期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 49, 页码 17572-17576出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201908471
关键词
copper monooxygenases; cupric superoxide; dioxygen reduction; H-atom transfer; hydrogen bonding
资金
- National Institutes of Health [GM 28962, DK031450]
- Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) [72110038]
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 degrees C in 2-methyltetrahydrofuran (MeTHF). Kinetic stabilization of the H-bonded [((X1)(X2) 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 [((X1)(X2) 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.
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