Rhodium-diphosphine catalysts for the hydroformylation of styrene:: the influence of the excess of ligand and the chelate ring size on the reaction selectivity

被引:38
作者
Diéguez, M
Pereira, MM
Masdeu-Bultó, AM
Claver, C
Bayón, JC
机构
[1] Univ Autonoma Barcelona, Dept Quim, E-08193 Barcelona, Spain
[2] Univ Rovira & Virgili, Dept Quim Fis & Inorgan, Tarragona 43005, Spain
[3] Univ Coimbra, Dept Quim, P-3046 Coimbra, Portugal
关键词
rhodium; hydroformylation; asymmetric catalysis; diphosphine; styrene; chelate; ring size;
D O I
10.1016/S1381-1169(98)00373-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study discusses the hydroformylation of styrene using rhodium systems containing four structurally related diphosphines: 1,2-bis(diphenylphosphine)ethane 1 (dppe), 1,3-bis(diphenylphosphine)propane 2 (dppp), (R,R)-2,3-bis(diphenylphosphine)butane 3 (chiraphos) and (S,S)-2,4-bis(diphenylphosphine)pentane 4 (bdpp). A systematic analysis of the effect of the pressure, temperature and the ligand to metal molar ratio for these catalytic systems shows that the five- and six-membered ring chelating diphosphines behave different. The regio- and enantioselectivity observed provide evidence of the catalytic species involved in the process. By analyzing the selectivity of the catalytic systems formed by mixing PEtPh2 and the chiral diphosphine ligands, we propose a model describing the equilibria among the catalytic species. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:111 / 122
页数:12
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