scispace - formally typeset
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

Reads0
Chats0
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

read more

Citations
More filters
Journal ArticleDOI

A copper(I) protein possibly involved in the assembly of CuA center of bacterial cytochrome c oxidase

TL;DR: A possible pathway for copper delivery to the Cu(A) center in bacteria is proposed using a class of proteins of unknown function displaying a conserved gene neighborhood to bacterial Sco1 genes, all sharing a potential metal binding motif H(M)X10MX21HXM.
Journal ArticleDOI

Ligand field effect on the chemical shift in XANES spectra of Cu(II) compounds

TL;DR: In this paper, the energy positions of the 2p1/2======→ 3d and 2p3/2』−3d transition peaks in the Cu L2,3 XANES spectra and the 1s → 3d transition peak (pre-edge peak) of the Cu K-edge X-ray absorption near-edge structure (XANES) were measured for a series of Cu(II) compounds.
Journal ArticleDOI

The Axial Oxygen Atom and Superconductivity in YBa2Cu3O7.

TL;DR: Changes in the copper K-edge x-ray absorption spectrum of YBa2Cu3O7 across the critical temperature indicate that, accompanying the superconducting transition, the mean square relative displacement of some fraction of the Cu2-O4 bonds becomes smaller or more harmonic, and that electronic states involving these atom pairs become more atomic-like.
Journal ArticleDOI

Defective Porous Carbon Polyhedra Decorated with Copper Nanoparticles for Enhanced NIR-Driven Photothermal Cancer Therapy.

TL;DR: In vivo experiments conducted with tumor bearing nude Balb/c mice confirm the efficacy of Cu@CPP-800 as a very promising NIR-driven phototherapy agent for cancer treatment and encourage the wider use of MOFs as low cost precursors for the synthesis of carbon-supported metal nanoparticle composites for photothermal therapy.
Journal ArticleDOI

The State of Cu Promoter Atoms in High-Temperature Shift Catalysts—An in Situ Fluorescence XAFS Study

TL;DR: In this paper, the state of the copper promoter (017-15 wt%) was studied in Fe-Cr-based high-temperature shift (HTS) catalysts by in situ fluorescence XAFS combined with on-line gas analysis.
Related Papers (5)