Water-stable organic mixed valence (MV) compounds have been prepared by the reaction of reduced bis(imino)pyridine ligands (I₂P) with the trichloride salts of Al, Ga, and In. The coordination of two tridentate ligands to each ion affords octahedral complexes that are accessible with five ligand charge states: [(I₂P⁰)(I₂P^–)M]²⁺, [(I₂P^–)₂M]⁺, (I₂P^–)(I₂P^2–)M, [(I₂P^2–)₂M]⁻, and [(I₂P^2–)(I₂P^3–)M]^2–, and for M = Al only, [(I₂P^3–)₂M]^3–. In solid-state structures, the anionic members of the redox series are stabilized by the intercalation of Na⁺ cations within the ligands. The MV members of the redox series, (I₂P^–)(I₂P^2–)M and [(I₂P^2–)(I₂P^3–)M]^2–, show characteristic intervalence transitions, in the near-infrared regions between 6800–7400 and 7800–9000 cm^–1, respectively. Cyclic voltammetry (CV), NIR spectroscopic, and X-ray structural studies support the assignment of class II for compounds [(I₂P^2–)(I₂P^3–)M]^2– and class III for M = Al and Ga in (I₂P^–)(I₂P^2–)M. All compounds containing a singly reduced I₂P^– ligand exhibit a sharp, low-energy transition in the 5100–5600 cm^–1 region that corresponds to a π*−π* transition. CV studies demonstrate that the electron-transfer events in each of the redox series, Al, Ga, and In, span 2.2, 1.4, and 1.2 V, respectively.