Search results for "Redox"

showing 10 items of 619 documents

Role of glutathione in plant signaling under biotic stress

2012

International audience; Glutathione (GSH) is a non-protein thiol compound which has been repeatedly reported to play an important role in plant responses during biotic stresses. However, our knowledge of glutathione-related molecular mechanisms underlying plant defense responses still remains limited. We first discovered that the Arabidopsis thaliana phytoalexin deficient 2-1 (pad2-1) mutant was linked to glutathione deficiency since the mutation was identified in the GSH1 gene encoding the first enzyme of glutathione biosynthesis: Glutamate Cysteine Ligase (GCL). Interestingly, this glutathione-deficient mutant pad2-1 also displays a high susceptibility to a wide range of invaders. We rece…

Hypersensitive responsePhytophthoraMini Reviewredox environment[SDV]Life Sciences [q-bio]ArabidopsisPlant ScienceBiologymedicine.disease_causeGenes Plantphytophthora brassicaechemistry.chemical_compoundpad2-1 mutantGene Expression Regulation PlantStress PhysiologicalArabidopsismedicineArabidopsis thalianaPlant ImmunityglutathionePlant Diseaseschemistry.chemical_classificationReactive oxygen speciesArabidopsis ProteinsPhytoalexinarabidopsis thalianaGlutathioneBiotic stressbiology.organism_classificationdefence responseOxidative StressBiochemistrychemistryMutation[SDE]Environmental SciencesOxidative stressSignal Transduction
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Monitoring pH and ORP in a SHARON reactor

2011

This paper analyses the valuable information provided by the on-line measurements of pH and oxidation reduction potential (ORP) in a continuous single high ammonia removal over nitrite (SHARON) reactor. A laboratory-scale SHARON reactor equipped with pH, ORP, electric conductivity and dissolved oxygen (DO) probes has been operated for more than one year. Nitrogen removal over nitrite has been achieved by adding methanol at the beginning of anoxic stages. Time evolution of pH and ORP along each cycle allows identifying the decrease in nitritation rate when ammonia is consumed during the aerobic phase and the end of the denitrification process during the anoxic phase. Therefore, monitoring pH…

INGENIERIA HIDRAULICADenitrificationPHLaboratory methodOxidation reduction potentialNitriteOxic conditionsWaste Disposal Fluidchemistry.chemical_compoundDissolved oxygenElectric conductivityBioreactorsElectrical conductivityAnaerobiosisNitriteControl systemWater Science and TechnologyTime evolutionsChemistryPH effectsHydrogen-Ion ConcentrationProbeAnoxic watersNitrificationAerobiosisPartial nitrificationReal timeNitritationEnvironmental chemistryPollutant removalDenitrificationSingle reactor system for high activity ammonium removal over nitrite reactorRedox potentialOxidation-ReductionEnvironmental MonitoringORPOptimizationDetection methodEnvironmental EngineeringOnline monitoringMonitoringAmmonia removalArticleSHARON reactorAnoxic sedimentsAmmoniaReduction potentialAmmoniaOxidationBioreactorAerobic phaseOn-line measurementNitritesTECNOLOGIA DEL MEDIO AMBIENTESHARONMethanolDenitrification processReactorNitrogen removalReal time controlLaboratory scaleMonitoring systemNitrificationProbesMethanolOxidation reduction reactionAnoxic conditions
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Extension of the potential intervals of high redox activity and electronic conductivity of polypyrrole films on electrode surface via their electroch…

2021

Abstract Thin polypyrrole films (thickness: about 30 nm) have been deposited at electrode surface via potentiostatic oxidation of dilute (1 mM) pyrrole solution in acetonitrile (AN). It has been shown that their subsequent treatment by means of multi-cycle voltammetry within a broad potential range (up to -2.0 V vs. Ag/Ag+ in AN) leads to their "activation", i.e. to a very strong extension of their redox response region in the negative direction as well as to almost uniform distribution of the redox activity within this potential range. Region of their high conductivity under in situ conditions has also extended significantly. Spectral and electrocatalytic properties of such PPy films befor…

In situMaterials scienceGeneral Chemical EngineeringAnalytical chemistryElectrochemistryPolypyrroleRedoxchemistry.chemical_compoundMonomerchemistryPolymerizationElectrodeElectrochemistryVoltammetryElectrochimica Acta
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A new cell for the study of in situ chemical reactions using X-ray absorption spectroscopy

2005

An in situ cell for reductive and oxidative treatments at different temperatures that allows the possibility of recording data as a function of temperature has been designed and constructed for X-ray absorption experiments at the GILDA beamline BM08 of ESRF. The cell is linked to a mass quadrupole spectrometer providing control of the reaction gases and monitoring of the products. The apparatus allows measurements to be performed both in transmission and fluorescence geometry. The cell was tested by studying the CO oxidation reaction promoted by a Pt/ceria-zirconia-supported catalyst. The CO(2) yield is correlated with the structural results confirming the existence of a strong metal-suppor…

In situNuclear and High Energy PhysicsAnalytical chemistryChemical reactionRedoxCatalysisSpecimen HandlingCatalysisthree-way catalystX-Ray DiffractionAbsorption (electromagnetic radiation)InstrumentationPlatinumX-ray absorption spectroscopyRadiationSpectrometerChemistryTemperatureSpectrometry X-Ray EmissionCarbon Dioxidein situ EXAFSOxygenYield (chemistry)Flow Injection AnalysisZirconiumOxidation-Reductionstrong metal support interaction
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A mixed-valence Cu(I)–Cu(II) and metal–metal bond containing coordination polymer obtained from an in situ oxidation reaction route

2006

Abstract A new mixed-valence copper coordination polymer with copper–copper metal bonds in a two-dimensional network was generated from an in situ oxidation reaction route under hydrothermal conditions. The synthesis of this coordination polymer demonstrated that the novel compounds that may not be accessible using the known methods could be synthesized via an oxidation reaction route. The reaction conditions are mild enough to keep the building blocks intact during the oxidation and self-assembly process under hydrothermal conditions.

In situValence (chemistry)Coordination polymerInorganic chemistrychemistry.chemical_elementCopperRedoxHydrothermal circulationInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryMetal metalPhysical and Theoretical ChemistryMetallic bondingInorganica Chimica Acta
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Redox intermediates of plant and mammalian peroxidases: a comparative transient-kinetic study of their reactivity toward indole derivatives.

2002

Abstract A comparative study on the reactivity of five indole derivatives (tryptamine, N-acetyltryptamine, tryptophan, melatonin, and serotonin), with the redox intermediates compound I (k2) and compound II (k3) of the plant enzyme horseradish peroxidase (HRP) and the two mammalian enzymes lactoperoxidase (LPO) and myeloperoxidase (MPO), was performed using the sequential-mixing stopped-flow technique. The calculated bimolecular rate constants (k2, k3) revealed substantial differences regarding the oxidizability of the substrates by redox intermediates at pH 7.0 and 25°C. With HRP it was shown that k2 and k3 are mainly determined by the reduction potential (E°′) of the substrate with k2 bei…

Indole testTryptamineMammalsIndolesbiologyStereochemistryLactoperoxidaseBiophysicsTryptophanSubstrate (chemistry)PlantsBiochemistryHorseradish peroxidaseRedoxchemistry.chemical_compoundKineticschemistryPeroxidasesbiology.proteinAnimalsLactoperoxidaseMolecular BiologyOxidation-ReductionHorseradish PeroxidasePeroxidaseArchives of biochemistry and biophysics
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A novel oxovanadate structural type – Synthesis, single crystal structure and magnetic properties of a mixed-valence polyoxovanadate formed by {V17O4…

2007

Abstract A novel polyoxovanadate structural type, with an average nuclearity of V16, formed by a mixture of two different polyoxovananadates: {V15O36(Cl)} and{V17O40(Cl)} has been synthesized and characterized. The title compound, formulated as [Ni(phen)3]2{[V15O36(Cl)]0.5[V17O40(Cl)]0.5} · H2O (1) (phen = 1,10′-phenanthroline), presents two different polyoxovanadate architectures: {V15O36(Cl)} and {V17O40(Cl)}, with the last one representing a new framework type in polyoxovanadate chemistry. Here, we present the synthesis of this novel polyoxovanadate under hydrothermal conditions and its characterization by IR and XPS spectroscopies, elemental and thermogravimetric analysis, redox titrati…

Inorganic ChemistryCrystallographyMagnetic measurementsThermogravimetric analysisValence (chemistry)X-ray photoelectron spectroscopyStructural typeChemistryRedox titrationMaterials ChemistryPhysical and Theoretical ChemistrySingle crystalHydrothermal circulationPolyhedron
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A Bis(tridentate)cobalt Polypyridine Complex as Mediator in Dye‐Sensitized Solar Cells

2015

Dye-sensitized solar cells equipped with cationic and neutral RuII-based sensitizers [Ru(ddpd){tpy(COOH)3}]2+ [12+; ddpd = N,N′-dimethyl-N,N′-di(pyridin-2-yl)pyridin-2,6-diamine, tpy(COOH)3 = 2,2″6′,2″-terpyridine-4,4′,4″-tricarboxylic acid] and [Ru(ddpd){tpy(COOH)(COO)2}] (2) with and without the coadsorbent chenodeoxycholic acid were constructed with I3–/I– or the CoIII/II-based redox mediators [Co(bpy)3]3+/2+ (33+/2+; bpy = 2,2′-bipyridine) and [Co(ddpd)2]3+/2+ (43+/2+) in the presence of LiClO4 and 4-tert-butylpyridine. The best photovoltaic performance was achieved by using the 43+/2+ shuttle and the neutral sensitizer 2 without coadsorbent. The higher short-circuit photocurrent densit…

Inorganic ChemistryElectron transferDye-sensitized solar cellCrystallographyPolypyridine complexChemistryKineticsCationic polymerizationchemistry.chemical_elementPhotochemistryRedoxCobaltRutheniumEuropean Journal of Inorganic Chemistry
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Front Cover: Redox‐Controlled Stabilization of an Open‐Shell Intermediate in a Bioinspired Enzyme Model (Eur. J. Inorg. Chem. 31/2018)

2018

Inorganic ChemistryFront coverChemical engineeringChemistryEnzyme modelOpen shellRedoxEuropean Journal of Inorganic Chemistry
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Effect of Peripheral Substitution and Extended Conjugation on the Redox Potentials of Nickel Porphycenes

1996

Eight different nickel porphycenes bearing substituents on the pyrrole β and/or ethylenic carbon positions of the macrocycle were investigated as to their redox properties in benzonitrile containin...

Inorganic ChemistryNickelBenzonitrilechemistry.chemical_compoundchemistrySubstitution (logic)chemistry.chemical_elementPhysical and Theoretical ChemistryPhotochemistryCarbonRedoxPyrroleInorganic Chemistry
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