A prototype hybrid 7π quinone-fused 1,3,2-dithiazolyl radical
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2011/DT/C0DT00967A
Reference80 articles.
1. Rings, Radicals, and Synthetic Metals: The Chemistry of SNS+
2. Quantitative preparations of 1,3,2-dithiazolium, 1,3,2,4-dithiadiazolium, and 1-halo-1,2,4,3,5-trithiadiazolium cations by the general, symmetry-allowed cycloadditions of SNSAsF6 with alkynes, nitriles, and thiazyl halides. Kinetics of cycloadditions of the 1,3-dipolar-like SNS+ with aliphatic and aromatic nitriles and alkynes
3. Cycloaddition reactions of SNSAsF6 with aryl nitriles and diphenylacetylene; the preparation and characterization of aryl 1,3,2,4- and 1,2,3,5-dithiadiazole radicals
4. The kinetics of the quantitative, symmetry allowed, reverse electron demand cycloadditions of the pseudo-1,3-dipole SNS+with alkynes and nitriles; the preparation and X-ray crystal structures of NCCSNSCHAsF6and SNSNC–CNSNS(AsF6)2: the precursor to a new class of S2N2C–CN2S2n+(n= 0,1,2) bicyclics
5. Evolution of the pseudo-1,3-dipolar cycloaddition chemistry of SNSMF6(M = As, Sb) leading to 2,5-dihydroxybenzo-1,3,2-dithiazolylium and 2,7-dicarbonylnaphtha-1,3,2-dithiazolylium salts and their corresponding radicals
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