Synthesis and properties of (4-hydroxy-5-methoxycarbonylthieno)-tetrathiafulvalenes

Autor: Sudmale, I. V., Khodorkovskii, V. Yu., Edzhinya, A. S., Neiland, O. Ya.
Zdroj: Chemistry of Heterocyclic Compounds; June 1993, Vol. 29 Issue: 6 p652-658, 7p
Abstrakt: 6-Hydroxy-5-methoxycarbonylthieno[2,3-d]-1,3-dithiol-2-thione, -2-one, and 2-selenone were prepared by intramolecular cyclocondensation of 4-methoxycarbonylmethylthio-1,3-dithiol-2-thione-, 2-one-, and 2-selenone-5-carboxylic acid methyl ester. 2,6(7)-Di(methoxycarbonylmethylthio)-3,7(6)-di(methoxycarbonyl)tetra-thiafulvalene, 2-methoxycarbonylmethylthio-3-methoxycarbonyl-6,7-ethylenedithiotetrathiafulvalene, and the corresponding thieno-condensed tetrafulvalene derivatives were synthesized from them. The electrochemical oxidation potentials of the new tetrafulvalene derivatives were determined.
Databáze: Supplemental Index