A highly efficient and recyclable catalyst-dendrimer supported chiral salen Mn(III) complexes for asymmetric epoxidation

被引:23
作者
Peng, Ming [1 ]
Chen, Yaju [1 ]
Tan, Rong [1 ]
Zheng, Weiguo [1 ]
Yin, Donghong [1 ,2 ]
机构
[1] Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med Res, Minist Educ, Inst Fine Catalysis & Synth, Changsha 410081, Hunan, Peoples R China
[2] China Tobacco Hunan Ind Co Ltd, Res & Dev Ctr, Changsha 410007, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
SCHIFF-BASE COMPLEXES; CARBON BOND FORMATION; ENANTIOSELECTIVE EPOXIDATION; MESOPOROUS MATERIALS; NANOPARTICLES; HYDROGENATION; SILICA;
D O I
10.1039/c3ra42470g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel series of PAMAM dendrimer-supported chiral salen Mn(III) complexes has been synthesized and applied to the enantioselective epoxidation of unfunctionalized olefins. Technologies of characterization clearly suggested the axial grafting of the chiral salen Mn(III) complex on the surface of PAMAM dendrimers through a phenoxy group spacer. It was found that the peripherally modified dendrimers benefited from the cooperativity between neighboring sites confined to the surface of the dendrimers, thereby enhancing the asymmetric induction of the catalyst. Higher enantioselectivity for PAMAM dendrimer-supported chiral salen Mn(III) complexes over the homogeneous counterpart was observed in the enantioselective epoxidation of unfunctionalized olefins. Furthermore, the dendritic supports imparted selective solubility properties to the catalysts. These catalysts could be easily recovered from the reaction solution by using solvent precipitation, and could be reused for several times without loss of activity and enantioselectivity.
引用
收藏
页码:20684 / 20692
页数:9
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