The reaction of the dinuclear species (mu-NH,NH)[Fe(III)(L(IP))(L(AP))](2) dissolved in CH(2)Cl(2) with dioxygen affords black microcrystals of diamagnetic (mu-S,S)[Fe(III)(L(IP))(L(ISQ))](2).n-hexane (6) upon the addition of n-hexane, where (L(IP))(2)(-) represents the dianion of 4,6-di-tert-butyl-2-aminothiophenol, (L(AP))(-) is the corresponding monoanion, and (L(ISQ))(-) is the corresponding o-iminothionebenzosemiquinonate(1-) pi radical monoanion; similarly, the dianion ('H(2)N(2)S(2)')(2)(-) is derived from 1,2-ethanediamine-N,N'-bis(2-benzenethiol), and ('N(2)S(2)(*)')(3)(-) is its monoradical trianion. The above reaction in a CH(2)Cl(2)/CH(3)OH (1:1) mixture yields the diamagnetic isomer (mu-NH,NH)[Fe(III)(L(IP))(L(ISQ))](2).5CH(3)OH (7), whereas air oxidation of (mu-S,S)[Fe(II)('H(2)N(2)S(2)')](2) in CH(3)CN yields diamagnetic (mu-S,S)[Fe(III)('N(2)S(2)(*)')](2) (8). Complexes 6 and 8 were shown to undergo addition reactions with phosphines, phosphites, or cyanide affording the following complexes: trans-[Fe(II)(L(ISQ))(2)(P(OPh)(3))] (9; S(t) = 0) and [N(n-Bu)(4)][Fe(II)(L(ISQ))(2)(CN)] (S(t) = 0). Oxidation of 6 in CH(2)Cl(2) with iodine, bromine, and chlorine respectively yields black microcrystals of [Fe(III)(L(ISQ))(2)X] (X = I, Br, or Cl) with S(t) = (1)/(2). The structures of complexes 6-9 have been determined by X-ray crystallography at 100 K. The oxidation level of the ligands and iron ions in all complexes has been unequivocally established, as indicated by crystallography; electron paramagnetic resonance, UV-vis, and Mössbauer spectroscopies; and magnetic-susceptibility measurements. The N,S-coordinated o-iminothionebenzosemiquinonate(1-) pi radicals have been identified in all new complexes. The electronic structures of the new complexes have been determined, and it is shown that no evidence for iron oxidation states >III is found in this chemistry.