Rh and Ir complexes containing multidentate, C2-symmetry ligands.: Structural and catalytic properties in asymmetric hydrogenation

被引:29
作者
Alcón, MJ
Iglesias, M
Sánchez, F
Viani, I
机构
[1] CSIC, Inst Ciencia Mat, E-28049 Madrid, Spain
[2] CSIC, Inst Quim Organ, E-28006 Madrid, Spain
关键词
rhodium; iridium; asymmetric hydrogenation; multidentate ligands;
D O I
10.1016/S0022-328X(00)00083-8
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A comparative investigation of the interaction of Rh(I) and Ir(I) with a series of mixed-donor multidentate, C-2-symmetry ligands has been carried out. The complexes have been prepared by the reaction of [MCl(cod)](2) (cod = 1,5-cyclooctadiene) with AgPF6 and further treatment with the ligand. All ligands form 1:1 (metal:ligand) species with the above metal ions although, in a few instances, species of type [M2L2](2+) were also detected. The structures of these complexes were elucidated by analytical and spectroscopic data (elemental analysis, mass spectroscopy, IR, H-1- and C-13-NMR). Complexes were tested in the asymmetric hydrogenation of prochiral olefins, providing enantioselectivities up to 36%. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
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页码:284 / 292
页数:9
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