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

28Citations
Citations of this article
29Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free