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X-ray absorption edge determination of the oxidation state and coordination number of copper: application to the type 3 site in Rhus vernicifera laccase and its reaction with oxygen

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TLDR
In this paper, a normalized difference edge analysis is used to quantitatively determine the oxidation states of the copper sites in type 2 copper-depleted (T2D) and native forms of the multicopper oxidase, Rhus vernicifera laccase.
Abstract
Cu X-ray absorption edge features of 19 Cu(I) and 40 Cu(II) model complexes have been systematically studied and correlated with oxidation state and geometry. Studies of Cu(I) model complexes with different coordination number reveal that an 8983-8984-eV peak (assigned as the Cu 1s ..-->.. 4p transition) can be correlated in energy, shape, and intensity with ligation and site geometry of the cuprous ion. These Cu(I) edge features have been qualitatively interpreted with ligand field concepts. Alternatively, no Cu(II) complex exhibits a peak below 8985.0 eV. The limited intensity observed in the 8983-8985-eV region for some Cu(II) complexes is associated with the tail of an absorption peak at approx. 8986 eV which is affected by the covalency of the equatorial ligands. These models studies allow accurate calibration of a normalized difference edge procedure which is used for the quantitative determination of Cu(I) content in copper complexes of mixed oxidation state composition. This normalized difference edge analysis is then used to quantitatively determine the oxidation states of the copper sites in type 2 copper-depleted (T2D) and native forms of the multicopper oxidase, Rhus vernicifera laccase. The type 3 site of the T2D laccase is found to be fully reduced and stable tomore » oxidation by O/sub 2/ or by 25-fold protein equivalents of ferricyanide, but it can be oxidized by reaction with peroxide. The increase in intensity of the 330-nm absorption feature which results from peroxide titration of T2D laccase is found to correlate linearly with the percent of oxidation of the binuclear copper site.« less

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Extended X-ray absorption fine structure study of mixed-ligand copper(II) complexes having analogous structures

TL;DR: X-ray absorption fine structure spectra have been studied at the Cu K-edge in five mixed-ligand copper(II) complexes, viz., [Cu(L-glu)(bipy)] 1, [Cu-L-glutamate dianion, L-tyro = Ltyrosinate anion, bipy = 2,2′-bipyridine, and phen = 1,10-phenanthroline), having essentially the same structure as discussed by the authors.
Journal ArticleDOI

Copper k-edge x-ray absorption studies of la2-xkxcuo4 superconductors, ba4nacuo4(co3)2, and ndcu2o4

TL;DR: In this paper, X-ray near-edge absorption spectroscopy (XANES) measurements are reported at the Cu K-edge for La{sub 2-x}K{sub x}CuO{sub 4} superconductors with x = 0.1 and 0.2.
Journal ArticleDOI

SO2 Poisoning of Cu-CHA deNOx Catalyst: The Most Vulnerable Cu Species Identified by X-ray Absorption Spectroscopy

TL;DR: In this article , the authors characterized a Cu-CHA catalyst under well-defined exposures to SO2 using in situ X-ray absorption spectroscopy and found that the highest reactivity toward SO2 was observed for CuII species coordinated to both NH3 and extraframework oxygen, in particular for [CuII2(NH3)4O2]2+ complexes.
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Mononuclear Copper Complexes with Tridentate Tris(N-heterocyclic carbene): Synthesis and Catalysis of Alkyne–Azide Cycloaddition

TL;DR: In this paper, the structures of the copper-triscarbene complexes were characterized using a tridentate tris(N-heterocyclic carbene) ligand.
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Local structure of Cu(I) ions in the MOR zeolite: A DFT-assisted XAS study

TL;DR: In this article, in situ XAS and DFT were combined to determine the local structure of Cu(I) ions in the Cu-exchanged mordenite (MOR) zeolite, one of the most promising materials for the selective oxidation of methane to methanol.
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