma, Xiaowei; Liu, Ping; Gu, Chengzhi; Dai, Bin; Chinese Journal of Chemistry; vol. 35; nb. 9; (2017); p. 1391 - 139, View in Reaxys; Ruzi, Rehanguli; Zhang, Muliang; Ablajan, Keyume; Zhu, Chengjian; Journal of Organic Chemistry; vol. 82; nb. 23; (2017); p. 12834 - 12839, View in Reaxys; Shipilovskikh, Sergei A.; Rubtsov, Aleksandr E.; Malkov, Andrei V.; Organic Letters; vol. 19; nb. 24; (2017); p. 6760 - 6762, View in Reaxys; Gao, Qian; Xu, Senmiao; Organic and Biomolecular Chemistry; vol. 16; nb. 2; (2018); p. 208 - 212, View in Reaxys; Huang, Tianzeng; Chen, Tieqiao; Han, Li-Biao; Journal of Organic Chemistry; vol. 83; nb. 5; (2018); p. 2959 - 2965, View in Reaxys; Laudadio, Gabriele; Govaerts, Sebastian; Wang, Ying; Ravelli, Davide; Koolman, Hannes F.; Fagnoni, Maurizio; Djuric, Stevan W.; Noël, Timothy; Angewandte Chemie - International Edition; vol. 57; nb.

15; (2018); p. 4078 - 4082; Angew. Chem.; vol. 130; nb. 15; (2018); p. 4142 - 4146,5, View in Reaxys 5 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

Maji, Arun; Rana, Sujoy; Akanksha; Maiti, Debabrata; Angewandte Chemie - International Edition; vol. 53; nb. 9; (2014); p. 2428 - 2432; Angew. Chem.; vol. 126; nb. 9; (2014); p. 2460 - 2464,5, View in Reaxys; Wang, Guang-Zu; Li, Xing-Long; Dai, Jian-Jun; Xu, Hua-Jian; Journal of Organic Chemistry; vol. 79; nb. 15; (2014); p. 7220 - 7225, View in Reaxys; Song, Juan; Wei, Fuliang; Sun, Wei; Li, Ke; Tian, Yanan; Liu, Chao; Li, Yali; Xie, Linghai; Organic Letters; vol. 17; nb. 9; (2015); p. 2106 - 2109, View in Reaxys; Dai, Wen; Lv, Ying; Wang, Lianyue; Shang, Sensen; Chen, Bo; Li, Guosong; Gao, Shuang; Chemical Communications; vol. 51; nb. 56; (2015); p. 11268 - 11271, View in Reaxys; Malekafzali; Malinovska; Patureau; New Journal of Chemistry; vol. 41; nb. 15; (2017); p. 6981 - 6985, View in Reaxys; Laudadio, Gabriele; Govaerts, Sebastian; Wang, Ying; Ravelli, Davide; Koolman, Hannes F.; Fagnoni, Maurizio; Djuric, Stevan W.; Noël, Timothy; Angewandte Chemie - International Edition; vol. 57; nb. 15; (2018); p. 4078 - 4082; Angew. Chem.; vol. 130; nb. 15; (2018); p.

4142 - 4146,5, View in Reaxys 6 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Fukuyama, Takahide; Maetani, Shinji; Miyagawa, Kazusa; Ryu, Ilhyong; Organic Letters; vol. 16; nb. 12; (2014); p. 3216 3219, View in Reaxys; Baars, Hannah; Unoh, Yuto; Okada, Takeshi; Hirano, Koji; Satoh, Tetsuya; Tanaka, Ken; Bolm, Carsten; Miura, Masahiro; Chemistry Letters; vol. 43; nb. 11; (2014); p. 1782 - 1784, View in Reaxys; Guo, Wei; Lu, LiangQiu; Wang, Yue; Wang, Ya-Ni; Chen, Jia-Rong; Xiao, Wen-Jing; Angewandte Chemie - International Edition; vol. 54; nb. 7; (2015); p. 2265 - 2269; Angew. Chem.; vol. 127; nb. 7; (2015); p. 2293 - 2297,5, View in Reaxys; Ravi Kumar, Devarapalli; Satyanarayana, Gedu; Organic Letters; vol. 17; nb. 23; (2015); p. 5894 - 5897, View in Reaxys; Sun, Denan; Li, Bijin; Lan,

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Jingbo; Huang, Quan; You, Jingsong; Chemical Communications; vol. 52; nb. 18; (2016); p. 3635 - 3638, View in Reaxys; Gülcemal, Süleyman; Gülcemal, Derya; Whitehead, George F. S.; Xiao, Jianliang; Chemistry - A European Journal; vol.

22; nb. 30; (2016); p. 10513 - 10522, View in Reaxys; Yang, Yiwen; Ma, Hongxia; Tetrahedron Letters; vol. 57; nb. 47; (2016); p. 5278 - 5280, View in Reaxys; Laha, Joydev K.; Patel, Ketul V.; Dubey, Gurudutt; Jethava, Krupal P.; Organic and Biomolecular Chemistry; vol. 15; nb. 10; (2017); p. 2199 - 2210, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys; Ramanathan, Mani; Liu, Yi-Hung; Peng, Shie-Ming; Liu, Shiuh-Tzung; Organic Letters; vol. 19; nb. 21; (2017); p. 5840 - 5843, View in Reaxys; Ruzi, Rehanguli; Zhang, Muliang; Ablajan, Keyume; Zhu, Chengjian; Journal of Organic Chemistry; vol. 82; nb. 23; (2017); p. 12834 - 12839, View in Reaxys; Shipilovskikh, Sergei A.; Rubtsov, Aleksandr E.; Malkov, Andrei V.; Organic Letters; vol. 19; nb. 24; (2017); p. 6760 - 6762, View in Reaxys; Gao, Qian; Xu, Senmiao; Organic and Biomolecular Chemistry; vol. 16; nb. 2; (2018); p. 208 - 212, View in Reaxys; Huang, Tianzeng; Chen, Tieqiao; Han, Li-Biao; Journal of Organic Chemistry; vol. 83; nb. 5; (2018); p. 2959 - 2965, View in Reaxys 7 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

23

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Konishi, Hideyuki; Futamata, Suguru; Wang, Xi; Manabe, Kei; Advanced Synthesis and Catalysis; vol. 360; nb. 9; (2018); p. 1805 - 1809, View in Reaxys 8 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

Paragraph 0064; 0068; 0072

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys 9 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

Paragraph 0064; 0068; 0072

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys 10 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Location

supporting information

Yi, Chae S.; Kwon, Ki-Hyeok; Lee, Do W.; Organic Letters; vol. 11; nb. 7; (2009); p. 1567 - 1569, View in Reaxys; Zarei, Amin; Khazdooz, Leila; Aghaei, Hamidreza; Gheisari, Mohammad Mehdi; Alizadeh, Shahrzad; Golestanifar, Laleh; Tetrahedron; vol. 73; nb. 49; (2017); p. 6954 - 6961, View in Reaxys 11 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys; Wei, Baosheng; Li, Heng; Zhang, Wen-Xiong; Xi, Zhenfeng; Organometallics; vol. 34; nb. 7; (2015); p.

1339 - 1344, View in Reaxys; Wang, Xiaolu; Liu, Mengjia; Wang, Yuqing; Fan, Hongyan; Wu, Jie; Huang, Chao; Hou, Hongwei; Inorganic Chemistry; vol. 56; nb. 21; (2017); p. 13329 - 13336, View in Reaxys 12 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Seo, Sangwon; Slater, Mark; Greaney, Michael F.; Organic Letters; vol. 14; nb. 10; (2012); p. 2650 - 2653, View in Reaxys; Seth, Saona; Jhulki, Samik; Moorthy, Jarugu Narasimha; European Journal of Organic Chemistry; nb. 12; (2013); p. 2445 2452, View in Reaxys; Ma, Jiaqi; Hu, Zhiming; Li, Meichao; Zhao, Weijuan; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Shen, Zhenlu; Tetrahedron; vol. 71; nb. 38; (2015); p. 6733 - 6739, View in Reaxys; Chebolu, Rajesh; Bahuguna, Ashish; Sharma, Reena; Mishra, Vivek Kumar; Ravikumar; Chemical Communications; vol. 51; nb. 84; (2015); p. 15438 15441, View in Reaxys; Komagawa, Hiromi; Maejima, Yukako; Nagano, Takashi; Synlett; vol. 27; nb. 5; (2016); p. 789 793, View in Reaxys; Furusawa, Takuma; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Tanimoto, Hiroki; Kakiuchi, Kiyomi; Chemistry - An Asian Journal; vol. 11; nb. 16; (2016); p. 2312 - 2315, View in Reaxys; Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p. 6972 - 6977, View in Reaxys 13 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 2745, View in Reaxys; Guo, Wei; Lu, Liang-Qiu; Wang, Yue; Wang, Ya-Ni; Chen, Jia-Rong; Xiao, Wen-Jing; Angewandte Chemie - International Edition; vol. 54; nb. 7; (2015); p. 2265 - 2269; Angew. Chem.; vol. 127; nb. 7; (2015); p. 2293 - 2297,5, View in Reaxys; Wang, Xing; Chen, Rui-Xi; Wei, Zeng-Feng; Zhang, Chen-Yang; Tu, Hai-Yang; Zhang, Ai-Dong; Journal of Organic Chemistry; vol. 81; nb. 1; (2016); p. 238 - 249, View in Reaxys; Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys 14 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, View in Reaxys; Liu, Li; Qiang, Jian; Bai, Shuhua; Li, Yang; Miao, Chunbao; Li, Jian; Applied Organometallic Chemistry; vol. 31; nb. 12; (2017); Art.No: E3817, View in Reaxys 15 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Lim, Chae Mi; Ha, Su Jeong; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 12; (2012); p. 4258 4260, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, View in Reaxys; Lim, Minkyung; Oh, Seungchan; Rhee, Hakjune; Bulletin of the Korean Chemical Society; vol. 32; (2011); p. 3179 - 3182, View in Reaxys; Obst, Martin; König, Burkhard; Beilstein Journal of Organic Chemistry; vol. 12; (2016); p.

2358 - 2363, View in Reaxys; Liu, Li; Qiang, Jian; Bai, Shuhua; Li, Yang; Miao, Chunbao; Li, Jian; Applied Organometallic Chemistry; vol. 31; nb. 12; (2017); Art.No: E3817, View in Reaxys 16 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

22.84

Frequency (NMR Spectro- 400.1 scopy) [MHz] Location

supporting information

Srivastava, Manish; Srivastava, Anamika; Goyal, Ashu; Mishra, Aakanksha; Tomer, Preeti; Dwivedi, Jaya; Kishore; Journal of Physical Organic Chemistry; vol. 30; nb. 2; (2017); Art.No: E3602, View in Reaxys 17 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 151 scopy) [MHz] Location

supporting information

Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys 18 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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2018-06-21 20:37:19

Laha, Joydev K.; Jethava, Krupal P.; Patel, Sagarkumar; Patel, Ketul V.; Journal of Organic Chemistry; vol. 82; nb. 1; (2017); p. 76 - 85, View in Reaxys 19 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 126 scopy) [MHz] Location

supporting information

Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p.

6972 - 6977, View in Reaxys 20 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Location

Paragraph 0088

Patent; Nanjing University of Posts and Telecommunications; Song Juan; Wei Fuliang; Sun Wei; Li Yali; Xie Linghai; (32 pag.); CN104844400; (2017); (B) Chinese, View in Reaxys 21 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Location

Paragraph 0088

Patent; Nanjing University of Posts and Telecommunications; Song Juan; Wei Fuliang; Sun Wei; Li Yali; Xie Linghai; (32 pag.); CN104844400; (2017); (B) Chinese, View in Reaxys 22 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25.84

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Ramanathan, Mani; Liu, Yi-Hung; Peng, Shie-Ming; Liu, Shiuh-Tzung; Organic Letters; vol. 19; nb. 21; (2017); p. 5840 5843, View in Reaxys 23 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys; Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys; Hossain, Md. Munkir; Shyu, Shin-Guang; Tetrahedron; vol. 72; nb. 29; (2016); p. 4252 - 4257, View in Reaxys 24 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

60/144

2018-06-21 20:37:19

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 2745, View in Reaxys; Wang, Xing; Chen, Rui-Xi; Wei, Zeng-Feng; Zhang, Chen-Yang; Tu, Hai-Yang; Zhang, Ai-Dong; Journal of Organic Chemistry; vol. 81; nb. 1; (2016); p. 238 - 249, View in Reaxys 25 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Puenner, Florian; Schieven, Justin; Hilt, Gerhard; Organic Letters; vol. 15; nb. 18; (2013); p. 4888 - 4891, View in Reaxys; Hossain, Md. Munkir; Shyu, Shin-Guang; Tetrahedron; vol. 72; nb. 29; (2016); p. 4252 - 4257, View in Reaxys; Mishra, Kalpana; Pandey, Ashok Kumar; Singh, Jay Bahadur; Singh, Radhey M.; Organic and Biomolecular Chemistry; vol. 14; nb. 26; (2016); p. 6328 - 6336, View in Reaxys; Alanthadka, Anitha; Devi, E. Sankari; Nagarajan, Subbiah; Sridharan, Vellaisamy; Suvitha, Ambigapathy; Maheswari, C. Uma; European Journal of Organic Chemistry; vol. 2016; nb. 28; (2016); p. 4872 - 4880, View in Reaxys; Wang, Huiqiao; Wang, Zhong; Huang, Hongchun; Tan, Jiajing; Xu, Kun; Organic Letters; vol. 18; nb. 21; (2016); p. 5680 - 5683, View in Reaxys 26 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Fukuda, Naohiro; Izumi, Minoru; Ikemoto, Tomomi; Tetrahedron Letters; vol. 56; nb. 25; (2015); p. 3905 - 3908, View in Reaxys; Evoniuk, Christopher J.; Hill, Sean P.; Hanson, Kenneth; Alabugin, Igor V.; Chemical Communications; vol. 52; nb. 44; (2016); p. 7138 - 7141, View in Reaxys 27 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Cai, Zhiqiang; Hou, Xu; Hou, Ling; Hu, Zhiquan; Zhang, Bo; Jin, Zhengsheng; Synlett; vol. 27; nb. 3; (2016); p. 395 398; Art.No: ST-2015-W0682-L, View in Reaxys 28 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

61/144

2018-06-21 20:37:19

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Evoniuk, Christopher J.; Hill, Sean P.; Hanson, Kenneth; Alabugin, Igor V.; Chemical Communications; vol. 52; nb. 44; (2016); p. 7138 - 7141, View in Reaxys 29 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

20.34

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Bhardwaj, Madhvi; Sharma, Harsha; Paul, Satya; Clark, James H.; New Journal of Chemistry; vol. 40; nb. 6; (2016); p.

4952 - 4961, View in Reaxys 30 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.14

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Bhardwaj, Madhvi; Sharma, Harsha; Paul, Satya; Clark, James H.; New Journal of Chemistry; vol. 40; nb. 6; (2016); p.

4952 - 4961, View in Reaxys 31 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Mishra, Kalpana; Pandey, Ashok Kumar; Singh, Jay Bahadur; Singh, Radhey M.; Organic and Biomolecular Chemistry; vol. 14; nb. 26; (2016); p. 6328 - 6336, View in Reaxys; Alanthadka, Anitha; Devi, E. Sankari; Nagarajan, Subbiah; Sridharan, Vellaisamy; Suvitha, Ambigapathy; Maheswari, C. Uma; European Journal of Organic Chemistry; vol. 2016; nb. 28; (2016); p. 4872 - 4880, View in Reaxys; Wang, Huiqiao; Wang, Zhong; Huang, Hongchun; Tan, Jiajing; Xu, Kun; Organic Letters; vol. 18; nb. 21; (2016); p. 5680 - 5683, View in Reaxys 32 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

62/144

2018-06-21 20:37:19

Temperature (NMR Spectroscopy) [°C]

21.8

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Furusawa, Takuma; Morimoto, Tsumoru; Oka, Nagato; Tanimoto, Hiroki; Nishiyama, Yasuhiro; Kakiuchi, Kiyomi; Chemistry Letters; vol. 45; nb. 4; (2016); p. 406 - 408, View in Reaxys 33 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

18.7

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Furusawa, Takuma; Morimoto, Tsumoru; Oka, Nagato; Tanimoto, Hiroki; Nishiyama, Yasuhiro; Kakiuchi, Kiyomi; Chemistry Letters; vol. 45; nb. 4; (2016); p. 406 - 408, View in Reaxys 34 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

20.84

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Guo, Shu; Zeng, Renyou; Li, Caiye; Synthetic Communications; vol. 46; nb. 17; (2016); p. 1446 - 1453, View in Reaxys 35 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.84

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Guo, Shu; Zeng, Renyou; Li, Caiye; Synthetic Communications; vol. 46; nb. 17; (2016); p. 1446 - 1453, View in Reaxys 36 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

63/144

2018-06-21 20:37:19

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys; Wei, Baosheng; Li, Heng; Zhang, Wen-Xiong; Xi, Zhenfeng; Organometallics; vol. 34; nb. 7; (2015); p.

1339 - 1344, View in Reaxys 37 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Location

supporting information

Li, Hu; Zhu, Ru-Yi; Shi, Wen-Juan; He, Ke-Han; Shi, Zhang-Jie; Organic Letters; vol. 14; nb. 18; (2012); p. 4850 - 4853,4, View in Reaxys; Motiwala, Hashim F.; Vekariya, Rakesh H.; Aubé, Jeffrey; Organic Letters; vol. 17; nb. 21; (2015); p. 5484 - 5487, View in Reaxys 38 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Li, Hu; Zhu, Ru-Yi; Shi, Wen-Juan; He, Ke-Han; Shi, Zhang-Jie; Organic Letters; vol. 14; nb. 18; (2012); p. 4850 - 4853,4, View in Reaxys; Motiwala, Hashim F.; Vekariya, Rakesh H.; Aubé, Jeffrey; Organic Letters; vol. 17; nb. 21; (2015); p. 5484 - 5487, View in Reaxys 39 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Ang, Wei Jie; Lam, Yulin; Organic and Biomolecular Chemistry; vol. 13; nb. 4; (2015); p. 1048 - 1052, View in Reaxys 40 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 126 scopy) [MHz] Location

supporting information

Ang, Wei Jie; Lam, Yulin; Organic and Biomolecular Chemistry; vol. 13; nb. 4; (2015); p. 1048 - 1052, View in Reaxys 41 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

64/144

2018-06-21 20:37:19

Temperature (NMR Spectroscopy) [°C]

20

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Urgoitia; Sanmartin; Herrero; Domínguez; Chemical Communications; vol. 51; nb. 23; (2015); p. 4799 - 4802, View in Reaxys 42 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

20

Frequency (NMR Spectro- 75.4 scopy) [MHz] Location

supporting information

Urgoitia; Sanmartin; Herrero; Domínguez; Chemical Communications; vol. 51; nb. 23; (2015); p. 4799 - 4802, View in Reaxys 43 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 151 scopy) [MHz] Location

supporting information

Fukuda, Naohiro; Izumi, Minoru; Ikemoto, Tomomi; Tetrahedron Letters; vol. 56; nb. 25; (2015); p. 3905 - 3908, View in Reaxys 44 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Dai, Wen; Lv, Ying; Wang, Lianyue; Shang, Sensen; Chen, Bo; Li, Guosong; Gao, Shuang; Chemical Communications; vol. 51; nb. 56; (2015); p. 11268 - 11271, View in Reaxys 45 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.84

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

65/144

2018-06-21 20:37:19

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Ravi Kumar, Devarapalli; Satyanarayana, Gedu; Organic Letters; vol. 17; nb. 23; (2015); p. 5894 - 5897, View in Reaxys 46 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Fang, Xin-Qiang; Xu, Hua-Jian; Jiang, Hong; Liu, You-Cheng; Fu, Yao; Wu, Yun-Dong; Tetrahedron Letters; vol. 50; nb.

3; (2009); p. 312 - 315, View in Reaxys; Kidwai, Mazaahir; Bhardwaj, Saurav; Applied Catalysis A: General; vol. 387; nb.

1-2; (2010); p. 1 - 4, View in Reaxys; Geraghty, Niall W.A.; McArdle, Patrick; Mullen, Laverne M.A.; Tetrahedron; vol. 67; nb. 19; (2011); p. 3546 - 3552, View in Reaxys; Lv, Xiao-Ming; Kong, Ling-Jie; Lin, Qi; Liu, Xiao-Feng; Zhou, Ya-Ming; Jia, Yu; Synthetic Communications; vol. 41; nb. 21; (2011); p. 3215 - 3222, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys 47 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectro- 303 scopy) [MHz] Location

supporting information

Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys 48 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 76.2 scopy) [MHz] Location

supporting information

Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys; Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys 49 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

66/144

2018-06-21 20:37:19

Sawama, Yoshinari; Morita, Kosuke; Yamada, Tsuyoshi; Nagata, Saori; Yabe, Yuki; Monguchi, Yasunari; Sajiki, Hironao; Green Chemistry; vol. 16; nb. 7; (2014); p. 3439 - 3443, View in Reaxys 50 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

water-d2; d(4)-methanol

Ghosh, Indrajit; Mukhopadhyay, Arindam; Koner, Apurba Lal; Samanta, Subhas; Nau, Werner M.; Moorthy, Jarugu Narasimha; Physical Chemistry Chemical Physics; vol. 16; nb. 31; (2014); p. 16436 - 16445, View in Reaxys 51 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 250 scopy) [MHz] Bellardita; Loddo; Mele; Panzeri; Parrino; Pibiri; Palmisano; RSC Advances; vol. 4; nb. 77; (2014); p. 40859 - 40864, View in Reaxys 52 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 62.5 scopy) [MHz] Bellardita; Loddo; Mele; Panzeri; Parrino; Pibiri; Palmisano; RSC Advances; vol. 4; nb. 77; (2014); p. 40859 - 40864, View in Reaxys 53 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys; Nguyen, Thanh Vinh; Hall, Michael; Tetrahedron Letters; vol. 55; nb. 50; (2014); p. 6895 - 6898, View in Reaxys 54 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

67/144

2018-06-21 20:37:19

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys; Nguyen, Thanh Vinh; Hall, Michael; Tetrahedron Letters; vol. 55; nb. 50; (2014); p. 6895 - 6898, View in Reaxys 55 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys 56 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectro- 303 scopy) [MHz] Location

supporting information

Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys 57 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Wang, Jin-Quan; He, Liang-Nian; New Journal of Chemistry; vol. 33; nb. 8; (2009); p. 1637 - 1640, View in Reaxys; Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys; Puenner, Florian; Schieven, Justin; Hilt, Gerhard; Organic Letters; vol. 15; nb. 18; (2013); p. 4888 - 4891, View in Reaxys 58 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Kidwai, Mazaahir; Bhardwaj, Saurav; Applied Catalysis A: General; vol. 387; nb. 1-2; (2010); p. 1 - 4, View in Reaxys; Geraghty, Niall W.A.; McArdle, Patrick; Mullen, Laverne M.A.; Tetrahedron; vol. 67; nb. 19; (2011); p. 3546 - 3552, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 2970, View in Reaxys

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

68/144

2018-06-21 20:37:19

59 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] An, Gwangil; Ahn, Hyunseok; De Castro, Kathlia A.; Rhee, Hakjune; Synthesis; nb. 3; (2010); p. 477 - 485; Art.No: F19009SS, View in Reaxys; Zhang, Xin; Ji, Xuan; Jiang, Shanshan; Liu, Lili; Weeks, Brandon L.; Zhang, Zhao; Green Chemistry; vol. 13; nb. 7; (2011); p. 1891 - 1896, View in Reaxys; Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p.

6488 - 6494, View in Reaxys 60 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Xu, Yuan; Yang, Zhenping; Hu, Jiantao; Yan, Jie; Synthesis (Germany); vol. 45; nb. 3; (2013); p. 370 - 374; Art.No: SS-2012-F0873-OP, View in Reaxys; Fukuda, Naohiro; Kajiwara, Takeshi; Katou, Tomoaki; Majima, Keisuke; Ikemoto, Tomomi; Synlett; vol. 24; nb. 11; (2013); p. 1438 - 1442; Art.No: ST-2013-U0273-L, View in Reaxys 61 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Xu, Yuan; Yang, Zhenping; Hu, Jiantao; Yan, Jie; Synthesis (Germany); vol. 45; nb. 3; (2013); p. 370 - 374; Art.No: SS-2012-F0873-OP, View in Reaxys; Fukuda, Naohiro; Kajiwara, Takeshi; Katou, Tomoaki; Majima, Keisuke; Ikemoto, Tomomi; Synlett; vol. 24; nb. 11; (2013); p. 1438 - 1442; Art.No: ST-2013-U0273-L, View in Reaxys 62 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys 63 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

69/144

2018-06-21 20:37:19

Frequency (NMR Spectro- 300 scopy) [MHz] Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys 64 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectro- 75.5 scopy) [MHz] Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys 65 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys; Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys; Cosner, Casey C.; Cabrera, Pablo J.; Byrd, Katherine M.; Adams Thomas, Asia M.; Helquist, Paul; Organic Letters; vol. 13; nb. 8; (2011); p.

2071 - 2073, View in Reaxys; Havare, Nizam; Plattner, Dietmar A.; Organic Letters; vol. 14; nb. 19; (2012); p. 5078 - 5081,4, View in Reaxys 66 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Wang, Congyang; Piel, Isabel; Glorius, Frank; Journal of the American Chemical Society; vol. 131; (2009); p. 4194 - 4195, View in Reaxys; Tilly, David; Fu, Jian-Min; Zhao, Bao-Ping; Alessi, Manlio; Castanet, Anne-Sophie; Snieckus, Victor; Mortier, Jacques; Organic Letters; vol. 12; nb. 1; (2010); p. 68 - 71, View in Reaxys; Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 67 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

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Wang, Congyang; Piel, Isabel; Glorius, Frank; Journal of the American Chemical Society; vol. 131; (2009); p. 4194 - 4195, View in Reaxys; Tilly, David; Fu, Jian-Min; Zhao, Bao-Ping; Alessi, Manlio; Castanet, Anne-Sophie; Snieckus, Victor; Mortier, Jacques; Organic Letters; vol. 12; nb. 1; (2010); p. 68 - 71, View in Reaxys; Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys; Lockner, Jonathan W.; Dixon, Darryl D.; Risgaard, Rune; Baran, Phil S.; Organic Letters; vol. 13; nb. 20; (2011); p. 5628 - 5631, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 68 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys; Nagano, Takashi; Kobayashi, Shu; Chemistry Letters; vol.

37; nb. 10; (2008); p. 1042 - 1043, View in Reaxys; Cui, Li-Qian; Liu, Kai; Zhang, Chi; Organic and Biomolecular Chemistry; vol. 9; nb. 7; (2011); p. 2258 - 2265, View in Reaxys; Su, Yijin; Zhang, Liangren; Jiao, Ning; Organic Letters; vol. 13; nb.

9; (2011); p. 2168 - 2171, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys 69 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys; Nagano, Takashi; Kobayashi, Shu; Chemistry Letters; vol.

37; nb. 10; (2008); p. 1042 - 1043, View in Reaxys; Wang, Jin-Quan; He, Liang-Nian; New Journal of Chemistry; vol. 33; nb.

8; (2009); p. 1637 - 1640, View in Reaxys; Cui, Li-Qian; Liu, Kai; Zhang, Chi; Organic and Biomolecular Chemistry; vol. 9; nb. 7; (2011); p. 2258 - 2265, View in Reaxys; Su, Yijin; Zhang, Liangren; Jiao, Ning; Organic Letters; vol. 13; nb. 9; (2011); p. 2168 - 2171, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol.

17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys; Wang, Lianyue; Li, Jun; Yang, Hua; Lv, Ying; Gao, Shuang; Journal of Organic Chemistry; vol. 77; nb. 1; (2012); p. 790 - 794, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys 70 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Location

supporting information

Wang, Lianyue; Li, Jun; Yang, Hua; Lv, Ying; Gao, Shuang; Journal of Organic Chemistry; vol. 77; nb. 1; (2012); p. 790 794, View in Reaxys 71 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

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Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.74

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Li, Dan-Dan; Yuan, Ting-Ting; Wang, Guan-Wu; Journal of Organic Chemistry; vol. 77; nb. 7; (2012); p. 3341 - 3347, View in Reaxys 72 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Location

supporting information

Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys 73 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys 74 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

benzene-d6

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte Chemie - International Edition; vol.

51; nb. 39; (2012); p. 9926 - 9930, View in Reaxys 75 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

benzene-d6

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte Chemie - International Edition; vol.

51; nb. 39; (2012); p. 9926 - 9930, View in Reaxys 76 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

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Original Text (NMR Spectroscopy)

1H

Location

supporting information

Signals [ppm]

7.29; 7.47 - 7.54; 7.66

Kind of signal

t, J=7.3 Hz, 2H; m, 4H; d, J=7.3 Hz, 2H

NMR (CDCl3, 400 MHz) β 7.29 (t, J=7.3 Hz, 2H), 7.47-7.54 (m, 4H), 7.66 (d, J=7.3 Hz, 2H)

Parida, Keshaba Nanda; Jhulki, Samik; Mandal, Susovan; Moorthy, Jarugu Narasimha; Tetrahedron; vol. 68; nb. 47; (2012); p. 9763 - 9768,6, View in Reaxys; Parida, Keshaba Nanda; Jhulki, Samik; Mandal, Susovan; Moorthy, Jarugu Narasimha; Tetrahedron; vol. 68; nb. 47; (2012); p. 9763 - 9768, View in Reaxys 77 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Tandon, Praveen K.; Singh, Santosh B.; Singh, Satpal; Kesarwani, Bhawana; Journal of the Indian Chemical Society; vol.

89; nb. 10; (2012); p. 1363 - 1367, View in Reaxys 78 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys 79 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Liu, Tao-Ping; Liao, Yuan-Xi; Xing, Chun-Hui; Hu, Qiao-Sheng; Organic Letters; vol. 13; nb. 9; (2011); p. 2452 - 2455, View in Reaxys 80 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Liu, Tao-Ping; Liao, Yuan-Xi; Xing, Chun-Hui; Hu, Qiao-Sheng; Organic Letters; vol. 13; nb. 9; (2011); p. 2452 - 2455, View in Reaxys

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81 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.5 scopy) [MHz] Zhang, Xin; Ji, Xuan; Jiang, Shanshan; Liu, Lili; Weeks, Brandon L.; Zhang, Zhao; Green Chemistry; vol. 13; nb. 7; (2011); p. 1891 - 1896, View in Reaxys 82 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300.1 scopy) [MHz] Location

supporting information

Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys 83 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.5 scopy) [MHz] Location

supporting information

Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys 84 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys; Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys 85 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.74

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

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Wang, Azhong; Jiang, Huanfeng; Journal of Organic Chemistry; vol. 75; nb. 7; (2010); p. 2321 - 2326, View in Reaxys 86 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.94

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Wang, Azhong; Jiang, Huanfeng; Journal of Organic Chemistry; vol. 75; nb. 7; (2010); p. 2321 - 2326, View in Reaxys 87 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Catir, Mustafa; Kilic, Hamdullah; Synlett; nb. 9; (2010); p. 1319 - 1322, View in Reaxys 88 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 50 scopy) [MHz] Catir, Mustafa; Kilic, Hamdullah; Synlett; nb. 9; (2010); p. 1319 - 1322, View in Reaxys 89 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Location

supporting information

Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys 90 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 50 scopy) [MHz] Location

supporting information

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Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys 91 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Location

supporting information

Yi, Chae S.; Kwon, Ki-Hyeok; Lee, Do W.; Organic Letters; vol. 11; nb. 7; (2009); p. 1567 - 1569, View in Reaxys 92 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

23.7

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Dohi, Toshifumi; Takenaga, Naoko; Goto, Akihiro; Fujioka, Hiromichi; Kita, Yasuyuki; Journal of Organic Chemistry; vol.

73; nb. 18; (2008); p. 7365 - 7368, View in Reaxys 93 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Jain, Nidhi; Kumar, Anil; Chauhan, Shive M.S.; Tetrahedron Letters; vol. 46; nb. 15; (2005); p. 2599 - 2602, View in Reaxys; Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys 94 of 155

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys 95 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz]

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Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys 96 of 155

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

tetradeuteriomethanol

Frequency (NMR Spectro- 500 scopy) [MHz] Nakamura, Hideyuki; Tomonaga, Yuzo; Miyata, Kana; Uchida, Mitsuo; Terao, Yoshiyasu; Environmental Science and Technology; vol. 41; nb. 7; (2007); p. 2190 - 2195, View in Reaxys 97 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

tetradeuteriomethanol

Frequency (NMR Spectro- 500 scopy) [MHz] Nakamura, Hideyuki; Tomonaga, Yuzo; Miyata, Kana; Uchida, Mitsuo; Terao, Yoshiyasu; Environmental Science and Technology; vol. 41; nb. 7; (2007); p. 2190 - 2195, View in Reaxys 98 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Tilly, David; Samanta, Subhendu S.; De, Asish; Castanet, Anne-Sophie; Mortier, Jacques; Organic Letters; vol. 7; nb. 5; (2005); p. 827 - 830, View in Reaxys; Qian, Weixing; Jin, Erlei; Bao, Weiliang; Zhang, Yongmin; Angewandte Chemie International Edition; vol. 44; nb. 6; (2005); p. 952 - 955, View in Reaxys; Sano, Yuki; Tanaka, Takanori; Hayashi, Masahiko; Chemistry Letters; vol. 36; nb. 12; (2007); p. 1414 - 1415, View in Reaxys 99 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100.6 scopy) [MHz] Sano, Yuki; Tanaka, Takanori; Hayashi, Masahiko; Chemistry Letters; vol. 36; nb. 12; (2007); p. 1414 - 1415, View in Reaxys 100 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Chvatal, Ivan; Vymetal, Jan; Pecha, Jaroslav; Simanek, Vilim; Dolejs, Ladislav; et al.; Collection of Czechoslovak Chemical Communications; vol. 48; nb. 1; (1983); p. 112 - 122, View in Reaxys; Diesveld, J. W.; Borkent, J.H.; Laarhoven, W. H.; Tetrahedron; vol. 38; nb. 12; (1982); p. 1803 - 1808, View in Reaxys; Chatani; Kamitani; Oshita; Fukumoto; Murai; Journal of the American Chemical Society; vol. 123; nb. 50; (2001); p. 12686 - 12687, View in Reaxys; Ibrahim, Yehia A.; Al-Awadi, Nouria A.; Kual, Kamini; Tetrahedron; vol. 59; nb. 29; (2003); p. 5425 - 5430, View in Reaxys; Yang, Guanyu; Zhang, Qiaohong; Miao, Hong; Tong, Xinli; Xu, Jie; Organic Letters; vol. 7; nb. 2; (2005); p. 263 - 266, View in Reaxys; Oota, Atsushi;

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Imai, Toshinobu; Yamazaki, Ayumi; Oba, Toru; Karikomi, Michinori; Minabe, Masahiro; Bulletin of the Chemical Society of Japan; vol. 79; nb. 2; (2006); p. 333 - 335, View in Reaxys; Singh, Krishna Nand; Kumar, Rajesh; Shukla, Ajay Kumar; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 46; nb. 8; (2007); p. 1347 - 1351, View in Reaxys 101 of 155

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol.

45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys 102 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol.

45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys 103 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol.

45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys 104 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz] Tilly, David; Samanta, Subhendu S.; De, Asish; Castanet, Anne-Sophie; Mortier, Jacques; Organic Letters; vol. 7; nb. 5; (2005); p. 827 - 830, View in Reaxys 105 of 155

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

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Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Tilly, David; Samanta, Subhendu S.; De, Asish; Castanet, Anne-Sophie; Mortier, Jacques; Organic Letters; vol. 7; nb. 5; (2005); p. 827 - 830, View in Reaxys 106 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CD3CN

Frequency (NMR Spectro- 50.3 scopy) [MHz] Kolano, Christoph; Bucher, Goetz; Schade, Olaf; Grote, Dirk; Sander, Wolfram; Journal of Organic Chemistry; vol. 70; nb.

17; (2005); p. 6609 - 6615, View in Reaxys 107 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Boberg, Friedrich; Schmidt, Wolfgang; Garming, Alfons; Phosphorus and Sulfur and the Related Elements; vol. 21; (1984); p. 315 - 320, View in Reaxys; Shaabani, Ahmad; Mirzaei, Peiman; Naderi, Soheila; Lee, Donald G.; Tetrahedron; vol. 60; nb. 50; (2004); p. 11415 - 11420, View in Reaxys 108 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

acetone-d6

Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectro- 270 scopy) [MHz] Kamata, Keigo; Kasai, Jun; Yamaguchi, Kazuya; Mizuno, Noritaka; Organic Letters; vol. 6; nb. 20; (2004); p. 3577 - 3580, View in Reaxys 109 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

acetone-d6

Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectro- 67.5 scopy) [MHz] Kamata, Keigo; Kasai, Jun; Yamaguchi, Kazuya; Mizuno, Noritaka; Organic Letters; vol. 6; nb. 20; (2004); p. 3577 - 3580, View in Reaxys 110 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

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Olah, Georgen A.; Nakajima, Tadashi; Prakash, G. K. Surya; Angewandte Chemie; vol. 92; nb. 10; (1980); p. 837 - 838, View in Reaxys; Majumder; Chakraborti; Journal of the Indian Chemical Society; vol. 66; nb. 11; (1989); p. 834 - 837, View in Reaxys; Ibrahim, Yehia A.; Al-Awadi, Nouria A.; Kual, Kamini; Tetrahedron; vol. 59; nb. 29; (2003); p. 5425 5430, View in Reaxys 111 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

benzene-d6

Branch, Catherine S.; Bott, Simon G.; Barron, Andrew R.; Journal of Organometallic Chemistry; vol. 666; nb. 1-2; (2003); p. 23 - 34, View in Reaxys 112 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

26.85

Frequency (NMR Spectro- 400.13 scopy) [MHz] Abraham, Raymond J.; Mobli, Mehdi; Smith, Richard J.; Magnetic Resonance in Chemistry; vol. 41; nb. 1; (2003); p. 26 36, View in Reaxys 113 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

dimethylsulfoxide

Temperature (NMR Spectroscopy) [°C]

26.85

Frequency (NMR Spectro- 400.13 scopy) [MHz] Abraham, Raymond J.; Mobli, Mehdi; Smith, Richard J.; Magnetic Resonance in Chemistry; vol. 41; nb. 1; (2003); p. 26 36, View in Reaxys 114 of 155

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

CDCl3

Chatani; Kamitani; Oshita; Fukumoto; Murai; Journal of the American Chemical Society; vol. 123; nb. 50; (2001); p. 12686 - 12687, View in Reaxys; Ibrahim, Yehia A.; Al-Awadi, Nouria A.; Kual, Kamini; Tetrahedron; vol. 59; nb. 29; (2003); p.

5425 - 5430, View in Reaxys 115 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 80 scopy) [MHz]

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Lukasiewicz, Marcin; Bogdal, Dariusz; Pielichowski, Jan; Advanced Synthesis and Catalysis; vol. 345; nb. 12; (2003); p.

1269 - 1272, View in Reaxys 116 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

20

Sancassan, Fernando; Petrillo, Giovanni; Abraham, Raymond J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 11; (1995); p. 1965 - 1972, View in Reaxys; Kalinovskii; Pogorelov; Gelbshtein; Akhmetov; Russian Journal of General Chemistry; vol. 71; nb. 9; (2001); p. 1457 - 1462, View in Reaxys 117 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

20

Sancassan, Fernando; Petrillo, Giovanni; Abraham, Raymond J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 11; (1995); p. 1965 - 1972, View in Reaxys; Kalinovskii; Pogorelov; Gelbshtein; Akhmetov; Russian Journal of General Chemistry; vol. 71; nb. 9; (2001); p. 1457 - 1462, View in Reaxys 118 of 155

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

20

Kalinovskii; Pogorelov; Gelbshtein; Akhmetov; Russian Journal of General Chemistry; vol. 71; nb. 9; (2001); p. 1457 - 1462, View in Reaxys 119 of 155

Description (NMR Spectroscopy)

Spin-lattice relaxation time (T1)

Sterk et al.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 118; (1979); p. 151,155, View in Reaxys; Wilson, Nancy K.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 12 - 15, View in Reaxys; Coletta, Flaviano; Gazzetta Chimica Italiana; vol. 127; nb. 4; (1997); p. 221 - 226, View in Reaxys 120 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

25

Coletta, Flaviano; Gazzetta Chimica Italiana; vol. 127; nb. 4; (1997); p. 221 - 226, View in Reaxys 121 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

solid

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Temperature (NMR Spectroscopy) [°C]

22

Fung; Tong, Tat-Hung; Dollase, Thilo; Magnuson, Matthew L.; Journal of Magnetic Resonance - Series A; vol. 123; nb. 1; (1996); p. 56 - 63, View in Reaxys 122 of 155

Description (NMR Spectroscopy)

NMR with shift reagents

Wolkowski,Z.W.; Tetrahedron Letters; (1971); p. 821 - 824, View in Reaxys; Ammon,H.L.; Mazzocchi,P.H.; Colicelli,E.J.; Organic Magnetic Resonance; vol. 11; (1978); p. 1, View in Reaxys; Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys; Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol.

36; (1980); p. 23 - 28, View in Reaxys; Abraham, Raymond J.; Bergen, Helen A.; Chadwick, Derek J.; Sancassan, Fernando; Journal of the Chemical Society, Chemical Communications; nb. 17; (1982); p. 998 - 1000, View in Reaxys; Sancassan, Fernando; Petrillo, Giovanni; Abraham, Raymond J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 11; (1995); p. 1965 - 1972, View in Reaxys 123 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

acetonitrile

Temperature (NMR Spectroscopy) [°C]

75

Baumstark; Graham; Boykin; Tetrahedron Letters; vol. 31; nb. 7; (1990); p. 957 - 960, View in Reaxys; Boykin, D. W.; Nowak-Wydra, Barbara; Magnetic Resonance in Chemistry; vol. 29; nb. 2; (1991); p. 152 - 155, View in Reaxys; Boykin, David W.; Kumar, Arvind; Journal of Molecular Structure; vol. 298; (1993); p. 121 - 128, View in Reaxys 124 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

dimethylsulfoxide

Temperature (NMR Spectroscopy) [°C]

90

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p.

2097 - 2104,1945 - 1951, View in Reaxys; Negrebetskii, Vad. V.; Russian Journal of General Chemistry; vol. 63; nb. 9.2; (1993); p. 1436 - 1440; Zhurnal Obshchei Khimii; vol. 63; nb. 9; (1993); p. 2059 - 2066, View in Reaxys 125 of 155

Description (NMR Spectroscopy)

Linewidth of NMR absorption

Negrebetskii, Vad. V.; Russian Journal of General Chemistry; vol. 63; nb. 9.2; (1993); p. 1436 - 1440; Zhurnal Obshchei Khimii; vol. 63; nb. 9; (1993); p. 2059 - 2066, View in Reaxys 126 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

various solvent(s)

Temperature (NMR Spectroscopy) [°C]

50

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p.

2097 - 2104,1945 - 1951, View in Reaxys 127 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

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Solvents (NMR Spectroscopy)

various solvent(s)

Temperature (NMR Spectroscopy) [°C]

20

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p.

2097 - 2104,1945 - 1951, View in Reaxys 128 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethylsulfoxide

Temperature (NMR Spectroscopy) [°C]

20

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p.

2097 - 2104,1945 - 1951, View in Reaxys 129 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

various solvent(s)

Temperature (NMR Spectroscopy) [°C]

20

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p.

2097 - 2104,1945 - 1951, View in Reaxys 130 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

dimethylsulfoxide

Temperature (NMR Spectroscopy) [°C]

20

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p.

2097 - 2104,1945 - 1951, View in Reaxys 131 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

acetone-d6

Krivdin, L. B.; Kalabin, G. A.; Journal of Organic Chemistry USSR (English Translation); vol. 24; nb. 11; (1988); p. 2045 2051; Zhurnal Organicheskoi Khimii; vol. 24; nb. 11; (1988); p. 2268 - 2275, View in Reaxys 132 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

acetone-d6

Krivdin, L. B.; Kalabin, G. A.; Journal of Organic Chemistry USSR (English Translation); vol. 24; nb. 11; (1988); p. 2045 2051; Zhurnal Organicheskoi Khimii; vol. 24; nb. 11; (1988); p. 2268 - 2275, View in Reaxys

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83/144

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133 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Hauser, A.; Thurner, J.-U.; Hinzmann, B.; Journal fuer Praktische Chemie (Leipzig); vol. 330; nb. 3; (1988); p. 367 - 378, View in Reaxys 134 of 155

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

acetone-d6

Comment (NMR Spectroscopy)

13C-13C.

Krivdin, L. B.; Kalabin, G. A.; Journal of Organic Chemistry USSR (English Translation); vol. 24; nb. 11; (1988); p. 2045 2051; Zhurnal Organicheskoi Khimii; vol. 24; nb. 11; (1988); p. 2268 - 2275, View in Reaxys 135 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Hirayama, Masatoshi; Suzuki, Hideto; Ohhata, Hiroshi; Chemistry Letters; (1987); p. 413 - 416, View in Reaxys; Hirayama, Masatoshi; Ohhata, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 60; nb. 8; (1987); p. 2751 - 2756, View in Reaxys 136 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

various solvent(s)

Hirayama, Masatoshi; Ohhata, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 60; nb. 8; (1987); p. 2751 - 2756, View in Reaxys 137 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

various solvent(s)

Hirayama, Masatoshi; Ohhata, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 60; nb. 8; (1987); p. 2751 - 2756, View in Reaxys 138 of 155

Description (NMR Spectroscopy)

2D-NMR

Hirayama, Masatoshi; Ohhata, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 60; nb. 8; (1987); p. 2751 - 2756, View in Reaxys 139 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

40

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Jaccard, Guy; Lauterwein, Juergen; Helvetica Chimica Acta; vol. 69; (1986); p. 1469 - 1485, View in Reaxys 140 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

28.7

Wilson, Nancy K.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 12 - 15, View in Reaxys 141 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

35

Mieloszynski, J. L.; Andrieu, C. G.; Schneider, M.; Paquer, D.; Recueil des Travaux Chimiques des Pays-Bas; vol. 104; nb.

1; (1985); p. 9 - 15, View in Reaxys 142 of 155

Description (NMR Spectroscopy)

NOE

Wilson, Nancy K.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 12 - 15, View in Reaxys 143 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Honzl, Jan; Lovy, Jan; Tetrahedron; vol. 40; nb. 10; (1984); p. 1885 - 1892, View in Reaxys 144 of 155

Description (NMR Spectroscopy)

CIDNP

Honzl, Jan; Lovy, Jan; Tetrahedron; vol. 40; nb. 10; (1984); p. 1885 - 1892, View in Reaxys 145 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

benzene-d6

Diesveld, J. W.; Borkent, J.H.; Laarhoven, W. H.; Tetrahedron; vol. 38; nb. 12; (1982); p. 1803 - 1808, View in Reaxys 146 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CS2

Temperature (NMR Spectroscopy) [°C]

24.9

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 147 of 155

Description (NMR Spectroscopy)

Chemical shifts

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Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

fluorosulfonic acid; not given

Temperature (NMR Spectroscopy) [°C]

-70

Olah, Georgen A.; Nakajima, Tadashi; Prakash, G. K. Surya; Angewandte Chemie; vol. 92; nb. 10; (1980); p. 837 - 838, View in Reaxys 148 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

-48.2 - 51.9

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 149 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

24.9

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 150 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

36.9

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 151 of 155

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CS2

Temperature (NMR Spectroscopy) [°C]

24.9

Comment (NMR Spectroscopy)

1H-1H.

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 152 of 155

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

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Temperature (NMR Spectroscopy) [°C]

36.9

Comment (NMR Spectroscopy)

1H-13C.

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 153 of 155

Description (NMR Spectroscopy)

NMR

Bartlett,P.D.; Landis,M.E.; Journal of the American Chemical Society; vol. 99; (1977); p. 3033 - 3037, View in Reaxys; Dehmlow,E.V. et al.; Justus Liebigs Annalen der Chemie; (1977); p. 1617 - 1624, View in Reaxys; Stothers,J.B.; Tan,C.T.; Wilson,N.K.; Organic Magnetic Resonance; vol. 9; (1977); p. 408, View in Reaxys; Giraud,J.; Marzin,C.; Organic Magnetic Resonance; vol. 12; (1979); p. 647, View in Reaxys; Knothe,L.; Prinzbach,H.; Justus Liebigs Annalen der Chemie; (1977); p.

687, View in Reaxys; Jackman,L.M.; Trewella,J.C.; Journal of the American Chemical Society; vol. 98; (1976); p. 5712, View in Reaxys; Koster,P.B.; Runsink,J.; Janssen,M.J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 393, View in Reaxys; Takeshita; Hirota; Journal of Chemical Physics; vol. 58; (1973); p. 3745, View in Reaxys; Balkau; Heffernan; Australian Journal of Chemistry; vol. 24; (1971); p. 2305,2308, View in Reaxys; Kuo; Nye; Canadian Journal of Chemistry; vol. 51; (1973); p. 1995,1999, View in Reaxys; Cardillo et al.; Synthesis; (1976); p.

394, View in Reaxys; Canters; de Boer; Molecular Physics; vol. 26; (1973); p. 1185,1194, View in Reaxys 154 of 155

Description (NMR Spectroscopy)

Spin-spin relaxation time (T2)

Liu; Edman; Journal of the American Chemical Society; vol. 90; (1968); p. 213, View in Reaxys 155 of 155

Description (NMR Spectroscopy)

Spectrum

Martin et al.; Tetrahedron; vol. 20; (1964); p. 1505,1513, 1514, View in Reaxys IR Spectroscopy (55) 1 of 55

Description (IR Spectroscopy)

Bands; Spectrum

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Eakins, Galen L.; Alford, Joshua S.; Tiegs, Brandon J.; Breyfogle, Bryan E.; Stearman, Chad J.; Journal of Physical Organic Chemistry; vol. 24; nb. 11; (2011); p. 1119 - 1128, View in Reaxys; Srivastava, Manish; Srivastava, Anamika; Goyal, Ashu; Mishra, Aakanksha; Tomer, Preeti; Dwivedi, Jaya; Kishore; Journal of Physical Organic Chemistry; vol. 30; nb. 2; (2017); Art.No: E3602, View in Reaxys 2 of 55

Description (IR Spectroscopy)

Spectrum

Location

supporting information

Eakins, Galen L.; Cooper, Matthew W.; Gerasimchuk, Nikolay N.; Phillips, Terry J.; Breyfogle, Bryan E.; Stearman, Chad J.; Canadian Journal of Chemistry; vol. 91; nb. 11; (2013); p. 1059 - 1071, View in Reaxys; Zarei, Amin; Khazdooz, Leila; Aghaei, Hamidreza; Gheisari, Mohammad Mehdi; Alizadeh, Shahrzad; Golestanifar, Laleh; Tetrahedron; vol. 73; nb. 49; (2017); p. 6954 - 6961, View in Reaxys 3 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Comment (IR Spectroscopy)

film

Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys 4 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Location

supporting information

Malekafzali; Malinovska; Patureau; New Journal of Chemistry; vol. 41; nb. 15; (2017); p. 6981 - 6985, View in Reaxys

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5 of 55

Description (IR Spectroscopy)

Intensity of IR bands; Bands

Solvent (IR Spectroscopy)

potassium bromide

Albertin, Gabriele; Antoniutti, Stefano; Bortoluzzi, Marco; Botter, Alessandra; Castro, Jesús; Inorganic Chemistry; vol.

55; nb. 11; (2016); p. 5592 - 5602, View in Reaxys 6 of 55

Description (IR Spectroscopy)

Intensity of IR bands; Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Albertin, Gabriele; Antoniutti, Stefano; Botter, Alessandra; Castro, Jesús; Inorganic Chemistry; vol. 54; nb. 5; (2015); p.

2091 - 2093, View in Reaxys 7 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

sodium chloride; chloroform

Location

supporting information

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys 8 of 55

Description (IR Spectroscopy)

Bands

Sieglitz,A.; Troester,H.; Chemische Berichte; vol. 96; (1963); p. 2577 - 2594, View in Reaxys; Godfroid,J.-J.; Bulletin de la Societe Chimique de France; (1964); p. 2929 - 2943, View in Reaxys; Bergmann,E.D.; Solomonovici,A.; Synthesis; (1970); p.

183 - 189, View in Reaxys; Flett,M.S.C.; Spectrochimica Acta; vol. 18; (1962); p. 1537 - 1556, View in Reaxys; Dunken; Fritzsche; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 249, View in Reaxys; Wiemann; Godefroid; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 255; (1962); p. 2608, View in Reaxys; Brown; Spectrochimica Acta; vol. 18; (1962); p. 1065,1066, View in Reaxys; Branch, Catherine S.; Bott, Simon G.; Barron, Andrew R.; Journal of Organometallic Chemistry; vol. 666; nb. 1-2; (2003); p. 23 - 34, View in Reaxys; Mohammadpoor-Baltork, Iraj; Sadeghi, Majid M. M.; Esmayilpour, Karim; Journal of Chemical Research - Part S; nb. 6; (2003); p. 348 - 350, View in Reaxys; Mohammadpoor-Baltork, Iraj; Memarian, Hamid Reza; Bahrami, Kiumars; Monatshefte fur Chemie; vol. 135; nb. 4; (2004); p. 411 - 418, View in Reaxys; Shaabani, Ahmad; Mirzaei, Peiman; Naderi, Soheila; Lee, Donald G.; Tetrahedron; vol. 60; nb. 50; (2004); p. 11415 - 11420, View in Reaxys; Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys; Saikia, Gunin; Iyer, Parameswar K.; Journal of Organic Chemistry; vol. 75; nb. 8; (2010); p. 2714 - 2717, View in Reaxys; Kidwai, Mazaahir; Bhardwaj, Saurav; Applied Catalysis A: General; vol. 387; nb. 1-2; (2010); p. 1 - 4, View in Reaxys; Geraghty, Niall W.A.; McArdle, Patrick; Mullen, Laverne M.A.; Tetrahedron; vol. 67; nb. 19; (2011); p. 3546 - 3552, View in Reaxys; Lv, Xiao-Ming; Kong, Ling-Jie; Lin, Qi; Liu, XiaoFeng; Zhou, Ya-Ming; Jia, Yu; Synthetic Communications; vol. 41; nb. 21; (2011); p. 3215 - 3222, View in Reaxys; Tandon, Praveen K.; Singh, Santosh B.; Singh, Satpal; Kesarwani, Bhawana; Journal of the Indian Chemical Society; vol. 89; nb. 10; (2012); p. 1363 - 1367, View in Reaxys; Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys 9 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

nujol

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys 10 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 2745, View in Reaxys 11 of 55

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys 12 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

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Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys 13 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Nagano, Takashi; Kobayashi, Shu; Chemistry Letters; vol. 37; nb. 10; (2008); p. 1042 - 1043, View in Reaxys; Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys; Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys; Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys 14 of 55

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent, solid phase)

Su, Yijin; Zhang, Liangren; Jiao, Ning; Organic Letters; vol. 13; nb. 9; (2011); p. 2168 - 2171, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys 15 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

nujol

Location

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 16 of 55

Description (IR Spectroscopy)

Intensity of IR bands; ATR (attenuated total reflectance); Bands

Solvent (IR Spectroscopy)

neat (no solvent, solid phase)

Location

supporting information

Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte Chemie - International Edition; vol.

51; nb. 39; (2012); p. 9926 - 9930, View in Reaxys 17 of 55

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent)

Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys 18 of 55

Description (IR Spectroscopy)

Bands

Location

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys 19 of 55

Description (IR Spectroscopy)

Mid IR (MIR); Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Dohi, Toshifumi; Takenaga, Naoko; Goto, Akihiro; Fujioka, Hiromichi; Kita, Yasuyuki; Journal of Organic Chemistry; vol.

73; nb. 18; (2008); p. 7365 - 7368, View in Reaxys

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20 of 55

Description (IR Spectroscopy)

Mid IR (MIR); Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent, solid phase)

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys 21 of 55

Description (IR Spectroscopy)

Reflection spectrum

Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys 22 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Lukasiewicz, Marcin; Bogdal, Dariusz; Pielichowski, Jan; Advanced Synthesis and Catalysis; vol. 345; nb. 12; (2003); p.

1269 - 1272, View in Reaxys; Jain, Nidhi; Kumar, Anil; Chauhan, Shive M.S.; Tetrahedron Letters; vol. 46; nb. 15; (2005); p.

2599 - 2602, View in Reaxys; Qian, Weixing; Jin, Erlei; Bao, Weiliang; Zhang, Yongmin; Angewandte Chemie - International Edition; vol. 44; nb. 6; (2005); p. 952 - 955, View in Reaxys; Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol. 45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys; Singh, Krishna Nand; Kumar, Rajesh; Shukla, Ajay Kumar; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 46; nb. 8; (2007); p. 1347 - 1351, View in Reaxys 23 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

cyclohexane

Temperature (IR Spectroscopy) [°C]

20

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb.

1-3; (2007); p. 44 - 48, View in Reaxys 24 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

cyclohexane

Temperature (IR Spectroscopy) [°C]

20

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb.

1-3; (2007); p. 44 - 48, View in Reaxys 25 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

octan-1-ol

Temperature (IR Spectroscopy) [°C]

19.84 - 49.84

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb.

1-3; (2007); p. 44 - 48, View in Reaxys 26 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

octan-1-ol

Temperature (IR Spectroscopy) [°C]

20

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb.

1-3; (2007); p. 44 - 48, View in Reaxys 27 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

KBr

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Comment (IR Spectroscopy)

ambient temperature

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 2408, View in Reaxys 28 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

ambient temperature

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 2408, View in Reaxys 29 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CD3CN

Comment (IR Spectroscopy)

ground state. Object(s) of Study: excited singlet state. Object(s) of Study: excited triplet state

Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys 30 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CD3CN

Comment (IR Spectroscopy)

ground state. Object(s) of Study: excited singlet state. Object(s) of Study: excited triplet state

Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys 31 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

heptane

Comment (IR Spectroscopy)

ground state. Object(s) of Study: excited triplet state

Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys 32 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

heptane

Comment (IR Spectroscopy)

ground state. Object(s) of Study: excited triplet state

Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys 33 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

vapour

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol.

69; nb. 3; (2002); p. 287 - 294, View in Reaxys 34 of 55

Description (IR Spectroscopy)

Vibrational energy transfer

Zalesskaya, G. A.; Yakovlev, D. L.; Sambor, E. G.; Prikhodchenko, D. V.; Journal of Applied Spectroscopy; vol. 68; nb. 1; (2001); p. 150 - 158; Zhurnal Prikladnoi Spektroskopii; vol. 68; nb. 1; (2001); p. 110 - 115, View in Reaxys 35 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

film

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Kalinovskii; Pogorelov; Gelbshtein; Akhmetov; Russian Journal of General Chemistry; vol. 71; nb. 9; (2001); p. 1457 - 1462, View in Reaxys 36 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CH2Cl2

Comment (IR Spectroscopy)

3056 - 747 cm**(-1)

Mirafzal, Gholam A.; Lozeva, Albena M.; Tetrahedron Letters; vol. 39; nb. 40; (1998); p. 7263 - 7266, View in Reaxys 37 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

1715 1/cm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb.

18; (1998); p. 3018 - 3024, View in Reaxys 38 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

nujol

Comment (IR Spectroscopy)

1950 - 645 cm**(-1)

Dutt, Sachchidananda; Banerjee, Santanu; Hazra, Banasri; Banerjee, Amalendu; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 64; (1987); p. 704 - 705, View in Reaxys; Dutta, Hasi; Hazra, Banasri; Banerjee, Amalendu; Banerjee, Santanu; Journal of the Indian Chemical Society; vol. 64; (1987); p. 706 - 707, View in Reaxys; Banerjee, Amalendu; Mandal, Dinabandhu; Ray, Arindam; Banerjee, Pulak; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 72; nb. 3; (1995); p. 205 - 208, View in Reaxys 39 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

polyethylene; potassium bromide

Kolev, Tsonko; Journal of Molecular Structure; vol. 349; (1995); p. 381 - 384, View in Reaxys 40 of 55

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1728 - 204 cm**(-1)

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys 41 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

1720 cm**(-1)

Zaitsev, B. E.; Zhdamarov, O. S.; Sheban, G. V.; Pleshakov, V. G.; Grigor'ev, G. V.; Prostakov, N. S.; Chemistry of Heterocyclic Compounds (New York, NY, United States); (1988); p. 294 - 299; Khimiya Geterotsiklicheskikh Soedinenii; vol. 24; nb.

3; (1988); p. 361 - 366, View in Reaxys 42 of 55

Description (IR Spectroscopy)

Intensity of IR bands

Zaitsev, B. E.; Zhdamarov, O. S.; Sheban, G. V.; Pleshakov, V. G.; Grigor'ev, G. V.; Prostakov, N. S.; Chemistry of Heterocyclic Compounds (New York, NY, United States); (1988); p. 294 - 299; Khimiya Geterotsiklicheskikh Soedinenii; vol. 24; nb.

3; (1988); p. 361 - 366, View in Reaxys 43 of 55

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1730 - 651 cm**(-1)

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Dunkin, Ian R.; Bell, Gordon A.; Tetrahedron; vol. 41; (1985); p. 339 - 348, View in Reaxys 44 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

3500 - 700 cm**(-1)

Chiu; Biemann; Krishnan; Hill; Analytical Chemistry; vol. 56; nb. 9; (1984); p. 1610 - 1615, View in Reaxys 45 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

1736 cm**(-1)

Chiu; Biemann; Krishnan; Hill; Analytical Chemistry; vol. 56; nb. 9; (1984); p. 1610 - 1615, View in Reaxys 46 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CS2

Comment (IR Spectroscopy)

1720 cm**(-1)

Chvatal, Ivan; Vymetal, Jan; Pecha, Jaroslav; Simanek, Vilim; Dolejs, Ladislav; et al.; Collection of Czechoslovak Chemical Communications; vol. 48; nb. 1; (1983); p. 112 - 122, View in Reaxys 47 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

1835 - 432 cm**(-1)

Banerjee, Amalendu; Dutt, Sachchidananda; Sengupta, Dipanjan; Adak, Mohini Mohan; Samaddar, Haraprasad; Journal of the Indian Chemical Society; vol. 60; (1983); p. 275 - 277, View in Reaxys 48 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

solid

Comment (IR Spectroscopy)

1800 - 1500 cm**(-1)

Zaitsev B. E.; Grekhova, N. G.; Sheban, G. V.; Dyumaev, K. M.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 18; nb. 10; (1982); p. 1079 - 1083; Khimiya Geterotsiklicheskikh Soedinenii; vol. 18; nb. 10; (1982); p. 1388 - 1392, View in Reaxys 49 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

solid

Comment (IR Spectroscopy)

1720 - 1610 cm**(-1)

Zaitsev B. E.; Grekhova, N. G.; Sheban, G. V.; Dyumaev, K. M.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 18; nb. 10; (1982); p. 1079 - 1083; Khimiya Geterotsiklicheskikh Soedinenii; vol. 18; nb. 10; (1982); p. 1388 - 1392, View in Reaxys 50 of 55

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1720 cm**(-1)

Saito, Takao; Oikawa, Isao; Motoki, Shinichi; Bulletin of the Chemical Society of Japan; vol. 53; nb. 4; (1980); p. 1023 1027, View in Reaxys 51 of 55

Description (IR Spectroscopy)

IR

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Juchnovski,I. et al.; Monatshefte fuer Chemie; vol. 101; (1970); p. 1712 - 1719, View in Reaxys; Tochtermann,W. et al.; Chemische Berichte; vol. 105; (1972); p. 1431 - 1438, View in Reaxys; Whitesides,G.M.; Ehmann,W.J.; Journal of the American Chemical Society; vol. 92; nb. 19; (1970); p. 5625 - 5640, View in Reaxys; Trost,B.M.; Kinson,P.L.; Journal of the American Chemical Society; vol. 97; nb. 9; (1975); p. 2438 - 2449, View in Reaxys; Bartlett,P.D.; Landis,M.E.; Journal of the American Chemical Society; vol. 99; (1977); p. 3033 - 3037, View in Reaxys; Akiba,K.-Y. et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 2674 - 2683, View in Reaxys; Battaglia et al.; Synthesis; (1971); p. 378, View in Reaxys; Olah; Welch; Journal of the American Chemical Society; vol. 100; (1978); p. 5396,5397, View in Reaxys; Kuo; Nye; Canadian Journal of Chemistry; vol. 51; (1973); p. 1995,1999, View in Reaxys; Minato; Bulletin of the Chemical Society of Japan; vol. 36; (1963); p. 1020, View in Reaxys; Schroeder; Mazur; Journal of the American Chemical Society; vol. 100; (1978); p.

7339,7345, View in Reaxys; Cardillo et al.; Synthesis; (1976); p. 394, View in Reaxys; Zwarich et al.; Journal of Molecular Spectroscopy; vol. 51; (1974); p. 38,42-47, View in Reaxys; Bostwick et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 1505,1506, 1508, View in Reaxys; Beelitz et al.; Chemiker-Zeitung; vol. 103; (1979); p. 179, View in Reaxys; Sahini; Ciurea; Revue Roumaine de Chimie; vol. 17; (1972); p. 273,276-279,282, View in Reaxys; Davies; Waring; Journal of the Chemical Society [Section] C: Organic; (1968); p. 2332, View in Reaxys 52 of 55

Description (IR Spectroscopy)

Polarization of IR bands

Zwarich et al.; Journal of Molecular Spectroscopy; vol. 51; (1974); p. 38,42-47, View in Reaxys 53 of 55

Description (IR Spectroscopy)

Spectrum

Demmering; Doerr; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 19; (1964); p. 365, View in Reaxys; Latham et al.; Analytical Chemistry; vol. 34; (1962); p. 311,312, View in Reaxys 54 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

tetrachloroethene

Comment (IR Spectroscopy)

2000 - 1250 cm**(-1)

Bruice; Sayigh; Journal of the American Chemical Society; vol. 81; (1959); p. 3416,3419, View in Reaxys 55 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

benzene

Comment (IR Spectroscopy)

10000 - 667 cm**(-1)

Ueberreiter; Rabel; Zeitschrift fuer Physikalische Chemie (Leipzig); <N.F.> 13 <1957> 95, 96, View in Reaxys Mass Spectrometry (39) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

References

gas chromatography mass spectrometry (GCMS); electron impact (EI); spectrum

Huang, Tianzeng; Chen, Tieqiao; Han, Li-Biao; Journal of Organic Chemistry; vol. 83; nb. 5; (2018); p. 2959 - 2965, View in Reaxys

gas chromatograParagraph 0064; phy mass spectrom- 0068; 0072 etry (GCMS); electron impact (EI); spectrum

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys

gas chromatograsupporting informaphy mass spectrom- tion etry (GCMS); electron impact (EI); spectrum

Havare, Nizam; Plattner, Dietmar A.; Organic Letters; vol. 14; nb. 19; (2012); p. 5078 - 5081,4, View in Reaxys; Wu, Jianglong; Liu, Yan; Ma, Xiaowei; Liu, Ping; Gu, Chengzhi; Dai, Bin; Synthetic Communications; vol. 46; nb. 21; (2016); p. 1747 - 1758, View in Reaxys; Wu, Jianglong; Liu, Yan; Ma, Xiaowei; Liu, Ping; Gu, Chengzhi; Dai, Bin; Chinese Journal of Chemistry; vol. 35; nb. 9; (2017); p. 1391 - 139, View in Reaxys

gas chromatography mass spectrometry (GCMS); spectrum

Sigrist, Rolf; Hansen, Hans-Juergen; Helvetica Chimica Acta; vol. 97; nb.

8; (2014); p. 1165 - 1175, View in Reaxys; Wu, Jianglong; Liu, Yan; Liu, Ping; Gu, Chengzhi; Letters in Organic Chemistry; vol. 14; nb. 4; (2017); p. 254 - 260, View in Reaxys

gas chromatograsupporting informaphy mass spectrom- tion

Sheet, Debobrata; Bhattacharya, Shrabanti; Paine, Tapan Kanti; Chemical Communications; vol. 51; nb. 36; (2015); p. 7681 - 7684,

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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etry (GCMS); spectrum

View in Reaxys; Chakraborty, Biswarup; Jana, Rahul Dev; Singh, Reena; Paria, Sayantan; Paine, Tapan Kanti; Inorganic Chemistry; vol. 56; nb. 1; (2017); p. 359 - 371, View in Reaxys; Zarei, Amin; Khazdooz, Leila; Aghaei, Hamidreza; Gheisari, Mohammad Mehdi; Alizadeh, Shahrzad; Golestanifar, Laleh; Tetrahedron; vol. 73; nb. 49; (2017); p. 6954 6961, View in Reaxys

high resolution mass spectrometry (HRMS); APCI (atmospheric pressure chemical ionization); liquid chromatography mass spectrometry (LCMS); time-offlight mass spectra (TOFMS); spectrum

Ruzi, Rehanguli; Zhang, Muliang; Ablajan, Keyume; Zhu, Chengjian; Journal of Organic Chemistry; vol. 82; nb. 23; (2017); p. 12834 - 12839, View in Reaxys

high resolution mass spectrometry (HRMS); spectrum

supporting information

spectrum

Malekafzali; Malinovska; Patureau; New Journal of Chemistry; vol. 41; nb. 15; (2017); p. 6981 - 6985, View in Reaxys Chiu; Biemann; Krishnan; Hill; Analytical Chemistry; vol. 56; nb. 9; (1984); p. 1610 - 1615, View in Reaxys; Wang, Charles C. -Y.; Ho, Douglas M.; Groves, John T.; Journal of the American Chemical Society; vol.

121; nb. 51; (1999); p. 12094 - 12103, View in Reaxys; Chatani; Kamitani; Oshita; Fukumoto; Murai; Journal of the American Chemical Society; vol. 123; nb. 50; (2001); p. 12686 - 12687, View in Reaxys; Lukasiewicz, Marcin; Bogdal, Dariusz; Pielichowski, Jan; Advanced Synthesis and Catalysis; vol. 345; nb. 12; (2003); p. 1269 - 1272, View in Reaxys; Istrati, Daniela; Marton, George; Draghici, Constantin; Grigore, Adriana; Banciu, Mircea D.; Revue Roumaine de Chimie; vol. 50; nb. 7-8; (2005); p.

719 - 724, View in Reaxys; Sano, Yuki; Tanaka, Takanori; Hayashi, Masahiko; Chemistry Letters; vol. 36; nb. 12; (2007); p. 1414 - 1415, View in Reaxys; Lim, Chae Mi; Ha, Su Jeong; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 12; (2012); p. 4258 - 4260, View in Reaxys; Wang, Xing; Chen, Rui-Xi; Wei, Zeng-Feng; Zhang, Chen-Yang; Tu, Hai-Yang; Zhang, Ai-Dong; Journal of Organic Chemistry; vol. 81; nb. 1; (2016); p. 238 - 249, View in Reaxys; Mendkovich, Andrey S.; Syroeshkin, Mikhail A.; Nasybullina, Darya V.; Mikhailov, Mikhail N.; Gultyai, Vadim P.; Elinson, Mikhail N.; Rusakov, Alexander I.; Electrochimica Acta; vol. 191; (2016); p. 962 - 973, View in Reaxys

high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); time-offlight mass spectra (TOFMS); spectrum

supporting information

Maji, Arun; Rana, Sujoy; Akanksha; Maiti, Debabrata; Angewandte Chemie - International Edition; vol. 53; nb. 9; (2014); p. 2428 - 2432; Angew. Chem.; vol. 126; nb. 9; (2014); p. 2460 - 2464,5, View in Reaxys; Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong; Chemical Communications; vol. 52; nb. 18; (2016); p. 3635 - 3638, View in Reaxys

spectrum

supporting information

Urgoitia; Sanmartin; Herrero; Domínguez; Chemical Communications; vol. 51; nb. 23; (2015); p. 4799 - 4802, View in Reaxys; Wang, Huiqiao; Wang, Zhong; Huang, Hongchun; Tan, Jiajing; Xu, Kun; Organic Letters; vol. 18; nb. 21; (2016); p. 5680 - 5683, View in Reaxys

electron impact (EI); spectrum

high resolution mass spectrometry (HRMS); time-offlight mass spectra (TOFMS); spectrum

Ma, Jiaqi; Hu, Zhiming; Li, Meichao; Zhao, Weijuan; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Shen, Zhenlu; Tetrahedron; vol.

71; nb. 38; (2015); p. 6733 - 6739, View in Reaxys; Obst, Martin; König, Burkhard; Beilstein Journal of Organic Chemistry; vol. 12; (2016); p. 2358 - 2363, View in Reaxys supporting information

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

Cai, Zhiqiang; Hou, Xu; Hou, Ling; Hu, Zhiquan; Zhang, Bo; Jin, Zhengsheng; Synlett; vol. 27; nb. 3; (2016); p. 395 - 398; Art.No: ST-2015W0682-L, View in Reaxys

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electrospray ionisa- supporting information (ESI); spection trum

Bhardwaj, Madhvi; Sharma, Harsha; Paul, Satya; Clark, James H.; New Journal of Chemistry; vol. 40; nb. 6; (2016); p. 4952 - 4961, View in Reaxys

high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); time-offlight mass spectra (TOFMS); spectrum

Mishra, Kalpana; Pandey, Ashok Kumar; Singh, Jay Bahadur; Singh, Radhey M.; Organic and Biomolecular Chemistry; vol. 14; nb. 26; (2016); p. 6328 - 6336, View in Reaxys

photoionization; spectrum

Soep, Benoît; Mestdagh, Jean-Michel; Briant, Marc; Gaveau, Marc-André; Poisson, Lionel; Physical Chemistry Chemical Physics; vol. 18; nb. 33; (2016); p. 22914 - 22920, View in Reaxys

high resolution mass spectrometry (HRMS); electron impact (EI); spectrum

supporting information

Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p.

9926 - 9930, View in Reaxys; Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p.

2742 - 2745, View in Reaxys; Baars, Hannah; Unoh, Yuto; Okada, Takeshi; Hirano, Koji; Satoh, Tetsuya; Tanaka, Ken; Bolm, Carsten; Miura, Masahiro; Chemistry Letters; vol. 43; nb. 11; (2014); p. 1782 - 1784, View in Reaxys; Ang, Wei Jie; Lam, Yulin; Organic and Biomolecular Chemistry; vol. 13; nb. 4; (2015); p. 1048 - 1052, View in Reaxys

high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); spectrum

supporting information

Guo, Wei; Lu, Liang-Qiu; Wang, Yue; Wang, Ya-Ni; Chen, Jia-Rong; Xiao, Wen-Jing; Angewandte Chemie - International Edition; vol. 54; nb. 7; (2015); p. 2265 - 2269; Angew. Chem.; vol. 127; nb. 7; (2015); p. 2293 2297,5, View in Reaxys

gas chromatograsupporting informaphy mass spectrom- tion etry (GCMS); timeof-flight mass spectra (TOFMS); fragmentation pattern

Paria, Sayantan; Chatterjee, Sayanti; Paine, Tapan Kanti; Inorganic Chemistry; vol. 53; nb. 6; (2014); p. 2810 - 2821, View in Reaxys

electrospray ionisation (ESI); gas chromatography mass spectrometry (GCMS); spectrum

Bellardita; Loddo; Mele; Panzeri; Parrino; Pibiri; Palmisano; RSC Advances; vol. 4; nb. 77; (2014); p. 40859 - 40864, View in Reaxys

GCMS (Gas chromatography mass spectrometry); Spectrum

supporting information

Du, Zhongtian; Sun, Zhiqiang; Zhang, Wei; Miao, Hong; Ma, Hong; Xu, Jie; Tetrahedron Letters; vol. 50; nb. 15; (2009); p. 1677 - 1680, View in Reaxys; Burange, Anand S.; Kale, Sandip R.; Jayaram, Radha V.; Tetrahedron Letters; vol. 53; nb. 24; (2012); p. 2989 - 2992, View in Reaxys; Yang, Xiu-Li; Xie, Ming-Hua; Zou, Chao; He, Yabing; Chen, Banglin; O'Keeffe, Michael; Wu, Chuan-De; Journal of the American Chemical Society; vol. 134; nb. 25; (2012); p. 10638 - 10645, View in Reaxys

HRMS (High resolution mass spectrometry); FAB (Fast atom bombardment); Spectrum

supporting information

Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 9381, View in Reaxys

electron impact (EI); spectrum

supporting information

Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p.

9926 - 9930, View in Reaxys

GCMS (Gas chromatography mass spectrometry); Spectrum

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

Matsumoto, Takahiro; Ohkubo, Kei; Honda, Kaoru; Yazawa, Akiko; Furutachi, Hideki; Fujinami, Shuhei; Fukuzumi, Shunichi; Suzuki, Masatatsu; Journal of the American Chemical Society; vol. 131; nb. 26; (2009); p. 9258 - 9267, View in Reaxys; Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys

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Spectrum

supporting information

Su, Yijin; Zhang, Liangren; Jiao, Ning; Organic Letters; vol. 13; nb. 9; (2011); p. 2168 - 2171, View in Reaxys

EI (Electron impact); Spectrum

supporting information

Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys

APCI (atmospheric pressure chemical ionization); IT (ion trap); Spectrum GCMS (Gas chromatography mass spectrometry); EI (Electron impact); Spectrum

Habicht, Steve C.; Vinueza, Nelson R.; Amundson, Lucas M.; Kenttaemaa, Hilkka I.; Journal of the American Society for Mass Spectrometry; vol. 22; nb. 3; (2011); p. 520 - 530, View in Reaxys supporting information

Wang, Congyang; Piel, Isabel; Glorius, Frank; Journal of the American Chemical Society; vol. 131; (2009); p. 4194 - 4195, View in Reaxys; Wang, Azhong; Jiang, Huanfeng; Journal of Organic Chemistry; vol. 75; nb. 7; (2010); p. 2321 - 2326, View in Reaxys

HRMS (High resolution mass spectrometry); TOFMS (Time of flight mass spectrum)

Kidwai, Mazaahir; Bhardwaj, Saurav; Applied Catalysis A: General; vol.

387; nb. 1-2; (2010); p. 1 - 4, View in Reaxys

EI (Electron impact); Spectrum

mol peak

Fang, Xin-Qiang; Xu, Hua-Jian; Jiang, Hong; Liu, You-Cheng; Fu, Yao; Wu, Yun-Dong; Tetrahedron Letters; vol. 50; nb. 3; (2009); p. 312 315, View in Reaxys

HRMS (High resolution mass spectrometry); Spectrum

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys

FAB (Fast atom bombardment); HRMS (High resolution mass spectrometry)

supporting informa- mol peak tion

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys

HRMS (High resolution mass spectrometry); ESI (Electrospray ionisation); Spectrum

supporting information

Nagano, Takashi; Kobayashi, Shu; Chemistry Letters; vol. 37; nb. 10; (2008); p. 1042 - 1043, View in Reaxys

spectrum; electron impact (EI)

Koenig, Johann; Balfanz, Eckhard; Funcke, Werner; Romanowski, Thomas; Analytical Chemistry; vol. 55; nb. 4; (1983); p. 599 - 603, View in Reaxys; Shevtsov, V. K.; Zvolinskii, V. P.; Zakharov, P. I.; Pleshakov, V. G.; Alekseeva, L. A.; Prostakov, N. S.; Journal of Organic Chemistry USSR (English Translation); vol. 18; (1982); p. 2140 - 2145; Zhurnal Organicheskoi Khimii; vol. 18; nb. 11; (1982); p. 2415 - 2421, View in Reaxys; Kamata, Keigo; Kasai, Jun; Yamaguchi, Kazuya; Mizuno, Noritaka; Organic Letters; vol. 6; nb. 20; (2004); p. 3577 - 3580, View in Reaxys

spectrum

collisional activation

Madhusudanan, K. P.; Durani, S.; Reddy, D. M.; Kapil, R. S.; Itagaki, Y.; Nojima, K.; Organic Mass Spectrometry; vol. 26; nb. 4; (1991); p. 298 304, View in Reaxys

fragmentation pattern; spectrum

metastable ions

Guidugli, F. H.; Ardanaz, C. E.; Kavka, J.; Garibay, M. E.; Joseph-Nathan, P.; Organic Mass Spectrometry; vol. 21; (1986); p. 117 - 124, View in Reaxys

spectrum

positive secondary ions

Ross, Mark M.; Colton, Richard J.; Analytical Chemistry; vol. 55; nb. 1; (1983); p. 150 - 153, View in Reaxys

ion current profiles; Proctor, C. J.; Kralj, B.; Larka, E. A.; Porter, C. J.; Maquestiau, A.; Bemetastable ions ynon, J. H.; Organic Mass Spectrometry; vol. 16; nb. 7; (1981); p. 312 322, View in Reaxys chemical ionization (CI)

IKE(S) (ion kinetic energy (spectrum))

Maquestiau, Andre; Flammang, Robert; Nielsen, Lawrence; Organic Mass Spectrometry; vol. 15; nb. 7; (1980); p. 376 - 379, View in Reaxys Beynon et al.; Journal of Physical Chemistry; vol. 63; (1959); p. 1861,1862, View in Reaxys; Eland; Danby; Journal of the Chemical Society; (1965); p.

5935,5936, View in Reaxys; Faust et al.; Zeitschrift fuer Naturforschung,

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 20; (1965); p.

1128,1133, View in Reaxys; Schwarz et al.; Journal of Heterocyclic Chemistry; vol. 13; (1976); p. 877, View in Reaxys; Beynon; Advances in Mass Spectrometry; (1959); p. 328,348, View in Reaxys; Koch; Markgraf; Journal of Heterocyclic Chemistry; vol. 8; (1971); p. 225,230, View in Reaxys; Krylowa et al.; Neftekhimiya; vol. 16; (1976); p. 581,582; Chem.Abstr.; vol. 85; nb. 159734; (1976), View in Reaxys; Gaines et al.; Analytical Chemistry; vol. 47; (1975); p. 1373, View in Reaxys; Patel; Politzer; Griffin; Laseter; Biomedical Mass Spectrometry; vol. 5; nb. 12; (1978); p. 664 670, View in Reaxys; Szabo et al.; Justus Liebigs Annalen der Chemie; (1977); p. 747,758, View in Reaxys; BELL JH; IRELAND S; SPEARS AW; Analytical Chemistry; vol. 41; nb. 2; (1969); p. 310 - 313, View in Reaxys; Beynon; Williams; Applied Spectroscopy; vol. 14; (1960); p. 156,158, View in Reaxys; Cheshire et al.; Tetrahedron; vol. 23; (1967); p. 1669, View in Reaxys UV/VIS Spectroscopy (115) 1 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Location

supporting information

Xia, Ji-Bao; Zhu, Chen; Chen, Chuo; Journal of the American Chemical Society; vol. 135; nb. 46; (2013); p. 17494 - 17500, View in Reaxys; Xia, Ji-Bao; Zhu, Chen; Chen, Chuo; Chemical Communications; vol. 50; nb. 79; (2014); p. 11701 - 11704, View in Reaxys; Bume, Desta Doro; Harry, Stefan Andrew; Pitts, Cody Ross; Lectka, Thomas; Journal of Organic Chemistry; vol. 83; nb. 3; (2018); p. 1565 - 1575, View in Reaxys 2 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Location

supporting information

Paul, Subhasis; Guin, Joyram; Green Chemistry; vol. 19; nb. 11; (2017); p. 2530 - 2534, View in Reaxys 3 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Location

supporting information

Absorption Maxima (UV/ VIS) [nm]

258; 295; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

22000; 950; 71

Li, Shuangjiang; Aljhdli, Merfat; Thakellapalli, Haresh; Farajidizaji, Behzad; Zhang, Yu; Akhmedov, Novruz G.; Milsmann, Carsten; Popp, Brian V.; Wang, Kung K.; Organic Letters; vol. 19; nb. 15; (2017); p. 4078 - 4081, View in Reaxys 4 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Absorption Maxima (UV/ VIS) [nm]

258

Tan, Ke Xin; Lintang, Hendrik O.; Maniam, Subashani; Langford, Steven J.; Bakar, Mohd Bakri; Tetrahedron; vol. 72; nb. 35; (2016); p. 5402 - 5413, View in Reaxys 5 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

377

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Ext./Abs. Coefficient [l·mol-1cm-1]

260

Ghosh, Indrajit; Mukhopadhyay, Arindam; Koner, Apurba Lal; Samanta, Subhas; Nau, Werner M.; Moorthy, Jarugu Narasimha; Physical Chemistry Chemical Physics; vol. 16; nb. 31; (2014); p. 16436 - 16445, View in Reaxys 6 of 115

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

379

Ext./Abs. Coefficient [l·mol-1cm-1]

260

Ghosh, Indrajit; Mukhopadhyay, Arindam; Koner, Apurba Lal; Samanta, Subhas; Nau, Werner M.; Moorthy, Jarugu Narasimha; Physical Chemistry Chemical Physics; vol. 16; nb. 31; (2014); p. 16436 - 16445, View in Reaxys 7 of 115

Solvent (UV/VIS Spectroscopy)

cyclohexane

Absorption Maxima (UV/ VIS) [nm]

382

Ext./Abs. Coefficient [l·mol-1cm-1]

280

Ghosh, Indrajit; Mukhopadhyay, Arindam; Koner, Apurba Lal; Samanta, Subhas; Nau, Werner M.; Moorthy, Jarugu Narasimha; Physical Chemistry Chemical Physics; vol. 16; nb. 31; (2014); p. 16436 - 16445, View in Reaxys 8 of 115

Description (UV/VIS Spectroscopy)

in the presence of additive(s); Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Location

supporting information

Xia, Ji-Bao; Zhu, Chen; Chen, Chuo; Chemical Communications; vol. 50; nb. 79; (2014); p. 11701 - 11704, View in Reaxys 9 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Zhu, Xiao-Qing; Chen, Xi; Mei, Lian-Rui; Organic Letters; vol. 13; nb. 9; (2011); p. 2456 - 2459, View in Reaxys; Samant, Vaishali; Varne, Mahendra; Palit, Dipak K.; Journal of Photochemistry and Photobiology A: Chemistry; vol. 264; (2013); p. 1 - 11, View in Reaxys 10 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Location

supporting information

Absorption Maxima (UV/ VIS) [nm]

393

Ext./Abs. Coefficient [l·mol-1cm-1]

300

Eakins, Galen L.; Cooper, Matthew W.; Gerasimchuk, Nikolay N.; Phillips, Terry J.; Breyfogle, Bryan E.; Stearman, Chad J.; Canadian Journal of Chemistry; vol. 91; nb. 11; (2013); p. 1059 - 1071, View in Reaxys 11 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

N,N-dimethyl acetamide

Absorption Maxima (UV/ VIS) [nm]

420; 520; 640; 510

Samant, Vaishali; Varne, Mahendra; Palit, Dipak K.; Journal of Photochemistry and Photobiology A: Chemistry; vol. 264; (2013); p. 1 - 11, View in Reaxys

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12 of 115

Description (UV/VIS Spectroscopy)

in the presence of additive(s); Spectrum

Samant, Vaishali; Varne, Mahendra; Palit, Dipak K.; Journal of Photochemistry and Photobiology A: Chemistry; vol. 264; (2013); p. 1 - 11, View in Reaxys 13 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Absorption Maxima (UV/ VIS) [nm]

309

Ext./Abs. Coefficient [l·mol-1cm-1]

1600

Robert, Patricia; Bolduc, Andreanne; Skene, W. G.; Journal of Physical Chemistry A: Molecules, Spectroscopy, Kinetics, Environment, and General Theory; vol. 116; nb. 37; (2012); p. 9305 - 9314,10, View in Reaxys 14 of 115

Solvent (UV/VIS Spectroscopy)

dichloromethane

Absorption Maxima (UV/ VIS) [nm]

258

Dufresne, Stephane; Skalski, Thomas; Skene; Canadian Journal of Chemistry; vol. 89; nb. 2; (2011); p. 173 - 180, View in Reaxys 15 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Location

supporting information

Dufresne, Stephane; Skalski, Thomas; Skene; Canadian Journal of Chemistry; vol. 89; nb. 2; (2011); p. 173 - 180, View in Reaxys 16 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

tetrachloromethane

Absorption Maxima (UV/ VIS) [nm]

425

Okamoto, Hideki; Yamaji, Minoru; Gohda, Shin; Kubozono, Yoshihiro; Komura, Noriko; Sato, Kaori; Sugino, Hisako; Satake, Kyosuke; Organic Letters; vol. 13; nb. 10; (2011); p. 2758 - 2761, View in Reaxys 17 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

chloroform

Okamoto, Hideki; Yamaji, Minoru; Gohda, Shin; Kubozono, Yoshihiro; Komura, Noriko; Sato, Kaori; Sugino, Hisako; Satake, Kyosuke; Organic Letters; vol. 13; nb. 10; (2011); p. 2758 - 2761, View in Reaxys 18 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Location

supporting information

Absorption Maxima (UV/ VIS) [nm]

393

Ext./Abs. Coefficient [l·mol-1cm-1]

262

Eakins, Galen L.; Alford, Joshua S.; Tiegs, Brandon J.; Breyfogle, Bryan E.; Stearman, Chad J.; Journal of Physical Organic Chemistry; vol. 24; nb. 11; (2011); p. 1119 - 1128, View in Reaxys 19 of 115

Description (UV/VIS Spectroscopy)

Spectrum

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Absorption Maxima (UV/ VIS) [nm]

286

Li, Zhuomin; Deng, Wenli; Journal of Chemical Crystallography; vol. 41; nb. 10; (2011); p. 1534 - 1538, View in Reaxys 20 of 115

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

290

Reddy, Sabbasani Rajasekhara; Titu, Devamani; Chadha, Anju; JAOCS, Journal of the American Oil Chemists' Society; vol. 87; nb. 7; (2010); p. 747 - 754, View in Reaxys 21 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CH2Cl2

Zhang, Kai; Chen, Zhao; Yang, Chuluo; Tao, Youtian; Zou, Yang; Qin, Jingui; Cao, Yong; Journal of Materials Chemistry; vol. 18; nb. 3; (2008); p. 291 - 298, View in Reaxys 22 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

Ramart-Lucas; Hoch; Bulletin de la Societe Chimique de France; vol. <5> 2; (1935); p. 1376,1378, View in Reaxys; Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 23 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 24 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Weininger; Ren; Wang; Chen; McGimpsey; Journal of Physical Chemistry A; vol. 103; nb. 28; (1999); p. 5477 - 5484, View in Reaxys; Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 25 of 115

Solvent (UV/VIS Spectroscopy)

pentane

Absorption Maxima (UV/ VIS) [nm]

413.993

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 26 of 115

Solvent (UV/VIS Spectroscopy)

hexane

Absorption Maxima (UV/ VIS) [nm]

413.993

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 27 of 115

Solvent (UV/VIS Spectroscopy)

heptane

Absorption Maxima (UV/ VIS) [nm]

415.007

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Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 28 of 115

Solvent (UV/VIS Spectroscopy)

toluene

Absorption Maxima (UV/ VIS) [nm]

425.007

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 29 of 115

Solvent (UV/VIS Spectroscopy)

butyl acetate

Absorption Maxima (UV/ VIS) [nm]

423.998

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 30 of 115

Solvent (UV/VIS Spectroscopy)

ethyl acetate

Absorption Maxima (UV/ VIS) [nm]

426.003

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 31 of 115

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Absorption Maxima (UV/ VIS) [nm]

424.628

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 32 of 115

Solvent (UV/VIS Spectroscopy)

1,2-dichloro-benzene

Absorption Maxima (UV/ VIS) [nm]

428.009

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 33 of 115

Solvent (UV/VIS Spectroscopy)

acetone

Absorption Maxima (UV/ VIS) [nm]

426.003

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 34 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

428.009

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 35 of 115

Description (UV/VIS Spectroscopy)

Triplet-triplet band

Comment (UV/VIS Spectroscopy)

Remark: 23 deg C

Lathioor, Edward C.; Leigh, William J.; Photochemistry and Photobiology; vol. 82; nb. 1; (2006); p. 291 - 300, View in Reaxys 36 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Comment (UV/VIS Spectroscopy)

Remark: 23 deg C

Absorption Maxima (UV/ VIS) [nm]

421

Lathioor, Edward C.; Leigh, William J.; Photochemistry and Photobiology; vol. 82; nb. 1; (2006); p. 291 - 300, View in Reaxys 37 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

toluene

Biczok, Laszlo; Berces, Tibor; Inoue, Haruo; Journal of Physical Chemistry A; vol. 103; nb. 20; (1999); p. 3837 - 3842, View in Reaxys; Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys 38 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

250; 294; 308; 324

Kolano, Christoph; Bucher, Goetz; Schade, Olaf; Grote, Dirk; Sander, Wolfram; Journal of Organic Chemistry; vol. 70; nb.

17; (2005); p. 6609 - 6615, View in Reaxys 39 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

380

Kolano, Christoph; Bucher, Goetz; Schade, Olaf; Grote, Dirk; Sander, Wolfram; Journal of Organic Chemistry; vol. 70; nb.

17; (2005); p. 6609 - 6615, View in Reaxys 40 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CHCl3

Comment (UV/VIS Spectroscopy)

ambient temperature

Chi, Chunyan; Im, Chan; Enkelmann, Volker; Ziegler, Andreas; Lieser, Guenter; Wegner, Gerhard; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6833 - 6845, View in Reaxys 41 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

film

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys 42 of 115

Solvent (UV/VIS Spectroscopy)

methanol

Absorption Maxima (UV/ VIS) [nm]

250; 295; 385

Ext./Abs. Coefficient [l·mol-1cm-1]

40738; 8317; 741

Kirichenko; Meshkova; Topilova; Kiriyak; Lyapunov; Kulygina; Luk'yanenko; Russian Journal of General Chemistry; vol.

75; nb. 2; (2005); p. 272 - 277, View in Reaxys 43 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

ambient temperature

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

103/144

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Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 2408, View in Reaxys 44 of 115

Description (UV/VIS Spectroscopy)

Singlet-triplet band

Comment (UV/VIS Spectroscopy)

Remark: absorption spectrum at 20 grad C; gas

Borisevich; Kazakov; Kukhto; Murtazaliev; Khristoforov; Artyukhov; Ivanov; Journal of Applied Spectroscopy; vol. 71; nb. 5; (2004); p. 681 - 685, View in Reaxys 45 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Comment (UV/VIS Spectroscopy)

Remark: 20 grad C

Borisevich; Kazakov; Kukhto; Murtazaliev; Khristoforov; Artyukhov; Ivanov; Journal of Applied Spectroscopy; vol. 71; nb. 5; (2004); p. 681 - 685, View in Reaxys 46 of 115

Description (UV/VIS Spectroscopy)

Singlet-triplet band

Comment (UV/VIS Spectroscopy)

Remark: Electron energy loss spectrum at 40 grad C; gas

Borisevich; Kazakov; Kukhto; Murtazaliev; Khristoforov; Artyukhov; Ivanov; Journal of Applied Spectroscopy; vol. 71; nb. 5; (2004); p. 681 - 685, View in Reaxys 47 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Comment (UV/VIS Spectroscopy)

Remark: Electron energy loss spectrum at 40 grad C

Borisevich; Kazakov; Kukhto; Murtazaliev; Khristoforov; Artyukhov; Ivanov; Journal of Applied Spectroscopy; vol. 71; nb. 5; (2004); p. 681 - 685, View in Reaxys 48 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Friedel,R.A.; Orchin,M.; Ultraviolet Spectra of Aromatic Compounds <New York 1951> Nr. 329, View in Reaxys; Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys 49 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

butan-1-ol; cyclohexane

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 1:4

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys 50 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

butan-1-ol; cyclohexane

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 1:3

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

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104/144

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51 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

butan-1-ol

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys 52 of 115

Solvent (UV/VIS Spectroscopy)

H2O

Comment (UV/VIS Spectroscopy)

in the presence of additives

Absorption Maxima (UV/ VIS) [nm]

256

Courtney, Michael C.; MacCormack, Aoife C.; More O'Ferrall, Rory A.; Journal of Physical Organic Chemistry; vol. 15; nb. 8; (2002); p. 529 - 539, View in Reaxys 53 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

vapour

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol.

69; nb. 3; (2002); p. 287 - 294, View in Reaxys 54 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

heptane

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 - 150, View in Reaxys 55 of 115

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Comment (UV/VIS Spectroscopy)

Remark: at 298 K

Absorption Maxima (UV/ VIS) [nm]

248.4; 256.9; 293.5; 307.2

Ext./Abs. Coefficient [l·mol-1cm-1]

57777; 84760; 3809; 1769

Behrendt, Andreas; Screttas, Constantinos G.; Bethell, Donald; Schiemann, Olav; Steele, Barry R.; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (1998); p. 2039 - 2045, View in Reaxys 56 of 115

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Comment (UV/VIS Spectroscopy)

Remark: at 298 K

Absorption Maxima (UV/ VIS) [nm]

322.7; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

847; 275

Behrendt, Andreas; Screttas, Constantinos G.; Bethell, Donald; Schiemann, Olav; Steele, Barry R.; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (1998); p. 2039 - 2045, View in Reaxys 57 of 115

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

Remark: 296 K

Absorption Maxima (UV/ VIS) [nm]

382

Ext./Abs. Coefficient [l·mol-1cm-1]

280

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105/144

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Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb.

18; (1998); p. 3018 - 3024, View in Reaxys 58 of 115

Solvent (UV/VIS Spectroscopy)

benzene

Comment (UV/VIS Spectroscopy)

Remark: 296 K

Absorption Maxima (UV/ VIS) [nm]

380

Ext./Abs. Coefficient [l·mol-1cm-1]

300

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb.

18; (1998); p. 3018 - 3024, View in Reaxys 59 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

Comment (UV/VIS Spectroscopy)

Remark: 296 K

Absorption Maxima (UV/ VIS) [nm]

377

Ext./Abs. Coefficient [l·mol-1cm-1]

260

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb.

18; (1998); p. 3018 - 3024, View in Reaxys 60 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

300 - 500 nm; Remark: 296 K

Absorption Maxima (UV/ VIS) [nm]

379

Ext./Abs. Coefficient [l·mol-1cm-1]

260

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb.

18; (1998); p. 3018 - 3024, View in Reaxys 61 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CH2Cl2

Comment (UV/VIS Spectroscopy)

300 - 450 nm

Biczok, Laszlo; Berces, Tibor; Linschitz, Henry; Journal of the American Chemical Society; vol. 119; nb. 45; (1997); p.

11071 - 11077, View in Reaxys 62 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile; aq. methanol

Absorption Maxima (UV/ VIS) [nm]

250; 258

Wischmann, Hartmut; Steinhart, Hans; Chemosphere; vol. 35; nb. 8; (1997); p. 1681 - 1698, View in Reaxys 63 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

270 - 480 nm

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

106/144

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Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb.

7; (1996); p. 1833 - 1839, View in Reaxys 64 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Comment (UV/VIS Spectroscopy)

270 - 480 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb.

7; (1996); p. 1833 - 1839, View in Reaxys 65 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

270 - 480 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb.

7; (1996); p. 1833 - 1839, View in Reaxys 66 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile; ethanol

Comment (UV/VIS Spectroscopy)

270 - 480 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb.

7; (1996); p. 1833 - 1839, View in Reaxys 67 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane; ethanol

Comment (UV/VIS Spectroscopy)

270 - 480 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb.

7; (1996); p. 1833 - 1839, View in Reaxys 68 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

200 - 500 nm

Lafleur, Arthur L.; Howard, Jack B.; Taghizadeh, Koli; Plummer, Elaine F.; Scott, Lawrence T.; Necula, Atena; Swallow, Kathleen C.; Journal of Physical Chemistry; vol. 100; nb. 43; (1996); p. 17421 - 17428, View in Reaxys 69 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

benzene

Comment (UV/VIS Spectroscopy)

280 - 333 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 70 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

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107/144

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Comment (UV/VIS Spectroscopy)

280 - 333 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 71 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CHCl3

Comment (UV/VIS Spectroscopy)

280 - 333 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 72 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol

Comment (UV/VIS Spectroscopy)

280 - 333 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 73 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

propan-1-ol

Absorption Maxima (UV/ VIS) [nm]

291.4

Ext./Abs. Coefficient [l·mol-1cm-1]

17989

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 74 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

hexane

Absorption Maxima (UV/ VIS) [nm]

289.9; 310.1

Ext./Abs. Coefficient [l·mol-1cm-1]

2931; 474

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 75 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

cyclohexane

Absorption Maxima (UV/ VIS) [nm]

290.5; 310.9

Ext./Abs. Coefficient [l·mol-1cm-1]

3243; 458

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 76 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

108/144

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Solvent (UV/VIS Spectroscopy)

methanol

Absorption Maxima (UV/ VIS) [nm]

291.7; 306.5

Ext./Abs. Coefficient [l·mol-1cm-1]

2904.01; 180

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 77 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

benzene

Absorption Maxima (UV/ VIS) [nm]

291.9; 307.6

Ext./Abs. Coefficient [l·mol-1cm-1]

5458; 1963

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 78 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Absorption Maxima (UV/ VIS) [nm]

292.1; 306.1

Ext./Abs. Coefficient [l·mol-1cm-1]

2449; 1262

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 79 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

292.4; 306.5

Ext./Abs. Coefficient [l·mol-1cm-1]

1968; 1007

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 80 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dioxane

Absorption Maxima (UV/ VIS) [nm]

292.5; 306.3

Ext./Abs. Coefficient [l·mol-1cm-1]

3013; 1439

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 81 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dimethylformamide

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109/144

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Absorption Maxima (UV/ VIS) [nm]

292.7; 308.5

Ext./Abs. Coefficient [l·mol-1cm-1]

5458; 2104

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 82 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

CH2Cl2

Absorption Maxima (UV/ VIS) [nm]

293.2; 307.6

Ext./Abs. Coefficient [l·mol-1cm-1]

2449; 1156.1

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 83 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

toluene

Absorption Maxima (UV/ VIS) [nm]

293.5; 307

Ext./Abs. Coefficient [l·mol-1cm-1]

7031; 1986.1

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 84 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

butan-1-ol

Absorption Maxima (UV/ VIS) [nm]

293.9; 312.8

Ext./Abs. Coefficient [l·mol-1cm-1]

597; 525

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 85 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

CHCl3

Absorption Maxima (UV/ VIS) [nm]

294.9; 307.8

Ext./Abs. Coefficient [l·mol-1cm-1]

1327; 679

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 86 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

propan-2-ol; H2O

Comment (UV/VIS Spectroscopy)

200 - 500 nm; Ratio of solvents: 4:1

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110/144

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Bauer, Rupert; Heisler, Guenter; Koenigstein, Christian; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 50; nb. 1; (1994); p. 57 - 68, View in Reaxys 87 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

propan-2-ol; H2O

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 4:1

Absorption Maxima (UV/ VIS) [nm]

205; 255; 298; 330

Ext./Abs. Coefficient [l·mol-1cm-1]

11000; 25000; 2000; 1800

Bauer; Heisler; Konigstein; Tetrahedron; vol. 49; nb. 30; (1993); p. 6591 - 6604, View in Reaxys; Bauer, Rupert; Heisler, Guenter; Koenigstein, Christian; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 50; nb. 1; (1994); p. 57 - 68, View in Reaxys 88 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

cyclohexane

Absorption Maxima (UV/ VIS) [nm]

374.95

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys 89 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

methylcyclohexane

Absorption Maxima (UV/ VIS) [nm]

374.95

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys 90 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

acetone

Absorption Maxima (UV/ VIS) [nm]

380.08

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys 91 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

380.08

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys 92 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Absorption Maxima (UV/ VIS) [nm]

450

McGimpsey, W. G.; Scaiano, J. C.; Tetrahedron Letters; vol. 27; nb. 5; (1986); p. 547 - 550, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

111/144

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93 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

249; 257; 296; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

53703; 72443; 2951; 245

Talapatra, Sunil K.; Bose, Srabani; Mallik, Asok K.; Talapatra, Bani; Tetrahedron; vol. 41; nb. 13; (1985); p. 2765 - 2770, View in Reaxys 94 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol; NaOH

Absorption Maxima (UV/ VIS) [nm]

249; 257; 296; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

53703; 72443; 2951; 245

Talapatra, Sunil K.; Bose, Srabani; Mallik, Asok K.; Talapatra, Bani; Tetrahedron; vol. 41; nb. 13; (1985); p. 2765 - 2770, View in Reaxys 95 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dioxane; H2O

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 1percent

Absorption Maxima (UV/ VIS) [nm]

258

Hoz, Shmaryahu; Gross, Zeev; Speizman, Dov; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1985); p. 1143 - 1146, View in Reaxys 96 of 115

Description (UV/VIS Spectroscopy)

Triplet-triplet band

Andrews; Journal of Physical Chemistry; vol. 82; (1978); p. 2304, View in Reaxys; Kobayashi; Nagakura; Chemical Physics Letters; vol. 43; (1976); p. 429, View in Reaxys; Engel, Paul S.; Woods, Treacy L.; Page, Matthew A.; Journal of Physical Chemistry; vol. 87; nb. 1; (1983); p. 10 - 13, View in Reaxys 97 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

249; 257; 296; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

56234; 87096; 3311; 263

Chvatal, Ivan; Vymetal, Jan; Pecha, Jaroslav; Simanek, Vilim; Dolejs, Ladislav; et al.; Collection of Czechoslovak Chemical Communications; vol. 48; nb. 1; (1983); p. 112 - 122, View in Reaxys 98 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

235 - 426 nm

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Frolova, E. P.; Akhvlediani, R. N.; Suvorov, N. N.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 18; nb. 10; (1982); p. 1049 - 1054; Khimiya Geterotsiklicheskikh Soedinenii; vol. 18; nb. 10; (1982); p. 1358 - 1362, View in Reaxys 99 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Absorption Maxima (UV/ VIS) [nm]

256

Carey, Edwin; O'Ferrall, Rory A. More; Vernon, Nicholas M.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1982); p. 1581 - 1586, View in Reaxys 100 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

benzene

Absorption Maxima (UV/ VIS) [nm]

420

Scaiano, J. C.; Wubbels, Gene G.; Journal of the American Chemical Society; vol. 103; nb. 3; (1981); p. 640 - 645, View in Reaxys 101 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

propan-2-ol

Comment (UV/VIS Spectroscopy)

450 - 700 nm

Peters, K. S.; Freilich, S. C.; Schaeffer, C. G.; Journal of the American Chemical Society; vol. 102; nb. 17; (1980); p. 5701 5702, View in Reaxys 102 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Stobbe; Seydel; Justus Liebigs Annalen der Chemie; vol. 370; (1909); p. 141, View in Reaxys; Stobbe; Justus Liebigs Annalen der Chemie; vol. 370; (1909); p. 97, View in Reaxys; Koster,P.B.; Runsink,J.; Janssen,M.J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 393, View in Reaxys; Lin; Topp; Chemical Physics; vol. 36; (1979); p. 365, View in Reaxys; Marchetti; Molecular Crystals and Liquid Crystals (1969-1991); vol. 16; (1972); p.

127, View in Reaxys; Filipescu et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 2276, View in Reaxys; Chen; Lin; Biochimica et Biophysica Acta; vol. 184; (1969); p. 634, View in Reaxys; Hayon et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 2072, View in Reaxys; Snyder; Testa; Journal of Physical Chemistry; vol. 83; (1979); p. 3041, View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p.

377,393, View in Reaxys; Zwarich; Bree; Journal of Molecular Spectroscopy; vol. 52; (1974); p. 329,331,333,339, View in Reaxys; Dehler; Doerr; Tetrahedron Letters; (1965); p. 2155,2157, View in Reaxys; Amand; Bensasson; Chemical Physics Letters; vol. 34; (1975); p. 44,46, 47, View in Reaxys; Mullen Orloff; Journal of Molecular Spectroscopy; vol. 30; (1969); p. 140, View in Reaxys; Huggenberger; Labhart; Helvetica Chimica Acta; vol. 61; (1978); p. 250,251, 253, 255, View in Reaxys; Treinin; Hayon; Journal of the American Chemical Society; vol. 98; (1976); p. 3884,3885, 3887, View in Reaxys; Moritani; Nagai; Nippon Kagaku Zasshi; vol. 86; (1965); p. 157; Chem.Abstr.; vol. 63; nb. 7789b, View in Reaxys; Yoshihara; Kearns; Journal of Chemical Physics; vol. 45; (1966); p. 1991,1999, View in Reaxys; McClelland; Transactions of the Faraday Society; vol. 57; (1961); p. 1458, View in Reaxys; Latham et al.; Analytical Chemistry; vol. 34; (1962); p. 311,312, View in Reaxys; Kadhim; Offen; Journal of Chemical Physics; vol. 47; (1967); p. 1289,1290, View in Reaxys; Kuboyama; Bulletin of the Chemical Society of Japan; vol. 37; (1964); p. 1540, View in Reaxys; Dehler; Fritz; Tetrahedron Letters; (1969); p. 2157, View in Reaxys 103 of 115

Description (UV/VIS Spectroscopy)

UV/VIS

Tochtermann,W. et al.; Chemische Berichte; vol. 105; (1972); p. 1431 - 1438, View in Reaxys; Akiba,K.-Y. et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 2674 - 2683, View in Reaxys; Godfroid,J.-J.; Bulletin de la Societe Chimique de France; (1964); p. 2929 - 2943, View in Reaxys; Borowitz,I.J. et al.; Journal of Organic Chemistry; vol. 36; (1971); p. 553 560, View in Reaxys; Akiba et al.; Synthesis; (1977); p. 862, View in Reaxys; Rehak et al.; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 697,702, View in Reaxys; Laemmle et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 5120,5122, View in Reaxys; Shida et al.; Journal of Physical Chemistry; vol. 78; (1974); p. 741,742, View in Reaxys; Hoshino et al.; Journal of Physical Chemistry; vol. 78; (1974); p. 1473,1474, View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys; Warren; Yandle; Journal of the Chemical Society; (1965); p. 5518, View in Reaxys; Zwarich; Bree; Journal of Molecular Spectroscopy; vol. 52; (1974); p. 329,331,333,339, View in Reaxys; Kuboyama; Chemical Physics Letters; vol.

41; (1976); p. 544, View in Reaxys; Mukherjee; Journal of Physical Chemistry; vol. 73; (1969); p. 4381, View in Reaxys; Rosencwaig; Hall; Analytical Chemistry; vol. 47; (1975); p. 548, View in Reaxys; BELL JH; IRELAND S; SPEARS AW;

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Analytical Chemistry; vol. 41; nb. 2; (1969); p. 310 - 313, View in Reaxys; Edward; Wong; Journal of the American Chemical Society; vol. 99; (1977); p. 4229,4231, View in Reaxys; Cheshire et al.; Tetrahedron; vol. 23; (1967); p. 1669, View in Reaxys; Harget et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 214, View in Reaxys 104 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Smith,G.G.; Bayer,R.P.; Tetrahedron; vol. 18; (1962); p. 323 - 331, View in Reaxys; Dahn; Nickel; Justus Liebigs Annalen der Chemie; vol. 667; (1963); p. 101,110, View in Reaxys; Osugi; Okishima; Nippon Kagaku Zasshi; vol. 92; (1971); p. 598,599, 600; Chem.Abstr.; vol. 75; nb. 156597; (1971), View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys; Wiemann; Godefroid; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 255; (1962); p. 2608, View in Reaxys; Parry; Warren; Journal of the Chemical Society; (1965); p. 4049, View in Reaxys; Stewart et al.; Canadian Journal of Chemistry; vol. 41; (1963); p.

1065,1066, View in Reaxys 105 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

220 - 420 nm

Anderson et al.; Journal of the Chemical Society; (1959); p. 3992,3996, View in Reaxys 106 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

230 - 450 nm; bei 100 K.

Doerr; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 61; (1957); p. 950,951, View in Reaxys 107 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dioxane

Absorption Maxima (UV/ VIS) [nm]

378

Bergmann et al.; Bulletin de la Societe Chimique de France; (1951); p. 669,680, View in Reaxys 108 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dioxane

Absorption Maxima (UV/ VIS) [nm]

258; 294; 308; 328

Bergmann et al.; Bulletin de la Societe Chimique de France; (1951); p. 669,680, View in Reaxys 109 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Chaix; Bulletin de la Societe Chimique de France; vol. <4> 53; (1933); p. 700,708, View in Reaxys; Ramart-Lucas; Hoch; Bulletin de la Societe Chimique de France; vol. <5> 2; (1935); p. 1376,1378, View in Reaxys; Jones; Journal of the American Chemical Society; vol. 67; (1945); p. 2127,2130, 2144; Chemical Reviews (Washington, DC, United States); vol. 41; (1947); p.

353,361, 364, View in Reaxys; Stobbe; Chemische Berichte; vol. 44; (1911); p. 1486; Chemische Berichte; vol. 48; (1915); p.

442, View in Reaxys; Boeeseken; Cohen; Langedijk; Recueil des Travaux Chimiques des Pays-Bas; vol. 44; (1925); p.

184,188, View in Reaxys; Friedel,R.A.; Orchin,M.; Ultraviolet Spectra of Aromatic Compounds <New York 1951> Nr. 329, View in Reaxys; Wittig; Lange; Justus Liebigs Annalen der Chemie; vol. 536; (1938); p. 266,269, 272, 278, 282, View in Reaxys 110 of 115

Description (UV/VIS Spectroscopy)

Spectrum

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Solvent (UV/VIS Spectroscopy)

benzene

Wittig; Lange; Justus Liebigs Annalen der Chemie; vol. 436; (1938); p. 266,271, View in Reaxys 111 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CCl4

Wittig; Lange; Justus Liebigs Annalen der Chemie; vol. 436; (1938); p. 266,271, View in Reaxys 112 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

light petroleum

Boeeseken; Cohen; Langedijk; Recueil des Travaux Chimiques des Pays-Bas; vol. 44; (1925); p. 184,188, View in Reaxys; Wittig; Lange; Justus Liebigs Annalen der Chemie; vol. 436; (1938); p. 266,271, View in Reaxys 113 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2SO4

Anderson; Gooding; Journal of the American Chemical Society; vol. 57; (1935); p. 999,1006, View in Reaxys 114 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

HCl; 1,2-dichloro-ethane

Anderson; Gooding; Journal of the American Chemical Society; vol. 57; (1935); p. 999,1006, View in Reaxys 115 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

SnCl4 / 1,2-dichloro-ethane; HCl / 1,2-dichloro-ethane

Anderson; Gooding; Journal of the American Chemical Society; vol. 57; (1935); p. 999,1006, View in Reaxys ESR Spectroscopy (6) 1 of 6

Description (ESR Spectro- CIDEP (chemically induced dynamic electron polarization) scopy) Comment (ESR Spectroscopy)

in the presence of additives

Kawai, Akio; Yamamoto, Tetsuya; Okutsu, Tetsuo; Kinichi, Obi; Bulletin of the Chemical Society of Japan; vol. 72; nb. 12; (1999); p. 2625 - 2632, View in Reaxys 2 of 6

Description (ESR Spectro- Spectrum scopy) Solvents (ESR Spectrosco- cyclohexane py) Comment (ESR Spectroscopy)

in the presence of additives

Kawai, Akio; Yamamoto, Tetsuya; Okutsu, Tetsuo; Kinichi, Obi; Bulletin of the Chemical Society of Japan; vol. 72; nb. 12; (1999); p. 2625 - 2632, View in Reaxys 3 of 6

Description (ESR Spectro- Spectrum scopy) Solvents (ESR Spectrosco- cyclohexane; ethanol py) Comment (ESR Spectroscopy)

Ratio of solvents: 5:1 v/v; in the presence of additives

Kawai, Akio; Yamamoto, Tetsuya; Okutsu, Tetsuo; Kinichi, Obi; Bulletin of the Chemical Society of Japan; vol. 72; nb. 12; (1999); p. 2625 - 2632, View in Reaxys

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4 of 6

Description (ESR Spectro- Spectrum scopy) Solvents (ESR Spectrosco- ethanol; KOH py) Comment (ESR Spectroscopy)

in the presence of additives

Kawai, Akio; Yamamoto, Tetsuya; Okutsu, Tetsuo; Kinichi, Obi; Bulletin of the Chemical Society of Japan; vol. 72; nb. 12; (1999); p. 2625 - 2632, View in Reaxys 5 of 6

Description (ESR Spectro- ESR scopy) Takeshita; Hirota; Journal of Chemical Physics; vol. 58; (1973); p. 3745, View in Reaxys; YAMANASHI BS; MAZZA C; BOWERS KW; Applied Spectroscopy; vol. 25; nb. 4; (1971); p. 460 - 465, View in Reaxys; Sahini; Ciurea; Revue Roumaine de Chimie; vol. 14; (1969); p. 689,692, View in Reaxys; Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 30; (1971); p. 41,46, View in Reaxys

6 of 6

Description (ESR Spectro- ESR-hyperfine coupling constants scopy) Broze; Luz; Journal of Chemical Physics; vol. 51; (1969); p. 738,742, View in Reaxys

NQR Spectroscopy (1) Description (NQR References Spectroscopy) Nuclear quadrupole Butler, Leslie G.; Cheng, C. P.; Brown, Theodore L.; Journal of Physical Chemistry; vol. 85; nb. 19; (1981); p. 2738 resonance 2740, View in Reaxys Rotational Spectroscopy (1) Description (Rota- References tional Spectroscopy) Microwave spectrum

Konishi, S.; Morioka, Y.; Nakagawa, I.; Journal of Molecular Structure; vol. 64; (1980); p. 157 - 162, View in Reaxys

Raman Spectroscopy (7) Description (Ram- Solvent (Raman an Spectroscopy) Spectroscopy)

Location

Bands; Spectrum

References Inada, Yuhi; Amaya, Toru; Hirao, Toshikazu; RSC Advances; vol. 5; nb.

24; (2015); p. 18523 - 18530, View in Reaxys

Spectrum

supporting informa- Eakins, Galen L.; Cooper, Matthew W.; Gerasimchuk, Nikolay N.; Philtion lips, Terry J.; Breyfogle, Bryan E.; Stearman, Chad J.; Canadian Journal of Chemistry; vol. 91; nb. 11; (2013); p. 1059 - 1071, View in Reaxys

Raman

supporting informa- Eakins, Galen L.; Alford, Joshua S.; Tiegs, Brandon J.; Breyfogle, Brytion an E.; Stearman, Chad J.; Journal of Physical Organic Chemistry; vol. 24; nb. 11; (2011); p. 1119 - 1128, View in Reaxys

Spectrum

solid

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Bands

solid

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Bands

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys; Kolev, Tsonko; Journal of Molecular Structure; vol. 349; (1995); p. 381 - 384, View in Reaxys

Raman

Zwarich et al.; Journal of Molecular Spectroscopy; vol. 51; (1974); p.

38,42-47, View in Reaxys

Luminescence Spectroscopy (21) Description (Lumi- Comment (Luminescence Spectronescence Spectroscopy) scopy)

References

Luminescence maximum(a)

Kirichenko; Meshkova; Topilova; Kiriyak; Lyapunov; Kulygina; Luk'yanenko; Russian Journal of General Chemistry; vol. 75; nb. 2; (2005); p. 272 - 277, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Luminescence spectrum

temperature dependence

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol.

10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Luminescence lifetime

ambient temperature. Object(s) of Study: solvent dependence

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol.

10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Luminescence spectrum

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol. 69; nb. 3; (2002); p. 287 - 294, View in Reaxys

Luminescence quantum yield

Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys; Andrews; Journal of Physical Chemistry; vol. 82; (1978); p. 2304, View in Reaxys; Mitchell et al.; Journal of Chemical Physics; vol. 67; (1977); p. 4832, View in Reaxys; Korol'kova, N. V.; Val'kova, G. A.; Shigorin, D. N.; Grekhova, N. G.; Andrievskii, A. M.; Russian Journal of Physical Chemistry; vol. 63; nb. 12; (1989); p. 1792 - 1795; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 3272 - 3277, View in Reaxys; Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys; Biczok, Laszlo; Berces, Tibor; Journal of Physical Chemistry; vol. 92; nb. 13; (1988); p. 3842 - 3845, View in Reaxys; Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys; Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Tachibana, Hiroshi; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 45; (1998); p. 8657 - 8663, View in Reaxys

Luminescence lifetime

Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys; Andrews; Journal of Physical Chemistry; vol. 82; (1978); p. 2304, View in Reaxys; Kobayashi; Nagakura; Chemical Physics Letters; vol. 43; (1976); p. 429, View in Reaxys; Scaiano, J. C.; Wubbels, Gene G.; Journal of the American Chemical Society; vol. 103; nb. 3; (1981); p. 640 - 645, View in Reaxys; Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys; Biczok, Laszlo; Berces, Tibor; Journal of Physical Chemistry; vol. 92; nb. 13; (1988); p. 3842 - 3845, View in Reaxys; Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys; Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Luminescence quenching

Quenching with alcohols

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys

Electroluminescence

Gruzinskii, V. V.; Kukhto, A. V.; Journal of Applied Spectroscopy; vol. 50; nb. 2; (1989); p. 165 168; Zhurnal Prikladnoi Spektroskopii; vol. 50; nb. 2; (1989); p. 232 - 236, View in Reaxys

Luminescence quenching

Herkstroeter; Hammond; Journal of the American Chemical Society; vol. 88; (1966); p. 4769, View in Reaxys; Guttenplan; Cohen; Tetrahedron Letters; (1972); p. 2163, View in Reaxys; Loutfy; Loutfy; Canadian Journal of Chemistry; vol. 50; (1972); p. 4052,4054, View in Reaxys; Parsons; Cohen; Journal of the American Chemical Society; vol. 96; (1974); p. 2948,2950,2951, View in Reaxys; Fry et al.; Journal of the American Chemical Society; vol. 88; (1966); p. 4781, View in Reaxys; Goerner; Schulte-Fronhlinde; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 88; nb. 12; (1984); p. 1208 - 1216, View in Reaxys

Luminescence quenching

Quenching with Ph-1N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p.

2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with Ph-2N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p.

2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with 1N-1N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p.

2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with 1N-2N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p.

2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with 2N-2N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p.

2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with dit-butyl peroxide

Scaiano, J. C.; Wubbels, Gene G.; Journal of the American Chemical Society; vol. 103; nb. 3; (1981); p. 640 - 645, View in Reaxys

Luminescence quenching

Quenching with βpyran

Cerfontain, Hans; Geenevasen, Jan A. J.; Noort, Paul C. M. van; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 1057 - 1062, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Luminescence

Pragst et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 257; (1976); p. 465,471, View in Reaxys; Andrews; Journal of Physical Chemistry; vol. 82; (1978); p. 2304, View in Reaxys; Yoshihara; Kearns; Journal of Chemical Physics; vol. 45; (1966); p. 1991,1999, View in Reaxys

Emission spectrum in the infrared region

Yoshihara; Kearns; Journal of Chemical Physics; vol. 45; (1966); p. 1991,1999, View in Reaxys

Degree of depolarization of luminescence

Krauss; Huber; Chemische Berichte; vol. 94; (1961); p. 2864,2869,2874, View in Reaxys

Luminescence quenching

Loeschung der Fluoreszenz in Ascorbinsaeure.

Luminescence quenching

Loeschung der Flu- Weber; Savic; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B>24; (1934); p. 68,71,73, oreszenz von Fluo- View in Reaxys renon-(9) in Benzol durch Phenol, oKresol und anderen organischen Verbindungen.

Fluorescence Spectroscopy (80) Description (Fluo- Solvent (Fluoresrescence Spectrocence Spectroscoscopy) py)

Weber; Radiologica; vol. 2; (1938); p. 57,61, View in Reaxys

Temperature (Fluorescence Spectroscopy) [°C]

Spectrum; Maxima

Location

supporting information

Comment (Fluores- References cence Spectroscopy) Li, Shuangjiang; Aljhdli, Merfat; Thakellapalli, Haresh; Farajidizaji, Behzad; Zhang, Yu; Akhmedov, Novruz G.; Milsmann, Carsten; Popp, Brian V.; Wang, Kung K.; Organic Letters; vol. 19; nb.

15; (2017); p. 4078 - 4081, View in Reaxys

Fluorescence quantum yield

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys; Andronico, Luca A.; Quintavalla, Arianna; Lombardo, Marco; Mirasoli, Mara; Guardigli, Massimo; Trombini, Claudio; Roda, Aldo; Chemistry - A European Journal; vol. 22; nb. 50; (2016); p.

18156 - 18168, View in Reaxys

Spectrum; Maxima; Fluorescence quantum yield

Tan, Ke Xin; Lintang, Hendrik O.; Maniam, Subashani; Langford, Steven J.; Bakar, Mohd Bakri; Tetrahedron; vol.

72; nb. 35; (2016); p. 5402 5413, View in Reaxys

Maxima; Fluorescence quantum yield; Fluorescence lifetime; Spectrum

Ghosh, Indrajit; Mukhopadhyay, Arindam; Koner, Apurba Lal; Samanta, Subhas; Nau, Werner M.; Moorthy, Jarugu Narasimha; Physical Chemistry Chemical Physics; vol. 16; nb. 31; (2014); p. 16436 - 16445, View in Reaxys

Spectrum; Maxima

Samant, Vaishali; Varne, Mahendra; Palit, Dipak K.; Journal of Photochemistry and Photobiology A: Chemistry; vol.

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264; (2013); p. 1 - 11, View in Reaxys Fluorescence quantum yield; Maxima; Spectrum; Fluorescence lifetime

Fluorescence

Robert, Patricia; Bolduc, Andreanne; Skene, W. G.; Journal of Physical Chemistry A: Molecules, Spectroscopy, Kinetics, Environment, and General Theory; vol. 116; nb. 37; (2012); p. 9305 - 9314,10, View in Reaxys supporting information

Fluorescence

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

Dufresne, Stephane; Skalski, Thomas; Skene; Canadian Journal of Chemistry; vol. 89; nb. 2; (2011); p. 173 - 180, View in Reaxys Dahn; Nickel; Justus Liebigs Annalen der Chemie; vol. 667; (1963); p. 101,110, View in Reaxys; Monroe; Groff; Tetrahedron Letters; (1973); p. 3955, View in Reaxys; Snyder; Testa; Journal of Physical Chemistry; vol. 83; (1979); p. 3041, View in Reaxys; Davidson; Lambeth; Journal of the Chemical Society [Section] D: Chemical Communications; (1969); p.

1098, View in Reaxys; Mitchell et al.; Journal of Chemical Physics; vol. 67; (1977); p.

4832, View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p.

377,393, View in Reaxys; Zwarich; Bree; Journal of Molecular Spectroscopy; vol. 52; (1974); p. 329,331,333,339, View in Reaxys; Huggenberger; Labhart; Helvetica Chimica Acta; vol. 61; (1978); p.

250,251, 253, 255, View in Reaxys; Moritani; Nagai; Nippon Kagaku Zasshi; vol. 86; (1965); p. 157; Chem.Abstr.; vol. 63; nb.

7789b, View in Reaxys; Davies; Ennis; Journal of the Chemical Society; (1960); p. 1488,1490, View in Reaxys; Davis et al.; Journal of the American Chemical Society; vol. 91; (1969); p.

2264, View in Reaxys; Caldwell; Tetrahedron Letters; (1969); p. 2121, View in Reaxys; Singer; Tetrahedron Letters; (1969); p. 923, View in Reaxys; Guttenplan; Cohen; Tetrahedron Letters; (1969); p. 2125, View in Reaxys; Singer et al.; Journal of the American Chemical Society; vol. 91; (1969); p.

897, View in Reaxys; Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and

119/144

2018-06-21 20:37:19

Biomolecular Spectroscopy; vol. 71; nb. 2; (2008); p. 537 542, View in Reaxys; Schneck, Crystal M.; Poncheri, Adam J.; Jennings, John T.; Snyder, Deanna L.; Worlinsky, Jill L.; Basu, Swarna; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 75; nb. 2; (2010); p. 624 628, View in Reaxys Spectrum

CH2Cl2

Zhang, Kai; Chen, Zhao; Yang, Chuluo; Tao, Youtian; Zou, Yang; Qin, Jingui; Cao, Yong; Journal of Materials Chemistry; vol. 18; nb. 3; (2008); p. 291 - 298, View in Reaxys

Spectrum

tetrahydrofuran

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Spectrum

acetonitrile

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Spectrum

hexane

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

pentane

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

hexane

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

heptane

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

toluene

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys; Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

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120/144

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Maxima

butyl acetate

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

ethyl acetate

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

tetrahydrofuran

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

1,2-dichloro-benzene

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

acetone

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

acetonitrile

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys; Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Spectrum

cyclohexane; tetrahydrofuran

-0.16 - 99.84

temperature dependence

Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p.

444 - 449, View in Reaxys

Spectrum

cyclohexane; ethanol

-0.16 - 99.84

temperature dependence

Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p.

444 - 449, View in Reaxys

Maxima

cyclohexane; tetrahydrofuran

Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p.

444 - 449, View in Reaxys

Maxima

cyclohexane; ethanol

Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p.

444 - 449, View in Reaxys

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Spectrum

toluene

Spectrum

CHCl3

Maxima

film

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys

Spectrum

film

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys

Biczok, Laszlo; Berces, Tibor; Inoue, Haruo; Journal of Physical Chemistry A; vol. 103; nb.

20; (1999); p. 3837 - 3842, View in Reaxys; Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys ambient temperature

Chi, Chunyan; Im, Chan; Enkelmann, Volker; Ziegler, Andreas; Lieser, Guenter; Wegner, Gerhard; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6833 - 6845, View in Reaxys

Spectrum

temperature dependence

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p.

2391 - 2408, View in Reaxys

Fluorescence excitation spectrum

temperature dependence

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p.

2391 - 2408, View in Reaxys

Maxima

cyclohexane

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

Maxima

butan-1-ol

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

Maxima

dioxane

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

Fluorescence quantum yield

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

solvent dependence

122/144

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

2018-06-21 20:37:19

Energy transfer from singlet state

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol. 69; nb. 3; (2002); p.

287 - 294, View in Reaxys

Fluorescence excitation spectrum

96.85

in the presence of rare gases

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

Fluorescence excitation spectrum

96.85

in the presence of organic compounds. Object(s) of Study: in the presence of rare gases

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

Spectrum

96.85

in the presence of rare gases

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

Spectrum

96.85

in the presence of organic compounds. Object(s) of Study: in the presence of rare gases

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

Fluorescence lifetime

96.85

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

26.85

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 150, View in Reaxys

Spectrum

acetonitrile

Fluorescence decay acetonitrile kinetics; Spectrum

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 150, View in Reaxys

Maxima

cyclohexane

472 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Maxima

benzene

485 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Maxima

acetonitrile

514 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Maxima

ethanol

562 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

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123/144

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Maxima

ethanol

Fluorescence quenching

490 nm, 512 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Quenching with ethanol

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Tachibana, Hiroshi; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 45; (1998); p. 8657 - 8663, View in Reaxys

Spectrum

acetonitrile

666.67 - 322.58 nm Demeter, Attila; Timari, Geza; Kotschy, Andras; Berces, Tibor; Tetrahedron Letters; vol.

38; nb. 29; (1997); p. 5219 5222, View in Reaxys

Spectrum

ethanol

400 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol.

69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

acetonitrile

400 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol.

69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

cyclohexane

400 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol.

69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

acetonitrile; ethanol

400 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol.

69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

acetonitrile; ethanol

440 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol.

69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

cyclohexane; ethanol

440 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol.

69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

benzene

320 - 600 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Spectrum

hexane

320 - 600 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molec-

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

124/144

2018-06-21 20:37:19

ular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys Spectrum

CHCl3

320 - 600 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Spectrum

methanol

320 - 600 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

hexane

341 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

propan-1-ol

346 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

cyclohexane

347 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

dioxane

347.5 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

butan-1-ol

350 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

methanol

353 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

acetonitrile

346.75 nm; 504.5 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

benzene

351 nm; 486 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

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125/144

2018-06-21 20:37:19

Maxima

toluene

Maxima

354 nm; 488.5 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

355.5 nm; 501 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

tetrahydrofuran

356.5 nm; 493.75 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

dimethylformamide

359.25 nm; 507.5 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

CH2Cl2

359.25 nm; 508.25 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

cyclohexane

505.08 nm

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p.

1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p.

2881 - 2890, View in Reaxys

Maxima

methylcyclohexane

505.08 nm

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p.

1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p.

2881 - 2890, View in Reaxys

Maxima

acetone

546.45 nm

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p.

1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p.

2881 - 2890, View in Reaxys

Maxima

acetonitrile

546.45 nm

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p.

1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p.

2881 - 2890, View in Reaxys

Spectrum

toluene

460 - 620 nm

Gruzinskii, V. V.; Kukhto, A. V.; Journal of Applied Spectroscopy; vol. 50; nb. 2; (1989); p.

165 - 168; Zhurnal Prikladnoi Spektroskopii; vol. 50; nb. 2;

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

126/144

2018-06-21 20:37:19

(1989); p. 232 - 236, View in Reaxys Maxima

benzene

Phosphorescence Spectroscopy (6) Description (Phos- Comment (Phosphorescence Spec- phorescence Spectroscopy) troscopy)

480 nm

Scaiano, J. C.; Wubbels, Gene G.; Journal of the American Chemical Society; vol. 103; nb.

3; (1981); p. 640 - 645, View in Reaxys

References

Triplet state energy

Yamaji, Minoru; Wakabayashi, Sayaka; Ueda, Shin-Ichi; Shizuka, Haruo; Tobita, Seiji; Chemical Physics Letters; vol. 368; nb. 1-2; (2003); p. 41 - 48, View in Reaxys

Triplet state quenching

Yamaji, Minoru; Wakabayashi, Sayaka; Ueda, Shin-Ichi; Shizuka, Haruo; Tobita, Seiji; Chemical Physics Letters; vol. 368; nb. 1-2; (2003); p. 41 - 48, View in Reaxys

Energy transfer from triplet state

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol. 69; nb. 3; (2002); p. 287 - 294, View in Reaxys

Triplet state decay kinetics

Zalesskaya, G. A.; Yakovlev, D. L.; Sambor, E. G.; Prikhodchenko, D. V.; Journal of Applied Spectroscopy; vol. 68; nb. 1; (2001); p. 150 - 158; Zhurnal Prikladnoi Spektroskopii; vol. 68; nb.

1; (2001); p. 110 - 115, View in Reaxys

Phosphorescence

Heller; Wasserman; Journal of Chemical Physics; vol. 42; (1965); p. 949,952, View in Reaxys; Huggenberger; Labhart; Helvetica Chimica Acta; vol. 61; (1978); p. 250,251, 253, 255, View in Reaxys; Yoshihara; Kearns; Journal of Chemical Physics; vol. 45; (1966); p. 1991,1999, View in Reaxys; Kadhim; Offen; Journal of Chemical Physics; vol. 47; (1967); p. 1289,1290, View in Reaxys

Spectrum

470 - 620 nm; bei 120 K.

Pesteil et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 239; (1954); p. 255, View in Reaxys

Other Spectroscopic Methods (2) Description (Other References Spectroscopic Methods) ESCA

Khel'mer, B. Yu.; Shelepin, O. E.; Shuvaev, A. T.; Mazalov, L. N.; Journal of Structural Chemistry; vol. 25; (1984); p.

325 - 327; Zhurnal Strukturnoi Khimii; vol. 25; nb. 2; (1984); p. 170 - 172, View in Reaxys

Photoelectron spec- Centineo et al.; Journal of Molecular Structure; vol. 44; (1978); p. 203,204, View in Reaxys trum Exposure Assessment (5) Exposure Sources

References

presence in carbonaceous aerosol particles

diesel soot and par- Matuschek, Georg; Karg, Erwin; Schroeppel, Andreas; Schulz, Holger; Schmid, Otmar; Enticles from tire and vironmental Science and Technology; vol. 41; nb. 24; (2007); p. 8406 - 8411, View in Reaxys break wear, diesel exhaust particles generated by a car at idle motor condition and laboratory generated aerosols (spark discharge C particles and diffusion flame soot)

presence in water in Lippe River (NorthRhine Westphalia, Germany)

samples taken on Dsikowitzky, Larissa; Schwarzbauer, Jan; Kronimus, Alexander; Littke, Ralf; Chemosphere; August 16-17, vol. 57; nb. 10; (2004); p. 1275 - 1288, View in Reaxys 1999; title comp. detected in 11 sites; GC-MS and GCFID analyses; biogenic or geogenic contribution; industrial influence

emission rates of 138.9 and 2.4 μg/L of gasoline-equivalent fuel burned for

motor vehicle traffic; Van Nuys Tunnel, Los Angeles, USA; 0600-1000

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Environmental Science and Technology; vol. 32; nb. 14; (1998); p. 2051 - 2060, View in Reaxys

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vapor and particle PDT, September phases, respectively 21, 1993; inside and outside tunnel; 7060 vehicles counted; average vehicle age: more than 7 years; catalyst and non-catalyst vehicles; average vehicle speed: ca. 64 km/h incineration of iodine bearing waste; presence in clean offgas; waste incineration plant; Germany depositions of aerosols and particulate matter as black crust; samples from the Sevilla cathedral (eastern side, major nave, and southern side); in limestone black weathering crust; percent intensity referenced to the highest peak of methyl n-docosanoate: <25

Jay, K.; Stieglitz, L.; Chemosphere; vol. 30; nb. 7; (1995); p. 1249 - 1260, View in Reaxys

air pollution in urFobe, Bart O.; Vleugels, Greta J.; Roekens, Eddy J.; Grieken, Rene E. Van; Hermosin, Berban environment of nardo; et al.; Environmental Science & Technology; vol. 29; nb. 6; (1995); p. 1691 - 1701, Sevilla, in Andalu- View in Reaxys cia (southwestern Spain); average temperatures: 10.7 deg C in January and 26.8 deg C in July; rain: 620 mm/ year; average relative humidity: 59 percent; effect of engine exhaust; GC/MS method

Concentration in the Environment (27) 1 of 27

Media (Concentration in the Environment)

wood

Contamination Concentration

27.5 μg/g CTW

Method, Remarks (Concentration in the Environment)

non-sterilized chipped creosote-contaminated wood samples collected; extracted with methanol in ultrasonic bath; GC-MS; conc. expressed as μg/g creosote treated wood (CTW); table

Polcaro; Brancaleoni; Donati; Frattoni; Galli; Migliore; Rapana; Bulletin of Environmental Contamination and Toxicology; vol. 81; nb. 2; (2008); p. 180 - 184, View in Reaxys 2 of 27

Media (Concentration in the Environment)

light-duty gasoline emission, gas-phase

Location

El Monte, California

Contamination Concentration

2.9 - 29 μg/l

Method, Remarks (Concentration in the Environment)

gas-phase emissions collec. from low-emission and three catalyst-equipped vehicles at HaagenSmit Laboratory during Aug.-Sep. 2002; ultrasonic extrac. in 1:1 hexane/DCM (v/v) and methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; tab.

Jakober, Chris A.; Robert, Michael A.; Riddle, Sarah G.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.; Environmental Science and Technology; vol. 42; nb. 13; (2008); p. 4697 - 4703, View in Reaxys 3 of 27

Media (Concentration in the Environment)

light-duty gasoline emission, particle-phase

Location

El Monte, California

Contamination Concentration

0 - 0.3 μg/l

Method, Remarks (Concentration in the Environment)

particle phase emissions collec. from low-emission, three catalyst-equipped vehicles at HaagenSmit Laboratory during Aug.-Sep. 2002; ultrasonic extrac. in 1:1 hexane/DCM (v/v), methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; table

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Jakober, Chris A.; Robert, Michael A.; Riddle, Sarah G.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.; Environmental Science and Technology; vol. 42; nb. 13; (2008); p. 4697 - 4703, View in Reaxys 4 of 27

Media (Concentration in the Environment)

heavy-duty diesel emission, gas-phase

Location

California

Contamination Concentration

190 - 1000 μg/l

Method, Remarks (Concentration in the Environment)

emissions from 1999 Freightliner Tractor operated under idle-creep, heavy heavy-duty diesel truck driving cycle condition; June 2003; ultrasonic extrac. in 1:1 hexane/DCM (v/v), methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; tab.

Jakober, Chris A.; Robert, Michael A.; Riddle, Sarah G.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.; Environmental Science and Technology; vol. 42; nb. 13; (2008); p. 4697 - 4703, View in Reaxys 5 of 27

Media (Concentration in the Environment)

heavy-duty diesel emission, particle-phase

Location

California

Contamination Concentration

0 - 24 μg/l

Method, Remarks (Concentration in the Environment)

emissions from 1999 Freightliner Tractor operated under idle-creep, heavy heavy-duty diesel truck driving cycle condition; June 2003; ultrasonic extrac. in 1:1 hexane/DCM (v/v), methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; tab.

Jakober, Chris A.; Robert, Michael A.; Riddle, Sarah G.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.; Environmental Science and Technology; vol. 42; nb. 13; (2008); p. 4697 - 4703, View in Reaxys 6 of 27

Media (Concentration in the Environment)

surface sediment

Location

river Elbe, Prelouc, Czech Republic

Contamination Concentration

20 ng/g dry wt

Method, Remarks (Concentration in the Environment)

samples (top 5 cm) collected using Van Veen grab; GCxGC-ToF-MS analyzed

Skoczynska, Ewa; Korytar, Peter; De Boer, Jacob; Environmental Science and Technology; vol. 42; nb. 17; (2008); p. 6611 6618, View in Reaxys 7 of 27

Media (Concentration in the Environment)

surface seawater

Location

Suruga Bay, Japan

Contamination Concentration

1.2 - 53.7 ng/l

Method, Remarks (Concentration in the Environment)

mean conc.; samples (2.7-11.5 m depth) collected from various sites on December 14-15, 2003; GC-MS

Hashimoto, Shinya; Ueda, Yasuhiro; Kurihara, Ryo; Shiraishi, Fujio; Environmental Toxicology and Chemistry; vol. 26; nb.

2; (2007); p. 279 - 286, View in Reaxys 8 of 27

Media (Concentration in the Environment)

ambient air

Location

Finokalia, Island of Crete, eastern Mediterranean

Contamination Concentration

46.3 fg/l

Method, Remarks (Concentration in the Environment)

average conc.; particulate phase conc.; samples collected using a modified high-volume sampler with 4 h sampling interval during 3-d intensive campaign on August 17-21, 2001; GC-MS analyzed; diagram

Tsapakis, Manolis; Stephanou, Euripides G.; Environmental Science and Technology; vol. 41; nb. 23; (2007); p. 8011 - 8017, View in Reaxys

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9 of 27

Media (Concentration in the Environment)

atmospheric particulate matter

Location

Lanzhou city, Gansu Province, Northwest of China

Contamination Concentration

0.64 pg/l air

Method, Remarks (Concentration in the Environment)

average conc.; total suspended particulate matter acquired from the Lanyuan hotel; 6 air samples collected in March 2003 during 24 h periods; flow rate: 0.8 m3/min; GC-MS and GC-FID analyses; triplicate measurements

Gao; Zhou; Ma; Chen; Hu; Bulletin of Environmental Contamination and Toxicology; vol. 72; nb. 5; (2004); p. 923 - 930, View in Reaxys 10 of 27

Media (Concentration in the Environment)

sediment

Location

Morava river basin, Czech Republic

Contamination Concentration

2.8 - 85.3 ng/g dry wt

Method, Remarks (Concentration in the Environment)

9 samples of surface sediment analyzed using GC/MS(EI)

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 11 of 27

Media (Concentration in the Environment)

soil

Location

Northern Germany (military existing material)

Contamination Concentration

4.1 mg/kg

Method, Remarks (Concentration in the Environment)

extraction by CH2Cl2/n-hexane; separation by acidity using solid-phase extraction (Chromaton SB/ silica gel column); elution by n-hexane/CH2Cl2, CH2Cl2/MeOH, MeOH/0.05 N HCl; cation-exchange solid-phase separation; GC, HPLC; matrix calibration

Steinhart; Meyer; Cartellieri; Analytical Chemistry; vol. 71; nb. 18; (1999); p. 4023 - 4029, View in Reaxys 12 of 27

Media (Concentration in the Environment)

sandy soil

Location

Northern Germany (wood-processing plant)

Contamination Concentration

1.6 mg/kg

Method, Remarks (Concentration in the Environment)

extraction by CH2Cl2/n-hexane; separation by acidity using solid-phase extraction (Chromaton SB/ silica gel column); elution by n-hexane/CH2Cl2, CH2Cl2/MeOH, MeOH/0.05 N HCl; cation-exchange solid-phase separation; GC, HPLC; matrix calibration

Steinhart; Meyer; Cartellieri; Analytical Chemistry; vol. 71; nb. 18; (1999); p. 4023 - 4029, View in Reaxys 13 of 27

Media (Concentration in the Environment)

airborne particulate

Location

Los Angeles; Southern California; USA

Contamination Concentration

10.5 - 49.2 mg/kg

Method, Remarks (Concentration in the Environment)

fine particulate matter; collected in 1993 at four urban sites with a different air pollution level: central Los-Angeles, Long Beach, Azuza and Roubidoux; extraction; fractionation; GC-SIMS analysis

Hannigan, Michael P.; Cass, Glen R.; Penman, Bruce W.; Crespi, Charles L.; Lafleur, Arthur L.; Busby Jr., William F.; Thilly, William G.; Simoneit, Bernd R. T.; Environmental Science and Technology; vol. 32; nb. 22; (1998); p. 3502 - 3514, View in Reaxys 14 of 27

Media (Concentration in the Environment)

air, vapor phase

Location

Southern California, USA

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Contamination Concentration

0.1 - 14.11 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993; volatile, semivolative and particle-phase organics collected over Long Beach, Central Los Angeles, Azusa and Claremont

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb.

12; (1998); p. 1760 - 1770, View in Reaxys 15 of 27

Media (Concentration in the Environment)

air, fine particulate matter

Location

Southern California, USA

Contamination Concentration

0 - 1.04 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993; volatile, semivolative and particle-phase organics collected over Long Beach, Central Los Angeles, Azusa and Claremont

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb.

12; (1998); p. 1760 - 1770, View in Reaxys 16 of 27

Media (Concentration in the Environment)

air

Location

San Nicolas Island, Los Angeles area, USA

Contamination Concentration

0.07 pg/l

Method, Remarks (Concentration in the Environment)

September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb.

12; (1998); p. 1760 - 1770, View in Reaxys 17 of 27

Media (Concentration in the Environment)

air

Location

Long Beach, Southern California, USA

Contamination Concentration

0.46 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb.

12; (1998); p. 1760 - 1770, View in Reaxys 18 of 27

Media (Concentration in the Environment)

air

Location

Claremont, Southern California, USA

Contamination Concentration

8.31 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb.

12; (1998); p. 1760 - 1770, View in Reaxys 19 of 27

Media (Concentration in the Environment)

air

Location

Azusa, Southern California, USA

Contamination Concentration

8.08 pg/l

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Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb.

12; (1998); p. 1760 - 1770, View in Reaxys 20 of 27

Media (Concentration in the Environment)

air

Location

Central Los Angeles, Southern California, USA

Contamination Concentration

0.73 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb.

12; (1998); p. 1760 - 1770, View in Reaxys 21 of 27

Media (Concentration in the Environment)

airborne particles

Location

Washington, DC, USA

Contamination Concentration

1.6 mg/kg

Method, Remarks (Concentration in the Environment)

in SRM 1649 from NIST (Gaithersburg, MD); collected over ca.12-months period in the late 1970s; baghouse sampler with canvas bags; Soxhlet extraction (CH2Cl2); GC-MS analysis; standards: authentic for identification, structural isomer for quantification

Durant, John L.; Lafleur, Arthur L.; Plummer, Elaine F.; Taghizadeh, Koli; Busby Jr., William F.; Thilly, William G.; Environmental Science and Technology; vol. 32; nb. 13; (1998); p. 1894 - 1906, View in Reaxys 22 of 27

Media (Concentration in the Environment)

air

Location

Kenmore Square, Boston, MA, U.S.A.

Contamination Concentration

2.072 pg/l

Method, Remarks (Concentration in the Environment)

average conc.; from the roof of a National Ambient Air Quality Standards monitoring station; five 24-h air samples; June 1994; 4 m above ground level; micro-orifice impactor; GC/MS; distribution with particle size in an urban aerosol

Allen, Jonathan O.; Dookeran, Nameeta M.; Taghizadeh, Koli; Lafleur, Arthur L.; Smith, Kenneth A.; Sarofim, Adel F.; Environmental Science and Technology; vol. 31; nb. 7; (1997); p. 2064 - 2070, View in Reaxys 23 of 27

Media (Concentration in the Environment)

distillate fuel oil

Contamination Concentration

25.0 - 32.3 pg kJ-1

Method, Remarks (Concentration in the Environment)

fine particulate matter collected from an industrial boiler burning no. 2; emission rates measured; 5 experiments; samples collected during tests 2 and 5 subjected to GC/MS analysis; time: 185-375 min; boiler operated at 54-58 percent of its rated capacity

Rogge, Wolfgang F.; Hildemann, Lynn M.; Mazurek, Monica A.; Cass, Glen R.; Simoneit, Bernd R. T.; Environmental Science and Technology; vol. 31; nb. 10; (1997); p. 2731 - 2737, View in Reaxys 24 of 27

Media (Concentration in the Environment)

wastewater

Location

Sweden

Contamination Concentration

0 - 0.5 μg/l

Method, Remarks (Concentration in the Environment)

daily composite samples; in the effluent wastewater from Henriksdal Sewage Treatment Plant, Stockholm (0.5 μg/l; Jan. 1994), Goeteborg Regional Sewage Works (not detected; Dec. 1993), and Sjoelunda Sewage Works, Malmoe (not detected; Dec. 1993); GC/MS

Paxeus, Nicklas; Water Research; vol. 30; nb. 5; (1996); p. 1115 - 1122, View in Reaxys

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25 of 27

Media (Concentration in the Environment)

clean offgas

Location

Germany

Contamination Concentration

1.69 ng/l

Method, Remarks (Concentration in the Environment)

municipal waste incineration plant; water vapor condensation; XAD-resin filters; adsorption/thermodesorption; adsorption/elution; GC-FID analysis

Jay, K.; Stieglitz, L.; Chemosphere; vol. 30; nb. 7; (1995); p. 1249 - 1260, View in Reaxys 26 of 27

Media (Concentration in the Environment)

smoke

Location

70 km north of Manaus, Amazonia

Contamination Concentration

4.0 ng/l

Method, Remarks (Concentration in the Environment)

smoke from burning forest litter; in northern forest reserve of Instituto Nacional de Pesquisas da Amazonia; November 1992; high volume filtration; extraction with CH2Cl2; methylation; separation by TLC; GC and GC-MS analysis

Radzi bin Abas, M.; Simoneit, B. R. T.; Elias, V.; Cabral, J. A.; Cardoso, J. N.; Chemosphere; vol. 30; nb. 5; (1995); p. 995 1016, View in Reaxys 27 of 27

Media (Concentration in the Environment)

urban atmosphere

Location

Barcelona, Spain

Contamination Concentration

2 - 7 pg*m-3

Method, Remarks (Concentration in the Environment)

two heavily trafficked sites; sampling in spring, fall, winter 1989-1990; Hi-Vol sampling system (MCV, Collbato, Spain); extraction with dichloromethane; GPC and NP-LC fractionation; cGC-MS analysis

Bayona, J. M.; Casellas, M.; Fernandez, P.; Solanas, A. M.; Albaiges, J.; Chemosphere; vol. 29; nb. 3; (1994); p. 441 - 450, View in Reaxys Biodegradation (3) 1 of 3

Type (Biodegradation)

aerobic

Inoculum

Pleurotus ostreatus (SMR 684)

Concentration (Biodegradation)

27.5 μg/g CTW

Degradation Rate (Biodegradation) [%]

Ca. 100 percent

Exposure Period (Biodegradation)

44 d

Method, Remarks (Biodegradation)

33percent of creosote treated wood (CTW) chips added to dry wheat straw inoculated with mycelium of Pleurotus ostreatus; pressed to eliminate water; extracted with methanol in ultrasonic bath; GC-MS; title comp. conc. after 44 d: 4.8 μg/g CTW; table

Polcaro; Brancaleoni; Donati; Frattoni; Galli; Migliore; Rapana; Bulletin of Environmental Contamination and Toxicology; vol. 81; nb. 2; (2008); p. 180 - 184, View in Reaxys 2 of 3

Type (Biodegradation)

aerobic

Inoculum

Pleurotus ostreatus (SMR 684)

Concentration (Biodegradation)

27.5 μg/g CTW

Method, Remarks (Biodegradation)

50percent of creosote treated wood (CTW) chips added to dry wheat straw inoculated with mycelium of Pleurotus ostreatus; pressed to eliminate water; extracted with methanol in ultrasonic bath; GC-MS; title comp. conc. after 60 d: 18.8 μg/g CTW; table

Polcaro; Brancaleoni; Donati; Frattoni; Galli; Migliore; Rapana; Bulletin of Environmental Contamination and Toxicology; vol. 81; nb. 2; (2008); p. 180 - 184, View in Reaxys

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3 of 3

Type (Biodegradation)

aerobic

Inoculum

Pleurotus ostreatus (SMR 684)

Concentration (Biodegradation)

27.5 μg/g CTW

Method, Remarks (Biodegradation)

60percent of creosote treated wood (CTW) chips added to dry wheat straw inoculated with mycelium of Pleurotus ostreatus; pressed to eliminate water; extracted with methanol in ultrasonic bath; GC-MS; title comp. conc. after 60 d: 8.4 μg/g CTW; table

Polcaro; Brancaleoni; Donati; Frattoni; Galli; Migliore; Rapana; Bulletin of Environmental Contamination and Toxicology; vol. 81; nb. 2; (2008); p. 180 - 184, View in Reaxys Abiotic Degradation, Photolysis (1) 1 of 1

Type (Abiotic Degradation, Photolysis)

photolysis

Concentration (Abiotic Degradation, Photolysis)

5 mg/l

Temperature (Abiotic Deg- 20 - 25 radation, Photolysis) [°C] Rate Constant

2.0E-2 1/min

Half-life Time (Abiotic Degradation, Photolysis) [h]

0.48

Method, Remarks (Abiotic photoreactor equipped with quartz immersion well; 125 W medium pressure mercury lamp; aqueDegradation, Photolysis) ous ethanolic solution of title comp.; photoreactor covered with aluminium foil; GC/MS; HPLC/UV; title comp. was practically stable during first 10 min Sabate; Bayona; Solanas; Chemosphere; vol. 44; nb. 2; (2001); p. 119 - 124, View in Reaxys Use (12) Laboratory Use and Use Pattern Handling

References

Pharmaceuticals

Li, Huifang; Hassona, Mohamed D.H.; Lack, Nathan A.; Axerio-Cilies, Peter; Leblanc, Eric; Tavassoli, Peyman; Kanaan, Natalia; Frewin, Kate; Singh, Kriti; Adomat, Hans; Boehm, Konrad J.; Prinz, Helge; Guns, Emma Tomlinson; Rennie, Paul S.; Cherkasov, Artem; Molecular Cancer Therapeutics; vol. 12; nb. 11; (2013); p. 2425 - 2435, View in Reaxys

treating antiandrogen-resistant prostate cancer

Li, Huifang; Hassona, Mohamed D.H.; Lack, Nathan A.; Axerio-Cilies, Peter; Leblanc, Eric; Tavassoli, Peyman; Kanaan, Natalia; Frewin, Kate; Singh, Kriti; Adomat, Hans; Boehm, Konrad J.; Prinz, Helge; Guns, Emma Tomlinson; Rennie, Paul S.; Cherkasov, Artem; Molecular Cancer Therapeutics; vol. 12; nb. 11; (2013); p. 2425 - 2435, View in Reaxys

Spectral sensitizer

Patent; CIBA HOLDING INC.; WO2009/47151; (2009); (A1) English, View in Reaxys

Sensitizer

Patent; FujiFilm Corporation; US2008/21223; (2008); (A1) English, View in Reaxys

Light stabilizer

Patent; FujiFilm Corporation; US2008/21223; (2008); (A1) English, View in Reaxys

aromatic ketone for generation enolates from 4,5-epoxymorphinan compounds in the presence of potassium tert-alkylate

Patent; Likhotvorik, Igor R.; Lisowski, Joseph J.; US2006/167258; (2006); (A1) English, View in Reaxys

Photoinitiator

Patent; KING PHARMACEUTICALS; WO2006/71844; (2006); (A2) English, View in Reaxys

determination of LiAlH4 in ether or THF solutions

Brown, Eric; Leze, Antoine; Touet, Joel; Tetrahedron Letters; vol. 32; nb. 34; (1991); p. 4309 4310, View in Reaxys

as sensitizer in the rearrangement of onitrobenzaldehyde to o-nitrosobenzoic acid

Filby, W. G.; Guenther, K.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol.

125; (1981); p. 21 - 26, View in Reaxys

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β, β* Sensibilisatorwirkung

Rehak et al.; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 697,702, View in Reaxys

Photosens. Decarboxylierung v. Phenoxyessigsaeure

Davidson et al.; Journal of the Chemical Society [Section] C: Organic; (1971); p. 3480, View in Reaxys

Photosens. Decarboxylierung v. N(o-Chlorphenyl)glycin

Davidson et al.; Journal of the Chemical Society [Section] C: Organic; (1971); p. 3480, View in Reaxys

Quantum Chemical Calculations (2) Calculated Proper- Method (Quantum ties Chemical Calculations) Molecular orbitals; Electronic energy levels; Transition energies

Ab initio calcns.

(LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)

Electronic energy levels; Molecular orbitals

Ab initio calcns.

(LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)

Location

References

supporting informa- Xie, Lili; Zhen, Xiaomeng; Huang, Shuping; Su, Xiaolong; Lin, Mai; Li, tion Yi; Green Chemistry; vol. 19; nb. 15; (2017); p. 3530 - 3534, View in Reaxys Spenst, Peter; Würthner, Frank; Angewandte Chemie - International Edition; vol. 54; nb. 35; (2015); p. 10165 - 10168; Angew. Chem.; vol. 127; nb.

35; (2015); p. 10303 - 10306,4, View in Reaxys

Medchem (29) 1 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

radioprotectant properties

Measurement Parameter

qualitative

Vatulina; Tuzhilkova; Bokova; Pharmaceutical Chemistry Journal; vol. 23; nb. 4; (1990); p. 325 - 329, View in Reaxys 2 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

LD 50: 2000 mg/kg, radioprotective activity, intraperitoneally (mouse)

Measurement Parameter

qualitative

Vatulina, G. G.; Bol'shakova, S. A.; Tuzhilkova, T. I.; Bokova, A. I.; Makhsudova, B.; et al.; Pharmaceutical Chemistry Journal; vol. 19; nb. 5; (1985); p. 326 - 330; Khimiko-Farmatsevticheskii Zhurnal; vol. 19; nb. 5; (1985); p. 552 - 557, View in Reaxys 3 of 29

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Biological Species/NCBI ID

rat

Substance RN

1636531View in Reaxys

Substance Name

21

Substance Dose

116 mg/kg

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

Cmax

Unit

ng/g

Quantitative value

255

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Dunn, Derek; Hostetler, Greg; Iqbal, Mohamed; Marcy, Val R.; Lin, Yin Guo; Jones, Bruce; Aimone, Lisa D.; Gruner, John; Ator, Mark A.; Bacon, Edward R.; Chatterjee, Sankar; Bioorganic and Medicinal Chemistry Letters; vol. 22; nb. 11; (2012); p. 3751 - 3753, View in Reaxys 4 of 29

Bioassay Category

Pharmacokinetic

Bioassay Name

Pharmacokinetic

Biological Species/NCBI ID

rat

Substance RN

1636531View in Reaxys

Substance Name

21

Substance Dose

116 mg/kg

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

tmax

Unit

hour

Quantitative value

0.8

Dunn, Derek; Hostetler, Greg; Iqbal, Mohamed; Marcy, Val R.; Lin, Yin Guo; Jones, Bruce; Aimone, Lisa D.; Gruner, John; Ator, Mark A.; Bacon, Edward R.; Chatterjee, Sankar; Bioorganic and Medicinal Chemistry Letters; vol. 22; nb. 11; (2012); p. 3751 - 3753, View in Reaxys 5 of 29

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Biological Species/NCBI ID

rat

Substance RN

1636531View in Reaxys

Substance Name

21

Substance Dose

116 mg/kg

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

AUC

Unit

ng.h/g

Quantitative value

2349

Dunn, Derek; Hostetler, Greg; Iqbal, Mohamed; Marcy, Val R.; Lin, Yin Guo; Jones, Bruce; Aimone, Lisa D.; Gruner, John; Ator, Mark A.; Bacon, Edward R.; Chatterjee, Sankar; Bioorganic and Medicinal Chemistry Letters; vol. 22; nb. 11; (2012); p. 3751 - 3753, View in Reaxys 6 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |growth inhibition Target : Lactuca sativa L. c. v. sacramento, lettuceBioassay : activity evaluation by measuring the length of hypocotyl and radicle of the lettuce lettuce petri dish test; placing 10 lettuce seeds onto moistened filter paper treated with the chemical; incubation at 25 deg C, rel. humidity 60 percent with 12-h light/dark photoperiod (PPFD of light 80 μE/m2/sec) or in the dark

Substance RN

1636531View in Reaxys

Substance Name

1448204

Substance Dose

5 ppm

Qualitative Results

growth inhibition in hypocotyls, 15 percent higher when light is present; growth enhancement effect in radicles at 5-20 ppm both in the light and in the dark

Measurement Parameter

qualitative

Tsao, Rong; Eto, Morifusa; Chemosphere; vol. 32; nb. 7; (1996); p. 1307 - 1317, View in Reaxys 7 of 29

Substance Effect

Estrogen

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Bioassay : rat liver S9: rat hepatic 9000-g supernatant; positive control: trans-stilbene in vitro; twohybrid system with or without rat liver S9

Biological Species/NCBI ID

Saccharomyces cerevisiae

Substance RN

1636531View in Reaxys

Substance Name

1448204

Substance Dose

100 µM

Measurement Parameter

qualitative

Qualitative value

NA

Measurement pX

1

Hashimoto, Shinya; Ueda, Yasuhiro; Kurihara, Ryo; Shiraishi, Fujio; Environmental Toxicology and Chemistry; vol. 26; nb.

2; (2007); p. 279 - 286, View in Reaxys 8 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : aryl hydrocarbon receptor-mediated activity; effect onTarget : rat hepatoma H4IIEGud.Luc1.1 cell lineBioassay : cells stably transfected with a luciferase reporter gene in the alpha modification of minimal essential medium supplemented with 10 percent heat-inactivated FBS; title comp. in DMSO (final conc. <= 0.4 percent v/v); incubated for 6 and 24 h chemical-activated luciferase expression (CALUX) assay; induction equivalency factor (IEF) calculated as the ratio between EC25 of benzo<a>pyrene (BaP) or TCDD and concentration of the title comp. induced the equal level

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

qualitative

Qualitative value

NA

Measurement pX

1

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 9 of 29

Substance Effect

Estrogen

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : MVLN cellsBioassay : stably transfected with the p-Vit-tk-Luc plasmid cells in a 1:1 mixture of Dulbecco's modified Eagle's medium and Ham's F-12 nutrient mixture supplemented with 5 percent heat-inactivated FBS, insulin and sodium pyruvate title comp. in DMSO (final conc. <= 0.1 percent v/v); incubated for 24 h; induction equivalency factor (IEF) calculated as the ratio between EC25 of 17β-estradiol and concentration of the title comp. induced the equal level of luciferase activity

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

qualitative

Qualitative value

NA

Measurement pX

1

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 10 of 29

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Target : MVLN cellsBioassay : cells in a 1:1 mixture of Dulbecco's modified Eagle's medium and Ham's F-12 nutrient mixture supplemented with 5 percent heat-inactivated FBS, insulin and sodium pyruvate; title comp. in DMSO (final conc. <= 0.1 percent v/v); incubated for 24 h

Substance RN

1636531View in Reaxys

Substance Name

1448204

Substance Dose

10 µM

Measurement Parameter

qualitative

Qualitative value

NA

Measurement pX

1

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 11 of 29

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : rat hepatoma H4IIEGud.Luc1.1 cell lineBioassay : cells in the alpha modification of minimal essential medium supplemented with 10 percent heat-inactivated FBS; title comp. in DMSO (final conc. <= 0.4 percent v/v); incubated for 24 h

Substance RN

1636531View in Reaxys

Substance Name

1448204

Substance Dose

10 µM

Measurement Parameter

qualitative

Qualitative value

NA

Measurement pX

1

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 12 of 29

Substance Effect

Antimutagenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : 6 different doses; means from 2 independent series in DMSO; mutagenicity induced by 1-nitropyrene (1-NP, 2.0 μg)

Biological Species/NCBI ID

Salmonella enterica serovar Typhimurium

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

qualitative

Qualitative value

NA

Measurement pX

1

Edenharder; Tang; Food and Chemical Toxicology; vol. 35; nb. 3-4; (1997); p. 357 - 372, View in Reaxys 13 of 29

Substance Effect

Antimutagenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : 6 different doses; means from 2 independent series in DMSO; mutagenicity induced by 2-nitrofluorene (2-NF, 6.0 μg)

Biological Species/NCBI ID

Salmonella enterica serovar Typhimurium

Substance RN

1636531View in Reaxys

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Substance Name

1448204

Qualitative Results

percent inhibition at the highest conc.: 4.8

Measurement Parameter

qualitative

Edenharder; Tang; Food and Chemical Toxicology; vol. 35; nb. 3-4; (1997); p. 357 - 372, View in Reaxys 14 of 29

Substance Effect

Antimutagenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : 6 different doses; means from 2 independent series in DMSO; mutagenicity induced by 3-nitrofluoranthene (3-NFA, 0.12 μg)

Biological Species/NCBI ID

Salmonella enterica serovar Typhimurium

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

percent inhibition at the highest conc.: 17.4

Measurement Parameter

qualitative

Edenharder; Tang; Food and Chemical Toxicology; vol. 35; nb. 3-4; (1997); p. 357 - 372, View in Reaxys 15 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : immobilityBioassay : 24 h old daphnids; 4 chambers with test solution and 4 chambers with control in aqueus medium; 5 daphnids in chamber filled with test solution for 24 h; temp. 20 deg C

Biological Species/NCBI ID

Daphnia magna

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

E(L)C50 15 mg/l

Measurement Parameter

qualitative

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 16 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Scenedesmus subspicatusBioassay : 12 h day/night photoperiod with blue and red wavelengths; for each concentration four replicate samples and one blank sample prepared in mineral medium; algal culture incubated with geometric dilution of 10 concentrations of title comp. for 7 days; at day 0 and after 7 days algal cells counted, biomass integral with interpolation used

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

31.4

Measurement pX

3.76

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 17 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Target : Scenedesmus subspicatusBioassay : 12 h day/night photoperiod with blue and red wavelengths; for each concentration four replicate samples and one blank sample prepared in mineral medium; algal culture incubated with geometric dilution of 10 concentrations of title comp. for 7 days; at day 0 and after 7 days algal cells counted, biomass integral with regression used

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

29.7

Measurement pX

3.78

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 18 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Scenedesmus subspicatusBioassay : 12 h day/night photoperiod with blue and red wavelengths; for each concentration four replicate samples and one blank sample prepared in mineral medium; algal culture incubated with geometric dilution of 10 concentrations of title comp. for 7 days; at day 0 and after 7 days algal cells counted, growth rate with interpolation used

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

21.8

Measurement pX

3.92

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 19 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Scenedesmus subspicatusBioassay : 12 h day/night photoperiod with blue and red wavelengths; for each concentration four replicate samples and one blank sample prepared in mineral medium; algal culture incubated with geometric dilution of 10 concentrations of title comp. for 7 days; at day 0 and after 7 days algal cells counted, growth rate with regression used

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

7.1

Measurement pX

4.4

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 20 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : immobilityBioassay : in standard water; 30 organisms exposured with dilution of title comp. for 24 h

Biological Species/NCBI ID

Thamnocephalus platyurus

Substance RN

1636531View in Reaxys

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Substance Name

1448204

Qualitative Results

E(L)C50 33 mg/l

Measurement Parameter

qualitative

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 21 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |growth inhibition Bioassay : logarithmic dilutions of metabolite in mineral medium; bacterial cultures incubated with title comp. in 26 deg C for cs. 16 h; turbidity of samples measured with spectrophotometer at 436 nm

Biological Species/NCBI ID

Pseudomonas putida

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

59

Measurement pX

3.49

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 22 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : receptor; activation ofTarget : mouse hepatoma H1L1.1c2 cellsBioassay : CALUX (chemical-activated luciferase expression) assay; cells incubated with title comp. in medium for 24 h at 37 deg C; luciferin added; aryl hydrocarbon receptor activity determined by luciferase activity

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

qualitative

Qualitative value

NA

Measurement pX

1

Misaki, Kentaro; Kawami, Hirofumi; Tanaka, Tota; Handa, Yoji; Nakamura, Masafumi; Matsui, Saburo; Matsuda, Tomonari; Environmental Toxicology and Chemistry; vol. 26; nb. 7; (2007); p. 1370 - 1379, View in Reaxys 23 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

Transactivation assay

Bioassay Details

Effect : receptor; activation ofTarget : Saccharomyces cerevisiae YCM3Bioassay : ECTCDD25: conc. producing galactosidase activity equal to 25% of maximum response to TCDD yeast assay; yeast incubated with title comp. in medium for 18 h at 30 deg C; aryl hydrocarbon receptor activity determined by β-galactosidase activity; ECTCDD25 calculated

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

ECTCDD25 2.9E3 nmol/l

Measurement Parameter

qualitative

Misaki, Kentaro; Kawami, Hirofumi; Tanaka, Tota; Handa, Yoji; Nakamura, Masafumi; Matsui, Saburo; Matsuda, Tomonari; Environmental Toxicology and Chemistry; vol. 26; nb. 7; (2007); p. 1370 - 1379, View in Reaxys 24 of 29

Target Name

Indoleamine 2,3-dioxygenase [human]

Target Synonyms

indoleamine 2,3-dioxygenase

Target, Subunit, Species

Indoleamine 2,3-dioxygenase [human]

Target Mutant/Chimera Details

Indoleamine 2,3-dioxygenase [human]:Wild

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25 of 29

Target Species (Bioactivity)

human

Substance Action on Target

Inhibitor

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Inhibitory concentration of the compound against purified recombinant human INDOLEAMINE 2,3-DIOXYGENASE (2 ng/ul) expressed in Escherichia coli BL21 AI upon incubation for 60 min at 37 degree C in 100 mM phosphate buffer (pH 6.5) in presence of L-Trp (200 uM)

Biological Species/NCBI ID

human

Substance RN

1636531View in Reaxys

Measurement Parameter

IC50

Unit

µM

Measurement Object

IC50

Qualitative value

>

Quantitative value

200

Measurement pX

1

Concomitants: Compound name

L-Trp

Concomitants: Compound role

COM

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lowest published toxic dose upon subcutaneous administration;Subcutaneous

Biological Species/NCBI ID

rat

Substance RN

1636531View in Reaxys

Substance Route of Adm.

subcutaneous administration

Measurement Parameter

TDLo

Unit

mg/kg

Qualitative value

=

Quantitative value

300

Material Safety Data Sheet, View in Reaxys 26 of 29

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose, 50% kill;Intraperitoneal;Acute toxicity

Biological Species/NCBI ID

mouse

Substance RN

1636531View in Reaxys

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

LD50

Unit

g/kg

Qualitative value

=

Quantitative value

2

Material Safety Data Sheet, View in Reaxys 27 of 29

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Mutagenic dose in Salmonella typhimurium;AMES test

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Biological Species/NCBI ID

Salmonella enterica serovar Typhimurium

Substance RN

1636531View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Not Published

Vasilieva; Tanirbergenov; Abilev; Migatchev; Huttunen; Mutation Research; vol. 244; nb. 4; (1990); p. 321 - 329, View in Reaxys 28 of 29

Target Name

Androgen receptor (T877A) [human]

Target Synonyms

androgen receptor (t877a)

Target, Subunit, Species

Androgen receptor (T877A) [human]

Target Mutant/Chimera Details

Androgen receptor (T877A) [human]:Wild

Target Species (Bioactivity)

human

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

Transactivation assay

Cells/Cell Lines

LNCaP cell line

Substance RN

1636531View in Reaxys

Substance Name

VPC-3002-table 1, VPC-ID 3002

Substance Dose

50 µM

Measurement Parameter

% Inhibition

Unit

%

Quantitative value

86.3

Measurement pX

5.1

Li, Huifang; Hassona, Mohamed D.H.; Lack, Nathan A.; Axerio-Cilies, Peter; Leblanc, Eric; Tavassoli, Peyman; Kanaan, Natalia; Frewin, Kate; Singh, Kriti; Adomat, Hans; Boehm, Konrad J.; Prinz, Helge; Guns, Emma Tomlinson; Rennie, Paul S.; Cherkasov, Artem; Molecular Cancer Therapeutics; vol. 12; nb. 11; (2013); p. 2425 - 2435, View in Reaxys 29 of 29

Target Name

androgen receptor

Target Synonyms

androgen receptor; androgen receptor activity; ar; bfar; dhtr; dihydrotestosterone receptor; nr3c4; nuclear receptor subfamily 3 group c member 4

Target, Subunit, Species

androgen receptor

Target Mutant/Chimera Details

androgen receptor:Wild

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

Binding

Substance RN

1636531View in Reaxys

Substance Name

VPC-3002-table 1, VPC-ID 3002

Measurement Parameter

IC50

Unit

µM

Quantitative value

5.9

Measurement pX

5.23

Concomitants: Compound name

Fluormone AL Green

Concomitants: Compound role

RAD

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Li, Huifang; Hassona, Mohamed D.H.; Lack, Nathan A.; Axerio-Cilies, Peter; Leblanc, Eric; Tavassoli, Peyman; Kanaan, Natalia; Frewin, Kate; Singh, Kriti; Adomat, Hans; Boehm, Konrad J.; Prinz, Helge; Guns, Emma Tomlinson; Rennie, Paul S.; Cherkasov, Artem; Molecular Cancer Therapeutics; vol. 12; nb. 11; (2013); p. 2425 - 2435, View in Reaxys

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