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

35 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.
LanguageEnglish
Pages649-652
Number of pages3
JournalTetrahedron Letters
Volume44
Issue number4
DOIs
Publication statusPublished - 20 Jan 2003

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Thiophenes
X-Rays
Electrons
X rays
tetrathiafulvalene

Keywords

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

Cite this

Leriche, P. ; Turbiez, M. ; Monroche, V. ; Frere, P. ; Blanchard, P. ; Skabara, P.J. ; Roncali, J. / Strong pi-electron donors based on a self-rigidified 2,2 '-bi(3,4-ethylenedioxy)thiophene-tetrathiafulvalene hybrid pi-conjugated system. In: Tetrahedron Letters. 2003 ; Vol. 44, No. 4. pp. 649-652.
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Strong pi-electron donors based on a self-rigidified 2,2 '-bi(3,4-ethylenedioxy)thiophene-tetrathiafulvalene hybrid pi-conjugated system. / Leriche, P.; Turbiez, M.; Monroche, V.; Frere, P.; Blanchard, P.; Skabara, P.J.; Roncali, J.

In: Tetrahedron Letters, Vol. 44, No. 4, 20.01.2003, p. 649-652.

Research output: Contribution to journalArticle

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KW - spacers

KW - oligomers

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