Ionic phosphine ligands with cobaltocenium backbone: Novel ligands for the highly selective, biphasic, rhodium-catalyzed hydroformylation of 1-octene in ionic liquids

被引:186
作者
Brasse, CC
Englert, U
Salzer, A
Waffenschmidt, H
Wasserscheid, P
机构
[1] Rhein Westfal TH Aachen, Inst Anorgan Chem, D-52056 Aachen, Germany
[2] Rhein Westfal TH Aachen, Inst Tech Chem & Petr Chem, D-52074 Aachen, Germany
关键词
D O I
10.1021/om000183y
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The use of electron-poor phosphine-substituted cobaltocenium salts as ligands for the biphasic hydroformylation in ionic liquids has been investigated. Using improved oxidation methods, 1,1'-bis(diphenylphosphino)cobaltocenium nitrate, 1,1'-bis(diphenylphosphino)cobaltocenium hexafluorophosphate, and 1,1'-bis[l-methyl(1-diphenylphosphino)ethyl]cobaltocenium hexafluorophosphate have been synthesized. 1.1'-Bis( diphenylphosphinocobaltocenium hexafluorophosphate in particular proved to be a very suitable ligand for the biphasic hydroformylation of 1-octene in 1-butyl-3-methylimidazolium hexafluorophosphate (BMIM PF6), enabling high catalyst activity, high selectivity to the n-product, and no detectable catalyst leaching. In contrast to aqueous biphasic systems, the ionic liquid BMIM PF6 provides for the rhodium catalyst a low-coordinating medium with limited but sufficient solubility for 1-octene to allow high reaction rates.
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页码:3818 / 3823
页数:6
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