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Turbiez, M., Frère, P., Allain, M., Videlot, C., Ackermann, J. and Roncali, J. (2005) Design of Organic Semiconductors: Tuning the Electronic Properties of π-Conjugated Oligothiophenes with the 3,4-Ethylenedioxythiophene (EDOT) Building Block. Chemistry: A European Journal, 11, 3742-3752.
http://dx.doi.org/10.1002/chem.200401058

has been cited by the following article:

• TITLE: Synthesis of Soluble Polythiophene Partially Containing 3,4-Ethylenedioxythiophene and 3-Hexylthiophene by Polycondensation

  AUTHORS: Ichiro Imae, Hitoshi Sagawa, Takahiro Mashima, Kenji Komaguchi, Yousuke Ooyama, Yutaka Harima

  KEYWORDS: Polycondensation, Polythiophene, Ethylenedioxythiophene, Alkylthiophene, Solubility

  JOURNAL NAME: Open Journal of Polymer Chemistry, Vol.4 No.3, August 20, 2014

  ABSTRACT: A novel poly(quinquethiophene) partially containing 3,4-ethylenedioxythiophene (EDOT) and 3-hexylthiophene, poly(3,3 ''''-dihexyl-3',4',3''',4'''-diethylenedioxy-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene), was synthesized by three types of polycondensations. Among them, direct C-H coupling reaction gave the polymer with the highest molecular weight. The resulting polymer was soluble in common organic solvents. Absorption and fluorescence spectra of the polymer showed a remarkable red-shift compared with the corresponding monomer due to the expansion of effective π-conjugation length.