Radical cation of helical, cross-conjugated β-oligothiophene

Jerzy K. Zak, Makoto Miyasaka, Suchada Rajca, Mieczyslaw Lapkowski, Andrzej Rajca

Research output: Contribution to journalArticlepeer-review

65 Scopus citations

Abstract

(Figure Presented) The radical cation of carbon-sulfur [7]helicene is configurationally stable in solution at room temperature. In contrast to the radical cations of α-oligothiophenes, which form diamagnetic π-dimers at low temperature, the radical cation of this helical, cross-conjugated β-oligothiophene shows a low propensity toward dimerization.

Original languageEnglish (US)
Pages (from-to)3246-3247
Number of pages2
JournalJournal of the American Chemical Society
Volume132
Issue number10
DOIs
StatePublished - Mar 17 2010

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

Fingerprint Dive into the research topics of 'Radical cation of helical, cross-conjugated β-oligothiophene'. Together they form a unique fingerprint.

Cite this