Poly-sulfur-nitrogen heterocycles via sulfur chlorides and nitrogen reagents

Authors
Citation
T. Torroba, Poly-sulfur-nitrogen heterocycles via sulfur chlorides and nitrogen reagents, J PRAK CH C, 341(2), 1999, pp. 99-113
Citations number
118
Categorie Soggetti
Chemistry
Journal title
JOURNAL FUR PRAKTISCHE CHEMIE-CHEMIKER-ZEITUNG
ISSN journal
09411216 → ACNP
Volume
341
Issue
2
Year of publication
1999
Pages
99 - 113
Database
ISI
SICI code
0941-1216(1999)341:2<99:PHVSCA>2.0.ZU;2-S
Abstract
The family of poly-sulfur-nitrogen heterocycles includes highly stable arom atic compounds that display physicochemical properties with relevance in th e design of new materials, especially those relating to molecular conductor s and magnets. The interesting characteristics found in many of these heter ocycles have led to the development of modern synthetic methods that are th e subject of this review. Heterocycles such as 1,2,3- and 1,2,5-thiadiazole s, 1,2,3- and 1,3,2-dithiazoles, 1,2,3,5-dithiadiazoles, thiatriazines, tri thiadiazines, dithia(and trithia)diazepines, trithiatriazepines, dithia(and trithia)tetrazozines, and fused systems are most commonly synthesized from tetrasulfur tetranitride and organic substrates (alkynes, diazomethanes), and from sulfenyl chlorides, sulfur or disulfur dichlorides and nitrogen co ntaining reagents such as bis(trimethylsilyl)surfurdiimide, trimethylsilyl azide, trisilylated amidines, N-imidoylamidines, hydrazones, oximes, and am ines.