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Salts of extended tetrathiafulvalene analogues: relationships between molecular structure, electrochemical properties and solid state organisation

Frere, P. and Skabara, P.J. (2005) Salts of extended tetrathiafulvalene analogues: relationships between molecular structure, electrochemical properties and solid state organisation. Chemical Society Reviews, 34 (1). pp. 69-98. ISSN 0306-0012

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Abstract

By considering the structures of many salts derived from extended TTF analogues, relationships between the molecular architecture of the donors with their electrochemical properties and their stacking mode in the salts are presented in this critical review. Three categories of donors corresponding to their extension modes have been considered. Firstly, for linearly extended TTFs the crucial role of the spacer in modifying the electrochemical properties and the packing mode in the salts is presented. Secondly, bidimentional extension of the donors obtained by linking several dithiafulvenyl units on a TTF core led to materials with increased dimensionality. Finally, the last class corresponds to the fusion, directly or across a benzene ring, of TTF frameworks. The former are the base of many salts with metallic behaviour.

Item type: Article
ID code: 881
Keywords: pi-electron donors, ray crystal-structures, charge-transfer salts, cation-radical salts, functionalized 9, 10-bis(1, 3-dithiol-2-ylidene)-9, 10-dihydroanthracene derivatives, metals (bedt-atd)(2)x(solvent) x, pressure organic superconductor, bis-fused tetrathiafulvalene, bedt-ttf, conducting properties, Chemistry, Chemistry(all)
Subjects: Science > Chemistry
Department: Faculty of Science > Pure and Applied Chemistry
Related URLs:
Depositing user: Mr Derek Boyle
Date Deposited: 24 Apr 2006
Last modified: 04 Sep 2014 13:15
URI: http://strathprints.strath.ac.uk/id/eprint/881

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