Search results for "Redox"

showing 10 items of 619 documents

In-situ transformation of iron-bearing minerals in marshland-derived paddy subsoil

2016

Transformations of Fe-bearing minerals under alternating redox conditions are not fully understood. In-situ approaches under field conditions have rarely been used. We exposed mesh bags containing ferrihydrite, goethite or nontronite to changing redox conditions in subsoil that had been under paddy management for 100, 700 and 2000 years. After 12 months, the minerals were retrieved and analysed for organic carbon and by X-ray diffraction; in addition, nontronite was analysed for cation exchange capacity and by Mossbauer spectroscopy at 278 and 4.2 K. Field exposure of the test minerals was complemented by measurements of soil redox potential and analyses of soil water. Minerals accumulated …

GoethiteMineralRecrystallization (geology)ChemistryInorganic chemistrySoil ScienceNontronite010501 environmental sciencesengineering.material010502 geochemistry & geophysics01 natural sciencesRedoxFerrihydritevisual_artvisual_art.visual_art_mediumCation-exchange capacityengineeringLepidocrocite0105 earth and related environmental sciencesEuropean Journal of Soil Science
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Closer to nature: an ATP-driven bioinspired catalytic oxidation process

2013

The capability of DNA to acquire enzyme-like properties has led to the emergence of the so-called DNAzyme field; herein, we take a further leap along this nature-inspired road, demonstrating that a template assembled synthetic G-quartet (TASQ) can act as a pre-catalyst for catalytic peroxidase-mimicking oxidation reactions, whatever its nature (guanine or guanosine-based G-quartets), in an ATP-dependent manner, thereby bringing this bioinspired TASQzyme process even closer to nature.

GuanineDeoxyribozymeGuanosineNanotechnology010402 general chemistry01 natural sciencesRedox[ CHIM ] Chemical SciencesCatalysisCatalysischemistry.chemical_compoundAdenosine TriphosphateMaterials Chemistry[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUS010405 organic chemistryMetals and AlloysDNA CatalyticGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsG-QuadruplexeschemistryCatalytic oxidationScientific methodCeramics and CompositesOxidation-Reduction
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Electronic characterisation of the oxidized state of the blue copper protein Rusticyanin by 1 H NMR: Is the axial methionine the dominant influence f…

2001

The oxidized state of rusticyanin, the blue copper protein with the highest redox potential in its class, has been investigated through (1)H nuclear magnetic resonance applied to its cobalt(II) derivative. The assignment of the protons belonging to the coordinated residues has been performed. Many other amino acids situated in the vicinity of the metal ion, including six hydrophobic residues (isoleucine140 and five phenylalanines) have also been identified. The orientation of the main axes of the magnetic susceptibility tensor for the cobalt(II)-rusticyanin as well as its axial, Deltachi(ax), and rhombic, Deltachi(rh), magnetic susceptibility anisotropy components have been determined. A co…

Half-reactionChemistryCopper proteinInorganic chemistrychemistry.chemical_elementCobaltLigandsBiochemistryMagnetic susceptibilityRedoxElectron TransportCrystallographyMethionineBacterial ProteinsAzurinMetalloproteinsRusticyaninProton NMRAnisotropyProtonsAzurinNuclear Magnetic Resonance BiomolecularOxidation-ReductionCobaltCopper
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Molecular docking and oxidation kinetics of 3-phenyl coumarin derivatives by human CYP2A13.

2021

CYP2A13 enzyme is expressed in human extrahepatic tissues, while CYP2A6 is a hepatic enzyme. Reactions catalysed by CYP2A13 activate tobacco-specific nitrosamines and some other toxic xenobiotics in lungs.To compare oxidation characteristics and substrate-enzyme active site interactions in CYP2A13 vs CYP2A6, we evaluated CYP2A13 mediated oxidation characteristics of 23 coumarin derivatives and modelled their interactions at the enzyme active site.CYP2A13 did not oxidise six coumarin derivatives to corresponding fluorescent 7-hydroxycoumarins. The Km-values of the other coumarins varied 0.85-97 µM, Vmax-values of the oxidation reaction varied 0.25-60 min-1, and intrinsic clearance varied 26-…

Health Toxicology and MutagenesisKineticsToxicology030226 pharmacology & pharmacyBiochemistryRedoxMedicinal chemistryCytochrome P-450 CYP2A603 medical and health scienceschemistry.chemical_compound0302 clinical medicineCytochrome P-450 Enzyme SystemCoumarinsHumansheterocyclic compoundsEnzyme kineticsCYP2A6Pharmacologychemistry.chemical_classificationbiologyChemistryActive siteGeneral MedicineCoumarinMolecular Docking SimulationKineticsEnzymeDocking (molecular)030220 oncology & carcinogenesisbiology.proteinAryl Hydrocarbon HydroxylasesXenobiotica; the fate of foreign compounds in biological systems
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Correspondence: Strongly-driven Re+CO2 redox reaction at high-pressure and high-temperature.

2016

Correspondence: Strongly-driven Re+CO 2 redox reaction at high-pressure and high-temperature

Hot TemperatureScienceGeneral Physics and AstronomyMineralogy010402 general chemistry01 natural sciencesRedoxCarbon-DioxideGeneral Biochemistry Genetics and Molecular BiologyHot Temperaturechemistry.chemical_compound0103 physical sciencesTEORIA DE LA SEÑAL Y COMUNICACIONESCorrespondencePressure010306 general physicsMultidisciplinaryChemistryQTemperatureOxidation reductionSilicaGeneral ChemistryCarbon Dioxide0104 chemical sciencesChemical engineeringHigh pressureCarbon dioxideOxidation-Reduction
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Chemistry of ?-hydridobis[pentacarbonylchromium(0)] species. Part III. Redox reactions with mercury(II) compounds and iodine

1981

[Cr2(CO)10(μ-H)]− undergoes ready hydride substitution on reaction with HgX2 (X = Cl, Br, I or SCN) or with iodine in acetone, yielding [Cr2(CO)10(μ-X)]− complex species which can be converted quantitatively into [Cr(CO)5X]− anions by reactions conducted in the presence of an excess of X−.

HydrideInorganic chemistryMetals and Alloyschemistry.chemical_elementIodineMedicinal chemistryRedoxMercury (element)CatalysisInorganic ChemistryPart iiichemistry.chemical_compoundchemistryMaterials ChemistryAcetoneOrganometallic chemistryTransition Metal Chemistry
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Au/TiO2-CeO2 Catalysts for Photocatalytic Water Splitting and VOCs Oxidation Reactions

2016

Photocatalytic water splitting for H2 production and photocatalytic oxidation of 2-propanol, an example of volatile organic compounds, were investigated over TiO2 catalysts loaded with gold and/or ceria. In the water splitting reaction the presence of gold only slightly affected the performance of TiO2 whereas the presence of CeO2 had a more remarkable positive effect. In the 2-propanol oxidation Au/TiO2 was the most active sample in terms of alcohol conversion whereas Au/TiO2-CeO2 exhibited the highest CO2 yield. On the basis of characterization experiments (X-Ray Diffraction (XRD), Energy Dispersive X-ray Analysis EDX, surface area measurements, Diffuse Reflectance Spectroscopy (DRS) and …

HydrogenDiffuse reflectance infrared fourier transformInorganic chemistrychemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistrylcsh:Chemical technology01 natural sciencesRedoxCatalysisCatalysiCatalysislcsh:Chemistrysymbols.namesakePhotocatalysilcsh:TP1-1185Physical and Theoretical ChemistryH2 productioncerium oxidetitanium dioxidegoldphotocatalysis; gold; titanium dioxide; cerium oxide; H<sub>2</sub> production021001 nanoscience & nanotechnology0104 chemical scienceschemistrylcsh:QD1-999PhotocatalysissymbolsWater splittingSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyRaman spectroscopyphotocatalysisPhotocatalytic water splittingCatalysts
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Direct involvement of acid centers of polyaniline in charge transfer on organic acceptor

1996

Abstract Electrochemical behavior of hydroquinone and 4F-hydroquinone has been studied on Pt/polyaniline (PANI) electrodes in 1 M H 2 SO 4 solution. Redox transformation of quinone/hydroquinone systems takes place on PANI practically without overpotential and, probably, the two-electron charge transfer processes are realized in such systems. Reaction currents depend on PANI quantities deposited on the Pt electrode and the molecular complex is formed. There exists a great electronic exchange between acid centers of PANI and quinone/hydroquinone molecules, resulting in electronic conjugation of this surface state (adsorbed molecule) with the polymer. Existence of such complexes was confirmed …

HydroquinoneMechanical EngineeringInorganic chemistryMetals and AlloysOverpotentialCondensed Matter PhysicsElectrochemistryAcceptorRedoxElectronic Optical and Magnetic MaterialsQuinonechemistry.chemical_compoundchemistryMechanics of MaterialsPolyanilineMaterials ChemistryMoleculeSynthetic Metals
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Deoxygenative Divergent Synthesis : En Route to Quinic Acid Chirons

2020

The installation of vicinal mesylate and silyl ether groups in a quinic acid derivative generates a system prone for stereoselective borane-catalyzed hydrosilylation through a siloxonium intermediate. The diversification of the reaction conditions allowed the construction of different defunctionalized fragments foreseen as useful synthetic fragments. The selectivity of the hydrosilylation was rationalized on the basis of deuteration experiments and computational studies. peerReviewed

Hydrosilylation010402 general chemistry01 natural sciencesBiochemistrySilyl etherchemistry.chemical_compoundredox reactionsPhysical and Theoretical Chemistryhapetus-pelkistysreaktioorgaaniset yhdisteeteetteritkemiallinen synteesi010405 organic chemistryreaction productsOrganic ChemistryhydrosilylationQuinic acidCombinatorial chemistry0104 chemical sciencesbond cleavageetherschemistryStereoselectivitySelectivityDivergent synthesisDerivative (chemistry)Vicinal
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Electrochemistry of hydrotalcite-supported bis(2-mercapto-2,2-diphenyl-ethanoate) dioxomolybdate complexes.

1998

The redox properties of the hydrotalcite-intercalated bis(2-mercapto-2,2-diphenyl-ethanoate) dioxomolybdate(VI) complex are investigated by cyclic voltammetry by using modified carbon paste electrodes and clay-modified electrodes. The electrochemical data provide evidence that boundary-associated species involving the VI, V and IV oxidation states of molybdenum are responsible for the electroactivity.

HydrotalciteGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementBuffer solutionSodium perchlorateElectrochemistryRedoxAnalytical Chemistrychemistry.chemical_compoundchemistryMolybdenumPolymer chemistryElectrochemistryCarboxylateCyclic voltammetryJournal of Electroanalytical Chemistry
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