Issue 8, 1992

Dalton communications. Convenient preparations of the mixed 1,3,2,4-/1,2,3,5-dithiadiazolylium salt [SNSNC–C6H4–CNSSN][AsF6]2 and the first mixed free radical, p-[SNSNC–C6H4–CNSSN]2˙

Abstract

The salt [p-NCC6H4–[graphic omitted]]Cl {prepared by reaction of Li[p-NCC6H4C(NSiMe3)2] with SCl2} was converted into [p-NCC6H4–[graphic omitted]]AsF6(with AgAsF6) and then reacted with [SNS]AsF6 to provide [[graphic omitted]–C6H4–[graphic omitted]][AsF6]2 in 92% recovered yield. Complete reduction of this material produced the first mixed 1,3,2,4-/1,2,3,5-dithiadiazole diradical, [[graphic omitted]–C6H4–[graphic omitted]]2˙.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1992, 1449-1450

Dalton communications. Convenient preparations of the mixed 1,3,2,4-/1,2,3,5-dithiadiazolylium salt [SNSNC–C6H4–CNSSN][AsF6]2 and the first mixed free radical, p-[SNSNC–C6H4–CNSSN]2˙

A. J. Banister, I. Lavender, J. M. Rawson and R. J. Whitehead, J. Chem. Soc., Dalton Trans., 1992, 1449 DOI: 10.1039/DT9920001449

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