Search results for " voltammetry"

showing 10 items of 295 documents

Studien zum Vorgang der Wasserstoffübertragung, 41. Elektroreduktion von Acetophenon unter Mitwirkung optisch aktiver Leitsalze

1977

Die Anderung des Carbinol/Pinakol-Verhaltnisses2) (C/P) und der optischen Induktion bei der Elektroreduktion von Acetophenon mit (1 R, 2S)-N-(3-Cyanpropyl)-N-methylephedriniumbromid (1) und (1 R, 2 S)-N,N-Dimethylephedriniumbromid (2) als Leitsalze wird untersucht in Abhangigkeit: a) vom Potential (Tabelle 1), b) von der Stromdichte (Tabelle 2), c) von Pulsbedingungen (Tabelle 3), d) vom pH (Tabelle 4), e) von der Anwesenheit anderer Kationen (Tabelle 5), f) vom Losungsmittel (Tabelle 6), g) von der Temperatur (Tabelle 7) und h) von der Art des Elektrodenmaterials (Tabelle 8). — Es werden tensammetrische und cyclovoltammetrische Messungen durchgefuhrt. Die in trockenem Dimethylformamid erha…

chemistry.chemical_compoundchemistryBromideSupporting electrolyteOrganic ChemistryHydrogen transferDimethylformamidePhysical and Theoretical ChemistryOptically activeCyclic voltammetryMedicinal chemistryAcetophenoneJustus Liebigs Annalen der Chemie
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Surface modification of graphite+polymer composite and ITO electrodes by Nafion®+cupromeronic phthalocyanine films

1999

Abstract The surface of indium tin oxide (ITO) and graphite+polymer composite electrodes can be modified by Nafion ® films containing a little amount of dispersed electroactive substances, such as phthalocyanines. This procedure allows the recovery of electroanalytical information on the electroactive deposited substance. The preparation methods for these types of modified electrodes are discussed from the voltammetric results obtained in this work. The Nafion ® net acts as a permeable membrane to the hydrogen ions. Furthermore, the presence of methylviologen within the Nafion ® film makes the electron transport throughout this membrane easy.

chemistry.chemical_compoundchemistryGeneral Chemical EngineeringNafionInorganic chemistryElectrochemistryPhthalocyanineSurface modificationGraphiteSemipermeable membraneCyclic voltammetryIndium tin oxideElectrode potentialElectrochimica Acta
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Novel electrolytes for electrochemical double layer capacitors based on 1,1,1,3,3,3-hexafluoropropan-2-ol

2012

Abstract 1,1,1,3,3,3-Hexafluoropropan-2-ol (HFIP) was tested for its applicability as solvent in electrolytes for energy storage devices. A comprehensive characterization with respect to solubility, conductivity, as well as chemical and electrochemical stability was carried out with different conducting salts. Furthermore, different HFIP solutions containing standard supporting electrolytes and alkali metal fluorides, respectively, were applied in electrochemical double layer capacitor cells. Their behavior was studied with impedance spectroscopy and cyclic voltammetry at low scan rates and compared to the current benchmark electrolytes based on propylene carbonate (PC) and acetonitrile (AN…

chemistry.chemical_compoundchemistryGeneral Chemical EngineeringPropylene carbonateElectrodeInorganic chemistryElectrochemistryElectrolyteCyclic voltammetryGlassy carbonSolubilityElectrochemistryDielectric spectroscopyElectrochimica Acta
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Mechanism of redox transformation of titanocene dichloride centers immobilized inside a polypyrrole matrix—EQCM and XPS evidences

2005

Abstract We report electrochemical quartz crystal microbalance (EQCM) results for electrodeposition of titanocene derivatized polypyrrole p(Tc3Py) films and redox transformation of polypyrrole matrix and titanocene centers immobilized in the film. Films of p(Tc3Py), Tc3Py = Tc(CH 2 ) 3 NC 4 H 4 (Tc = Cl 2 TiCpCp′, Cp = C 5 H 5 , Cp′ = C 5 H 4 ) were obtained from acetonitrile solutions of monomer on a Pt disc or thin Au layer evaporated on 10 MHz quartz crystals. Polymerization efficiency, derived from the slope of the change of resonant frequency as a function of the deposition charge ranged from 54% to 75%. A gradual loss of redox activity of Tc centers during consecutive redox cycles of …

chemistry.chemical_compoundchemistryPolymerizationGeneral Chemical EngineeringInorganic chemistryElectrochemistryTitanocene dichlorideQuartz crystal microbalanceCyclic voltammetryPolypyrroleElectrochemistryAcetonitrileRedoxElectrochimica Acta
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Cathodic behaviour of dicationic imidazolium bromides: the role of the spacer

2019

The cathodic reduction of dicationic imidazolium bromides, whose spacer is either an aliphatic chain or a xylyl group, leads to the formation of the corresponding N-heterocyclic carbenes (NHCs), which were isolated as the corresponding thiones, after reaction with elemental sulfur. The behaviour of the dications was compared with the corresponding monocations. The behaviour of dicarbenes depends on the nature of the spacer. This study evidenced that dicarbenes deriving from xylyl dications are less stable than the corresponding aliphatic ones (giving lower yields in thiones), due to a debenzylation reaction. On the other hand, the yields in thiones starting from aliphatic dications are high…

chemistry.chemical_compoundchemistryimidazolium dications; cathodic reduction; imidazole-2-thione; N-heterocyclic carbene; electroorganic chemistryIonic liquidInorganic chemistryElectrochemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologieSettore CHIM/06 - Chimica OrganicaCyclic voltammetryCatalysisionic liquids electrochemistry cyclic voltammetryCathodic protection
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Non-covalent graphene nanobuds from mono- and tripodal binding motifs.

2017

Graphene nanobuds were prepared via the non-covalent anchoring of C60-based molecules endowed with one or three pyrene units, respectively. TGA, FTIR, UV-Vis and TEM investigations confirmed the formation of nanohybrids. For the two molecular derivatives, striking differences were determined in their interaction with graphene or carbon surfaces by Raman, cyclic voltammetry and molecular mechanics calculations, revealing the important role of pyrene adsorption in modulating the electronic properties of the nanohybrids.

chemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysislaw.inventionsymbols.namesakechemistry.chemical_compoundAdsorptionlawMaterials ChemistryOrganic chemistryMoleculeFourier transform infrared spectroscopyGrapheneMetals and Alloystechnology industry and agricultureQuímica orgánicaGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryCeramics and CompositessymbolsPyreneCyclic voltammetry0210 nano-technologyRaman spectroscopyCarbonChemical communications (Cambridge, England)
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Synthesis, crystallographic and electrochemical study of ethynyl[2.2]paracyclophane derived cobalt metallatetrahedranes

2012

Abstract A series of alkynyl cobalt complexes [Co2(μ-η2-HCC–PCP)(CO)6−nLn] [n = 0 (2); n = 2, L2 = dppa (3), dppm (4), dcpm (6), 2 P(OPh)3 (7)] and [Co2(CO)4L2]2(μ-η2:μ-η2-HCC–PCP–CCH)] (L2 = dppm (8), dcpm (9); (PCP = [2.2]paracyclophane) has been prepared and characterized. The molecular structures of 3 and 4, as well as that of [Co2(CO)4(μ-CO)2(μ2-dcpm)] (5), have been determined by X-ray diffraction. Electrochemical studies (Cyclic Voltammetry, Rotating Disk Electrode) and luminescence spectroscopy have been used to evaluate the extent of the electronic communication through the PCP motif using the “Co2C2” centres as a probe. No electronic coupling between the Co2(CO)n centres via the b…

chemistry.chemical_elementAlkyne[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistry01 natural sciencesBiochemistryInorganic ChemistryMaterials ChemistryluminescencealkyneElectronic communication[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryRotating disk electrodeSpectroscopyComputingMilieux_MISCELLANEOUSchemistry.chemical_classification010405 organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistrycobalt0104 chemical sciencesCrystallographychemistryelectrochemistryCyclic voltammetry[2.2]paracyclophaneLuminescenceCobalt
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Influences of Chemical Functionalities on Crystal Structures and Electrochemical Properties of Dihydro-benzoxazine Dimer Derivatives

2021

Dihydro-1,3,2H-benzoxazine dimer derivatives or dihydro-benzoxazine dimers are a class of compounds typically prepared by ring-opening reactions between dihydro-benzoxazines and phenols. Dihydro-benzoxazine dimers act as chelating agents for several transition and rare-earth cations. To better understand the chelating properties, it is necessary to examine their structural features and electrochemical characteristics thoroughly. However, the electrochemical properties of dihydro-benzoxazine dimers have not been tremendously examined. Herein, eight derivatives of dihydro-benzoxazine dimers possessing different substituents on the benzene ring and the tertiary-amine nitrogen were synthesized …

crystal structureCrystallographyHydrogen bondGeneral Chemical EngineeringDimerHirshfeld surfaceIntermolecular forceCrystal structureCondensed Matter PhysicsRedoxInorganic ChemistryCrystalelectrochemical propertychemistry.chemical_compoundCrystallographychemistryQD901-999General Materials SciencebenzoxazineCyclic voltammetryMethyleneCrystals
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Synthesis of phosphine derivatives of [Fe2(CO)6(μ-sdt)] (sdt = SCH2SCH2S) and investigation of their proton reduction capabilities

2023

The reactions of [Fe2(CO)6(μ-sdt)] (1) (sdt = SCH2SCH2S) with phosphine ligands have been investigated. Treatment of 1 with dppm (bis(diphenylphosphino)methane) or dcpm (bis(dicyclohexylphosphino)methane) affords the diphosphine-bridged products [Fe2(CO)4(μ-sdt)(μ-dppm)] (2) and [Fe2(CO)4(μ-sdt)(μ-dcpm)] (3), respectively. The complex [Fe2(CO)4(μ-sdt)(κ2-dppv)] (4) with a chelating diphosphine was obtained by reacting 1 with dppv (cis-1,2-bis(diphenylphosphino)ethene). Reaction of 1 with dppe (1,2-bis(diphenylphosphino)ethane) produces [{Fe2(CO)4(μ-sdt)}2(μ-κ1-dppe)] (5) in which the diphosphine forms an intermolecular bridge between two diiron cluster fragments. Three products were obtaine…

elektrokatalyysielectrocatalysisphosphinehydrogenaseiron carbonyl complexkompleksiyhdisteetproton reductioncyclic voltammetry
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Physical chemical properties and kinetics of redox processes in water/soybean oil microemulsions

2008

Microemulsoes de agua em oleo (ME w/o) constituidas de agua, oleo de soja, SDS (dodecil sulfato de sodio) e diversos alcoois de cadeia curta foram caracterizadas sob o ponto de vista fisico-quimico e de propriedades eletroanaliticas. Foram testados diferentes co-surfactantes e razoes surfactante:cosurfactante, sendo a ME com a composicao mais favoravel utilizada para estudar a cinetica de processos redox. Para tanto, realizaram-se medidas de voltametria ciclica utilizando como eletrodo de trabalho um ultramicroeletrodo de disco de Pt e, como eletrodo de referencia e auxiliar, foram usados Ag/AgCl e Pt, respectivamente, e ferroceno como uma sonda. Verificou-se que a estabilidade termodinâmic…

food.ingredientAqueous solutionChemistryStereochemistryKineticsGeneral ChemistryReference electrodeRedoxSoybean oilchemistry.chemical_compoundfoodMicroemulsionSodium dodecyl sulfateCyclic voltammetryNuclear chemistryJournal of the Brazilian Chemical Society
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