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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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Identifying the active redox oxygen sites in a mixed Cu and Ce oxide catalyst by in situ X-ray absorption spectroscopy and anaerobic reactions with CO in concentrated H2

TL;DR: In this paper, the active redox oxygen site of a mixed copper cerium oxide catalyst (Cu 0.07 Ce 0.93 O 2 ) and the active copper species for CO preferential oxidation in rich H 2 were investigated by in situ X-ray absorption spectroscopy (XAS) at Cu K-edge during anaerobic reaction.
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In-situ DRIFTS and XANES identification of copper species in the ternary composite oxide catalysts CuMnCeO during CO preferential oxidation

TL;DR: A series of CuMnCeO catalysts with 10% CuO (weight loading) and variable atomic ratios of Mn/Mn+Ce (0, 002, 005 or 010) were synthesized by co-precipitation and employed for CO preferential oxidation (CO PROX).
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Conjugated Polyrotaxanes Incorporating Mono- or Divalent Copper Complexes

TL;DR: A conjugated polyrotaxane poly[Cu(1.2)+] has been synthesized via copper-I-templated strategy and electropolymerization as mentioned in this paper.
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Electronic Structural Analysis of Copper(II)–TEMPO/ABNO Complexes Provides Evidence for Copper(I)–Oxoammonium Character

TL;DR: The emergent electronic structure picture reveals that Cu coordination confers appreciable oxoammonium character to the aminoxyl ligand and has important implications for the mechanism of alcohol oxidation and the underlying basis for cooperativity in this co-catalyst system.
Journal ArticleDOI

The Lumenal Loop Met672–Pro707 of Copper-transporting ATPase ATP7A Binds Metals and Facilitates Copper Release from the Intramembrane Sites

TL;DR: It is demonstrated that the characteristic His/Met-rich segment Met672–Pro707 (HM-loop) that connects the first two transmembrane segments of ATP7A is important for copper release and that copper binding within the HM-loop stabilizes Cu(I) and protects it from oxidation, which may further aid the transfer of copper from ATP 7A to acceptor proteins.
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