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Extensive quinoidal oligothiophenes with dicyanomethylene groups at terminal positions as highly amphoteric redox molecules. | LitMetric

Extensive quinoidal oligothiophenes with dicyanomethylene groups at terminal positions as highly amphoteric redox molecules.

J Am Chem Soc

Department of Applied Chemistry, Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527, Japan.

Published: June 2005

AI Article Synopsis

  • A series of quinoidal oligothiophenes with dicyanomethylene groups at both ends were synthesized.
  • These structures exhibit amphoteric properties and strong electronic absorption in the visible to near-infrared region.
  • Longer versions like quinquethiophene and sexithiophene exist in equilibrium with biradical species.

Article Abstract

A series of highly extensive quinoidal oligothiophenes carrying a dicyanomethylene group at both terminal positions is synthesized. As the quinoidal structures extend, they have highly amphoteric abilities and show strong electronic absorptions in the visible to near-infrared region. The higher homologues, quinquethiophene and sexithiophene, exist as equilibrium mixtures with the biradical species.

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Source
http://dx.doi.org/10.1021/ja051840mDOI Listing

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