Search results for "Anode"

showing 10 items of 317 documents

Single and Twofold Metal- and Reagent-Free Anodic C-C Cross-Coupling of Phenols with Thiophenes.

2017

The first electrochemical dehydrogenative C-C cross-coupling of thiophenes with phenols has been realized. This sustainable and very simple to perform anodic coupling reaction enables access to two classes of compounds of significant interest. The scope for electrochemical C-H-activating cross-coupling reactions was expanded to sulfur heterocycles. Previously, only various benzoid aromatic systems could be converted, while the application of heterocycles was not successful in the electrochemical C-H-activating cross-coupling reaction. Here, reagent- and metal-free reaction conditions offer a sustainable electrochemical pathway that provides an attractive synthetic method to a broad variety …

Coupling010405 organic chemistryChemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesSulfurCatalysisCoupling reaction0104 chemical sciencesAnodeMetalchemistry.chemical_compoundReagentvisual_artvisual_art.visual_art_mediumOrganic chemistryPhenolsAngewandte Chemie (International ed. in English)
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Unexpected high robustness of electrochemical cross-coupling for a broad range of current density

2017

Solvent effect enables electrosynthesis of organic compounds with strong variation of electric current at constant efficacy.

CouplingMultidisciplinaryMaterials science010405 organic chemistrySciAdv r-articlesNanotechnologyElectrolyte010402 general chemistry01 natural sciences0104 chemical sciencesAnodeChemical physicsRobustness (computer science)Yield (chemistry)ElectrochemistryConstant currentCurrent densityOrder of magnitudeResearch ArticlesResearch ArticleScience Advances
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DNA-Based Enzyme Reactors and Systems

2016

During recent years, the possibility to create custom biocompatible nanoshapes using DNA as a building material has rapidly emerged. Further, these rationally designed DNA structures could be exploited in positioning pivotal molecules, such as enzymes, with nanometer-level precision. This feature could be used in the fabrication of artificial biochemical machinery that is able to mimic the complex reactions found in living cells. Currently, DNA-enzyme hybrids can be used to control (multi-enzyme) cascade reactions and to regulate the enzyme functions and the reaction pathways. Moreover, sophisticated DNA structures can be utilized in encapsulating active enzymes and delivering the molecular…

DNA sensorsGeneral Chemical EngineeringeducationNanotechnologyDNA nanodevice02 engineering and technologyReviewBiology010402 general chemistry01 natural scienceslcsh:Chemistrychemistry.chemical_compoundDna nanostructuresDNA nanotechnologyDNA origamiGeneral Materials ScienceDNA nanotechnologychemistry.chemical_classificationPhysicsfood and beveragesself-assemblycascade reactions021001 nanoscience & nanotechnologyBiocompatible materialnanolääketiedenanomedicineDrug-deliveryMaterials science0104 chemical sciencesdrug-deliveryChemistryenzymeEnzymechemistrylcsh:QD1-999drug deliveryNanomedicineDNA origami0210 nano-technologyDNABiotechnologyNanomaterials
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Latest improvements of microchannel-plate PMTS

2020

Abstract The DIRC detectors of the PANDA experiment at FAIR will use multi-anode MCP-PMTs as photon sensors. After long and extensive R&D work the performance parameters of the recent 2” MCP-PMT models are converging towards the required values. The lifetime of most ALD-coated MCP-PMTs is well surpassing the DIRC requirements with the best tube currently reaching > 22 C/cm2 integrated anode charge without aging. The performance of the most advanced MCP-PMTs from PHOTONIS and Hamamatsu fulfill basically all requirements with a highlight being the high detective quantum efficiency (DQE) of almost 30% for the PHOTONIS 9002108. The improvements of the latest MCP-PMT models compared to former tu…

Detective quantum efficiencyPhysicsNuclear and High Energy PhysicsPhotonOpticsbusiness.industryDetectorMicrochannel plate detectorTube (fluid conveyance)Charge (physics)businessInstrumentationAnodeNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
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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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Direct Methane Oxidation on La1-xSrxCr1-yFeyO3-δ perovskite-type oxides as Potential Anode for Intermediate Temperature Solid Oxide Fuel Cells

2016

Abstract La1−xSrxCr1−yFeyO3−δ (x = 0, 0.1, 0.15, 0.2; y = 0, 0.3, 0.5) perovskite-type oxide powders were synthesized by solution combustion synthesis and characterized by X-ray diffraction, X-ray photoelectron spectroscopy and H2-temperature programmed reduction. Selected compositions were studied by CH4-temperature programmed reduction in the absence and in the presence of H2S. Temperature programmed oxidation and structural characterizations were performed in order to discriminate the nature of residual deposits on the catalyst surface. The study about reduction in different methane-based mixture revealed that total and partial methane oxidation occurred in the range ∼450–1000 °C indepen…

Doped-LaCrO3; IT-SOFC; Direct methane oxidation; H2SInorganic chemistryOxide02 engineering and technology010402 general chemistry01 natural sciencesCatalysisMethaneCatalysischemistry.chemical_compoundX-ray photoelectron spectroscopyGeneral Environmental SciencePerovskite (structure)Range (particle radiation)IT-SOFCChemistryH2SProcess Chemistry and Technologydirect methane oxidation021001 nanoscience & nanotechnologydoped-LaCrO30104 chemical sciencesAnodedoped-LaCrO3; IT-SOFC; direct methane oxidation; H2SSettore CHIM/03 - Chimica Generale E InorganicaAnaerobic oxidation of methane0210 nano-technology
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Thermogalvanic effects on the corrosion of copper in heavy brine LiBr solutions

2012

Thermogalvanic corrosion of copper in heavy brine LiBr solutions has been investigated using a zero-resistance ammeter (ZRA). The temperature gradients between copper electrodes immersed in the same LiBr solution result in the formation of thermogalvanic cells with hot anodes, leading to high and sustained thermogalvanic currents. Copper loss rates, calculated using Faraday's law, substantially exceed 0.025mmyear -1, a value regarded as the threshold of low corrosion rates. The effects of thermogalvanic coupling on the surface properties of the anode and the cathode have been analysed by means of electrochemical impedance spectroscopy (EIS). The results obtained in this analysis have been r…

EISAnodic dissolutionChemistryGeneral Chemical EngineeringInorganic chemistryMetallurgychemistry.chemical_elementGeneral ChemistryCopperCopper lossCathodeINGENIERIA QUIMICAAnodeCorrosionDielectric spectroscopylaw.inventionElectroquímicachemistry.chemical_compoundBrineBromidelawGeneral Materials ScienceCopperPolarisation
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Twofold Electrochemical Amination of Naphthalene and Related Arenes

2017

The twofold, electrochemical amination reaction of polycyclic arenes, e.g. naphthalene (4), via Zincke intermediates is demonstrated for the first time. The installation of the nitrogen functionalities occurs regioselectively in positions 1 and 5 of naphthalene (4). The key for this electro-conversion is boron-doped diamond as anode material. The method of the multi-amination reaction is expanded to other aromatic substrates. A detailed study is provided, covering electrolysis parameters, e.g. anode material, electrolyte system, current density, separator, etc. Despite the moderate yields, this approach offers the first direct electro-synthetic access to diaminated products.

Electrolysis010405 organic chemistryChemistryInorganic chemistryDiamondElectrolyteengineering.material010402 general chemistryElectrochemistry01 natural sciencesCatalysis0104 chemical sciencesAnodelaw.inventionchemistry.chemical_compoundlawElectrochemistryengineeringAminationSeparator (electricity)NaphthaleneChemElectroChem
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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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Synthesis ofmeta-Terphenyl-2,2′′-diols by Anodic C−C Cross-Coupling Reactions

2016

The anodic C-C cross-coupling reaction is a versatile synthetic approach to symmetric and non-symmetric biphenols and arylated phenols. We herein present a metal-free electrosynthetic method that provides access to symmetric and non-symmetric meta-terphenyl-2,2''-diols in good yields and high selectivity. Symmetric derivatives can be obtained by direct electrolysis in an undivided cell. The synthesis of non-symmetric meta-terphenyl-2,2''-diols required two electrochemical steps. The reactions are easy to conduct and scalable. The method also features a broad substrate scope, and a large variety of functional groups are tolerated. The target molecules may serve as [OCO](3-) pincer ligands.

Electrolysis010405 organic chemistrySubstrate (chemistry)General Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reaction0104 chemical scienceslaw.inventionPincer movementAnodechemistry.chemical_compoundchemistrylawTerphenylOrganic chemistryMoleculeAngewandte Chemie International Edition
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