4.8 Article

Radical Cation of Helical, Cross-Conjugated β-Oligothiophene

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 132, Issue 10, Pages 3246-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja910076n

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Funding

  1. National Science Foundation [CHE-0718117]
  2. Direct For Mathematical & Physical Scien
  3. Division Of Chemistry [1012578] Funding Source: National Science Foundation
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [0718117] Funding Source: National Science Foundation

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

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