Direct observation of chiral oligo(p-phenylenevinylene)s with scanning tunneling microscopy

被引:27
|
作者
Gesquière, A
Jonkheijm, P
Schenning, APHJ
Mena-Osteritz, E
Bäuerle, P
De Feyter, S
De Schryver, FC
Meijer, EW
机构
[1] Eindhoven Univ Technol, Lab Macromol & Organ Chem, NL-5600 MB Eindhoven, Netherlands
[2] Univ Ulm, Dept Organ Chem 2, D-89081 Ulm, Germany
[3] Katholieke Univ Leuven, Dept Chem, Lab Mol Dynam & Spect, B-3001 Heverlee, Belgium
关键词
D O I
10.1039/b304517j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Oligo(p-phenylenevinylene) (OPV) dimers, tetramers and hexamers, have been organized in highly organized 2D crystals on graphite by spontaneous self-assembly. The unit cell parameters of these monolayers could be determined and a profound effect of the length of the pi-conjugated backbone on the adlayer structure was discovered. For all oligomers, the OPV-units were aligned in rows, with the alkyl chains residing in between the rows. Only trans-vinylene bonds were observed. In the hexamer, the organization was strongly determined by the pi-system. Shortening the pi-conjugated moiety led to monolayer structures controlled by the alkyl side chains. The chiral oligomers (hexamer and tetramer) formed chiral monolayers. In the case of the tetramer, the pi-conjugated backbone was oriented clockwise with respect to the normal of the rows while in the case of the hexamer this orientation was counterclockwise.
引用
收藏
页码:2164 / 2167
页数:4
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