Abstract
The reaction of azide ion with cyclo-octasulphur in tris(dimethylamino)phosphine oxide produces the [S4N] ion, whereas lithium nitride yields the trisulphur radical ion, S3 ·, predominantly. The azide reaction provides a convenient and direct synthesis of S7NH. PO(NMe2)3 Is superior to NN-dimethylformamide (dmf) as a solvent for the S2Cl2–NH3 route to cyclic sulphur imides. Equilibria of the type [S7N]⇌[S4N]+⅜S8⇌½[S6N2]2–+½S8 are invoked to explain the formation and relatively low yields of S6(NH)2 isomers in these syntheses.
Keywords

This publication has 0 references indexed in Scilit: