Rigid oligomers based on the combination of 3,6-dimethoxythieno[3,2-b]thiophene and 3,4-ethylenedioxythiophene
作者:Mathieu Turbiez、Noémie Hergué、Philippe Leriche、Pierre Frère
DOI:10.1016/j.tetlet.2009.10.021
日期:2009.12
New oligomers based on the combination of the 3,6-dimethoxythieno[3,2-b]thiophene and 3,4-ethylenedioxythiophene (EDOT) moieties have been prepared and studied by UV-vis spectroscopy and cyclic voltammetry. The use of the intrinsically rigid thienothiophene units in addition to the S center dot center dot center dot O intramolecular interactions leads to planar conformation of the conjugated chains. While the radical cations of oligomers end capped by n-hexyl chains show a tendency to the dimerization, those substituted by n-hexylsulfanyl chains present a high stability. (c) 2009 Elsevier Ltd. All rights reserved.