4.6 Article

Synthesis and Electropolymerization of Bis(phenylthieno[3,2-b]thiophenes)- (4,4′-dinonyl-2,2′-bithiazole) co-monomer

Journal

ELECTROCHIMICA ACTA
Volume 222, Issue -, Pages 1592-1603

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2016.11.145

Keywords

4,4 '-Dinonyl-2,2 '-bithiazole and 3-phenylthieno[3,2-b]thiophene; Stille cross coupling; Electropolymerization; DFT

Funding

  1. Istanbul Technical University (ITU), Turkey
  2. Scientific and Technological Research Council of Turkey (TUBITAK)
  3. Unsped Global Logistic

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Synthesis of comonomer possessing 4,4'-dinonyl-2,2'-bithiazole and 3-phenylthieno[3,2-b] thiophene units (PhTT-NBT-PhTT) was performed under Stille cross coupling condition. Its electropolymerization was conducted in the presence of trifluroborate-diethyl ether (BF3 center dot DEE) to lower the electrochemical polymerization potential through a complex formation between heteroaromatic monomers and boron trifluoride. Electrochemical properties of obtained P[PhTT] and P[PhTT-NBT-PhTT] films, such as effect of electrolyte, polymerization charge, potential limits on the redox behaviour were investigated. They were further characterized by UV-visible spectrophotometric measurements. Corresponding electrical equivalent circuit was applied to the experimental electrochemical impedance spectroscopy (EIS) data to explain the parameters of each element and the interface between the Pt/P[PhTT]/BF3 center dot DEE and Pt/P[PhTT-NBT-PhTT]/BF3 center dot DEE systems. The band gap of P[PhTT-NBT-PhTT was obtained as 2.04 eV by insitu spectroelectrochemical measurements. Frontier molecular orbitals and electropolymerization of the comonomer were assessed computationally. (C) 2016 Elsevier Ltd. All rights reserved.

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