Search results for "ELECTROCHEMICAL"

showing 10 items of 574 documents

Recent Scientific and Technological Developments in Electrochemical Carboxylation Based on Carbon Dioxide

2010

chemistry.chemical_compoundMaterials scienceCarbon dioxidechemistryChemical engineeringCarboxylationGalvanic anodeCarbon dioxideInorganic chemistryElectrocatalystElectrochemistryElectrochemical reduction of carbon dioxide
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Room-temperature ionic liquid-based electrochemical nanobiosensors

2012

Abstract Room-temperature ionic liquids (RTILs) have proved to be excellent materials for applications in electrochemistry. We review progress in constructing high-performance electrochemical biosensors. We also discuss: • different modified electrodes based on RTILs for biosensing applications; • different routes for enzyme biosensing based on RTIL-modified electrodes; • incorporation of biorecognition elements into RTIL-based electrodes; • electroanalytical applications of RTIL-based modified electrodes; and, • recent developments in which the advantages of ILs as a medium for biosensing were realized. We also summarize the latest developments in the applications of RTIL-based electrochem…

chemistry.chemical_compoundMaterials sciencechemistryIonic liquidElectrodeElectrochemical biosensorNanotechnologyElectrochemistryBiosensorSpectroscopyAnalytical ChemistryTrAC Trends in Analytical Chemistry
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Electrochemical Syntheses of Carboxylic Acids from Carbon Dioxide

1987

The first report on the reduction of carbon dioxide is due to the venerable name of Hermann Kolbe, who, in 1861, published with R. Schmitt the reduction of carbon dioxide to formate with metallic potassium (1). Seven years later he introduced to the Chemical Society in London his assistant E. Drechsel, who “after many unsuccessful experiments, made during several years” (2) at the end succeeded in reducing carbon dioxide to oxalate with metallic sodium or with potassium amalgam in anhydrous conditions. Soon afterwards Beketov (3) and Royer (4) opened the series of papers dealing with the direct involvement of carbon dioxide in electrolytic processes. Since then the reduction of carbon dioxi…

chemistry.chemical_compoundchemistryPotassiumCarbon dioxideInorganic chemistryAnhydrouschemistry.chemical_elementOrganic chemistryFormateAmalgam (chemistry)ElectrochemistryOxalateElectrochemical reduction of carbon dioxide
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Electrochemical Characterization of Corrosion Products in Leaded Bronze Sculptures Considering Ohmic Drop Effects on Tafel Analysis

2015

[EN] The characterization of corrosion products in leaded bronze based on the voltammetry of immobilized particles methodology is described. Voltammetric data, supported by Fourier transform infra-red spectroscopy, field emission scanning electron microscopy-energy dispersive X-ray microanalysis (FESEM-EDX) and scanning electrochemical microscopy (SECM) allow the identification of copper and lead corrosion materials. The mutual influence of such products is modeled upon considering uncompensated ohmic drops in the Tafel analysis of the rising portion of the respective voltammetric signals for their electrochemical reduction.

chemistry.chemical_element02 engineering and technologyLeaded copper and bronzeengineering.material01 natural sciencesMicroanalysisUncompensated ohmic dropsAnalytical ChemistryCorrosionScanning electrochemical microscopyElectrochemistryBronzeTafel analysisVoltammetryOhmic contactTafel equationVoltammetry of immobilized particles010401 analytical chemistryMetallurgy021001 nanoscience & nanotechnologyCopper0104 chemical scienceschemistryPINTURAengineering0210 nano-technologySECM
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The first copper(I)-olefin complexes bearing a 1,3,4-oxadiazole core: Alternating-current electrochemical crystallization, X-ray experiment and DFT s…

2017

By means of alternating-current electrochemical technique, four new π-complexes, namely [Cu2(C11H10N2OS)2Br1.91Cl0.09] (1), [Cu(C11H10N2OS)NO3] (2), [Cu2(C11H10N2OS)2(H2O)2](BF4)2 (3) and [Cu2(C11H10N2OS)2(H2O)2](ClO4)2 (4), were obtained using copper(II) salts and the 2-(allylthio)-5-phenyl-1,3,4-oxadiazole (C11H10N2OS) ligand. The metal and halogen centers in 1 form Cu2X2 dimers; the N-atom from the oxadiazole ring and the Cdouble bond; length as m-dashC bond of the allyl group from the same ligand complete the copper coordination environment, giving [Cu(C11H10N2OS)X]2 isolated fragments. The ligand plays the same chelating role in 2, whereas the O (NO3) atom occupies the third position i…

crystal structure3Stereochemistry1chemistry.chemical_elementOxadiazolekupariCrystal structure134-oxadiazole derivatives4-oxadiazole derivatives010402 general chemistryElectrochemistryRing (chemistry)DFT01 natural sciencesolefinpi-complexInorganic ChemistryMetalchemistry.chemical_compoundraman spectroscopyMaterials ChemistryMoleculePhysical and Theoretical Chemistryta116010405 organic chemistryLigandac-electrochemical techniquekompleksiyhdisteetCoppercopper(I)0104 chemical sciencesCrystallographychemistryvisual_artvisual_art.visual_art_mediumPolyhedron
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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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On the mechanistic behavior of highly efficient palladium-tetraphosphine catalytic systems for cross-coupling reactions: first spectroscopic and elec…

2008

Electrochemical studies carried out in conjunction with 31P NMR spectroscopy on the palladium(II)/palladium(0) halogeno complexes of the tetraphosphine 1,1′,2,2′-tetrakis(diphenylphosphino)-4,4′-di...

crystal structureDenticityredox reactionoxidative additiontetraphosphinechemistry.chemical_elementmechanism010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesCoupling reactionCatalysisInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysiscross-coupling reactionsferrocenylpolyphosphine complexesPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSelectrochemical studies010405 organic chemistryChemistryOrganic Chemistry[CHIM.CATA]Chemical Sciences/CatalysispalladiumCombinatorial chemistryOxidative addition0104 chemical sciences3. Good healthcatalytic systemsreaction kinetics31p nmr spectroscopyPalladium
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Origin of the large spectral shift in electroluminescence in a blue light emitting cationic iridium(III) complex

2007

A new, but archetypal compound [ Ir( ppy- F-2) (2)Me(4)phen] PF6, where ppy- F2 is 2-(2',4'- fluorophenyl) pyridine and Me(4)phen is 3,4,7,8- tetramethyl- 1,10- phenanthroline, was synthesized and used to prepare a solid-state light-emitting electrochemical cell (LEEC). This complex emits blue light with a maximum at 476 nm when photoexcited in a thin film, with a photoluminescence quantum yield of 52%. It yields an efficient single-component solid-state electroluminescence device with a current efficiency reaching 5.5 cd A(-1) and a maximum power efficiency of 5.8 Lm Watt(-1). However, the electroluminescence spectrum is shifted with respect to the photoluminescence spectrum by 80 nm resul…

education.field_of_studyFunctional Response TheoryPhotoluminescenceExcitation-EnergiesTransition-Metal-ComplexesChemistryPopulationQuantum yieldSolid-StateGeneral ChemistryExcited-State PropertiesElectroluminescencePhotochemistryOptical SpectroscopyExcited stateMaterials ChemistryLight emissionEmission spectrumElectrochemical-CellsTriplet stateeducationRoom-TemperatureSingle-LayerPhotophysical Properties
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effect of the temperature on the electrochemical incineration of organic pollutants

2009

effect of temperature carboxylic acids electrochemical incineration
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Innovative chemical processes for the treatment of water polluted by recalcitrant organic substances

2012

In the last years, many research groups have focused their attention on the innovative chemical processes adopted for the treatment of water effluents polluted by recalcitrant organic substances, i.e., substances resistant to biological treatment. The electrochemical oxidation is one of the most studied technologies because it presents high versatility and low cost, it is realized under mild conditions of pressure and temperature and generally it does not involve the use of toxic substances [1]. In this work, the comparative performance of different electrochemical approaches such as direct oxidation processes, oxidation by means of electrogenerated chlorine and electro-Fenton was investiga…

electro-fentonelectrochemical incinerationcarboxylic acidBDDDSA
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