Aliphatic Hydroxylation by a Bis(μ-oxo)dicopper(III) Complex

Abstract
By using molecular oxygen bis(μ‐oxo)dicopper(III) complexes can be produced from CuI complexes with ligand LX (LX=p‐substituted N‐ethyl‐N‐[2‐(2‐pyridyl)ethyl]‐2‐phenylethylamine; X=OMe, Me, H, Cl, NO2) in which the benzylic position of the ligand is activated and hydroxylated by the Cu2O2 core (see reaction scheme). Detailed characterization of this new C−H bond activation reaction by the bis(μ‐oxo)dicopper(III) core reveals important information on the fundamental chemistry underlying copper monooxygenase reactivity.

This publication has 0 references indexed in Scilit: