Search results for "oxidation"

showing 10 items of 1913 documents

"Partial oxidation of methane and methanol on FeOx-, MoOx- and FeMoOx -SiO2 catalysts prepared by sol-gel method: a comparative study"

2020

[EN] FeOx-, MoOx and FeMoOx-SiO2 materials prepared by a sol-gel procedure have been evaluated as catalysts for the partial oxidation of methane and methanol. The effect of decreasing the pH of the synthesis gel on the chemical nature of FeOx and MoOx species has been investigated. Characterization results show that low pH improves the dispersion of metal oxide species present in SiO2 matrix. For FeOx/SiO2 materials, the presence of dispersed FeOx species (rather than bulk Fe2O3) improves the selectivity to formaldehyde in the partial oxidation of methane and methanol. For FeMoOx/SiOx catalysts, dispersed species favor the selectivity to formaldehyde only for methane oxidation. In contrast,…

CatalizadorFormaldehydeOxideEstudio comparativo010402 general chemistry01 natural sciencesAldehydeCatalysisMethaneCatalysischemistry.chemical_compoundFormaldehydeIron oxidePartial oxidationPhysical and Theoretical Chemistrychemistry.chemical_classification010405 organic chemistryProcess Chemistry and TechnologyMethanolFormaldehídoMolybdenum oxide0104 chemical scienceschemistryChemical engineeringAnaerobic oxidation of methaneMethanolMethane
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A Thermophilic Tetramolecular G-Quadruplex/Hemin DNAzyme.

2017

International audience; The quadruplex-based DNAzyme system is one of the most useful artificial enzymes or catalysts; their unique properties make them reliable alternatives to proteins for performing catalytic transformation. The first prototype of a thermally stable DNAzyme system is presented. This thermophilic DNAzyme is capable of oxidizing substrates at high temperatures (up to 95 degrees C) and long reaction times (up to 18 h at 75 degrees C). The catalytic activity of the DNAzymes were investigated with the standard peroxidase-mimicking oxidation of 2,2'-azino-bis(3-ethylbenzothiozoline-6-sulfonic acid) (ABTS) by H2O2. The step-by-step design of this unique heat-activated G-quadrup…

Catalytic transformationDNAzymeoxidationDeoxyribozymeaptamersspecificityNanotechnologyBiocompatible MaterialsdnainsightsG-quadruplex010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesperoxidase-mimicking dnazymesCatalysisCatalysischemistry.chemical_compoundOxidizing agent[CHIM]Chemical SciencesBenzothiazolesthermophilicityComputingMilieux_MISCELLANEOUSPeroxidaseChemistry010405 organic chemistryThermophileperoxidase activityGeneral Chemistry[CHIM.CATA]Chemical Sciences/CatalysisGeneral MedicineDNA CatalyticHydrogen PeroxideCombinatorial chemistry0104 chemical sciencesG-QuadruplexesMethylene BluekineticsHeminactivity enhancementSulfonic AcidsporphyrinOxidation-ReductioncomplexHeminAngewandte Chemie (International ed. in English)
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Electrochemical treatment of aqueous solutions of catechol by various electrochemical advanced oxidation processes: Effect of the process and of oper…

2017

Abstract Catechol, one of the most abundant compounds in olive mills wastewaters, which is generated in the Fenton degradation of various aromatic compounds, is a toxic, possible carcinogen, persistent pollutant and it is not readily biodegradable. Hence, its degradation requires the utilization of advanced oxidation processes (AOPs). Here, the electrochemical treatment of aqueous solutions of catechol was investigated. The utilization of various electrochemical processes, such as electro-Fenton (EF), direct anodic oxidation (AO), indirect oxidation by electro-generated active chlorine and coupled processes was investigated. Furthermore, the effect of various operating conditions (including…

CatecholAqueous solutionChemistryGeneral Chemical EngineeringAdvanced oxidation processInorganic chemistrychemistry.chemical_element02 engineering and technology010501 environmental sciences021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesCatechol; Advanced oxidation process electro-Fenton anodic oxidation; BDDAnalytical ChemistryAnodeCatalysischemistry.chemical_compoundCatecholElectrochemistryChlorineDegradation (geology)Advanced oxidation process electro-Fenton anodic oxidation0210 nano-technologyBDD0105 earth and related environmental sciences
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Efficient electroorganic synthesis of 2,3,6,7,10,11-hexahydroxytriphenylene derivatives

2012

2,3,6,7,10,11-Hexahydroxytriphenylene of good quality and purity can be obtained via anodic treatment of catechol ketals and subsequent acidic hydrolysis. The electrolysis is conducted in propylene carbonate circumventing toxic and expensive acetonitrile. The protocol is simple to perform and superior to other chemical or electrochemical methods. The key of the method is based on the low solubility of the anodically trimerized product. The shift of potentials is supported by cyclic voltammetry studies.

CatecholElectrolysishexahydroxytriphenyleneketalsOrganic Chemistrycatecholpropylene carbonateElectrochemistryFull Research Paperlaw.inventionlcsh:QD241-441Chemistrychemistry.chemical_compoundHydrolysischemistrylcsh:Organic chemistrylawPropylene carbonateOrganic chemistrylcsh:QCyclic voltammetrySolubilityelectrochemical oxidationAcetonitrilelcsh:ScienceBeilstein Journal of Organic Chemistry
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Chemistry and reactivity of dinuclear manganese oxamate complexes: Aerobic catechol oxidation catalyzed by high-valent bis(oxo)-bridged dimanganese(I…

2006

[EN] The high-valent bis(oxo)-bridged dimanganese(IV) complexes with the series of binucleating 4.5-X-2-o-phenylenebis(oxamate) ligands (opbaX(2); X = H, Cl, Me) (1a-c) have been synthesized and characterized structurally, spectroscopically and magnetically. Complexes la-c possess unique Mn-2(mu-O)(2) core structures with two o-phenylenediamidate type additional bridges which lead to exceptionally short Mn-Mn distances (2.63-2.65 angstrom) and fairly bent Mn-O-Mn angles (94.1 degrees-94.6 degrees). The cyclovoltammograms of la-c in acetonitrile (25 degrees C, 0.1 M Bu4NPF6) show an irreversible one-electron oxidation peak at moderately high anodic potentials (E-ap = 0.50-0.85 V versus SCE),…

CatecholManganeseLigandStereochemistryProcess Chemistry and TechnologyCatecholschemistry.chemical_elementElectron donorManganeseMedicinal chemistryCatalysisQuinonechemistry.chemical_compoundHomologous serieschemistryO-O Bond activationOxidationsFISICA APLICADAReactivity (chemistry)Physical and Theoretical ChemistryAcetonitrileRedox properties
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Structural Characterization of Isomeric Dimers from the Oxidative Oligomerization of Catechol with a Biomimetic Catalyst

2007

In a previous paper, it has been reported about the formation of catechol di-, tri- and tetramers within an oxidative polymerization catalyzed by synthetic water-soluble iron-porphyrin as an efficient alternative to bio-labile natural peroxidase. It has also been demonstrated the occurrence of both C-C and C-O-C coupling mechanisms. However, since the coupling products were determined by mass spectroscopy, the exact bonding position could not have been precisely ascertained for the C-C bonded isomeric dimers that are the dominant products of catechol oligomerization. Therefore, here isolation and characterization of catechol isomeric dimers, obtained by oxidative coupling under the catalysi…

CatecholPolymers and PlasticsDimerMolecular MimicrySettore AGR/13 - Chimica AgrariaCatecholsRegioselectivityBioengineeringOxidative phosphorylationOxidative cathecolOligomerCatalysisCatalysisBiomaterialschemistry.chemical_compoundIsomerismPhenolschemistryPolymer chemistryMaterials ChemistryMoleculeOxidative coupling of methaneDimerizationOxidation-Reduction
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Solid-State Electrochemical Assay of Heme-Binding Molecules for Screening of Drugs with Antimalarial Potential

2013

The interaction between heme and ligands is the basis for a variety of tests aimed at the discovery of antiplasmodial molecules. Two electrochemical methods for the screening of molecules with potential antimalarial activity through heme-binding mechanism are described. The first method is applicable to lipophilic environment, by using solution phase electrochemistry in DMSO solutions of Fe(III)-heme plus the tested compounds at carbon electrodes. This method provides well-defined voltammetric signals, characteristic of the heme-ligand (L) interaction. The second method involves aqueous media at biological pH and the use of voltammetry of immobilized particles, by means of microparticulate …

Cell ExtractsErythrocytesHeme bindingStereochemistryHemeLigandsElectrochemistryFerric CompoundsPraziquantelAnalytical ChemistryAntimalarialsHemoglobinsStructure-Activity Relationshipchemistry.chemical_compoundDrug DiscoveryHumansMoleculeElectrodesHemeVoltammetryQuinineElectrochemical TechniquesHydrogen-Ion ConcentrationCombinatorial chemistryArtemisininsCarbonchemistryElectrodeHemoglobinOxidation-ReductionMacromoleculeAnalytical Chemistry
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Membrane protein oxidation determines neuronal degeneration

2015

Oxidative stress is an early hallmark in neurodegenerative disorders such as Alzheimer's and Parkinson's diseases. However, the critical biochemical effector mechanisms of oxidative neurotoxicity have remained surprisingly elusive. In screening various peroxides and potential substrates of oxidation for their effect on neuronal survival, we observed that intramembrane compounds were significantly more active than aqueous or amphiphilic compounds. To better understand this result, we synthesized a series of competitive and site-specific membrane protein oxidation inhibitors termed aminoacyllipids, whose structures were designed on the basis of amino acids frequently found at the protein-lipi…

Cell SurvivalBiologyProtein oxidationmedicine.disease_causeBiochemistryProtein Structure SecondaryRats Sprague-DawleyCellular and Molecular Neurosciencechemistry.chemical_compoundmedicineAnimalsLipid bilayerCells CulturedNeuronsSphingosineNeurodegenerationNeurotoxicityMembrane Proteinsmedicine.diseaseTransmembrane proteinRatsCell biologyOxidative StressMembrane proteinchemistryNerve DegenerationReactive Oxygen SpeciesOxidation-ReductionOxidative stressJournal of Neurochemistry
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Induction of apoptosis by arachidonic acid in human retinoblastoma Y79 cells: involvement of oxidative stress

2000

Arachidonic acid administration caused apoptosis in Y79 cells, as shown by typical morphological changes, phosphatidylserine externalization, chromatin condensation, processing and activation of caspase-3 and cleavage of the endogenous caspase substrate poly-(ADP-ribose)-polymerase. Arachidonic acid also caused lamin B cleavage, suggesting caspase-6 activation. Arachidonic acid treatment was accompanied by increased formation of the lipid peroxidation end products malondialdehyde and 4-hydroxy-2-nonenal, lowering in reduced glutathione content and in mitochondrial membrane potential. Inhibiting glutathione synthesis sensitized Y79 cells to apoptosis-inducing stimuli, whilst replenishing red…

Cell SurvivalBlotting WesternApoptosisCell Countmedicine.disease_causeMembrane PotentialsLipid peroxidationCellular and Molecular Neurosciencechemistry.chemical_compoundPhospholipase A2medicineTumor Cells Culturedarachidonic acidHumansCYP2C8biologyDose-Response Relationship DrugRetinoblastomaGlutathioneTrypan BlueMalondialdehydeFlow CytometryGlutathioneSensory SystemsCell biologyMitochondriaOphthalmologyOxidative StressBiochemistrychemistryMitochondrial permeability transition poreCaspasesbiology.proteinArachidonic acidColorimetryPoly(ADP-ribose) PolymerasesOxidative stress
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Genotoxicity of 1,4-benzoquinone and 1,4-naphthoquinone in relation to effects on glutathione and NAD(P)H levels in V79 cells.

1989

1,4-Benzoquinone is cytotoxic in V79 Chinese hamster cells and induces gene mutations and micronuclei. The cell-damaging effects of quinones are usually attributed to thiol depletion, oxidation of NAD(P)H, and redox-cycling involving the formation of semiquinone radicals and reactive oxygen species. To elucidate the role of these mechanisms in the genotoxicity of 1,4-benzoquinone, we measured various genotoxic effects, cytotoxicity, and the levels of glutathione, NADPH, NADH, and their oxidized forms all in the same experiment. 1,4-Naphthoquinone, which does not induce gene mutations in V79 cells, was investigated for comparative reasons. The quinones had a similar effect on the levels of c…

Cell SurvivalHealth Toxicology and MutagenesisGlutathione reductaseGene mutationBiologymedicine.disease_causeCell Linechemistry.chemical_compoundBenzoquinonesmedicineAnimalschemistry.chemical_classificationReactive oxygen speciesMutagenicity TestsQuinonesPublic Health Environmental and Occupational HealthGlutathioneNADGlutathioneBiochemistrychemistryMicronucleus testNAD+ kinaseOxidation-ReductionNADPGenotoxicityOxidative stressMutagensNaphthoquinonesResearch ArticleEnvironmental Health Perspectives
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