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- W2970819209 abstract "Abstract The dioxygen reactivity of a series of TMPA‐based copper(I) complexes (TMPA=tris(2‐pyridylmethyl)amine), with and without secondary‐coordination‐sphere hydrogen‐bonding moieties, was studied at −135 °C in 2‐methyltetrahydrofuran (MeTHF). Kinetic stabilization of the H‐bonded [( TMPA)Cu II (O 2 .− )] + cupric superoxide species was achieved, and they were characterized by resonance Raman (rR) spectroscopy. The structures and physical properties of [( TMPA)Cu II (N 3 − )] + azido analogues were compared, and the O 2 .− reactivity of ligand–Cu I complexes when an H‐bonding moiety is replaced by a methyl group was contrasted. A drastic enhancement in the reactivity of the cupric superoxide towards phenolic substrates as well as oxidation of substrates possessing moderate C−H bond‐dissociation energies is observed, correlating with the number and strength of the H‐bonding groups." @default.
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- W2970819209 date "2019-10-23" @default.
- W2970819209 modified "2023-10-16" @default.
- W2970819209 title "Impact of Intramolecular Hydrogen Bonding on the Reactivity of Cupric Superoxide Complexes with O−H and C−H Substrates" @default.
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- W2970819209 doi "https://doi.org/10.1002/anie.201908471" @default.
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