Chiral Recognition at One-Dimensional Metal-Organic Coordination Networks Initiates the Ordering of Prochiral Catalytic Reagent Methylacetoacetate on Au{111}

被引:14
作者
Trant, Aoife G. [1 ]
Baddeley, Christopher J. [1 ]
机构
[1] Univ St Andrews, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
基金
英国工程与自然科学研究理事会;
关键词
ENANTIOSELECTIVE HYDROGENATION; ASYMMETRIC HYDROGENATION; METHYL ACETOACETATE; SURFACE; ADSORPTION; REACTIVITY; GLYCINE; NI;
D O I
10.1021/la1040097
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A scanning tunnelling microscopy investigation is reported of the adsorption of methylacetoacetate on Au{111} surfaces templated by the growth of 1-D chains of nickel pyroglutamate. The symmetry of the Au{111}-herringbone reconstruction and the chirality of the pyroglutamate species influence the preferred growth directions of pyroglutamate chains. The interaction of methylacetoacetate with the various chain types reveals details of the symmetry and conformation of the chains. In addition, the docking of methylacetoacetate initiates the growth of ordered domains of methylacetoacetate not observed on either Au{111} or Ni/Au{111} surfaces. The possibilities to utilize such chiral recognition and amplification effects in the design of enantioselective heterogeneous catalysts are discussed.
引用
收藏
页码:1788 / 1795
页数:8
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