Synthesis, Structure, and Redox Reactivity of Ni Complexes Bearing a Redox and Acid–Base Non-innocent Ligand with NiII, NiIII, and NiIV Formal Oxidation States

A series of Ni complexes bearing a redox and acid-base noninnocent tetraamido macrocyclic ligand, H4-(TAML-4) {H4-(TAML-4) = 15,15-dimethyl-5,8,13,17-tetrahydro-5,8,13,17-tetraaza-dibenzo[a,g]cyclotridecene-6,7,14,16-tetraone}, with formal oxidation states of NiII, NiIII, and NiIV were synthesized and characterized structurally and spectroscopically. The X-ray crystallographic analysis of the Ni complexes revealed a square planar geometry, and the [Ni(TAML-4)] complex with the formal oxidation state of NiIV was characterized to be [NiIII(TAML-4•+)] with the oxidation state of the NiIII ion and the one-electron oxidized TAML-4 ligand, TAML-4•+. The NiIII oxidation state and the TAML-4 radical cation ligand, TAML-4•+, were supported by X-ray absorption spectroscopy and density functional theory calculations. The reversible interconversions between [NiII(TAML-4)]2- and [NiIII(TAML-4)]- and between [NiIII(TAML-4)]- and [NiIII(TAML-4•+)] were demonstrated in spectroelectrochemical measurements as well as in chemical oxidation and reduction reactions. The reactivities of [NiIII(TAML-4)]- and [NiIII(TAML-4•+)] were then investigated in hydride transfer reactions using NADH analogs. Hydride transfer from 9,10-dihydro-10-methylacridine (AcrH2) to [NiIII(TAML-4•+)] was found to proceed via electron transfer (ET) from AcrH2 to [NiIII(TAML-4•+)] with no deuterium kinetic isotope effect (kH/kD = 1.0(2)). In contrast, hydride transfer from AcrH2 to [NiIII(TAML-4)]- proceeded much more slowly via a concerted proton-coupled electron transfer (PCET) process with kH/kD = 7.0(5). In the latter reaction, an electron and a proton were transferred to the NiIII center and the TAML-4 ligand, respectively. The mechanisms of the ET by [NiIII(TAML-4•+)] and the concerted PCET by [NiIII(TAML-4)]- were ascribed to the different redox potentials of the Ni complexes.