Induction of Chirality in an Achiral Monolayer at the Liquid/Solid Interface by a Supramolecular Chiral Auxiliary

被引:64
作者
De Cat, Inge [2 ]
Guo, Zongxia [2 ]
George, Subi J. [1 ]
Meijer, E. W. [1 ]
Schenning, Albertus P. H. J. [1 ]
De Feyter, Steven [2 ]
机构
[1] Eindhoven Univ Technol, Lab Macromol & Organ Chem, NL-5600 MB Eindhoven, Netherlands
[2] KU Leuven Univ Leuven, Dept Chem, Div Mol Imaging & Photon, B-3001 Heverlee, Belgium
关键词
SCANNING-TUNNELING-MICROSCOPY; ABSOLUTE ASYMMETRIC SYNTHESIS; MOLECULAR CHIRALITY; SOLDIERS PRINCIPLE; AMPLIFICATION; EXPRESSION; HELICITY; SURFACE; MEMORY; POLYMERIZATION;
D O I
10.1021/ja2106652
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An achiral oligo(p-phenylene vinylene) derivative with a ureido-triazine hydrogen bonding unit self-assembles into rows of hydrogen bonded dimers at the liquid/solid interface. Scanning tunneling microscopy reveals the formation of chiral domains, but overall, the surface remains racemic. Addition of a chiral auxiliary which is able to interact with the dimers through hydrogen bonding, showed that global organizational chirality could be achieved since a majority of the domains show the same handedness. After removing the chiral auxiliary with a volatile solvent, the global organizational chirality could be trapped, revealing a memory effect. With this straightforward supramolecular approach, we were able to create a chiral surface with preferred handedness composed of achiral molecules at the air/solid interface.
引用
收藏
页码:3171 / 3177
页数:7
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