Bd. Gupta et al., Homolytic displacements at two reactive centers: organodicobaloximes and organodisulfonyl chloride, J ORGMET CH, 582(2), 1999, pp. 279-281
The reactions of 1,3 xylylene dicobaloxime with PhSSPh, PhSeSePh, ArSO2Cl a
t 0 degrees C under irradiation form the corresponding disulfides, diseleni
de and the disulfones but the 2,5 thiophene dicobaloxime form the methyl su
bstituted mono sulfides, selenides and sulfones. The 3-methylallylcobaloxim
e with biphenyldisulfonyl chloride and mesitylene disulfonyl chloride forms
exclusively the corresponding disulfones whereas 3-thienylmethyl cobaloxim
e forms a mixture of products. (C) 1999 Elsevier Science S.A. All rights re
served.