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Intermediates of photolysis of 1,3,2,4-benzodithiadiazines studied by matrix isolation spectroscopy and quantum chemistry Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 2001, Volume: 50, Number: 11, Pages: 2064-2070 Pages count : 7 DOI: 10.1023/A:1015032814197
Tags 1,3,2,4-benzodithiadiazine; 1,2,3-benzodithiazolyl radical; 1,2,3-benzodithiazol-2-ylnitrene; photolysis; UV spectroscopy; IR spectroscopy; ESR spectroscopy; matrix isolation; quantum yield; ab initio quantum-chemical calculations
Authors Gritsan N.P. 1,2 , Bagryansky V.A. 1,2 , Vlasyuk I.V. 2 , Molin Yu.N. 1,2 , Makarov A.Yu. 3 , Platz M.S. 4 , Zibarev A.V. 3
Affiliations
1 (Данные Web of science) Russian Acad Sci, Inst Chem Kinet & Combust, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
3 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
4 (Данные Web of science) Ohio State Univ, Dept Chem, Columbus, OH 43210 USA

Abstract: Photolysis of 12pi-electron, formally antiaromatic, 1,3,2,4-benzodithiadiazine (1a) and its tetrafluoro-substituted derivative (1b) was studied in glassy matrices at 77 K and in an argon matrix at 14 K by UV, IR, and ESR spectroscopy. In these matrices, a diamagnetic species (3a,b) is formed as a persistent species. It is product of the intramolecular transformations of heterocycles 1a,b and the precursor of 1,2,3-benzodithiazolyl radicals (2a,b). The nitrenoid structure, intermediate between the structures of singlet 1,2,3-benzodithiazol-2-ylnitrene RS-N: and the corresponding thiazyl RSequivalent toN, was ascribed to intermediate 3a,b in agreement with the data of IR spectroscopy.
Cite: Gritsan N.P. , Bagryansky V.A. , Vlasyuk I.V. , Molin Y.N. , Makarov A.Y. , Platz M.S. , Zibarev A.V.
Intermediates of photolysis of 1,3,2,4-benzodithiadiazines studied by matrix isolation spectroscopy and quantum chemistry
Russian Chemical Bulletin. 2001. V.50. N11. P.2064-2070. DOI: 10.1023/A:1015032814197 WOS Scopus РИНЦ OpenAlex
Identifiers:
Web of science: WOS:000175056400017
Scopus: 2-s2.0-84961982080
Elibrary: 41767088
OpenAlex: W70384320
Citing:
DB Citing
Web of science 19
Scopus 17
Elibrary 14
OpenAlex 13
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