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• W2895834514 abstract "Investigations of small molecule copper-dioxygen chemistry can and have provided fundamental insights into enzymatic processes (e.g., copper metalloenzyme dioxygen binding geometries and their associated spectroscopy and substrate reactivity). Strategically designing copper-binding ligands has allowed for insight into properties that favor specific (di)copper-dioxygen species. Herein, the tetradentate tripodal TMPA-based ligand (TMPA = tris((2-pyridyl)methyl)amine) possessing a methoxy moiety in the 6-pyridyl position on one arm (OCH3TMPA) was investigated. This system allows for a trigonal bipyramidal copper(II) geometry as shown by the UV-vis and EPR spectra of the cupric complex [(OCH3TMPA)CuII(OH2)](ClO4)2. Cyclic voltammetry experiments determined the reduction potential of this copper(II) species to be -0.35 V vs. Fc+/0 in acetonitrile, similar to other TMPA-derivatives bearing sterically bulky 6-pyridyl substituents. The copper-dioxygen reactivity is also analogous to these TMPA-derivatives, affording a bis-μ-oxo dicopper(III) complex, [{(OCH3TMPA)CuIII}2(O2-)2]2+, upon oxygenation of the copper(I) complex [(OCH3TMPA)CuI](B(C6F5)4) at cryogenic temperatures in 2-methyltetrahydrofuran. This highly reactive intermediate is capable of oxidizing phenolic substrates through a net hydrogen atom abstraction. However, after bubbling of the precursor copper(I) complex with dioxygen at very low temperatures (-135 °C), a cupric superoxide species, [(OCH3TMPA)CuII(O2•-)]+, is initially formed before slowly converting to [{(OCH3TMPA)CuIII}2(O2-)2]2+. This appears to be the first instance of the direct conversion of a cupric superoxide to a bis-μ-oxo dicopper(III) species in copper(I)-dioxygen chemistry." @default.
• W2895834514 created "2018-10-26" @default.
• W2895834514 creator A5057340442 @default.
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• W2895834514 date "2019-01-01" @default.
• W2895834514 modified "2023-10-12" @default.
• W2895834514 title "Unprecedented direct cupric-superoxo conversion to a bis-μ-oxo dicopper(III) complex and resulting oxidative activity" @default.
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• W2895834514 doi "https://doi.org/10.1016/j.ica.2018.10.015" @default.
• W2895834514 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6461407" @default.
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