| Автор | Phan, Nam T. S. |
| Автор | Brown, David H. |
| Автор | Adams, Harry |
| Автор | Spey, Sharon E. |
| Автор | Styring, Peter |
| Дата выпуска | 2004 |
| dc.description | Solid-supported catalysts derived from homogeneous nickel(ii) and palladium(ii) non-symmetrical salen-type coordination complexes have been prepared and shown to be effective in the heterogeneous catalysis of carbonâ carbon cross-coupling reactions. The nickel catalyst has been used in room-temperature Tamaoâ Kumadaâ Corriu reactions and the palladium catalyst in the Heck reaction at elevated temperatures. The complexes were prepared by improved methods and characterised by spectroscopic techniques. Comparisons between the solid-supported catalysts and their homogeneous analogues are reported. The single-crystal structure determination of the nickel and palladium complexes [M(salenac-OH)] [M = Ni, Pd; salenac-OH = 9-(2â ²,4â ²-dihydroxyphenyl)-5,8-diaza-4-methylnona-2,4,8-trienato](2â )] is reported. |
| Формат | application.pdf |
| Издатель | Royal Society of Chemistry |
| Название | Solid-supported cross-coupling catalysts derived from homogeneous nickel and palladium coordination complexesElectronic supplementary information (ESI) available: Synthesis of the complexes and crystallographic data for 1 and 2. See http://www.rsc.org/suppdata/dt/b3/b316553c/ |
| Тип | research-article |
| DOI | 10.1039/b316553c |
| Electronic ISSN | 1477-9234 |
| Print ISSN | 1477-9226 |
| Журнал | Dalton Transactions |
| Первая страница | 1348 |
| Последняя страница | 1357 |
| Аффилиация | Phan Nam T. S.; Department of Chemical and Process Engineering, The University of Sheffield |
| Аффилиация | Brown David H.; Department of Chemical and Process Engineering, The University of Sheffield |
| Аффилиация | Adams Harry; Department of Chemistry, The University of Sheffield |
| Аффилиация | Spey Sharon E.; Department of Chemistry, The University of Sheffield |
| Аффилиация | Styring Peter; Department of Chemical and Process Engineering, The University of Sheffield |
| Выпуск | 9 |
| Библиографическая ссылка | Y. R. D. Miguel, J. Chem. Soc., Perkin Trans. 1, 2000, 24, 4213 |
| Библиографическая ссылка | P. Styring, C. Grindon, C. M. Fisher, Catal. Lett., 2001, 77, 219 |
| Библиографическая ссылка | K. Kasuga, T. Tanaka, K. Tsukahara, Inorg. Chim. Acta, 1989, 157, 267 |
| Библиографическая ссылка | X. R. Bu, C. R. Jackson, D. V. Derveer, X. Z. You, Q. J. Meng, R. X. Wang, Polyhedron, 1997, 16, 2991 |
| Библиографическая ссылка | S. Di Bella, I. Fragalà , I. Ledoux, M. A. Diaz-Garcia, T. J. Marks, J. Am. Chem. Soc., 1997, 119, 9550 |
| Библиографическая ссылка | I. M. Saez, G. H. Mehl, E. Sinn, P. Styring, J. Organomet. Chem., 1998, 551, 299 |
| Библиографическая ссылка | J. Sparling, D. Fung, S. Safe, Biomed. Mass Spectrom., 1980, 7, 13 |
| Библиографическая ссылка | I. Klement, H. Lütjens, P. Knochel, Tetrahedron, 1997, 53, 9135 |
| Библиографическая ссылка | L. A. Jones, S. L. Kirby, D. M. Kean, G. L. Campbell, J. Organomet. Chem., 1985, 284, 159 |
| Библиографическая ссылка | M. S. Kharasch, W. B. Reynolds, J. Am. Chem. Soc., 1943, 65, 501 |
| Библиографическая ссылка | H. Gilman, A. Wood, J. Am. Chem. Soc., 1926, 48, 806 |
| Библиографическая ссылка | I. P. Beletskaya, A. V. Cheprakov, Chem. Rev., 2000, 100, 3009 |
| Библиографическая ссылка | M. Feuerstein, H. Doucet, M. Santelli, Tetrahedron Lett., 2002, 43, 2191 |
| Библиографическая ссылка | R. M. Roberts, M. B. Abdel-Baset, J. Org. Chem., 1976, 41, 1698 |
| Библиографическая ссылка | J. A. Loch, M. Albrecht, E. Peris, J. Mata, J. W. Faller, R. H. Crabtree, Organometallics, 2002, 21, 700 |
