A triangular prismatic hexanuclear iridium(iii) complex bridged by flavin analogues showing reversible redox processes

[Ir₆(μ-alloCl₂^2-)₃(Cp* )₆(OH)₃](PF₆)₃ (1) having 7,8-dichloroalloxazine dianion (alloCl₂^2-) as bridging ligands was synthesized and characterized by X-ray crystallography, spectroscopic and electrochemical measurements. The alloxazine ligands showed unprecedented coordination modes to link the six Ir(iii) centres. The complex exhibited remarkable stability and reversible six-electron redox processes at the bridging alloxazine ligands in organic solvents. The first reversible reduction process occurred on each of three alloxazine ligands in 1 to produce a three-electron-reduced species, [Ir^III₆Cp* ₆(μ-alloCl₂^3-)₃(OH)₃], and was observed as an apparent one-step reduction process at -0.65 V (vs. Fc^0/+). The second reversible reduction process on each of the three alloxazine ligands in 1 was recorded at almost the same potential, -0.78 V (vs. Fc^0/+), to afford the six-electron-reduced form, [Ir ^III₆Cp*₆(μ-alloCl₂ ^4-)₃(OH)₃]^3-. The radical anion of the alloxazine derivative was detected by EPR measurements at room temperature. After the six-electron reduction of 1 with cobaltocene, the backward oxidation processes of reduced forms with p-chloranil were traced by UV-Vis spectroscopy to confirm the recovery of the original spectrum of 1.