Chiral salen Mn(III) complexes immobilized onto crystalline aluminium oligo-styrenyl phosphonate-hydrogen phosphate (AlSPP) for heterogeneous asymmetric epoxidation

被引:17
|
作者
Huang, Xuemei [1 ]
Fu, Xiangkai [1 ]
Jia, Ziyong [1 ]
Miao, Qiang [1 ]
Wang, Guoming [1 ]
机构
[1] Southwest Univ, Key Lab Ecoenvironm Three Gorges Reservoir Reg, Coll Chem & Chem Engn,Res Inst Appl Chem, Key Lab Appl Chem Chongqing Municipal,Minist Educ, Chongqing 400715, Peoples R China
关键词
HIGHLY ENANTIOSELECTIVE EPOXIDATION; CATALYTIC EPOXIDATION; ALKENE EPOXIDATION; JACOBSEN CATALYST; MODIFIED MCM-41; OLEFINS; ZIRCONIUM; EFFICIENT; SBA-15; CLAY;
D O I
10.1039/c2cy20394d
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
A novel type of organic polymer-inorganic hybrid material layered crystalline aluminium oligo-styrenyl phosphonate-hydrogen phosphate (AlSPP) was designed and prepared in the absence of any template. The chiral salen Mn(III) complex immobilized onto alkoxy-modified AlSPP was synthesized and characterized by FT-IR, diffusion reflection UV-vis, AAS, N-2 volumetric adsorption, SEM, TEM, XRD, TG and AFM. The supported catalysts displayed superior catalytic activities in the asymmetric epoxidation of alpha-methylstyrene and indene with m-CPBA as an oxidant. Delightfully, the heterogeneous catalysts afforded a remarkable increase in conversion and ee values without the expensive O-coordinating axial bases for the asymmetric epoxidation of olefins. The catalysts can be easily recovered and reused with a slight decrease in activity and enantioselectivity after ten cycles. Furthermore, they could also be efficiently used in large-scale reactions with the enantioselectivity being maintained at the same level, which provided the potentiality for application in industry.
引用
收藏
页码:415 / 424
页数:10
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