中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective hydrogenation of pyruvates over polymer-stabilized and supported platinum nanoclusters

文献类型:期刊论文

作者Zuo, XB; Liu, HF; Guo, DW; Yang, XZ
刊名TETRAHEDRON
出版日期1999-06-18
卷号55期号:25页码:7787-7804
关键词Enantioselective Hydrogenation Pyruvate Platinum Nanocluster Molecular Mechanics
ISSN号0040-4020
英文摘要The cinchonidine-modified enantioselective hydrogenation of pyruvates has been studied over polyvinylpyrrolidone-stabilized platinum (PVP-Pt) and the corresponding alumina-supported platinum (Al2O3-Pt) clusters. It is shown that the catalysts with particle size less than 2.0 nm demonstrate >90% enantioselectivity in favor of (R)-lactates. The solvent effect is similar to that over the conventional supported platinum catalyst except for tetrahydrofuran. These colloidal and supported clusters are stable with no obvious loss of activity and enantioselectivity even after 18 months standing in air at room temperature. Molecular mechanics calculations of the modifier-reactant interaction on the platinum surface suggest that it is possible to obtain good enantioselectivity on the small clusters. (C) 1999 Elsevier Science Ltd. All rights reserved.
语种英语
WOS记录号WOS:000080894100008
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://ir.iccas.ac.cn/handle/121111/74927]  
专题中国科学院化学研究所
通讯作者Liu, HF
作者单位1.Chinese Acad Sci, Polymer Chem Lab, Beijing 100080, Peoples R China
2.Chinese Acad Sci, China Petrochem Corp, Inst Chem, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Zuo, XB,Liu, HF,Guo, DW,et al. Enantioselective hydrogenation of pyruvates over polymer-stabilized and supported platinum nanoclusters[J]. TETRAHEDRON,1999,55(25):7787-7804.
APA Zuo, XB,Liu, HF,Guo, DW,&Yang, XZ.(1999).Enantioselective hydrogenation of pyruvates over polymer-stabilized and supported platinum nanoclusters.TETRAHEDRON,55(25),7787-7804.
MLA Zuo, XB,et al."Enantioselective hydrogenation of pyruvates over polymer-stabilized and supported platinum nanoclusters".TETRAHEDRON 55.25(1999):7787-7804.

入库方式: OAI收割

来源:化学研究所

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