Search results for "Voltammetry"
showing 10 items of 404 documents
Synthesis and electrochemical study of a new doubly-metallated compound with the ferrocene-labelled phosphine PPh2(C5H4)Fe(C5H5)
1993
Abstract Direct reaction of the metalled compound Rh 2 (μ 2 -O 2 CCH 3 ) 3 [μ 2 -(C 6 H 4 ) PPh 2 ]·(H 2 O) 2 with PPh 2 Fc [Fc = (C 5 H 4 )Fe(C 5 H 5 )] in chloroform solution yields the corresponding mono-adduct Rh 2 (O 2 CCH 3 ) 3 [(C 6 H 4 )PPh 2 ]·(PPh 2 Fc) ( 1 ), which has been characterized by 31 P NMR spectroscopy. Photochemical irradiation of 1 in chloroform gives the compound Rh 2 (μ-O 2 CCH 3 ) 2 (η 2 -O 2 CCH 3 )[μ 2 -(C 6 H 4 )PPh 2 ][PPh 2 Fc]·(H 2 O) ( 2 ) in practically quantitative yield. Compound 2 , by thermal treatment in chloroform solution, yields cleanly the doubly-metallated compound Rh 2 (μ 2 -O 2 CCH 3 ) 2 [μ 2 -(C 6 H 4 )PPhFc][μ 2 -(C 6 H 4 )PPh 2 ]·(H 2 O) 2 ( …
Channel flow at an immobilised liquid|liquid interface
2000
A novel rectangular channel flow electrochemical cell for the study of liquid | liquid interfaces is presented. The organic phase is immobilised by the use of a gelling agent, while the aqueous phase flows past the interface. This creates an asymmetric setup that allows us to establish diagnostic criteria to determine, for example, the direction of the ion transfer. The effects of varying flow rate and sweep rate have been considered both theoretically and experimentally. By comparison with two-dimensional simulations, it is demonstrated that a simple one-dimensional theory can be used to describe the cyclic voltammetry response of the channel flow cell.
Ion-exchange voltammetry at a surfactant-doped electrode: model of mass transfer kinetics to an anionic surface-charged electrode and its application…
2000
cited By 10; International audience; A theoretical model of mass transfer kinetics was developed for investigating the accumulation of cationic compounds at an anionic surfactant-doped screen-printed electrode. It was extended to an enzyme-generated cationic product for the indirect determination of alkaline phosphatase (AP). The model takes into account the analyte depletion, the kinetics of the ion-exchange reaction-diffusion and the kinetics of the enzymatic reaction. The relationship between the ion-exchange voltammetric anodic peak current and the enzyme incubation/accumulation time for a given concentration of AP was established and the validity of the theoretical model was verified e…
Electrochemistry-based chemotaxonomy in plants using the voltammetry of microparticles methodology
2015
A methodology for characterizing vegetal taxonomic groups using microextraction-assisted voltammetry of microparticles is described. It is based on recording the voltammetric response of microparticulate films of polyphenolic compounds of leaf extracts using different organic solvents. As a result, characteristic voltammetric profiles, tentatively defining an electrochemolomic response, are obtained. Bivariant and multivariant chemometric evaluation of the voltammetric responses of such films allows characterizing vegetal families. Analysis of voltammetric responses for a set of species of the Rosales order suggests that electrochemical data can be correlated with phylogenetic trees.
Reduction of ferricytochrome c catalyzed by optically active chromium(III) complexes
2009
The reduction rates of horse heart ferricytochrome c by amalgamated zinc or by electrolysis at fixed potential on a mercury pool as the cathode have been measured in a buffered solution at pH 7.5 by absorption spectrophotometry. In both cases, the reaction was strongly accelerated by the presence of the optically active complexes Lambda-[Cr(III)((S,S)-promp)H(2)O](+) (H(2)promp = N,N'-[(pyridine-2,6-diyl)bis(methylene)]-bis[(S)-proline]), Delta-[Cr(III)((R,R)-alamp)H(2)O](+) (H(2)alamp = N,N'-[(pyridine-2,6-diyl)bis(methylene)]-bis[(R)-alanine]) and Lambda-[Cr(III)((S,S)-alamp)(H(2)O)(2)](+). These were shown to undergo reversible one-electron reduction to the corresponding labile chromium(…
Spectroscopic and electrochemical study of interactions between DNA and different salts of 1,4-dihydropyridine AV-153
2020
1,4-dihydropyridines (1,4-DHP) possess important biochemical and pharmacological properties, including antimutagenic and DNA-binding activity. The latter activity was first described for water-soluble 1,4-DHP with carboxylic group in position 4, the sodium salt of the 1,4-DHP derivative AV-153 among others. Some data show the modification of physicochemical properties and biological activities of organic compounds by metal ions that form the salts. We demonstrated the different affinity to DNA and DNA-protecting capacity of AV-153 salts, depending on the salt-forming ion (Na, K, Li, Rb, Ca, Mg). This study aimed to use different approaches to collate data on the DNA-binding mode of AV-153-N…
Synthesis, photochemistry, and electrochemistry of (P)Ge(R)2 and (P)Ge(R)X (P = TPP or OEP, R = CH3, CH2C6H5, or C6H5, and X = Cl-, OH-, or ClO4-)
1987
Chaque complexe est caracterise par spectroscopie RMN de H1, UV-visible, IR et aussi par l'etude electrochimique
Pb(II) adsorption by a novel activated carbon - alginate composite material. A kinetic and equilibrium study.
2016
The adsorption capacity of an activated carbon – calcium alginate composite material (ACAA-Ca) has been tested with the aim of developing a new and more efficient adsorbent material to remove Pb(II) ion from aqueous solution. The study was carried out at pH = 5, in NaCl medium and in the ionic strength range 0.1–0.75 mol L−1. Differential Pulse Anodic Stripping Voltammetry (DP-ASV) technique was used to check the amount of Pb(II) ion removed during kinetic and equilibrium experiments. Different kinetic (pseudo first order, pseudo second order and Vermuelen) and equilibrium (Langmuir and Freundlich) models were used to fit experimental data, and were statistically compared. Calcium alginate …
Evaluation of the electrochemical anion recognition ofNO3−-imprinted poly(Azure A) inNO3−/Cl−mixed solutions by ac-electrogravimetry
2016
Abstract During the reversible electrochemical reactions of the intrinsically conducting polymer (ICP) films, ions are inserted in them to balance the inner charge site of the polymer. For this reason, doped ICP films with anions or cations can be good candidates for the electrochemical removal of contaminant ions from wastewater. In this work, a polymer of a phenothiazine derivative (poly(Azure A or PAA)) was electrosynthesized by cyclic voltammetry in aqueous solutions using nitrate ions as a structural template. After that, PAA film was repeatedly cycled in identical conditions in a monomer-free solution. The electrochemical anion recognition of the nitrate-imprinted poly(Azure A) ( N O …
Charging process in electron conducting polymers: dimerization model
2001
Abstract Theory of the charging and discharging process in electron-conducting polymer films at an electrode surface has been presented. It is based on the concept of two coexisting subsystems at the polymer matrix, ‘usual’ sites P which can exchange with the electrode by the electronic charge in a quasi-reversible manner, and sites D where intermolecular bonds between neighboring polymer molecules can be formed. The charging and discharging of the latter subsystem may be realized along different reaction pathways, e.g. via the bond formation after the generation of two cation radicals within such site D in the course of the anodic scan while the bond dissociation may take place via a parti…