We have prepared a series of gallium(III) complexes of the redox active iminopyridine ligand (IP). Reaction of GaCl₃ with iminopyridine ligand (IP) in the presence of either two or four equivalents of sodium metal resulted in the formation of deep green (IP⁻)₂GaCl (1), or deep purple [(DME)₃Na][(IP²⁻)₂Ga] (2a), respectively. Complex 1 is paramagnetic with a room temperature magnetic moment of 2.3 μ_B which falls to 0.5 μ_B at 5 K. These observations indicate that two ligand radicals comprise a triplet at room temperature which becomes a singlet due to antiferromagnetic coupling at low temperature. Complex 2 is diamagnetic. Cyclic voltammograms recorded on 0.3 M Bu₄NPF₆ THF solutions of [Na(THF)₆][(IP²⁻)₂Ga]⁻ (2b) indicate that oxidation of 2b occurs in two two-electron steps at −1.31 V and −0.54 V vs. SCE. The observation of two-electron redox events indicates that electronic coupling through the gallium(III) center is minimal and that the two IP ligand on 2b are oxidized concurrently. Oxidation of 2 with one equivalent of MeS–SMe afforded the two-electron oxidized product (IP⁻)₂Ga(SMe) (3). This complex has an electronic structure analogous to 1. Accordingly, both 1 and 3 are deep green in color and magnetic susceptibility measurements performed on 3 confirm the triplet character of the complex at room temperature. Electron paramagnetic resonance experiments on 1 and 3 display a quartet signal at g = 2.0 which confirmed the triplet nature of the compounds, and a half field signal consistent with the integer spin state.