Preparation and Catalytic Performances of a Molecularly Imprinted Ru-Complex Catalyst with an NH2 Binding Site on a SiO2 Surface

被引:32
|
作者
Yang, Yong [1 ]
Weng, Zhihuan [1 ,3 ]
Muratsugu, Satoshi [1 ,2 ,4 ]
Ishiguro, Nozomu [1 ,5 ]
Ohkoshi, Shin-ichi [5 ]
Tada, Mizuki [1 ,2 ,4 ]
机构
[1] Natl Inst Nat Sci, Inst Mol Sci, Okazaki, Aichi 4448585, Japan
[2] JST, Res Seeds Program, Chiyoda Ku, Tokyo 1020075, Japan
[3] Univ Electrocommun, Dept Appl Phys & Chem, Chofu, Tokyo 1828585, Japan
[4] Grad Univ Adv Studies SOKENDAI, Okazaki, Aichi 4448585, Japan
[5] Univ Tokyo, Grad Sch Sci, Dept Chem, Tokyo 1130033, Japan
关键词
hydrogenation; imprinting; molecular recognition; ruthenium; supported catalysts; ASYMMETRIC TRANSFER HYDROGENATION; SHAPE-SELECTIVE HYDROGENATION; HETEROGENEOUS CATALYSIS; BIOMIMETIC CATALYSIS; FOOTPRINT CATALYSIS; METAL-COMPLEXES; LIQUID-CHROMATOGRAPHY; HOMOGENEOUS CATALYSIS; METATHESIS CATALYSTS; EPOXIDATION CATALYST;
D O I
10.1002/chem.201100529
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A catalyst surface with an active metal site, a shape-selective reaction space, and an NH2 binding site for o-fluorobenzophenone was designed and prepared by the molecular imprinting of a supported metal complex on a SiO2 surface. A ligand of a SiO2-supported Ru complex that has a similar shape to the product of o-fluorobenzophenone hydrogenation was used as a template. An NH2 binding site for o-fluorobenzophenone was spatially arranged on the wall of a molecularly imprinted cavity with a similar shape to the template. The structures of the SiO2-supported and molecularly imprinted Ru catalysts were characterized in a step-by-step manner by means of solid-state magic angle spinning (MAS) NMR, XPS, UV/Vis, N2 adsorption, XRF, and Ru K-edge EXAFS. The molecularly imprinted Ru catalyst exhibited excellent shape selectivity for the transfer hydrogenation of benzophenone derivatives. It was found that the NH2 binding site on the wall of the molecularly imprinted cavity enhanced the adsorption of o-fluorobenzophenone, of which the reduction product was imprinted, whereas there was no positive effect in the case of o-methylbenzophenone, which cannot interact with the NH2 binding site through hydrogen bonding.
引用
收藏
页码:1142 / 1153
页数:12
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