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Zachary S. Parr, Roman Halaksa, Peter A. Finn, Reem B. Rashid,Jonathan Rivnay, Jozef Krajčovič, Christian B. Nielsen
Original Title
Glycolated Thiophene-Tetrafluorophenylene Copolymers for Bioelectronic Applications: Synthesis by Direct Heteroarylation Polymerisation
Type
journal article in Web of Science
Language
English
Original Abstract
A series of copolymers contg. a glycolated 1,4-dithienyl-2,3,5,6-tetrafluorophenylene unit copolymd. with thiophene, bithiophene, thienothiophene and 1,2,4,5-tetrafluorobenzene comonomer units were designed and synthesized by direct heteroarylation polymn. The optical, electrochem., electrochromic and solid-state structural properties of the copolymers were investigated. The copolymers exhibit stable redox properties in org. solvents and promising redox properties in thin film configuration with an aq. electrolyte. Finally, the potential of the copolymers as active materials in org. electrochem. transistors (OECTs) was assessed, and promising performance was shown as an accumulation-mode OECT material with a peak transconductance of 0.17 mS and a good on/off ratio of 105 for the thiophene copolymer.
Keywords
bioelectronic applications, glycolated copolymers, organic electrochemical transistors
Authors
Released
17. 6. 2019
Publisher
WILEY-V C H VERLAG GMBH
Location
Německo
ISBN
2192-6506
Periodical
ChemPlusChem
Year of study
84
Number
9
State
Federal Republic of Germany
Pages from
1384
Pages to
1390
Pages count
7
URL
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cplu.201900254
BibTex
@article{BUT157970, author="Jozef {Krajčovič} and Alexander {Kovalenko} and Martin {Weiter} and Roman {Halaksa}", title="Glycolated Thiophene-Tetrafluorophenylene Copolymers for Bioelectronic Applications: Synthesis by Direct Heteroarylation Polymerisation", journal="ChemPlusChem", year="2019", volume="84", number="9", pages="1384--1390", doi="10.1002/cplu.201900254", issn="2192-6506", url="https://onlinelibrary.wiley.com/doi/pdf/10.1002/cplu.201900254" }