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Zachary S. Parr, Roman Halaksa, Peter A. Finn, Reem B. Rashid,Jonathan Rivnay, Jozef Krajčovič, Christian B. Nielsen
Originální název
Glycolated Thiophene-Tetrafluorophenylene Copolymers for Bioelectronic Applications: Synthesis by Direct Heteroarylation Polymerisation
Typ
článek v časopise ve Web of Science, Jimp
Jazyk
angličtina
Originální abstrakt
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.
Klíčová slova
bioelectronic applications, glycolated copolymers, organic electrochemical transistors
Autoři
Vydáno
17. 6. 2019
Nakladatel
WILEY-V C H VERLAG GMBH
Místo
Německo
ISSN
2192-6506
Periodikum
ChemPlusChem
Ročník
84
Číslo
9
Stát
Spolková republika Německo
Strany od
1384
Strany do
1390
Strany počet
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" }