• Medientyp: E-Artikel
  • Titel: Polyvinyl‐Locked versus Free Quaterthiophene: Effect of Spatial Constraints on the Electronic Properties of n‐Hexylquaterthiophene
  • Beteiligte: Melucci, Manuela; Zambianchi, Massimo; Zanelli, Alberto; Camaioni, Nadia; Gazzano, Massimo; Bongini, Alessandro; Barbarella, Giovanna
  • Erschienen: Wiley, 2007
  • Erschienen in: ChemPhysChem
  • Sprache: Englisch
  • DOI: 10.1002/cphc.200700459
  • ISSN: 1439-4235; 1439-7641
  • Schlagwörter: Physical and Theoretical Chemistry ; Atomic and Molecular Physics, and Optics
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  • Beschreibung: <jats:title>Abstract</jats:title><jats:p>A soluble, low‐weight fraction of poly(α‐vinyl,ω‐<jats:italic>n</jats:italic>‐hexyl‐quaterthiophene), PT4Hex, having <jats:italic>n</jats:italic>‐hexylquaterthiophenes as side‐chain groups, is prepared by free‐radical polymerization of α‐vinyl,ω‐n‐hexyl‐quaterthiophene and the corresponding properties compared to those of free di‐<jats:italic>n</jats:italic>‐hexylquaterthiophene (T4Hex). Optical analysis (absorption and emission) and X‐ray diffraction data indicate that in the polyvinyl‐locked architecture the quaterthiophene pendants adopt a cofacial arrangement with a mutual distance close enough for π–π orbitals to overlap (∼4 Å). As a consequence of the close chain packing, a shift of the reduction potential of about 0.5 V toward less negative values with respect to free T4Hex, is found for PT4Hex films. Due to its enhanced electron affinity, PT4Hex displays an electron‐acceptor behavior when blended with alkylated and silylated quaterthiophenes acting as donors.</jats:p>