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A novel layered organic polymer-inorganic hybrid zinc poly (styrene-phenylvinylphosphonate)-phosphate immobilized chiral salen Mn(III) catalyst large-scale asymmetric epoxidation of unfunctionalized olefins
被引:21
作者:
Hu, Xiaoyan
[2
]
Fu, Xiangkai
[1
,2
]
Xu, Jiangwei
[2
]
Wang, Changwei
[2
]
机构:
[1] Minist Educ, Key Lab Ecoenvironm Gorges Reservoir Reg 3, Chongqing 400715, Peoples R China
[2] Southwest Univ, Key Lab Appl Chem Chongqing Municipal, Coll Chem & Chem Engn, Res Inst Appl Chem, Chongqing 400715, Peoples R China
关键词:
Layered zinc poly (styrene-phenylvinylphosphonate)-phosphate;
Diphenol-modified;
Heterogeneous chiral salen Mn(III) catalysts;
Asymmetric epoxidation;
Large-scale reaction;
HIGHLY ENANTIOSELECTIVE EPOXIDATION;
ZIRCONIUM PHOSPHONATES;
COMPLEXES;
PHOSPHATE;
EFFICIENT;
OXIDATION;
D O I:
10.1016/j.jorganchem.2011.04.027
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
A novel layered organic polymer-inorganic hybrid zinc poly (styrene-phenylvinylphosphonate)-phosphate (ZnPS-PVPA) has been synthesized under mild conditions and diphenol-modified ZnPS-PVPA was used to successfully immobilize the chiral salen Mn(III) by axial coordination. The obtained heterogeneous chiral catalysts exhibited excellent activities and enantioselectivities using sodium periodate as an oxidant for asymmetric epoxidation of unfunctionalized olefins, especially for the epoxidation of a-methylstyrene (conversion: up to 97%; ee: exceed 99%). Moreover, these synthesized catalysts were relatively stable and could be expediently separated from the reaction system, and could be recycled at least ten times without obvious loss of activity and enantioselectivity. These novel catalysts could be efficiently used in large-scale reactions with the enantioselectivity being maintained at the same level, which offer a great possibility for application in industry. (C) 2011 Elsevier B.V. All rights reserved.
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页码:2797 / 2804
页数:8
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