Imidazolate-Stabilized Cu(III): Dioxygen to Oxides at Type 3 Copper Sites.
Autor: | Large TAG; Department of Chemistry, Stanford University Stanford, California, 94305, USA., Keown W; Department of Chemistry, Stanford University Stanford, California, 94305, USA., Gary JB; Department of Chemistry, Stanford University Stanford, California, 94305, USA.; Department of Chemistry & Biochemistry, Stephen F. Austin State University Nacogdoches, TX, 75962, USA., Chiang L; Department of Chemistry, Stanford University Stanford, California, 94305, USA.; Department of Chemistry, University of the Fraser Valley Abbotsford, BC, Canada., Stack TDP; Department of Chemistry, Stanford University Stanford, California, 94305, USA. |
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Jazyk: | angličtina |
Zdroj: | Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2024 Oct 17, pp. e202416967. Date of Electronic Publication: 2024 Oct 17. |
DOI: | 10.1002/anie.202416967 |
Abstrakt: | Imidazole ligation of metals through histidine is extensive among metalloproteins, yet the role of the imidazolate conjugate base is often neglected, despite its potential accessibility when bonded to an oxidized metal center. Using synthetic models of oxygenated tyrosinase enzymes ligated exclusively by monodentate imidazoles, we find that deprotonation of the μ (© 2024 Wiley-VCH GmbH.) |
Databáze: | MEDLINE |
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