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 0040-4039Full text not available in this repository. (Request a copy from the Strathclyde author)
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.
|Keywords:||cation-radical salts, tetrathiafulvalene analogs, spacers, oligomers, Chemistry, Biochemistry, Organic Chemistry, Drug Discovery|
|Subjects:||Science > Chemistry|
|Department:||Faculty of Science > Pure and Applied Chemistry|
|Depositing user:||Mr Derek Boyle|
|Date Deposited:||20 Apr 2006|
|Last modified:||22 Mar 2017 09:14|