Exploring the Redox Properties of Bench-Stable Uranyl(VI) Diamido–Dipyrrin Complexes

[Image: see text] The uranyl complexes UO(2)(OAc)(L) and UO(2)Cl(L) of the redox-active, acyclic diamido–dipyrrin anion L(–) are reported and their redox properties explored. Because of the inert nature of the complexes toward hydrolysis and oxidation, synthesis of both the ligands and complexes was conducted under ambient conditions. Voltammetric, electron paramagnetic resonance spectroscopy, and density functional theory studies show that one-electron chemical reduction by the reagent CoCp(2) leads to the formation of a dipyrrin radical for both complexes [Cp(2)Co][UO(2)(OAc)(L(•))] and [Cp(2)Co][UO(2)Cl(L(•))]