Myoglobin modified electrodes as anchors for d metal cationic complexes.

The capability of adsorption of different electroactive cationic Re(V)-amine complexes onto myoglobin-containing electrodes has been investigated. The goal of this work was the development of an Au/thiol/myo electrode and, after incubation of such ensemble in the presence of three different Re(V)-amine complexes, the evaluation of the extent of surface coverage by the complexes (as a way to evaluate the interaction complex-protein) using electrochemical techniques. Our results showed that a protein-containing electrode could therefore be used for the detection of the interaction of small electroactive cationic complexes and the biomolecule.

Redox behavior of Re(V)-amino acid containing complexes.

Three cationic complexes containing the [Re((V))O](3+) core (general formula [ReO(dien-H)(aa)](+), dien=diethylenetriamine, aa=glycine, alanine, valine) were studied on polycrystalline Au electrodes employing cyclic voltammetry techniques. The electrochemical behavior of the amino acids (aa) was also evaluated. Experiments were performed at pH 7.

Voltammetric studies of the interaction between Re(V) complexes and proteins.

A reliable method based on electrochemical measurements for the evaluation of protein interaction with small electroactive coordination compounds is proposed. Protein binding capacity of five different cationic Re(V) complexes was evaluated by means of voltammetric techniques in the absence and the presence of bovine serum albumin. The percentage of interaction between the complex and the protein was estimated from the quantitative decrease of the diffusion coefficient for the sole complex due to the addition of the protein, and therefore the formation of the protein-complex molecular ensemble.

Electrochemical behavior of aqueous acid perrhenate-containing solutions on noble metals: critical review and new experimental evidence.

The actual state of the art in the reduction of perrhenate ions on noble metals is reviewed and discussed. Also, with the aim of contributing to better knowledge of this process, results of several experiments are presented. For the first time, spectroscopic evidence on the nature of the deposited rhenium layer on Pt and Rh and the detection of an intermediate in the reduction pathway toward metallic rhenium is provided.

Voltammetric Characterization of trans-Dioxo Ethylenediamine Complexes of Re(V) in Aqueous Solutions.

The electrochemical behavior of trans-[Re((V))O(2)(en)(2)]I and trans-[Re((V))O(2) (en)(2)]ClO(4) (en=ethylenediamine) complexes was studied by cyclic voltammetry on Au electrodes. Experiments were performed in aqueous solutions at pH 7.0 and at room temperature.