Search results for "Electrosynthesi"

showing 10 items of 105 documents

Comprehensive Study of Poly(2,3,5,6-tetrafluoroaniline): From Electrosynthesis to Heterojunctions and Ammonia Sensing.

2018

In this work, we report for the first time on a comprehensive study of poly(2,3,5,6-tetrafluoroaniline) (PTFANI). Contrary to the nonfluorinated polyaniline (PANI) or its analogues bearing one fluorine atom, PTFANI is a poorly conductive material. We present a comprehensive study of the electrosynthesized PTFANI from its monomer in an acidic aqueous medium. PTFANI was fully characterized by a potential-pH diagram, spectroelectrochemistry, and electrochemical quartz crystal microbalance (EQCM) measurements, as well as by a morphological study. Combined with the X-ray photoelectron spectroscopy (XPS) analysis, it allowed us to understand the redox properties of this polymer compared to those …

Conductive polymerMaterials scienceInorganic chemistry02 engineering and technologyQuartz crystal microbalance010402 general chemistry021001 nanoscience & nanotechnologyElectrosynthesisElectrochemistry01 natural sciencesRedox0104 chemical scienceschemistry.chemical_compoundElectron transferchemistryX-ray photoelectron spectroscopyPolyaniline[CHIM]Chemical SciencesGeneral Materials Science0210 nano-technologyComputingMilieux_MISCELLANEOUSACS applied materialsinterfaces
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Nanostructured Ni Based Anode and Cathode for Alkaline Water Electrolyzers

2019

Owing to the progressive abandoning of the fossil fuels and the increase of atmospheric CO2 concentration, the use of renewable energies is strongly encouraged. The hydrogen economy provides a very interesting scenario. In fact, hydrogen is a valuable energy carrier and can act as a storage medium as well to balance the discontinuity of the renewable sources. In order to exploit the potential of hydrogen it must be made available in adequate quantities and at an affordable price. Both goals can be potentially achieved through the electrochemical water splitting, which is an environmentally friendly process as well as the electrons and water are the only reagents. However, these devices stil…

Control and OptimizationMaterials scienceNanostructureHydrogen020209 energyEnergy Engineering and Power Technologychemistry.chemical_elementNanotechnology02 engineering and technologyElectrocatalystElectrosynthesiselectrocatalystslcsh:Technologynickeliridium oxideHydrogen economySettore ING-IND/17 - Impianti Industriali Meccanicinanostructures0202 electrical engineering electronic engineering information engineeringalkaline electrolyzersElectrical and Electronic EngineeringEngineering (miscellaneous)Energy carrierRenewable Energy Sustainability and the Environmentbusiness.industrylcsh:TOxygen evolutionElectrocatalyst021001 nanoscience & nanotechnologypalladiumcobaltAnodeNanowireSettore ING-IND/23 - Chimica Fisica Applicatachemistrynanowiresni-alloyWater splitting0210 nano-technologybusinessAlkaline electrolyzerfoamEnergy (miscellaneous)Energies
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Template electrosynthesis of aligned Cu2O nanowires

2008

Abstract Large arrays of aligned copper oxide nanowires were produced by electrodeposition, using anodic alumina membranes as template. We have studied the effect of two fundamental parameters involved in fabrication process: potential perturbation and bath composition. Performing electrodeposition from a copper acetate/sodium acetate bath (pH 6.5), we found that chemical composition of nanowires varied in dependence on the shape of the applied potential perturbation: pure copper oxide nanowires were produced by pulsed potential, whilst continuous electrodeposition resulted in a co-deposition of Cu and Cu 2 O. In a copper lactate bath, buffered at pH 10, the shape of perturbation did not in…

Copper oxideMaterials scienceScanning electron microscopeGeneral Chemical EngineeringNanowirechemistry.chemical_elementNanotechnologyElectrosynthesisElectrochemistryCopperchemistry.chemical_compoundChemical engineeringchemistryElectrochemistryCrystalliteVapor–liquid–solid methodElectrochimica Acta
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Direct Anodic Dehydrogenative Cross- and Homo-Coupling of Formanilides

2018

Coupling (electronics)Green chemistry010405 organic chemistryChemistryElectrochemistryFormamides010402 general chemistryElectrosynthesisPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesAnodeChemElectroChem
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Boron-Doped Diamond Electrodes for Electroorganic Chemistry

2011

Boron-doped diamond (BDD) electrodes provide an unusually wide electrochemical window in protic media, since there exist large offset potentials for the evolution of molecular hydrogen and oxygen, respectively. At the anode, alcohols are specifically converted to alkoxyl radicals. These can be used for chemical synthesis. When the enormous reactivity of such intermediate spin centers is not controlled, mineralization or electrochemical incineration dominates. Efficient strategies include either high substrate concentrations or fluorinated alcohols which seem to stabilize the spin centers in the course of reaction.

Diamondchemistry.chemical_elementengineering.materialElectrosynthesisPhotochemistryElectrochemistryCathodelaw.inventionAnodechemistrylawElectrodeengineeringBoronElectrochemical window
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Electrochemical synthesis of 2-arylimino-4,5-di(2-furyl)-1,3-dioxoles and (E)-1,2-di(2-furyl)vinylene bis(N-arylchloroformimidates). HF and B3LYP com…

2009

Abstract Cathodic reductions of 2,2′-furils in the presence of N-arylcarbonimidoyl dichlorides lead to 2-arylimino-4,5-di(2-furyl)-1,3-dioxoles in high yields, along with minor amounts of (E)-1,2-di(2-furyl)vinylene bis(N-arylchloroformimidates). HF and B3LYP density functional theory methods have been applied to the determination of molecular geometries and to study the topomerization mechanism of aryliminodioxoles. The molecular structure of (E)-1,2-di(2-furyl)vinylene bis[N-(2-chloro-4-methylphenyl)chloroformimidate] has been determined by X-ray crystallography and compared with the calculated structure.

DiketoneReaction mechanismChemistryOrganic ChemistryImineElectrosynthesisBiochemistryMedicinal chemistryChemical synthesischemistry.chemical_compoundMolecular geometryDrug DiscoveryMoleculeDensity functional theoryTetrahedron
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Control over the oxidative reactivity of metalloporphyrins. Efficient electrosynthesis of meso,meso-linked zinc porphyrin dimer.

2011

The electrochemical oxidation of zinc(II) 5,15-p-ditolyl-10-phenylporphyrin at its first oxidation potential leads to the formation of the corresponding meso-meso porphyrin dimer as the main product. The number of electrons abstracted, the addition of the hindered base 2,6-lutidine as well as operating in DMF, instead of a CH(2)Cl(2)/CH(3)CN mixture are the key parameters to obtain high yields of the desired coupling product. Indeed, when the electrolyses are carried out in the CH(2)Cl(2)/CH(3)CN mixture, the unexpected zinc(II) 5-chloro-10,20-p-ditolyl-15-phenyl porphyrin is produced as a by-product, the chlorine atom originating from the CH(2)Cl(2) solvent. The monomer and the dimer are c…

Dimerchemistry.chemical_elementZincElectrosynthesisElectrochemistryPhotochemistryPorphyrinInorganic ChemistrySolventchemistry.chemical_compoundMonomerchemistryPolymer chemistryReactivity (chemistry)Dalton transactions (Cambridge, England : 2003)
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ELECTROSYNTHESIS IN MICROFLUIDIC CELLS: PRELIMINARY INVESTIGATIONS

2013

ELECTROSYNTHESIS IN MICROFLUIDIC CELLS
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Selective and Scalable Dehydrogenative Electrochemical Synthesis of 3,3′,5,5′-Tetramethyl-2,2′-biphenol

2019

3,3′,5,5′-Tetramethyl-2,2′-biphenol is a compound of high technical significance, as it exhibits superior properties as building block for ligands in the transition-metal catalysis. However, side reactions and overoxidation are challenging issues in the conventional synthesis of this particular biphenol. Here, an electrochemical method is presented as powerful and sustainable alternative to conventional chemical strategies, which gives good yields up to 51%. Despite using inexpensive and well-available bromide-containing supporting electrolytes, the issue of bromination and general byproduct formation is effectively suppressed by adding water to the electrolyte. Additionally, the scalabilit…

Electrolysis010405 organic chemistryOrganic ChemistryHalogenationElectrolyte010402 general chemistryElectrosynthesisElectrochemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesAnodelaw.inventionCatalysischemistry.chemical_compoundchemistrylawPhenolSynlett
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Solvent Control in Electro-Organic Synthesis

2018

Exploiting the solvent control within electro-organic conversions is a far underestimated parameter in prep-scale electrolysis. The beneficial application in several transformations is outlined and in particular discussed for the dehydrogenative coupling of arenes and heteroarenes. This simple electrolytic strategy in fluorinated solvents allows the modulation of the substrate’s nucleophilicity and the stabilization of the intermediates as well as of the final product from over-oxidation.1 Introduction2 Solvent Effects in Kolbe Electrolysis and Anodic Fluorination3 Unique Solvent Effects of 1,1,1,3,3,3-Hexafluoropropan-2-ol (HFIP)4 Anodic Dehydrogenative Coupling Reactions with Use of HFIP …

ElectrolysisKolbe electrolysis010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryElectrosynthesis01 natural sciencesCombinatorial chemistryCoupling reactionElectrochemical fluorination0104 chemical scienceslaw.inventionSolventchemistry.chemical_compoundlawOrganic synthesisSolvent effectsSynlett
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