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Convenient regioselective syntheses of isomeric bis(tetrathiafulvalenylethenyl)naphthalene π-donors

Authors
Journal
Tetrahedron Letters
0040-4039
Publisher
Elsevier
Publication Date
Volume
39
Issue
19
Identifiers
DOI: 10.1016/s0040-4039(98)00355-4

Abstract

Abstract Novel highly soluble isomeric tetrathiafulvalene (TTF) dimers with unusual divinylnaphthalene spacers have been prepared from Wittig reactions. The cyclic voltammetry of the new TTF dimers reveals an independent behaviour of the two TTF units which show different oxidation potential values depending upon the substitution pattern.

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