Molecular
cobalt(III) complexes of bis-amidate-bis-alkoxide ligands,
(Me4N)[CoIII(L1)] (1) and (Me4N)[CoIII(L2)] (2), are synthesized and assessed through a range of characterization
techniques. Electrocatalytic water oxidation activity of the Co complexes
in a 0.1 M phosphate buffer solution revealed a ligand-centered 2e–/1H+ transfer event at 0.99 V followed by
catalytic water oxidation (WO) at an onset overpotential of 450 mV.
By contrast, 2 reveals a ligand-based oxidation event
at 0.9 V and a WO onset overpotential of 430 mV. Constant potential
electrolysis study and rinse test experiments confirm the homogeneous
nature of the Co complexes during WO. The mechanistic investigation
further shows a pH-dependent change in the reaction pathway. On the
one hand, below pH 7.5, two consecutive ligand-based oxidation events
result in the formation of a CoIII(L2–)(OH) species, which, followed by a proton-coupled electron transfer
reaction, generates a CoIV(L2–)(O) species
that undergoes water nucleophilic attack to form the O–O bond.
On the other hand, at higher pH, two ligand-based oxidation processes
merge together and result in the formation of a CoIII(L2–)(OH) complex, which reacts with OH– to yield the O–O bond. The ligand-coordinated reaction intermediates
involved in the WO reaction are thoroughly studied through an array
of spectroscopic techniques, including UV–vis absorption spectroscopy,
electron paramagnetic resonance, and X-ray absorption spectroscopy.
A mononuclear CoIII(OH) complex supported by the one-electron
oxidized ligand, [CoIII(L3–)(OH)]−, a formal CoIV(OH) complex, has been characterized,
and the compound was shown to participate in the hydroxide rebound
reaction, which is a functional mimic of Compound II of Cytochrome
P450.