RCNSSS+[rad]: A novel class of stable sulfur rich radical cations

Abstract

The current review provides up-to-date information on the structures, solution and solid state electron paramagnetic resonance (EPR), electronic and magnetic properties, and computational analysis of the novel 1,2,3,4-trithiazolium RCNSSS+ radical cation. The stable 7π radical cation RCNSSS+, derived from RCNSSN by isoelectronic substitution of N by S+, is a rare example of a main group radical with ca. 96% of the spin density residing exclusively on the sulfur atoms. In the solid state it forms a great variety of structures, which, depending on the nature of the substituent group, range from dimeric to monomeric. This results in markedly different magnetic properties in which the magnetic coupling varies from −2100cm−1 to −2cm−1, respectively. An important highlight in the chemistry of RCNSSS+ is the preparation of (CNSSS+)22+, which contains two radical centers directly joined by a single bond and is paramagnetic in all states, making it the only O2-like species in main group chemistry. Also important is the observation, by EPR, of a triplet excited state in the [RCNSSS]22+ dimers and estimation of the dimerisation energy of the very weak inter-molecular S⋯S bonds as ca. −11 to −3kJ/mol. The radical pairs [RCNSSS]22+ also possess a high diradical character, ranging from 45 to 32%, thus lying on the borderline between conventional open shell and closed shell species.