Noncovalent Immobilization of Enantioselective Catalysts

被引:297
作者
Fraile, Jose M. [1 ]
Garcia, Jose I.
Mayoral, Jose A.
机构
[1] Univ Zaragoza, CSIC, Inst Ciencia Mat Aragon, Dept Quim Organ, E-50009 Zaragoza, Spain
关键词
ASYMMETRIC HETEROGENEOUS AZIRIDINATION; RHODIUM-DIPHOSPHINE COMPLEXES; IN-A-BOTTLE; MN(III) SALEN COMPLEXES; DIELS-ALDER REACTIONS; ANCHORED HOMOGENEOUS CATALYSTS; HYDROLYTIC KINETIC RESOLUTION; SUPPORTED CHIRAL CATALYSTS; HYDROXIDE-HOSTED CATALYSTS; METAL-ORGANIC FRAMEWORK;
D O I
10.1021/cr800363y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Various methods of immobilization applied to enantioselective catalysts that do not require the covalent link of the chiral ligand to a solid support are presented. The first noncovalent immobilization method, an anionic support to immobilize a positively charged chiral catalytic complex, included the direct cationic exchange of the complex performed in solution and the formation of the complex on a pre-exchanged metal center. The immobilization of PhBox-CuCl 2 and BnBox-CuCl2 complexes result in the loss of chloride couteranion during the exchange process, so that catalytic complex is firmly bound to the anionic support through electrostatic interactions. The immobilization of Mn complex resulted in catalyst that led to moderate enantioselectivity in the epoxidation and a slight reduction from the value obtained in the solution.
引用
收藏
页码:360 / 417
页数:58
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