Issue 39, 2015

exo-Methylene-BEDT-TTF and alkene-functionalised BEDT-TTF derivatives: synthesis and radical cation salts

Abstract

Hydroxymethyl-BEDT-TTF is converted by tosylation and elimination into exo-methylene-BEDT-TTF whose exocyclic double bond leads to a small increase in the oxidation potential, and from which radical cation salts with perchlorate and triiodide have been prepared, the latter showing semiconductor properties. Allyloxymethyl- and allylthiomethyl-BEDT-TTF, the first BEDT-TTF derivatives with an alkene in the side chain, have been prepared, along with a 1 : 2 radical cation perchlorate salt of the former, an insulator which contains a donor dication.

Graphical abstract: exo-Methylene-BEDT-TTF and alkene-functionalised BEDT-TTF derivatives: synthesis and radical cation salts

Supplementary files

Article information

Article type
Paper
Submitted
05 Mar 2015
Accepted
25 Mar 2015
First published
25 Mar 2015
This article is Open Access
Creative Commons BY license

RSC Adv., 2015,5, 31104-31112

Author version available

exo-Methylene-BEDT-TTF and alkene-functionalised BEDT-TTF derivatives: synthesis and radical cation salts

M. Zecchini, J. R. Lopez, S. W. Allen, S. J. Coles, C. Wilson, H. Akutsu, L. Martin and J. D. Wallis, RSC Adv., 2015, 5, 31104 DOI: 10.1039/C5RA03921E

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