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Issue 13, 2004
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Surface-controlled self-assembly of chiral sexithiophenes

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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.

Graphical abstract: Surface-controlled self-assembly of chiral sexithiophenes

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Article information

16 Dec 2003
20 Apr 2004
First published
19 May 2004

J. Mater. Chem., 2004,14, 1959-1963
Article type

Surface-controlled self-assembly of chiral sexithiophenes

P. Leclère, M. Surin, R. Lazzaroni, A. F. M. Kilbinger, O. Henze, P. Jonkheijm, F. Biscarini, M. Cavallini, W. J. Feast, E. W. Meijer and A. P. H. J. Schenning, J. Mater. Chem., 2004, 14, 1959
DOI: 10.1039/B316399G

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