A copper complex supported by an N2S-tridentate ligand inducing efficient heterolytic O-O bond cleavage of alkylhydroperoxide

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Abstract

We have recently reported a copper(ii)-superoxide complex supported by an N3-tridentate ligand (LN3), which exhibits a similar structure and reactivity to those of a putative reactive intermediate involved in the catalytic reactions of copper monooxygenases such as peptidylglycine α-hydroxylating monooxygenase (PHM) and dopamine β-monooxygenase (DβM). In this study, we have synthesised and characterised copper complexes supported by a related sulphur-containing ligand (LN2S) to get insight into the notable electronic effect of the sulphur donor atom in the reaction with cumene hydroperoxide, inducing efficient heterolytic O-O bond cleavage. © 2014 The Royal Society of Chemistry.

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Tano, T., Mieda, K., Sugimoto, H., Ogura, T., & Itoh, S. (2014). A copper complex supported by an N2S-tridentate ligand inducing efficient heterolytic O-O bond cleavage of alkylhydroperoxide. Dalton Transactions, 43(12), 4871–4877. https://doi.org/10.1039/c3dt52952e

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