Surface-controlled self-assembly of chiral sexithiophenes

被引:54
作者
Leclère, P
Surin, M
Lazzaroni, R
Kilbinger, AFM
Henze, O
Jonkheijm, P
Biscarini, F
Cavallini, M
Feast, WJ
Meijer, EW
Schenning, APHJ
机构
[1] Eindhoven Univ Technol, Lab Macromol & Organ Chem, NL-5600 MB Eindhoven, Netherlands
[2] Univ Mons, Serv Chim Mat Nouveaux, B-7000 Mons, Belgium
[3] Univ Durham, IRC Polymer Sci & Technol, Durham DH1 3LE, England
[4] CNR, Ist Studio Mat Nanostrutturati, I-40129 Bologna, Italy
关键词
D O I
10.1039/b316399g
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
We report on the self-assembly of two enantiomeric sexithiophenes in solution and on surfaces. Circular dichromism of aggregated sexithiophenes and drop-cast films reveals, as expected, mirror image spectra for both enantiomers. The aggregation in thin deposits from sexithiophenes molecularly dispersed in a solution on different types of substrates was investigated by atomic force microscopy (AFM). On graphite, one-dimensional objects (nanowires) are formed while on mica platelets are generated. Remarkably, we found that both enantiomers form left-handed helices on silicon. This observation depends on the hydrophilicity of the silicon. Furthermore, the achiral sexithiophene did not form helical aggregates suggesting that the stereocenter is required to obtain chirality in the fibers.
引用
收藏
页码:1959 / 1963
页数:5
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