Formation of stable 1,2,3-benzodithiazolyl radicals by thermolysis of 1,3,2,4-benzodithiadiazines
Mild thermolysis (at 110–150 °C) of 1,3,2,4-benzodithiadiazine 1 and its derivatives 2–6 in hydrocarbon solvents quantitatively yielded stable 1,2,3-benzodithiazolyl π-radicals via a first-order reaction ( Ea = 76.2 kJ mol –1, k 0 = 4.34×10 5 s–1 for 1).
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Veröffentlicht in: | Mendeleev communications 2000, Vol.10 (1), p.5-7 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Mild thermolysis (at 110–150 °C) of 1,3,2,4-benzodithiadiazine 1 and its derivatives 2–6 in hydrocarbon solvents quantitatively yielded stable 1,2,3-benzodithiazolyl π-radicals
via a first-order reaction (
Ea = 76.2 kJ mol
–1,
k
0 = 4.34×10
5
s–1 for 1). |
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ISSN: | 0959-9436 |
DOI: | 10.1070/MC2000v010n01ABEH001198 |