Selective hydroxylation of benzene to phenol via Cu II (μ-O˙)Cu II intermediate using a nonsymmetric dicopper catalyst.

The one-step oxidation of benzene to phenol represents a significant and promising advancement in modern industries focused on the production of high-value-added chemical products. Nevertheless, challenges persist in achieving sufficient catalytic selectivity and preventing over-oxidation. Inspired by copper enzymes, we present a nonsymmetric dicopper complex ([CuII2(TPMAN)(μ-OH)(H ₂ O)] ³⁺ , 1) for the selective oxidation of benzene to phenol. Utilizing H ₂ O ₂ as the oxidant, complex 1 demonstrates remarkable catalytic activity (a TON of 14 000 within 29 hours) and selectivity exceeding 97%, comparable to the finest homogeneous catalyst derived from first-row transition metals. It is noteworthy that the significant substituent effect, alongside a negligible kinetic isotope effect (KIE = 1.05), radical trapping experiments, and an inconsistent standard selectivity test of the ˙OH radicals, all contradict the conventional Fenton mechanism and rebound pathway. Theoretical investigations indicate that the active Cu ^II (μ-O˙)Cu ^II -OH species generated through the cleavage of the O-O bond in the Cu ^II (μ-1,1-OOH)Cu ^I intermediate facilitates the hydroxylation of benzene via an electrophilic attack mechanism. The nonsymmetric coordination geometry is crucial in activating H ₂ O ₂ and in the process of O-O bond cleavage.