CONVENIENT REGIOSELECTIVE SYNTHESES OF ISOMERIC BIS(TETRATHIAFULVALENYLETHENYL)NAPHTHALENE PI-DONORS

Authors
GONZALEZ S MARTIN N SEGURA JL SEOANE C
Citation
S. Gonzalez et al., CONVENIENT REGIOSELECTIVE SYNTHESES OF ISOMERIC BIS(TETRATHIAFULVALENYLETHENYL)NAPHTHALENE PI-DONORS, Tetrahedron letters, 39(19), 1998, pp. 3051-3054
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
39
Issue
19
Year of publication
1998
Pages
3051 - 3054
Database
ISI
SICI code
0040-4039(1998)39:19<3051:CRSOIB>2.0.ZU;2-N
Abstract
Novel highly soluble isomeric tetrathiafulvalene (TTF) dimers with unu sual divinylnaphthalene spacers have been prepared from Wittig reactio ns. The cyclic voltammetry of the new TTF dimers reveals an independen t behaviour of the two TTF units which show different oxidation potent ial values depending upon the substitution pattern. (C) 1998 Elsevier Science Ltd. All rights reserved.