Unxepected dimerization of oxidized fullerene-oligothiophene-fullerene triads

  • J.J. Apperloo
  • , B.M.W. Langeveld-Voss
  • , J. Knol
  • , J.C. Hummelen
  • , R.A.J. Janssen

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Can bulky fullerene substituents reduce the dimerization tendency of oligothiophene radical cations? These authors prepared the dumbbell-shaped bis-C60-substituted oligothiophene shown in the Figure in order to address this question. Contrary to expectation, the molecules display extensive dimerization, even at room temperature, in remarkable contrast to the corresponding unsubstituted oligothiophenes.
Original languageEnglish
Pages (from-to)908-911
Number of pages3
JournalAdvanced Materials
Volume12
Issue number12
DOIs
Publication statusPublished - 2000

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