Search results for "supporting electrolyte"

showing 10 items of 49 documents

Cathodic reduction of hexavalent chromium coupled with electricity generation achieved by reverse-electrodialysis processes using salinity gradients

2014

Abstract A new approach for the simultaneous generation of electric energy and the treatment of waters contaminated by recalcitrant pollutants using salinity gradients was proposed. Reverse electrodialysis allows for the generation of electric energy from salinity gradients. Indeed, the utilization of different salt concentrations gives a potential difference between the electrodes which allows the generation of electric energy by using suitable electrolytes and an external circuit. The simultaneous generation of electric energy and the treatment of waters contaminated by Cr(VI) was successfully achieved for the first time by reverse electrodialysis processes using salinity gradients and pr…

Cr(VI)ChemistrySupporting electrolyteGeneral Chemical EngineeringElectrolytesalinity gradientVolumetric flow rateSalinitychemistry.chemical_compoundElectricity generationChemical engineeringStack (abstract data type)Waste water treatmentenergy generationEnvironmental chemistryReversed electrodialysisElectrochemistryreverse electrodialisyHexavalent chromium
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Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups

2019

Abstract We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity for additional supporting electrolyte. As such, this conversion is efficient, practical, and thereby environmentally friendly, as production of waste is minimized. The method features a broad substrate scope, and a variety of functional groups are tolerated, providing easy access to precursors for novel polydentate ligands and even heterocycles such as dibenzofurans.

Denticityoxidation010405 organic chemistryChemistrySupporting electrolyteCommunicationC−C couplingoxygen heterocyclesSubstrate (chemistry)General Chemistry010402 general chemistryElectrochemistry01 natural sciencesEnvironmentally friendlyCombinatorial chemistryCommunicationsCatalysisCoupling reaction0104 chemical scienceschemistry.chemical_compoundElectrochemistry | Hot Paperelectrochemistrycross-couplingPolar effectPhenolsAngewandte Chemie International Edition
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Electrochemical impedance spectroscopy of thin films with two mobile charge carriers: effects of the interfacial charging

1999

In the electrochemical systems containing an excess of the background electrolyte, the faradaic process and the interfacial (‘double-layer’) charging are coupled to the fluxes of different charge carriers, the former being related to the diffusional transport of electroactive entities while the latter being realized mostly by ions of the supporting electrolyte. As a result, the interfacial capacitance Cdl may simply be added in parallel to the faradaic impedance specific for each particular system (Randles & Ershler). This simple treatment is not justified in the absence of an indifferent electrolyte, if the same charged species take part in both the electrode reaction and the double layer …

Double layer (biology)ChemistrySupporting electrolyteGeneral Chemical EngineeringFaradaic impedanceAnalytical chemistryElectrolyteConductivityAnalytical ChemistryDielectric spectroscopyIonChemical physicsElectrochemistryCharge carrierJournal of Electroanalytical Chemistry
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Supporting-Electrolyte-Free and Scalable Flow Process for the Electrochemical Synthesis of 3,3′,5,5′-Tetramethyl-2,2′-biphenol

2020

The most efficient electrochemical synthesis of 3,3′,5,5′-tetramethyl-2,2′-biphenol by dehydrogenative coupling is reported. The electrolysis is performed supporting-electrolyte-free in 1,1,1,3,3,3...

ElectrolysisMaterials science010405 organic chemistrySupporting electrolyteOrganic ChemistryFlow cell010402 general chemistryElectrochemistry01 natural sciences0104 chemical scienceslaw.inventionCoupling (electronics)Chemical engineeringlawPhysical and Theoretical ChemistryFlow processOrganic Process Research & Development
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The Pd3(dppm)3(CO)2+ Cluster: An Efficient Electrochemically Assisted Lewis Acid Catalyst for the Fluorination and Alcoholysis of Acyl Chlorides.

2002

The dicationic palladium cluster Pd3(dppm)3(CO)2+ (dppm = bis(diphenylphosphino)methane) reacts with acid chlorides RCOCl (R = n-C6H13, t-Bu, Ph) to afford quantitatively the chloride adduct Pd3(dppm)3(CO)(Cl)+ and the acyl cation RCO+ as the organic counterpart. The dicationic reactive cluster can be reformed by electrolyzing the chloride complex with a copper anode leaving CuCl as a byproduct. The combination of these two reactions provides an electrocatalytic way to form the acylium from the acid chloride. Indeed, in CH2Cl2, 0.2 M NBu4PF6, or NBu4BF4, the electrolysis of the acid chloride in the presence of a catalytic amount of the cluster (1%) gives in good yields the acid fluoride RCO…

ElectrolysisSupporting electrolyteOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral MedicineElectrochemistryMedicinal chemistryChlorideAdductlaw.inventionLewis acid catalysisCatalysischemistry.chemical_compoundAcyl chloridechemistryNucleophilelawmedicineLewis acids and basesPalladiummedicine.drugChemInform
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Electrochemical incineration of oxalic acid at boron doped diamond anodes: Role of operative parameters

2008

The electrochemical incineration of oxalic acid (OA) at boron doped diamond (BDD) anodes was investigated both theoretically and experimentally in order to find the influence of the operative parameters on the performances of the process. Polarization curves and chronoamperometric measurements indicate the probable occurrence of a direct electrochemical oxidation of OA at the surface of the BDD anode at low pH and of a hydroxyl radical-mediated reaction at high pH. When incineration electrolyses are performed at low pH with potentiostatic alimentation, a dramatic influence of the potential is observed. In amperostatic incineration, high CE are obtained when most part of the process was unde…

ElectrolysisSynthetic diamondChemistrySupporting electrolyteGeneral Chemical EngineeringInorganic chemistryOxalic acidElectrochemical incinerationChronoamperometryElectrochemistryCarboxylic acidAnodelaw.inventionchemistry.chemical_compoundlawOxalic acidElectrochemistryPolarization (electrochemistry)Oxidation of organicsBDD
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Electrochemical Synthesis of 5-Aryl-phenanthridin-6-one by Dehydrogenative N,C Bond Formation.

2018

Currently, the general synthesis of 5-aryl-phenanthridin-6-ones relies on the involvement of metal catalysis. Despite the urgent demand for green alternatives, avoiding synthetic routes that require transition metals for key roles is still challenging. Electrochemical efforts employing a constant potential protocol in divided cells revealed a possible alternative to the catalytic approach. A constant current protocol, undivided cells, and a remarkably low supporting electrolyte concentration enable a novel access to N-aryl-phenanthridin-6-ones by anodic N,C bond formation using directly generated amidyl radicals. Easy accessible starting materials, a broad scope of applicable functional gro…

Green chemistry010405 organic chemistrySupporting electrolyteArylRadicalOrganic ChemistryGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisMetalchemistry.chemical_compoundTransition metalchemistryvisual_artvisual_art.visual_art_mediumChemistry (Weinheim an der Bergstrasse, Germany)
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Electrochemical synthesis of carbazoles by dehydrogenative coupling reaction

2020

Abstract A constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N‐protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.

Green chemistry540 Chemistry and allied sciencesDeblocking filterSupporting electrolyteRadicalSustainable Chemistry010402 general chemistryElectrochemistry01 natural sciencesCatalysisCoupling reactionNC couplingProtecting groupgreen chemistry010405 organic chemistryChemistryCommunicationOrganic Chemistryheterocyclic chemistryGeneral ChemistryCombinatorial chemistryCommunications0104 chemical sciencesAnodecarbazoleselectrochemistry540 Chemie
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Electrochemical nitration with nitrite

2021

Aromatic nitration has tremendous importance in organic chemistry as nitroaromatic compounds serve as versatile building blocks. This study represents the electrochemical aromatic nitration with NBu4 NO2 , which serves a dual role as supporting electrolyte and as a safe, readily available, and easy-to-handle nitro source. Stoichiometric amounts of 1,1,1-3,3,3-hexafluoroisopropan-2-ol (HFIP) in MeCN significantly increase the yield by solvent control. The reaction mechanism is based on electrochemical oxidation of nitrite to NO2 , which initiates the nitration reaction in a divided electrolysis cell with inexpensive graphite electrodes. Overall, the reaction is demonstrated for 20 examples w…

Green chemistryReaction mechanism540 Chemistry and allied sciencesSupporting electrolyteGeneral Chemical EngineeringElectrochemistryCombinatorial chemistrySolventchemistry.chemical_compoundGeneral EnergychemistryNitrationYield (chemistry)540 ChemieEnvironmental ChemistryGeneral Materials ScienceNitrite
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Electrochemical processes in macro and microfluidic cells for the abatement of chloroacetic acid from water

2014

Abstract The remediation of solutions contaminated with monochloroacetic acid (CAA), which is one of the most resistant haloacetic acids (HAAs) to chemical degradation, dramatically depends on the adopted electrochemical approach: (i) CAA is only poorly oxidized either by homogeneous hydroxyl radical in electro-Fenton (EF), electrogenerated active chlorine or electro-oxidation on Pt anode; (ii) it is moderately abated by direct reduction on silver or compact graphite cathodes (from 30% in macro cells to 60% in the microfluidic devices); (iii) it is quantitatively removed by direct electro-oxidation on a boron-doped diamond (BDD) anode. The use of a microreactor enables operation in the abse…

Haloacetic acidsSupporting electrolyteGeneral Chemical EngineeringInorganic chemistryChloroacetic acidchemistry.chemical_elementElectrochemistryAnodechemistry.chemical_compoundchemistryElectrochemistryChlorinemedicineMicroreactorChemical decompositionmedicine.drugElectrochimica Acta
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