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Copper(I)-Dioxygen Adducts and Copper Enzyme Mechanisms

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Journal Isr J Chem
Specialty Chemistry
Date 2016 Dec 3
PMID 27909346
Citations 26
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Abstract

Primary copper(I)-dioxygen (O) adducts, cupric-superoxide complexes, have been proposed intermediates in copper-containing dioxygen-activating monooxygenase and oxidase enzymes. Here, mechanisms of C-H activation by reactive copper-(di)oxygen intermediates are discussed, with an emphasis on cupric-superoxide species. Over the past 25 years, many synthetically derived cupric-superoxide model complexes have been reported. Due to the thermal instability of these intermediates, early studies focused on increasing their stability and obtaining physical characterization. More recently, in an effort to gain insight into the possible substrate oxidation step in some copper monooxygenases, several cupric-superoxide complexes have been used as surrogates to probe substrate scope and reaction mechanisms. These cupric superoxides are capable of oxidizing substrates containing weak O-H and C-H bonds. Mechanistic studies for some enzymes and model systems have supported an initial hydrogen-atom abstraction via the cupric-superoxide complex as the first step of substrate oxidation.

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References
1.
Klinman J . Mechanisms Whereby Mononuclear Copper Proteins Functionalize Organic Substrates. Chem Rev. 1996; 96(7):2541-2562. DOI: 10.1021/cr950047g. View

2.
Chen P, Root D, Campochiaro C, Fujisawa K, Solomon E . Spectroscopic and electronic structure studies of the diamagnetic side-on CuII-superoxo complex Cu(O2)[HB(3-R-5-iPrpz)3]: antiferromagnetic coupling versus covalent delocalization. J Am Chem Soc. 2003; 125(2):466-74. DOI: 10.1021/ja020969i. View

3.
Weitzer M, Schindler S, Brehm G, Schneider S, Hormann E, Jung B . Reversible binding of dioxygen by the copper(I) complex with tris(2-dimethylaminoethyl)amine (Me6tren) ligand. Inorg Chem. 2003; 42(6):1800-6. DOI: 10.1021/ic025941m. View

4.
Jazdzewski B, Reynolds A, Holland P, Young Jr V, Kaderli S, Zuberbuhler A . Copper(I)-phenolate complexes as models of the reduced active site of galactose oxidase: synthesis, characterization, and O2 reactivity. J Biol Inorg Chem. 2003; 8(4):381-93. DOI: 10.1007/s00775-002-0420-9. View

5.
Evans J, Ahn K, Klinman J . Evidence that dioxygen and substrate activation are tightly coupled in dopamine beta-monooxygenase. Implications for the reactive oxygen species. J Biol Chem. 2003; 278(50):49691-8. DOI: 10.1074/jbc.M300797200. View