Exo-Methylene-BEDT-TTF and alkene-functionalised BEDT-TTF derivatives: Synthesis and radical cation salts

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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.

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Zecchini, M., Lopez, J. R., Allen, S. W., Coles, S. J., Wilson, C., Akutsu, H., … Wallis, J. D. (2015). Exo-Methylene-BEDT-TTF and alkene-functionalised BEDT-TTF derivatives: Synthesis and radical cation salts. RSC Advances, 5(39), 31104–31112. https://doi.org/10.1039/c5ra03921e

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