This article describes the synthesis and reactivity studies of three cobalt complexes bearing aminophenol-derived ligands without nitrogen substitution: CoII(tBu2APH)2(tBu2AP)2 (1), Co2III(tBu2APH)2(tBu2AP)2(μ-tBu2BAP)2 (2), and CoIII(tBu2AP)3 (3) (tBu2APH = 2-amino-4,6-di-tert-butylphenol, tBu2AP = 2-amino-4,6-di-tert-butylphenolate, μ-tBu2BAP = bridging 2-amido-4,6-di-tert-butylphenolate). Stoichiometric reactivity studies of these well-defined complexes demonstrate the catalytic com-petency of both CoII and CoIII complexes in the aerobic oxidative cyclization of tBu2APH with tert-butyl isonitrile. Reactions with O2 reveal the aerobic oxidation of CoII complex 1 to generate the CoIII species 2 and 3. UV-visible time-course studies and EPR spectroscopy indicate that this oxidation proceeds through a ligand-based radical intermediate. These studies repre-sent the first example of well-defined cobalt-aminophenol complexes that participate in catalytic aerobic oxidation reactions and highlight a key role for a ligand radical in the oxidation sequence.
Aerobic Oxidation Reactivity of Well-Defined CoII and CoIII Aminophenol Complexes
