Issue 9, 1990

New symmetrical and unsymmetrical tetrathiafulvalene π-donors containing the dithiinoquinoxaline ring system

Abstract

2,3-Dichloroquinoxaline when treated with the multi-sulphur dithiolate (1) gave the thione (2), which was coupled using neat triethyl phosphite to give the bisquinoxalinodithiin-fused tetrathiafulvalene, BQDT-TTF (3). Cross-coupling of thione (2) with 4,5-bis(methylthio)-1,3-dithiole-2-thione and 5,6-dihydro-1,3-dithiol[4,5-b][1,4]dithiin-2-thione afforded the unsymmetrical donors (4) and (5) respectively. The oxidation potentials of donors (4) and (5) are reported along with the preparation and electrical conductivity measurement of a tri-iodide cation-radical salt of BQDT-TTF (3).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 2563-2565

New symmetrical and unsymmetrical tetrathiafulvalene π-donors containing the dithiinoquinoxaline ring system

K. S. Varma, S. Edge, A. E. Underhill, J. Becher and G. Bojesen, J. Chem. Soc., Perkin Trans. 1, 1990, 2563 DOI: 10.1039/P19900002563

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