3-Dithiolthione-substituted polythiophene and its redox activities

Ichiro Takemura, Tomokazu Iwasaki, Shinji Takeoka, Hiroyuki Nishide

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

We synthesized 3-dithiolthione-substituted polythiophene, poly[3-(1′,2′-dithiol-3′-thione-4′-yl)thiophene], by cyclization reaction of poly[3-bis(methoxycaronyl)methyl thiophene]. Its redox behavior and electronic states showed that the oxidation of the polythiophene followed the oxidation of the dithiolthione ring to the radical cation of the dithiolthione ring.

Original languageEnglish
Pages (from-to)1482-1483
Number of pages2
JournalChemistry Letters
Volume33
Issue number11
DOIs
Publication statusPublished - 2004 Nov 5

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Thiophenes
Oxidation
Cyclization
Electronic states
Cations
Oxidation-Reduction
polythiophene
1,2-dithiol-3-thione

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

3-Dithiolthione-substituted polythiophene and its redox activities. / Takemura, Ichiro; Iwasaki, Tomokazu; Takeoka, Shinji; Nishide, Hiroyuki.

In: Chemistry Letters, Vol. 33, No. 11, 05.11.2004, p. 1482-1483.

Research output: Contribution to journalArticle

Takemura, Ichiro ; Iwasaki, Tomokazu ; Takeoka, Shinji ; Nishide, Hiroyuki. / 3-Dithiolthione-substituted polythiophene and its redox activities. In: Chemistry Letters. 2004 ; Vol. 33, No. 11. pp. 1482-1483.
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