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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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X-ray absorption studies of copper (II) mixed ligand complexes with ethylenediamine (en) as one of the ligands

TL;DR: In this paper, the X-ray K-absorption spectra of six biologically important copper (II) complexes having ethylenediamine (en) as primary ligand and nitrate, thio-cynate, perchlorate, bromide, chloride and sulphate as secondary ligands have been studied using a bent crystal 0.4 m Cauchois-type transmission spectrograph.
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Cu- and Fe-speciation in a composite zeolite catalyst for selective catalytic reduction of NOx: insights from operando XAS

TL;DR: In this article, the authors investigated temperature-driven Cu-speciation in the pure Cu-CZC and mechanical mixture under standard NH3-SCR conditions and showed that the presence of Fe-MOR component in the mixed catalyst can result in the increase of NH3 and NO concentration in the proximity of Cu-sites at a low temperature regime.
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Mechanisms of the Cu(I)-Catalyzed Intermolecular Photocycloaddition Reaction Revealed by Optical and X-ray Transient Absorption Spectroscopies.

TL;DR: In this paper, the authors used a combination of optical and X-ray transient absorption spectroscopies to elucidate the mechanism of the Cu(I)-catalyzed intermolecular photocycloaddition reaction using norbornene and cyclohexene as model substrates.
Journal ArticleDOI

Joint X-ray absorption and far infrared spectroscopic studies on zeolite surfaces – exchange and siting of copper ions and their redox behavior during NO decomposition in zeolite ZSM-5

TL;DR: In this paper, Far Infrared (FIR) and X-ray absorption spectroscopy (XAS) assisted by computer modelling were tested for their aptitude to study ion exchange, cation siting, NO adsorption and redox behavior of CuZSM-5.
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