Journal
SYNTHESIS-STUTTGART
Volume -, Issue 6, Pages 1000-1006Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0028-1087974
Keywords
Wittig-Horner reaction; 1,4-dithiafulvenes; ferrocene; oxidative dimerization; sunlight; pi-extended tetrathiafulvalenes; organic conductors; electrochemical properties; charge-transfer complex
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Funding
- Alexander von Humboldt Stiftung
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A new method for the synthesis of pi-extended tetrathiafulvalenes developed. The protocol is based on the exposure of 1,4-dithiafulvenes to sunlight or UV light at ambient temperature. In the resulting chalcogenofulvalenes the 1.3-dithiole ring systems are separated by conjugated spacers. Extended TTF analogues are obtained by insertion of linear pi-conjugated spacers (C=C-C=C) of increasing dimensions between the two 1,4-dithiafulvenyl moieties.
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