Synthetic methods of selenium- and tellurium variants of tetrathiafulvalene electron donors

Citation
T. Otsubo et al., Synthetic methods of selenium- and tellurium variants of tetrathiafulvalene electron donors, PHOSPHOR SU, 171, 2001, pp. 231-253
Citations number
43
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
ISSN journal
10426507 → ACNP
Volume
171
Year of publication
2001
Pages
231 - 253
Database
ISI
SICI code
1042-6507(2001)171:<231:SMOSAT>2.0.ZU;2-Q
Abstract
Two very useful, versatile reactions applicable to the synthesis of TTF-typ e electron donors are presented: the one-pot preparation of 1,3-dichalcogen ole-2-chalcogenones from readily available terminal alkynes and the ready f ormation of heterocyclic rings fused on TTF by transalkylation on a chalcog en atom. These reactions in combination with a conventional trialkyl phosph ite-promoted coupling reaction of 1,3-dichalcogenole-2-chalcogenones provid e a ready access to novel selenium- and tellurium- variants of TTF-type ele ctron donors. A variety of synthetic examples of these compounds, especiall y inaccessible ones of six-membered heterocycle-fused type, five-membered h eterocycle-fused type, dimeric type, and cyclophane type, are demonstrated.