Synthesis, Characterization and Electrochemical Properties of Polymers Based on Dithienothiophene and Bithiazole

Fatma Dikcal, Sebahat Topal, Murat Unal, Turan Ozturk*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Conjugated polymers are promising cost-effective, lightweight, and flexible electrode materials. 3,5-Dinonyl-2,6-di(thiophene-2-yl)dithieno[3,2-b : 2′,3′d]thiophene (M1) as a donor and 4,4′-dinonyl-5,5′-di(thiophen-2-yl)-2,2′-bithiazole (M2) as an acceptor were synthesized and their polymers poly(3,5-dinonyl-2,6-di(thiophene-2-yl)dithieno[3,2 b : 2′,3′-d]thiophene) (P1) and poly(4,4′-dinonyl-5,5′-di(thiophen-2-yl)-2,2′-bithiazole) (P2) were obtained via electropolymerization on ITO/glass electrode surface in ACN : DCM (1 : 3 v/v) solution, containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF6). Then, a third polymer as a co-polymer (P3) was synthesized through electropolymerization of a mixture of the monomers M1 and M2 in 1 : 1 ratio. All the polymers were characterized by UV-Vis, CV and CV-UV measurements. Moreover, capacitor properties of the polymers by potentiostatic electrochemical impedance spectroscopy (EIS) was performed. The polymers P1, P2 and P3 exhibited absorptions at 456, 453 and 519 nm in neutral state and their optical band gaps were determined to be 2.17, 2.53 and 1.95 eV, respectivetly. EIS measurements indicated that P3 had the highest current density, having lower resistance.

Original languageEnglish
Pages (from-to)1309-1317
Number of pages9
JournalAsian Journal of Organic Chemistry
Volume9
Issue number9
DOIs
Publication statusPublished - 1 Sept 2020

Bibliographical note

Publisher Copyright:
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Funding

This work was supported by the ITU BAP (TGA‐2018‐41123). M. U. acknowledges financial support from the Scientific and Technological Research Council of Turkey (TUBITAK)‐ BIDEB 2218 for the Postdoctoral Research fellowship. F.D. would like to thanks İstanbul Sisli Vocational School for their valuable assistance. We thank Higher Education Council of Turkey (YOK) and TUBITAK for grants to S. T. (PhD, 100/2000 YOK and BIDEP TUBİTAK). We thank to Prof Esma Sezer of ITU for her scientific discussions. This work was supported by the ITU BAP (TGA-2018-41123). M. U. acknowledges financial support from the Scientific and Technological Research Council of Turkey (TUBITAK)- BIDEB 2218 for the Postdoctoral Research fellowship. F.D. would like to thanks ?stanbul Sisli Vocational School for their valuable assistance. We thank Higher Education Council of Turkey (YOK) and TUBITAK for grants to S. T. (PhD, 100/2000 YOK and BIDEP TUB?TAK). We thank to Prof Esma Sezer of ITU for her scientific discussions.

FundersFunder number
BIDEP TUBİTAK
Higher Education Council of Turkey
ITU BAPTGA‐2018‐41123
TUBITAK
YOK
International Technological University
Türkiye Bilimsel ve Teknolojik Araştirma Kurumu

    Keywords

    • bithiazoles
    • dithienothiophene based polymers
    • dithienothiophenes

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