期刊
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
卷 -, 期 13, 页码 1806-1815出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.200801163
关键词
Carbenes; P ligands; Ferrocenes; Rhodium; Hydrosilylation
资金
- Centre National de la Recherche Scientifique (CNRS)
- Institut Universitaire de France (IUF)
N-[(1-Phosphanylferrocen-1'-yl)methyl]-N'-[(2,4,6-trimethylphenyl)methyl]-5,6-di-X-benzimidazolium tetrafluoroborate salts (X = H, 5a and Me, 5b), precursors of new phosphane-benzimidazol-2-ylidene bifunctional ligands, and related ferrocenyl 5,6-di-X-benzimidazol-2-ylidene iodide salts (X = H, 6a and Me, 6b), precursors of monodentate benzimidazol-2-ylidene ligands, have been prepared for the first time. Cationic rhodium(I) complexes 7a and 7b and neutral rhodium(I) complexes 8a and 8b have been obtained in good yields and have been fully characterised. Cationic rhodium(I) complexes 10a and 10b were prepared from 8a and 8b, for comparison with complexes 7, but not isolated. All complexes showed good activities for the catalytic hydrosilylation of acetophenone derivatives. The activities are much greater than for related imidazol-2-ylidene systems, and the cationic complexes are more active than the neutral complexes; the highest activity is observed for the more soluble complex 7b. The use of bidentate ligands proved to be essential for obtaining good selectivities of the desired alcohol. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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