The sulfur diimide dianion

The salt K2[SN2] is an important reagent for the preparation of other sulfur diimide derivatives when MesSiNSNSiMes is not sufficiently reactive. For example, both acyclic and cyclic arsenic(Iir) compounds, Bu2AsNSNAs Bu2 and BuAs(NSN)2As Bu, respectively, have been obtained in this way.  

Salts of mono-alkylated or arylated sulfur diimide anion [RNSN] (R = aryl, Bu, SiMcs) are prepared by Si-N cleavage of RNSNSiMcs with [(Me2N)3S][Mc3SiF2]. ° ° These anions adopt cis configurations with very short terminal S-N bond lengths (1.44 - 1.49 A) indicative of a thiazylamide anion, [RNS N] (5.21).  

The orange-red [SsN] anion Xm2.x 465 nm) is obtained by the addition of triphenylphosphine to a solution of a [S4N] salt in acetonitrile.It can be isolated as a salt in combination with large counterions, e.g., [Ph4As] or [N(PPh3)2] , but it is unstable with respect to the formation of the blue [S4N] anion in solution or in the solid state under the influence of heat or pressure. 

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