Distinct Reactivity of a Mononuclear Peroxocobalt(III) Species toward Activation of Nitriles

A mononuclear side-on peroxocobalt­(III) complex with a tetradentate macrocyclic ligand, [CoIII(TBDAP)­(O2)]+ (1), shows a novel and facile mode of dioxygenase-like reactivity with nitriles (RCN; R = Me, Et, and Ph) to produce the corresponding mononuclear hydroximatocobalt­(III) complexes, [CoIII(TBDAP)­(RC­(NO)­O)]+, in which the nitrile moiety is oxidized by two oxygen atoms of the peroxo group. The overall reaction proceeds in one-pot under ambient conditions (ca. 1 h, 40 °C). 18O-Labeling experiments confirm that both oxygen atoms are derived from the peroxo ligand. The structures of all products, hydroximatocobalt­(III) complexes, were confirmed by X‑ray crystallography and various spectroscopic techniques. Kinetic studies including the Hammett analysis and isotope labeling experiments suggest that the mechanistic mode of 1 for activation of nitriles occurs via a concerted mechanism. This novel reaction would be significantly valuable for expanding the chemistry for nitrile activation and utilization.