Issue 1, 2006

Photochemistry of 1,3,2,4-benzodithiadiazines: formation and oxidation of 1,2,3-benzodithiazolyl radicals

Abstract

Photolysis of 1,3,2,4-benzodithiadiazine and its derivatives in hydrocarbon solutions yields dinitrogen and stable 1,2,3-benzodithiazolyls (Herz radicals) whose interaction with dioxygen leads finally to O[double bond, length as m-dash]S[double bond, length as m-dash]N-substituted diphenyl disulfides via a self termination-like process with an effective second-order rate constant depending linearly on the concentration of dissolved O2.

Graphical abstract: Photochemistry of 1,3,2,4-benzodithiadiazines: formation and oxidation of 1,2,3-benzodithiazolyl radicals

Article information

Article type
Paper
Submitted
18 Jul 2005
Accepted
11 Oct 2005
First published
11 Nov 2005

Photochem. Photobiol. Sci., 2006,5, 95-101

Photochemistry of 1,3,2,4-benzodithiadiazines: formation and oxidation of 1,2,3-benzodithiazolyl radicals

N. P. Gritsan, S. N. Kim, A. Yu. Makarov, E. N. Chesnokov and A. V. Zibarev, Photochem. Photobiol. Sci., 2006, 5, 95 DOI: 10.1039/B510188C

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