Search results for "halogenation"

showing 10 items of 111 documents

Nanocomposite antimicrobials prevent bacterial growth through the enzyme-like activity of Bi-doped cerium dioxide (Ce1−xBixO2−δ)

2020

Preventing bacterial adhesion on materials surfaces is an important problem in marine, industrial, medical and environmental fields and a topic of major medical and societal importance. A defense strategy of marine organisms against bacterial colonization relies on the biohalogenation of signaling compounds that interfere with bacterial communication. These reactions are catalyzed by haloperoxidases, a class of metal-dependent enzymes, whose activity can be emulated by ceria nanoparticles. The enzyme-like activity of ceria was enhanced by a factor of 3 through bismuth substitution (Ce1−xBixO2−δ). The solubility of Bi3+ in CeO2 is confined to the range 0 < x < 0.25 under quasi-hydrothermal c…

NanocompositeChemistryNanoparticleHalogenation02 engineering and technologyBacterial growth010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysisMembraneChemical engineeringGeneral Materials ScienceSolubility0210 nano-technologyBET theoryNanoscale
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Elemental Bromine Production by TiO2 Photocatalysis and/or Ozonation

2016

Significant production of elemental bromine (Br2 ) was observed for the first time when treating bromide containing solutions at acidic pH, with TiO2 photocatalyst, ozone, or a combination thereof. Br2 selectivities up to approximately 85 % were obtained and the corresponding bromine mass balance values satisfied. The process is general and may be applied at a laboratory scale for green bromination reactions, or industrially as a cheap, safe, and environmentally sustainable alternative to the currently applied bromine production methods.

Ozone010504 meteorology & atmospheric sciencesbromineozonationInorganic chemistrychemistry.chemical_element010501 environmental sciencesLaboratory scale010402 general chemistry01 natural sciencesCatalysisCatalysiphotocatalysichemistry.chemical_compoundNitric acidBromideTiO20105 earth and related environmental sciencesSettore ING-IND/24 - Principi Di Ingegneria ChimicaBromineChemistry (all)HalogenationTio2 photocatalystGeneral MedicineGeneral Chemistry0104 chemical sciencesnitric acidchemistryPhotocatalysisAngewandte Chemie International Edition
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X-ray snapshot observation of palladium-mediated aromatic bromination in a porous complex

2014

Pd-mediated aromatic bromination is intriguing to synthetic and organometallic chemists due to both its synthetic utility and, more importantly, a proposed mechanism involving an uncommon Pd(IV)/Pd(II) catalytic cycle. Here, we report an X-ray snapshot observation of a Pd reaction center during a Pd-mediated aromatic bromination in a single crystal of a porous coordination network crystalline scaffold. Upon treatment of a single crystal with N-bromosuccinimide, sequential X-ray snapshots revealed that the aryl-Pd(II)-L species embedded in the network pores was converted to the brominated aryl product through a transient aryl-Pd(II)-Br species, which is normally unobservable because of its r…

Photosynthetic reaction centreChemistryArylX-rayHalogenationchemistry.chemical_elementGeneral ChemistryBiochemistryCombinatorial chemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryCatalytic cycleOrganic chemistryPorositySingle crystalta116PalladiumJournal of the American Chemical Society
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Phytoscreening as an efficient tool to delineate chlorinated solvent sources at a chlor-alkali facility

2017

Chlorinated ethenes (CE) are among the most common volatile organic compounds (VOC) that contaminate groundwater, currently representing a major source of pollution worldwide. Phytoscreening has been developed and employed through different applications at numerous sites, where it was generally useful for detection of subsurface chlorinated solvents. We aimed at delineating subsurface CE contamination at a chlor-alkali facility using tree core data that we compared with soil data. For this investigation a total of 170 trees from experimental zones was sampled and analyzed for perchloroethene (PCE) and trichloroethene (TCE) concentrations, measured by solid phase microextraction gas chromato…

PollutionEnvironmental EngineeringHalogenation010504 meteorology & atmospheric sciencesTrichloroethyleneHealth Toxicology and Mutagenesismedia_common.quotation_subjectAlkalies010501 environmental sciencesSolid-phase microextraction01 natural sciencesGas Chromatography-Mass SpectrometryTrees[ SDV.EE ] Life Sciences [q-bio]/Ecology environmentchemistry.chemical_compoundEnvironmental ChemistryGroundwaterSolid Phase MicroextractionComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesmedia_common[SDV.EE]Life Sciences [q-bio]/Ecology environmentVolatile Organic CompoundsSoil gasPublic Health Environmental and Occupational HealthSampling (statistics)General MedicineGeneral Chemistry15. Life on landContaminationPollutionTrichloroethylenechemistry13. Climate actionEnvironmental chemistrySolventsGas chromatographyWater Pollutants ChemicalGroundwater
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One-Pot Synthesis of Pyrrole-2-carboxylates and -carboxamides via an Electrocyclization/Oxidation Sequence

2014

An electrocyclic ring closure is the key step of an efficient one-pot method for the synthesis of pyrrole-2-carboxylates and -carboxamides from chalcones and glycine esters or amides. The 3,4-dihydro-2H-pyrrole intermediates generated in situ are oxidized to the corresponding pyrroles by stoichiometric oxidants or by catalytic copper(II) and air in moderate to high yields. A wide range of functional groups are tolerated, and further combination with an in situ bromination gives access to polyfunctional pyrrole scaffolds.

ProlineOrganic ChemistryOne-pot synthesischemistry.chemical_elementHalogenationEstersStereoisomerismStereoisomerismElectrochemistryRing (chemistry)Combinatorial chemistryCopperCatalysisCatalysischemistry.chemical_compoundchemistryCyclizationElectrochemistryPyrrolesOxidation-ReductionCopperPyrroleThe Journal of Organic Chemistry
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Synthese und eigenschaften von einem nitrosubstituierten p-polyphenylen und von nitrosubstituierten p-oligophenylenen. 15. Mitteilung1

1964

Bei aromatischen Nitrojodverbindungen nimmt die ULLMANN-Reaktion unter verhaltnismasig milden Bedingungen einen praktisch quantitativen Verlauf, wenn sich das Jod in der o-Stellung zu einer Nitrogruppe befindet. Mit einer entsprechenden bifunktionellen Verbindung, dem 4,4′-Dijod-3,3′-dinitrobiphenyl, konnte unter den gleichen Bedingungen ein nitrosubstituiertes p-Polyphenylen erhalten werden, ein hellgelbes, unlosliches und unschmelzbares Pulver, das sich bei hoherer Temperatur (> 250°C) zersetzt. Auf Grund des Jodgehaltes (Endgruppen) wurde ein mittlerer Kondensationsgrad von 52 berechnet; das entspricht einer p-Phenylenkette aus 104 Benzolringen. Das Polymere ist kristallin und besitzt ei…

Reaction conditionsChemistryLong periodPolymer chemistryNitroHalogenationSolubilityIodine compoundsUllmann reactionDie Makromolekulare Chemie
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Palladium‐Catalyzed Electrophilic C–H‐Bond Fluorination: Mechanistic Overview and Supporting Evidence

2018

International audience; Palladium-catalyzed electrophilic fluorination is a particularly attractive and challenging synthetic issue. Because of the rapid evolution of this topic, a critical point on the mechanistic and experimental advances is provided herein. In the present review, we focused on current mechanistic understanding in electrophilic fluorination (and related halogenations) catalyzed by palladium, mainly with N-directing group. Our discussion is based on the well-characterized or calculated pertinent metal species and intermediates used for analyzing the plausible catalytic cycles. A particular effort has been devoted to gathering supporting data for the putative species involv…

Reaction mechanismC h bond[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistryReaction mechanismsOrganic Chemistrychemistry.chemical_element[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistry01 natural sciencesMedicinal chemistryCatalysis Fluorination0104 chemical sciencesCatalysisC–H halogenationElectrophilePhysical and Theoretical ChemistryFluorinated compoundsPalladiumPalladiumEuropean Journal of Organic Chemistry
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Enantioselective Palladium-Catalyzed Oxidative β,β-Fluoroarylation of α,β-Unsaturated Carbonyl Derivatives

2016

© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim The site-selective palladium-catalyzed three-component coupling of deactivated alkenes, arylboronic acids, and N-fluorobenzenesulfonimide is disclosed herein. The developed methodology establishes a general, modular, and step-economical approach to the stereoselective β-fluorination of α,β-unsaturated systems.

Reaction mechanismHydrocarbons FluorinatedHalogenationStereochemistrychemistry.chemical_elementStereoisomerismAlkenes010402 general chemistry01 natural sciencesArticleCatalysisCatalysisFluorinatedfluorineOrganic chemistrychemistry.chemical_classificationSulfonamidesMolecular StructurealkenesAlkene010405 organic chemistryOrganic ChemistryEnantioselective synthesisHalogenationStereoisomerismGeneral ChemistryGeneral MedicinepalladiumBoronic AcidsHydrocarbons0104 chemical sciencesreaction mechanismschemistryChemical Sciencessynthetic methodsStereoselectivityOxidation-ReductionPalladiumPalladium
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cis-bromination of alkynes without cationic intermediates

2005

Reaction mechanismMolecular StructureAcetyleneHydrocarbons HalogenatedChemistryElectrophilic additionStatic ElectricityCationic polymerizationHalogenationGeneral ChemistryBromineCatalysisBromine CompoundsIsomerismModels ChemicalAlkynesSolventsThermodynamicsOrganic chemistry
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Electroreduction of aliphatic chlorides at silver cathodes in water

2010

The effect of water on the reduction of aliphatic chlorides at silver cathodes was investigated by cyclovoltammetric experiments in acetonitrile, water and their mixture and focused electrolyses in water solutions. The addition of water to acetonitrile gives rise to the formation of new peaks and/or the displacement of pre-existent peaks at dramatically less negative potentials. In a water medium, silver shows a very large electrocatalytic effect towards the reduction of chlorinated aliphatic compounds belonging to the classes of chloromethanes, chloroethanes and chloroethenes, dramatically higher than that observed in aprotic solvents such as dimethylformamide (DMF) or acetonitrile (ACN). …

Reaction mechanismSilverAqueous solutionChemistryGeneral Chemical EngineeringElectrocatalysiInorganic chemistryDe-halogenationSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryElectrocatalystAnalytical Chemistrychemistry.chemical_compoundElectrochemistryDimethylformamideWater treatmentElectrochemical remediationAliphatic compoundAcetonitrileAliphatic chlorideJournal of Electroanalytical Chemistry
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