Search results for "CYCLIC VOLTAMMETRY"

showing 10 items of 238 documents

The Radical Trap in Atom Transfer Radical Polymerization Need Not Be Thermodynamically Stable. A Study of the MoX3(PMe3)3 Catalysts

2005

The molybdenum(III) coordination complexes MoX(3)(PMe(3))(3) (X = Cl, Br, and I) are capable of controlling styrene polymerization under typical atom transfer radical polymerization (ATRP) conditions, in conjunction with 2-bromoethylbenzene (BEB) as an initiator. The process is accelerated by the presence of Al(OPr(i))(3) as a cocatalyst. Electrochemical and synthetic studies aimed at identifying the nature of the spin trap have been carried out. The cyclic voltammogram of MoX(3)(PMe(3))(3) (X = Cl, Br, I) shows partial reversibility (increasing in the order ClBrI) for the one-electron oxidation wave. Addition of X(-) changes the voltammogram, indicating the formation of MoX(4)(PMe(3))(3) f…

AnionsReaction mechanismRadical polymerization010402 general chemistryPhotochemistry01 natural sciencesBiochemistryRedoxCatalysisStyreneCatalysisStyreneschemistry.chemical_compoundColloid and Surface ChemistryRadical polymerizationOxidationOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryRedox reactions010405 organic chemistryAtom-transfer radical-polymerizationGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersPolymerizationchemistryCyclic voltammetry
researchProduct

The different redox-activity of dianthrylbenzene and dianthrylbiphenyl

1989

Abstract The reduction of dianthrylbenzene and dianthrylbiphenyl to stable tetraanion salts is described by NMR spectroscopy and cyclic voltammetry. The significantly different Coulomb interactions between the anthracene units are compared with those in dianthrylalkanes.

Anthracenechemistry.chemical_compoundchemistryOrganic ChemistryDrug DiscoveryInorganic chemistryNuclear magnetic resonance spectroscopyCyclic voltammetryBiochemistryRedox ActivityTetrahedron Letters
researchProduct

Electronic Interactions in a New π-Extended Tetrathiafulvalene Dimer

2006

The first pi-extended tetrathiafulvalene (exTTF) dimer in which the two exTTF units are covalently connected by 1,3-dithiole rings has been obtained in a multistep synthetic procedure involving the Ullmann cross-coupling reaction by using copper(I) thiophene-2-carboxylate (CuTC). The electronic spectrum reveals a significant electronic interaction between the exTTF units. The electrochemical study carried out by cyclic voltammetry in solution and in thin-layer conditions, and the electrochemical simulation and spectroelectrochemical (SEC) measurements confirm the electronic communication and show that the oxidation of dimer 14 occurs as two consecutive 2 e(-) processes D(0)-D(0)-->D(2+)-D(0…

AnthracenesAnthraceneDimerOrganic Chemistrychemistry.chemical_elementStereoisomerism[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryPhotochemistryElectrochemistryCopperCatalysisDelocalized electronchemistry.chemical_compoundCrystallographyModels ChemicalchemistryHeterocyclic CompoundsCovalent bondElectrochemistryElectronicsCyclic voltammetryDimerizationOxidation-ReductionTetrathiafulvaleneChemistry - A European Journal
researchProduct

Vis/NIR spectroelectrochemical analysis of poly-(Azure A) on ITO electrode

2006

Electrochromic behavior of poly-(Azure A) on indium–tin oxide electrode is analyzed in an aqueous potassium nitrate solution. The dependence of the absorbance on the applied potential during cyclic voltammograms proves very interesting at two selected characteristic wavelengths: at 925 nm, attributed to an intermediate species and another at 735 nm, attributed to the oxidized form of the polymer. Molar absorptivity coefficients for both species have been calculated from the relationship between current and the derivative of absorbance with respect to time. Voltammograms of formation of the intermediate are simulated from spectroelectrochemical results. Keywords: Poly-(Azure A), Spectroelect…

Aqueous solutionAnalytical chemistryAzure APotassium nitrateMolar absorptivitylcsh:ChemistryAbsorbancechemistry.chemical_compoundlcsh:Industrial electrochemistrylcsh:QD1-999chemistryElectrochromismElectrodeElectrochemistryCyclic voltammetrylcsh:TP250-261
researchProduct

Calculation of the surface concentration of Zn(I) from the anodic voltammetric peak of zinc combined with the QCM results

2004

Deconvolution of voltammograms of anodic dissolution of zinc has proved to be possible through the electrochemical quartz crystal microbalance data and the F(dm/dQ) function. This deconvolution allows to calculate the surface concentration of Zn(I) and to obtain an estimation for the kinetic constant of the second single-electron transfer. Keywords: Zinc anodic dissolution, EQCM, Surface concentration, Deconvolution and kinetic constant

Aqueous solutionChemistryAnalytical chemistrychemistry.chemical_elementQuartz crystal microbalanceZincElectrochemistryAnodelcsh:Chemistrylcsh:Industrial electrochemistrylcsh:QD1-999Transition metalElectrochemistryDeconvolutionCyclic voltammetrylcsh:TP250-261Electrochemistry Communications
researchProduct

The role of lithium, perchlorate and water during electrochemical processes in poly(3,4-ethylenedioxythiophene) films in LiClO4 aqueous solutions

2021

Abstract Thin films of poly(3,4-ethylendioxythiophene) (PEDOT) were electrochemically deposited on gold electrodes in aqueous media. The role of perchlorate, lithium, and water during the charge/discharge of PEDOT films was investigated by cyclic voltammetry together with EQCM, vis − NIR spectroscopy, and acoustic impedance, also by means of ac-electrogravimetry in a 0.1 M LiCl O 4 aqueous solutions. In this way, it has been possible to correlate the electrical, mass, color and electromechanical properties changes during the electrochemical reactions of this polymer. Both, hydrated lithium cations and perchlorate anions can act as counterions during the electrochemical reactions, however, a…

Aqueous solutionChemistryGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementElectrochemistryLithium perchlorateAnalytical ChemistryPerchloratechemistry.chemical_compoundPEDOT:PSSElectrochemistryLithiumsense organsCyclic voltammetryPoly(34-ethylenedioxythiophene)Journal of Electroanalytical Chemistry
researchProduct

Preparation of nanostructures composed of dextran sulfate/ruthenium nanoparticles and their interaction with phospholipid monolayers at a liquid–liqu…

2007

Abstract Nanostructures composed of dextran sulfate (DS)/ruthenium (Ru) nanoparticles (NPs) adsorbed on phospholipid monolayers at a liquid–liquid interface were prepared and characterized electrochemically in relation to their potential use in drug delivery systems. First, positively charged Ru NPs were prepared, and then negatively charged DS was adsorbed on the surface of the NPs, thus forming well-defined and organized structures, as observed under the transmission electron microscope, which are referred to composite nanoclusters. The lipid monolayers were formed by depositing either 1-palmitoyl-2-oleoyl- sn -glycero-3-phosphatidylcholine or 1-palmitoyl-2-oleoyl- sn -glycero-3-phospho- …

Aqueous solutionChromatographyGeneral Chemical Engineeringtechnology industry and agricultureNanoparticlechemistry.chemical_elementAnalytical ChemistryRutheniumNanoclustersAdsorptionchemistryChemical engineeringMonolayerElectrochemistrylipids (amino acids peptides and proteins)Cyclic voltammetryDrug carrierJournal of Electroanalytical Chemistry
researchProduct

Oxamidato complexes. Part 4. Electrochemical study of the copper(III)/copper(II) couple in monomeric N,N?-bis(substituent)oxamidatocopper(II) complex…

1993

The electrochemical behaviour of a series of monomeric N,N′-bis(substituent)oxamidato copper(II) complexes of formula Na2[Cu(3,5,3′,5′-X4obbz)]·4H2O [X = Cl (1), Br (2), I (3) and obbz = oxamidobis(benzoato)], Na2-[Cu(obbz)]·4H2O (4), Na2[Cu(5,5′-Me2obbz)]·4H2O (5), Na2[Cu(4,5,4,5′-(MeO)4obbz)]·4H2O(6),Na2[Cu(obp)]· 3.5H2O (7) (obp = oxamidobis(propionato)) and Na2[Cu(pba)]·6H2O (8), [pba = propylenebis(oxamate)] has been investigated by cyclic voltammetry, rotating disk electrode and coulometry in water and dimethylsulphoxide (dmso) solutions. NaNO3 (0.1 M) and n-Bu4NPF6 (0.1 M) were used as supporting electrolytes in H2O and dmso respectively, all solutions being thermostatted at 25 °C. I…

Aqueous solutionLigandOxamideInorganic chemistryMetals and AlloysSubstituentchemistry.chemical_elementMedicinal chemistryCopperInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryRotating disk electrodeCyclic voltammetryOrganometallic chemistryTransition Metal Chemistry
researchProduct

Magnetoelectrochemistry of 4,4′-bis(dimethylamino)biphenyl and 4,4′-dinitrobiphenyl azacrown macrocyclic lactams

2005

Abstract The voltammetric behaviour at carbon fibre microelectrodes under the application of static magnetic fields of two series of macrolactams containing in their structure 4,4′-bis(dimethylamino)biphenyl or 4,4′-dinitrobiphenyl groups in MeCN solution is described. The response of 4,4′-dinitrobiphenyl receptors is dominated by two successive one-electron reduction processes at −0.9 and −1.6 V versus AgCl/Ag. 4,4′-bis(dimethylamino)biphenyl-containing receptors display two one-electron oxidations above +0.8 and +1.0 V. In both cases, a dihedral/planar interconversion precedes the second electron transfer step. Upon application of moderate (0.05–0.2 T) static magnetic fields to the electr…

BiphenylStereochemistryGeneral Chemical EngineeringReaction intermediateDihedral angleElectrochemistrychemistry.chemical_compoundElectron transferCrystallographychemistryElectrochemistryCyclic voltammetryAcetonitrileConformational isomerismElectrochimica Acta
researchProduct

Sensor Properties of Pristine and Functionalized Carbon Nanohorns

2016

Nanodispersions of pristine single-wall carbon nanohorns (i.e., p-SWCNHs) and oxidized-SWCNHs (i.e.; o-SWCNHs) were used to modify screen printed electrode (SPE). p-SWCNHs and o-SWCNHs were fully characterized by using several analytical techniques, as: HR-TEM (High Resolution-Transmission Electron Microscopy), FE-SEM/EDX (Field Emission-Scanning Electron Microscopy/Energy Dispersive X-ray Analysis), Raman spectroscopy, thermogravimetric analysis, differential thermal analysis (DTA), and the Brunauer-Emmett-Teller (BET) method. The chemically modified SPEs were also characterized with Cyclic Voltammetry (CV), using several different electro-active targets. In all cases, p-SWCNHs showed bett…

Carbon NanohornThermogravimetric analysisScreen Printed ElectrodesMaterials scienceAnalytical chemistrychemistry.chemical_element02 engineering and technologyGlassy carbon010402 general chemistryElectrochemistry01 natural sciencesCarbon NanohornsAnalytical Chemistrysymbols.namesakeDifferential thermal analysisElectrochemistrySettore CHIM/01 - Chimica AnaliticaSingle-WallCarbon Nanohorns; Screen Printed Electrodes; Single-Wall; Analytical Chemistry; ElectrochemistryScreen Printed Electrode021001 nanoscience & nanotechnology0104 chemical scienceschemistryElectrodesymbolsCyclic voltammetry0210 nano-technologyRaman spectroscopyCarbonElectroanalysis
researchProduct