Organic charge transfer complex

Details Organic charge transfer complex Organic charge transfer complex

1995-10-06

1997-04-01

Dees, Jose G.

Organic compounds -- part of the class 532-570 series

Organic compounds

Heterocyclic carbon compounds containing a hetero ring...

552303, C07D33906, C07C 5006

Patent

active

056167288

ABSTRACT:
An organic charge transfer complex comprising an electron donor and an electron acceptor, the electron donor is at least one of bis(oxapropylenedithio)tetrathiafulvalene represented by formula (1): ##STR1## and bis(thiapropylenedithio)tetrathiafulvalene represented by formula (2): ##STR2##

REFERENCES:
Synthetic Metals, vol. 42, No. 1-2, 1991, Amsterdam NL, pp. 1963-1970, R.P. Shibaeva et al, "New cation-radical salts based on BEDT-TTF Analogs with Polyhalide Anions" *pp. 1963-1965*.
Synthetic Metals, vol. 2, No. 3, 1991, Amsterdam NL, pp. 2409-2413, H. Nakano et al "Synthesis of multi-chalcogen TTF-derivatives and electrical conductivities of their radical-ion salts" *pp. 2409-2411; table 2*.
Chemistry Letters No. 11, 1990, Tokyo JP, pp. 2129-2132, H. Nakano et al "Synthesis of 4,5-ethylene dithio-4'5'-(2-oxatrimethylenedithio)-tetrathiafulvalene (EOTT) and electrical conductivities of their ion-radical salts" *p. 2130; table 1*.
Journal of Molecular Electronics, vol. 5, No. 1, 1989, Chichester GB, pp. 33-36, V. Khodorkovsy et al, "Electron-donating ability of tetrathiafulvalene derivatives invedtigated by cyclic voltammetry" *pp. 33-34; table 1*.
Chemical Abstracts, vol. 111, No. 13, 25 Sep. 1989, Columbus, Ohio, US; abstract No. 115150b.
R. Medne et al "Synthesis and crystal structure of bis(oxapropylenedithio) tetrathiafulvalene hexyfluorophosphate", p. 661; *abstract* & Izv. Akad. Nauk SSSR, Ser. Khim. No. 1, 1989, pp. 174-176.
Bulletin of the Chemical Society of Japan, vol. 66, No. 6, Jun. 1993, Tokyo JP, pp. 1773-1777.
H. Muller et al "Synthesis and properties of bis(oxybid(Methylenethio)tetrathiafulvalene ad its sulfur analog: pi-donor for organic metals" *pp. 1773-1775*.

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