Skip to Main Content (Press Enter)

Logo CNR
  • ×
  • Home
  • People
  • Outputs
  • Organizations
  • Expertise & Skills

UNI-FIND
Logo CNR

|

UNI-FIND

cnr.it
  • ×
  • Home
  • People
  • Outputs
  • Organizations
  • Expertise & Skills
  1. Outputs

Surface-controlled self-assembly of chiral sexithiophenes

Academic Article
Publication Date:
2004
abstract:
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.
Iris type:
01.01 Articolo in rivista
List of contributors:
Biscarini, Fabio; Cavallini, Massimiliano
Authors of the University:
CAVALLINI MASSIMILIANO
Handle:
https://iris.cnr.it/handle/20.500.14243/14121
Published in:
JOURNAL OF MATERIALS CHEMISTRY (PRINT)
Journal
  • Use of cookies

Powered by VIVO | Designed by Cineca | 26.5.0.0 | Sorgente dati: PREPROD (Ribaltamento disabilitato)