4.2 Article

Preparation of MCM-41-supported chiral Salen Mn(III) catalysts and their catalytic properties in the asymmetric epoxidation of olefins

Journal

CHINESE SCIENCE BULLETIN
Volume 52, Issue 17, Pages 2337-2344

Publisher

SCIENCE CHINA PRESS
DOI: 10.1007/s11434-007-0333-7

Keywords

MCM-41; heterogenization; alpha-methylstyrene; Salen Mn (III); asymmetric epoxidation; 1,2-dihydronaphthalene

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A secondary amino-modified mesoporous molecular sieve MCM-41 was obtained by reaction of bis(3-(triethoxysilyl)propyl)amine with MCM-41. The chiral Salen-Mn (III) complex was anchored onto the modified MCM-41 by a multi-step grafting method and two heterogenized catalysts with different Mn contents were obtained. The catalysts were characterized by XRD, N-2 adsorption, ICP, FT-IR and DR UV-Vis. Their catalysis on asymmetric epoxidation of several olefins was studied with NaCIO and m-CPBA as oxidants respectively. It was found that both the activity and enantioselectivity of the catalysts decreased after the homogeneous catalyst was heterogenized. The reasons resulting in the decrease of catalytic performance were discussed.

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