Search results for "Kinetic"

showing 10 items of 3064 documents

Transient absorption studies of the Ru(dcbpy)2(NCS)2 excited state and the dye cation on nanocrystalline TiO2 film

2001

We have measured dynamics of the Ru(dcbpy)2(NCS)2 [dcbpy = 4,4′-dicarboxy-2,2′-bipyridine] excited state and the dye cation on nanocrystalline TiO2 film in the wavelength region 700–900 nm. The dye in ethanol solution and Ru(dcbpy)2(NCS)2 sensitized nanocrystalline Al2O3 films were used as non-injecting reference samples for excited state identification. For TiO2/Ru(dcbpy)2(NCS)2 film the `reactant' decay and `product' formation kinetics observed at different probe wavelengths showed that the resolved transient absorption picosecond components (1.1±0.2), (12±2) and (100±5) ps are related to electron injection from the excited states of the dye to the semiconductor TiO2.

Electron transferAbsorption spectroscopyNanocrystalChemistryExcited statePicosecondUltrafast laser spectroscopyKineticsGeneral Physics and AstronomyPhysical and Theoretical ChemistryPhotochemistryNanocrystalline materialChemical Physics Letters
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Photoinduced interfacial electron injection in RuN3–TiO2 thin films: Resolving picosecond timescale injection from the triplet state of the protonate…

2008

Using femtosecond transient absorption spectroscopy we have studied light-induced electron injection from the sensitizer RuN3 and its partly deprotonated tetrabutylamonium salt to nano-structured TiO2 film. Previous studies have suggested significant differences in electron injection dynamics for these dyes and some results have indicated that aggregation of the sensitizer may lead to slow injection. By measuring transient absorption spectra and kinetics of RuN3 and RuN3-TBA in solution and attached to TiO2 film we show that the electron injection dynamics are very similar for the two forms of the dye and that aggregation has only moderate effects on the electron transfer dynamics. (c) 2008…

Electron transferChemistryPicosecondFemtosecondUltrafast laser spectroscopyKineticsGeneral Physics and AstronomyPhysical and Theoretical ChemistryTriplet stateThin filmSpectroscopyPhotochemistryChemical Physics Letters
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Decreased Electron Transfer Rates of Manganese Porphyrins with Conformational Distortion of the Macrocycle

1998

Slow electron transfer to manganese(iii) porphyrins results when the macrocycle deviates from planarity. This was demonstrated by measuring the kinetics of homogeneous electron transfer from a series of semiquinone radical anions to synthetic manganese porphyrins (shown schematically; R1 =H, Cl, F; R2 =H, F). Three of the four porphyrins studied have nonplanar macrocycles. These results could have implications for the role of manganese in biological electron transfer processes.

Electron transferchemistrySemiquinoneHomogeneousKineticschemistry.chemical_elementGeneral ChemistryManganesePhotochemistryCatalysisPlanarity testingAngewandte Chemie International Edition
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Asymmetric Homoaldol Reactions with Cyclohex-2-enylN,N-Diisopropylcarbamate: Kinetic Resolution, Elucidation of the Stereochemical Course and Applica…

2007

Enantio-enriched cyclohex-2-enyl N,N-diisopropylcarbamate (5) is stereospecifically deprotonated by sec-butyllithium/(–)-sparteine (9) to form the configurationally stable lithium complex 7·9. A kinetic resolution of rac-5 by n-butyllithium/(–)-sparteine (9) yielded (R)-5 with up to 99 % ee. Electrophilic substitution with tin electrophiles proceeds in a anti-SE′ fashion as shown by chemical correlations. The synthesized allylstannanes 10 undergo a highly stereospecific TiCl4-mediated homoaldol reaction with various aldehydes, yielding syn-configured homoaldol products 12. These were transferred into all-cis-configured hexahydroisobenzofuran-4(1H)-ones 22 by BF3·OEt2-mediated reactions with…

Electrophilic substitutionStereospecificityDeprotonationChemistryStereochemistryOrganic ChemistryElectrophileEnantioselective synthesischemistry.chemical_elementLithiumPhysical and Theoretical ChemistryTinKinetic resolutionEuropean Journal of Organic Chemistry
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LACTATE DEHYDROGENASE ISOENZYMES IN THE NERVOUS TISSUE?V..

1965

ElectrophoresisAgingBiologyBiochemistryCellular and Molecular Neurosciencechemistry.chemical_compoundLactate dehydrogenasemedicinePyruvateschemistry.chemical_classificationL-Lactate DehydrogenaseResearchX-RaysNervous tissueBrainMetabolismRat brainMolecular biologyRatsLactic acidIsoenzymesRadiation EffectsKineticsMetabolismmedicine.anatomical_structureEnzymechemistryBiochemistryNeurogliaPyruvic acidNeurogliaJournal of Neurochemistry
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A novel approach for analysis of oligonucleotide-cisplatin interactions by continuous elution gel electrophoresis coupled to isotope dilution inducti…

2008

In this work we present a novel approach for in vitro studies of cisplatin interactions with 8-mer oligonucleotides. The approach is based on the recently developed coupling of continuous elution gel electrophoresis (GE) to an inductively coupled plasma-sector field mass spectrometer (ICP-SFMS) with the aim of monitoring the interaction process between this cytostatic drug and the nucleotides. In contrast to existing methods, the electrophoretic separation conditions used here allow both the determination of the reaction kinetics in more detail as well as the observation of dominant intermediates. Two different nucleotides sequences have been investigated for comparison purposes, one contai…

ElectrophoresisChromatographyProtein mass spectrometryElutionChemistryClinical BiochemistryAnalytical chemistryOligonucleotidesAntineoplastic AgentsMass spectrometryBiochemistryCapillary electrophoresis–mass spectrometrySample preparation in mass spectrometryAnalytical ChemistrySurface-enhanced laser desorption/ionizationMatrix-assisted laser desorption/ionizationKineticsSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationCisplatinInductively coupled plasma mass spectrometryElectrophoresis
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Ettringite surface chemistry: Interplay of electrostatic and ion specificity

2011

International audience; This paper presents a detailed experimental study combined with Monte Carlo (MC) simulations within the primitive model of the physical chemistry at the ettringite-water interface over a wide range of pH and bulk conditions for which ettringite exists thanks to its solubility in aqueous solutions. Ettringite, which is an important phase in hydrated cement-based systems, bears a permanent and positive structural charge. In contrast with previous studies, electrokinetic measurements together with the careful chemical analysis of the equilibrium solutions of the dispersions have brought strong support to designate sulfate as being the ion determining the potential. Simu…

ElectrophoresisEttringiteSurface PropertiesStatic Electricity02 engineering and technology010402 general chemistryEttringite01 natural sciencesMonte Carlo simulationsIonBiomaterialschemistry.chemical_compoundElectrokinetic phenomenaColloid and Surface ChemistryPhase (matter)Computer SimulationSulfateSolubilityIonsMineralsAqueous solutionSulfatesChemistryAdsorption potentialWaterHydrogen-Ion Concentration021001 nanoscience & nanotechnologyElectrostaticsSulfate0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Models ChemicalChemical physicsPhysical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyMonte Carlo MethodJournal of Colloid and Interface Science
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Cadmium induces the expression of specific stress proteins in sea urchin embryos.

2004

Abstract Marine organisms are highly sensitive to many environmental stresses, and consequently, the analysis of their bio-molecular responses to different stress agents is very important for the understanding of putative repair mechanisms. Sea urchin embryos represent a simple though significant model system to test how specific stress can simultaneously affect development and protein expression. Here, we used Paracentrotus lividus sea urchin embryos to study the effects of time-dependent continuous exposure to subacute/sublethal cadmium concentrations. We found that, between 15 and 24 h of exposure, the synthesis of a specific set of stress proteins (90, 72–70, 56, 28, and 25 kDa) was ind…

Embryo NonmammalianBiophysicschemistry.chemical_elementWestern blotBiologyEmbryo developmentBiochemistryGel electrophoresiParacentrotus lividusStress proteins; Embryo development; Gel electrophoresis; Western blotWestern blotCadmium ChloridemedicineMorphogenesisStress ProteinsAnimalsElectrophoresis Gel Two-DimensionalSettore BIO/06 - Anatomia Comparata E CitologiaMolecular BiologyCells CulturedHeat-Shock ProteinsGel electrophoresisCadmiummedicine.diagnostic_testStress proteinEmbryogenesisCell BiologyGastrulaSea urchin embryoBlastulabiology.organism_classificationMolecular biologyCell biologyHighly sensitiveKineticschemistryFertilizationSea UrchinsFemaleBiochemical and biophysical research communications
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Endoribonuclease IV. A poly(A)-specific ribonuclease from chick oviduct. 1. Purification of the enzyme.

1976

A new endoribonuclease, termed endoribonuclease IV, has been described. This enzyme has been isolated from chick oviducts and purified 15 000-fold in a 25% yield nearly to homogeneity. The nuclease, which specifically degrades poly(A), forms oligonucleotides of an average chain length of 10. These (A)-10 fragments are terminated by 3'-hydroxyl and 5'-phosphate groups. The enzyme has a pH optimum at 8.7, requires Mn2+ or Mg2+ as a cofactor, and has a molecular weight of about 45 000.

EndoribonucleaseOviductsBiologyBiochemistryCofactorStructure-Activity RelationshipRibonucleasesAnimalsMagnesiumchemistry.chemical_classificationNucleaseManganeseOligoribonucleotidesOligonucleotideEndoribonuclease IVEndonucleasesMolecular biologyEnzyme ActivationMolecular WeightKineticsEnzymeBiochemistrychemistryYield (chemistry)biology.proteinOviductFemalePoly AChickensEuropean journal of biochemistry
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Unjamming overcomes kinetic and proliferation arrest in terminally differentiated cells and promotes collective motility of carcinoma.

2019

During wound repair, branching morphogenesis and carcinoma dissemination, cellular rearrangements are fostered by a solid-to-liquid transition, known as unjamming. The biomolecular machinery behind unjamming and its pathophysiological relevance remain, however, unclear. Here, we study unjamming in a variety of normal and tumorigenic epithelial two-dimensional (2D) and 3D collectives. Biologically, the increased level of the small GTPase RAB5A sparks unjamming by promoting non-clathrin-dependent internalization of epidermal growth factor receptor that leads to hyperactivation of the kinase ERK1/2 and phosphorylation of the actin nucleator WAVE2. This cascade triggers collective motility effe…

EndosomeCellular differentiationmedia_common.quotation_subjectMotility02 engineering and technologySettore MED/08 - Anatomia Patologica010402 general chemistry01 natural sciencesExtracellular matrixCell MovementCell Line TumorHumansGeneral Materials ScienceSmall GTPaseEpidermal growth factor receptorInternalizationActinmedia_commonCell Proliferationrab5 GTP-Binding ProteinsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3biologyChemistryMechanical EngineeringCell DifferentiationGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesCell biologyErbB ReceptorsKineticscarcinoma differentiated neoplastic cellsMechanics of Materialsbiology.protein0210 nano-technologyNature materials
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