Strong pi-electron donors based on a self-rigidified 2,2 '-bi(3,4-ethylenedioxy)thiophene-tetrathiafulvalene hybrid pi-conjugated system

P. Leriche, M. Turbiez, V. Monroche, P. Frere, P. Blanchard, P.J. Skabara, J. Roncali

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

Strong pi-donors based on the association of TTF and 2,2'-bi(3,4-ethylenedioxy)thiophene conjugating unit have been synthesised, optical and an X-ray data show that intramolecular interactions lead to full rigidification of the conjugated system. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)649-652
Number of pages3
JournalTetrahedron Letters
Volume44
Issue number4
DOIs
Publication statusPublished - 20 Jan 2003

Keywords

  • cation-radical salts
  • tetrathiafulvalene analogs
  • spacers
  • oligomers

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