Skeletal Scrambling of Sulfur Diimide Radical-Anions
by Bestari, K.; Oakley, R. T.; Cordes, A. W.
In the presence of a catalytic quantity of alkali metal mixtures of sulphur diimides RNSNR and R'NSNR' (R, R' = Ph, 4-C6H4Me, 4-C6H4OMe, SiMe3, SPh) undergo a rapid scrambling of the R and R' groups. When R and R' are significantly different (e.g., R = Ph, R' = SiMe3 or SPh) the equilibrium is shifted to favour the unsymmetrical sulphur dimmide (R not-equal R'); the procedure thus represents an effective method for preparing such derivatives. A mechanism involving the centrosymmetric association and rearrangement of two sulphur diimide radical anions is suggested for the observed ligand scrambling. The synthesis and X-ray structure determination of the mixed diimide (4-NO2C6H4)SNSN(4-C6H4OMe) is reported. The crystals are monoclinic, space group P2(1)/n; the molecules stack as plates along the a axis in a head-to-head fashion, producing an interplanar spacing between consecutive S2N2 units of 3.421 angstrom.
- Journal
- Canadian Journal of Chemistry-Revue Canadienne de Chimie
- Volume
- 69
- Issue
- 1
- Year
- 1991
- Start Page
- 94-99
- URL
- https://dx.doi.org/10.1139/v91-014
- ISBN/ISSN
- 1480-3291; 0008-4042
- DOI
- 10.1139/v91-014