Leriche, P. and Turbiez, M. and Monroche, V. and Frere, P. and Blanchard, P. and Skabara, P.J. and Roncali, J. (2003) Strong pi-electron donors based on a self-rigidified 2,2 '-bi(3,4-ethylenedioxy)thiophene-tetrathiafulvalene hybrid pi-conjugated system. Tetrahedron Letters, 44 (4). pp. 649-652. ISSN 0040-4039
Full text not available in this repository. (Request a copy from the Strathclyde author)Official URL: http://dx.doi.org/10.1016/S0040-4039(02)02702-8
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.
| Item type: | Article |
|---|---|
| ID code: | 828 |
| Keywords: | cation-radical salts, tetrathiafulvalene analogs, spacers, oligomers, Chemistry |
| Subjects: | Science > Chemistry |
| Department: | Faculty of Science > Pure and Applied Chemistry |
| Related URLs: | |
| Depositing user: | Mr Derek Boyle |
| Date Deposited: | 20 Apr 2006 |
| Last modified: | 12 Mar 2012 10:36 |
| URI: | http://strathprints.strath.ac.uk/id/eprint/828 |
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