Ionic liquids containing anionic selenium species: Applications for the oxidative carbonylation of aniline

Angewandte Chemie - International Edition

Volumn 41, Issue 22, 2002, Pages 4300-4303

  Kim, Hoon Sik ^a   Kim, Yong Jin ^c   Lee, Hyunjoo ^a   Park, Kun You ^a   Lee, Chongmok ^b   Chin, Chong Shik ^c  

^a Korea Institute of Science and Technology   (South Korea)

^b Ewha Womans University   (South Korea)

^c Sogang University   (South Korea)

Author keywords

Carbonylation; Cyclic voltammetry; Homogeneous catalysis; Ionic liquids; Selenium

Indexed keywords

CARBONYLATION; OXIDATION; SELENIUM;

IONIC LIQUIDS;

AROMATIC COMPOUNDS;

ANILINE DERIVATIVE; ANION; CARBONYL DERIVATIVE; IMIDAZOLE DERIVATIVE; SELENIUM DERIVATIVE;

ARTICLE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL REACTION; LIQUID; MATERIALS; MATERIALS TESTING; TEMPERATURE;

EID: 0037112582     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3773(20021115)41:22<4300::AID-ANIE4300>3.0.CO;2-V     Document Type: Article

References (22)

1. (a) A. M. Tafesh, J. Weiguny, Chem. Rev. 1996, 96, 2035-2052;
2. (b) J. D. Gargulak, W. L. Gladfelter, Organometallics 1994, 13, 698-705;
3. (c) I. Vauthey, F. Valot, C. Gozzi, F. Fache, M. Lemaire, Tetrahedron Lett. 2000, 41, 6347-6350.
4. (a) T. W. Leung, B. D. Dombek, J. Chem. Soc. Chem. Commun. 1992, 205-206;
5. (b) K. V. Prasad, R. V. Chaudhari, J. Catal. 1994, 145, 204-215.
6. (a) H. S. Kim, Y. J. Kim, H. Lee. K. Y. Park, C. S. Chin, J. Catal. 1998, 176, 264-266;
7. (b) H. S. Kim, Y. J. Kim, H. Lee, S. D. Lee. C. S. Chin, J. Catal. 1999, 184, 526-534.
8. (a) R. Sheldon, Chem. Commun. 2001, 2399-2407;
9. (b) C. M. Gordon, Appl. Catal. A 2001, 222, 101-117;
10. (c) R. J. C. Brown, P. J. Dyson, D. J. Ellis, T. Welton, Chem. Commun. 2001, 1862-1863;
11. (d) J. E. L. Dullius, P. A. Z. Suarez, S. Einloft, R. F. de Souza, J. Dupont, Organometallics 1998, 17, 815-819;
12. (e) C. J. Adams, M. J. Earle, K. R. Seddon, Chem. Commun. 1999, 1043-1044.
13. -1, R1 = 0.0332, wR2 = 0.0886, (1 > 2σ1); R1 = 0.0340, wR2 = 0.0893 (all data). CCDC-185119 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12. Union Road, Cambridge CB21EZ, UK; fax: (+44) 1223-336-033; or deposit@ccdc.cam.ac.uk).
14. R. Hagiwara, Y. Ito, J. Fluorine Chem. 2000, 105, 221-227.
15. S. Fukuoka, M. Chono, M. Kohno, J. Chem. Soc. Chem. Commun. 1984, 399-400.
16. (a) S. A. Akyüz, A. B. Dempster, R. L. Morehouse, N. Zengin, J. Chem. Soc. Chem. Commun. 1972, 307-308;
17. (b) N. Sonoda, T. Yasuhara, K. Kondo, T. Ikeda, S. Tsutsumi, J. Am. Chem. Soc. 1971, 93, 6344;
18. (c) K. Kondo, N. Sonoda, K. Yoshida, M. Koishi, S. Tsutsumi, Chem. Lett. 1972, 401-404;
19. (d) J. G. Zajacek, J. J. McCoy, K. E. Fuger, USP 3956360 1976.
20. (a) M. Hasan, I. V. Kozhevnikov, M. R. H. Siddiqui, A. Steiner, N. Winterton, Inorg. Chem. 1999, 38, 5637-5641;
21. (b) J. S. Wilkes, J. A. Levisky, R. A. Wilson, C. L. Hussey, Inorg. Chem. 1982, 21, 1263-1264.
22. 1H NMR data of the transformation reactions of 3a into 3b, 3c, and 3d.