Issue 11, 2005

Hexyl-substituted oligothiophenes with a central tetrafluorophenylene unit: crystal engineering of planar structures for p-type organic semiconductors

Abstract

Rigidification has been achieved in thiophene–tetrafluorophenylene architectures through strong S⋯F and H⋯F intramolecular interactions; the resulting materials are promising candidates for p-type organic field effect transistors.

Graphical abstract: Hexyl-substituted oligothiophenes with a central tetrafluorophenylene unit: crystal engineering of planar structures for p-type organic semiconductors

Supplementary files

Article information

Article type
Communication
Submitted
23 Nov 2004
Accepted
22 Dec 2004
First published
24 Jan 2005

Chem. Commun., 2005, 1465-1467

Hexyl-substituted oligothiophenes with a central tetrafluorophenylene unit: crystal engineering of planar structures for p-type organic semiconductors

D. J. Crouch, P. J. Skabara, M. Heeney, I. McCulloch, S. J. Coles and M. B. Hursthouse, Chem. Commun., 2005, 1465 DOI: 10.1039/B417642A

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