Search results for "Redox"

showing 10 items of 619 documents

Chemistry and reactivity of dinuclear iron oxamate complexes: alkane oxidation with hydrogen peroxide catalysed by an oxo-bridged diiron(III) complex…

2004

[EN] A new dinuclear iron(III) complex with the tetradentate ligand N,N'-o-phenylenebis(oxamate) (opba) has been synthesised, and structurally, magnetically and electrochemically characterised. It possesses an unprecedented triply bridged Fe-2(mu-O)(mu-RCO2...H2O...O2CR)(2) core, whereby two N-amides from the opba ligand complete the square-pyramidal coordination sphere of the O-carboxylate rich iron site (Fe-N = 2.053 Angstrom and Fe-O = 2.015 Angstrom), The antiferromagnetic exchange interaction between the two high-spin Fe-III ions through the oxo bridge (J = -190 cm(-1); H = -JS(1)(.)S(2)) is weaker than that found in related mu-oxo singly bridged diiron(III) complexes. The lessened ant…

Coordination sphereLigandIronAdamantanePhotochemistryAmidesMedicinal chemistryRedoxCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundCarboxylateschemistryOxidationsFISICA APLICADAAlkanesMaterials ChemistryReactivity (chemistry)CarboxylatePhysical and Theoretical ChemistryAcetonitrileInorganica Chimica Acta
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FERULIC ACID INHIBITS OXIDATE STRESS AND CELL DEATH INDUCED BY Ab OLIGOMERS: IMPROVED DELIVERY BY SOLID LIPID NANOPARTICLES.

2009

Oxidative stress and dysfunctional mitochondria are among the earliest events in AD, triggering neurodegeneration. The use of natural antioxidants could be a neuroprotective strategy for blocking cell death. Here, the antioxidant action of ferulic acid (FA) on different paths leading to degeneration of recombinant beta-amyloid peptide (rAbeta42) treated cells was investigated. Further, to improve its delivery, a novel drug delivery system (DDS) was used. Solid lipid nanoparticles (SLNs), empty or containing ferulic acid (FA-SNL), were developed as DDS. The resulting particles had small colloidal size and highly negative surface charge in water. Using neuroblastoma cells and rAbeta42 oligome…

Coumaric AcidsMitochondrionmedicine.disease_causeBiochemistryAntioxidantsFerulic acidchemistry.chemical_compoundAlzheimer DiseaseCell Line TumorSolid lipid nanoparticlemedicineHumansViability assayMembrane Potential MitochondrialNeuronsAmyloid beta-PeptidesCell DeathbiologyCytochrome cCytochromes cFERULIC ACID Ab OLIGOMERS LIPID NANOPARTICLES DELIVERY SYSTEM.General MedicineLipidsPeptide FragmentsRecombinant ProteinsMitochondriaOxidative StressBiochemistrychemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryBiophysicsbiology.proteinNanoparticlesPeroxiredoxinOxidative stress
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A multiphase multiobjective dynamic genome-scale model shows different redox balancing among yeast species of the saccharomyces genus in fermentation

2021

Yeasts constitute over 1,500 species with great potential for biotechnology. Still, the yeast Saccharomyces cerevisiae dominates industrial applications, and many alternative physiological capabilities of lesser-known yeasts are not being fully exploited. While comparative genomics receives substantial attention, little is known about yeasts’ metabolic specificity in batch cultures. Here, we propose a multiphase multiobjective dynamic genome-scale model of yeast batch cultures that describes the uptake of carbon and nitrogen sources and the production of primary and secondary metabolites. The model integrates a specific metabolic reconstruction, based on the consensus Yeast8, and a kinetic …

Cryotolerant speciesPhysiologySaccharomyces cerevisiaeBatch fermentationsSaccharomyces speciesBiochemistryRedoxSaccharomycesMicrobiologyRedox balance03 medical and health sciencesSaccharomycesDynamic genome-scale modelsGeneticsMolecular BiologyEcology Evolution Behavior and Systematics030304 developmental biologyComparative genomics0303 health sciencesbiologyKinetic model030306 microbiologyChemistryKinetic modelbiology.organism_classificationYeastQR1-502YeastComputer Science ApplicationsFlux balance analysisMetabolismModeling and SimulationFermentationBiochemical engineeringBatch cultures
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Syntheses, X-ray structures, and redox behaviour of the group 14 bis-boraamidinates M[PhB(μ-N-t-Bu)2]2 (M = Ge, Sn) and Li2M[PhB(μ-N-t-Bu)2]2 (M = Sn…

2009

The solid-state structures of the complexes M[PhB(μ-N-t-Bu)2]2 (1a, M= Ge; 1b, M = Sn) were determined to be spirocyclic with two orthogonal boraamidinate (bam) ligands N,N′-chelated to the group 14 centre. Oxidation of 1b with SO2Cl2 afforded the thermally unstable, blue radical cation {Sn[PhB(μ-N-t-Bu)2]2}•+, identified by electron paramagnetic resonance (EPR) spectroscopy supported by density functional theory (DFT) calculations, whereas the germanium analogue 1a was inert towards SO2Cl2. The reaction between Li2[PhB(μ-N-t-Bu)2]2 and SnCl2 or PbI2 in 2:1 molar ratio in diethyl ether produced the novel heterotrimetallic complexes Li2Sn[PhB(μ-N-t-Bu)2]2 (2b) and (Et2O·Li)LiPb[PhB(μ-N-t-Bu…

CrystallographyGroup (periodic table)ChemistryOrganic ChemistryX-rayGeneral ChemistryRedoxCatalysisNuclear chemistryCanadian Journal of Chemistry
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Structural effects of Co and Cr substitution in LaMnO3 + δ

2000

Series of perovskite oxides with the composition LaMn1 − xMxO3 + δ (M = Cr, Co; 0 ≤ x ≤ 1) have been synthesized by thermal treatment of precursors obtained by freeze-drying of acetic acid solutions. The oxides have been characterized by X-ray diffraction, and the Mn4+ content and, thus, the oxygen excess, δ, has been determined by redox back-titration. LaMnO3.14 and LaCrO3 phases have the rhombohedral-LaAlO3 and the orthorhombic-GdFeO3 structures, respectively. The LaMn1 − xCrxO3 + δ phases have the rhombohedral structure for x ≤ 0.3, and the orthorhombic structure for x ≥ 0.5. LaCoO3 has, as LaMnO3.14, the rhombohedral structure. However, the LaMn1 − xCoxO3 + δ phases have orthorhombic st…

CrystallographyIonic radiusChemistryInorganic chemistryMaterials ChemistryOrthorhombic crystal systemGeneral ChemistryCrystal structureThermal treatmentChemical compositionRedoxPerovskite (structure)Solid solutionJournal of Materials Chemistry
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Model of the catalyticA+B→0reaction with surface reconstruction

2002

The $A+\stackrel{\ensuremath{\rightarrow}}{B}0$ reaction model with a surface reconstruction is analyzed. It is compared with another similar model for the ${A+1/2B}_{2}\ensuremath{\rightarrow}0$ reaction [V. N. Kuzovkov et al., J. Chem. Phys. 108, 5571 (1998)], which mimics the CO oxidation reaction on the Pt surfaces. The effect of monomer B adsorption instead of dimer ${B}_{2}$ is examined. It is shown that qualitative system features such as reactant concentration oscillations are independent of this substitution.

Crystallographychemistry.chemical_compoundMonomerMaterials scienceAdsorptionchemistryReaction modelDimerRedoxSurface reconstructionCatalysisPhysical Review E
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Novel Phases in the V-P-O Catalytic System from Oxovanadium Hydrogenphosphate Precursors

1994

ABSTRACTSeveral biphasic VOP04/(VO)2P2O7 redox partners seem to be active in the catalytic cycles involved in the mild oxidation of simple hydrocarbons to maleic anhydride. The present X-ray time resolved thermal-diffractometric study reveals the existence of a new anhydrous variety of the oxidized form, ω-VOPO4, which may appear as an intermediate in the formation of the well known β-VOPO4. This new phase only remains well crystallized at relatively high temperatures, and when it is allowed to cool down in wet air VOPO4·2H2O results. In turn, another well defined phase, VOPO4·1.58H2O, can be recognized in the course of the hydration process.

Crystallographychemistry.chemical_compoundlawChemistryPhase (matter)AnhydrousMaleic anhydrideCrystal structureCrystallizationRedoxChemical reactionlaw.inventionCatalysisMRS Proceedings
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Electrocatalytic Behavior of Tetrathiafulvalene (TTF) and Extended Tetrathiafulvalene (exTTF) [FeFe] Hydrogenase Mimics

2021

TTF- and exTTF-containing [(μ-S2)Fe2(CO)6] complexes have been prepared by the photochemical reaction of TTF or exTTF and [(μ-S2)Fe2(CO)6]. These complexes are able to interact with PAHs. In the absence of air and in acid media an electrocatalytic dihydrogen evolution reaction (HER) occurs, similarly to analogous [(μ-S2)Fe2(CO)6] complexes. However, in the presence of air, the TTF and exTTF organic moieties strongly influence the electrochemistry of these systems. The reported data may be valuable in the design of [FeFe] hydrogenase mimics able to combine the HER properties of the [FeFe] cores with the unique TTF properties

Cultural StudiesHistoryHydrogenaseLiterature and Literary TheoryChemistryFerredoxin HydrogenaseDithiol-Iron(III)-Sulphide ComplexOrganic chemistryQuímicaCombinatorial chemistrychemistry.chemical_compoundQD241-441ComplexTetrathiafulvaleneInorganic chemistryQD146-197ACS Organic & Inorganic Au
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Thermal frontal polymerization with a thermally released redox catalyst

2012

ABSTRACT: We studied thermal frontal polymerization using a re-dox systeminan attempt to lower the temperature of thefrontallypolymerizable system while increasing the front velocity so as toobtain a self-sustaining front in a thinner layer than without theredox components. A cobalt-containing polymer with a meltingpoint of 63 C (Intelimer 6050X11) and cumene hydroperoxidewere used with a triacrylate. The use of the Intelimer decreasedthe front velocity but allowed fronts to propagate in thinner layersand with more filler while still having a pot life of days. Nonplanarmodes of propagation occurred. Fronts propagated faster when6-O-palmitoyl- L -ascorbic acid was used as a reductant. Intere…

CumeneMaterials sciencePolymers and PlasticsRadical polymerizationkineticfrontal polymerizationchemistry.chemical_compoundPolymer chemistryMaterials ChemistryFront velocityredox polymersSettore CHIM/02 - Chimica Fisicaaddition polymerizationchemistry.chemical_classificationAcrylateOrganic ChemistryacrylatePolymeracrylate; addition polymerization; frontal polymerization; kinetics; radical polymerization; redox polymersAscorbic acidradical polymerizationchemistryPolymerizationChemical engineeringAddition polymerJournal of Polymer Science Part A: Polymer Chemistry
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Model for Solid State Voltammetry of Zeolite-Associated Species

2004

The electrochemical reduction/oxidation of zeolite-associated species is described from the model of Lovric and Scholz for redox conductive microcrystals and the model of Andrieux and Saveant for redox polymers. It is assumed that the reaction starts at the three-phase boundary between electrode, zeolite particle, and electrolyte. From this point, the reaction zone grows while electrons and charge-balancing cations diffuse perpendicularly along the zeolite. As a result, at short times, a Cottrell-type behavior, controlled by the diffusion of electrolyte countercations in the zeolite can be expected. At larger times, a thin-layer response in which electron hopping between adjacent redox site…

CyclohexaneDiffusionInorganic chemistryElectrolyteElectrochemistryRedoxSurfaces Coatings and Filmschemistry.chemical_compoundchemistryElectrodeMaterials ChemistryPhysical and Theoretical ChemistryZeoliteVoltammetryThe Journal of Physical Chemistry B
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