The tuning of heterocyclic isomerization: Additional routes to extended donors

Citation
Rl. Meline et Rl. Elsenbaumer, The tuning of heterocyclic isomerization: Additional routes to extended donors, SYNTH METAL, 102(1-3), 1999, pp. 1658-1661
Citations number
27
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
SYNTHETIC METALS
ISSN journal
03796779 → ACNP
Volume
102
Issue
1-3
Year of publication
1999
Pages
1658 - 1661
Database
ISI
SICI code
0379-6779(199906)102:1-3<1658:TTOHIA>2.0.ZU;2-Y
Abstract
Tetrathianaphthalene: A precursor easily synthesized in bulk, is utilized i n: the synthesis of tetrathiafulvalene, and extended chalcogenated tetrathi anaphthalenes and tetrathiafulvalenes. The donor syntheses dependant upon c ore heterocycle configuration retention or isomerization are controlled via the use of novel solvent systems and new classes of disulfide building blo cks.