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Journal ArticleDOI

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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Journal ArticleDOI

Single-ion magnetism in the extended solid-state: insights from X-ray absorption and emission spectroscopy.

TL;DR: The results demonstrate that dopant sites within solid-state host lattices could offer a viable alternative to rare-earth bulk magnets and high-performance SIMs, where the host matrix can be tailored to impose high symmetry and control lattice induced relaxation effects.
Journal ArticleDOI

An X-ray absorption spectroscopic study at the mercury LIII edge on phenylmercury(II) oxygen species

TL;DR: In this article, the X-ray absorption spectra of the reference and model compounds HgCl2, PhHgCl 2, PhGCl 2 and HgOAc have been analyzed in both the XANES and EXAFS regions.
Journal ArticleDOI

On the Nanostructure of Cu in TixCu1-x and TiN/Cu Films: A XAFS Study

TL;DR: In this paper, the effect of chemical composition on the bonding environment of Cu, in a series of Ti1-x Cux and TiN/Cu films, was studied using X-Ray Absorption Spectroscopies (XAFS) at the Cu-K-edge.
Reference EntryDOI

X‐Ray Absorption Spectroscopy

TL;DR: X-ray absorption spectroscopy (XAS) is a powerful technique available for determining the local coordination site structure and electronic properties of specific atoms in molecules as mentioned in this paper, which can be performed on molecules in the gaseous, solution, or solid states, and generally every element is spectroscopically active.
Book ChapterDOI

Combined Use of XAFS and Crystallography for Studying Protein-Ligand Interactions in Metalloproteins

TL;DR: X-ray absorption spectroscopy can yield atomic resolution three-dimensional structural models of the metal sites, thus providing the level of structural detail necessary for understanding the chemical mechanisms involved in the active states of metalloproteins.
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