Search results for "Activation"

showing 10 items of 2079 documents

Temperature and excitation energy dependence of decay processes of luminescence in Ge-doped silica

2003

We report experimental results on the time decay of photoluminescence at 4.2 eV in Ge-doped silica. This optical emission is assigned to a singlet-singlet transition between electronic states localized on an oxygen deficiency nearby a Ge atom and its radiative decay rate is in competition with an intersystem crossing mechanism that populates an excited triplet state. We investigate the dependence of the lifetime of this photoluminescence on the temperature, in the 6--295 K range, and on the excitation energy, in the ultraviolet and vacuum ultraviolet region. The mean value of the decay time decreases on increasing the temperature, in agreement with the phonon-assisted nature of the intersys…

Range (particle radiation)Materials scienceIntersystem crossingPhotoluminescenceExcited stateAtomActivation energyAtomic physicsTriplet stateExcitation
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Photoluminescence study of radiative transitions in ZnTe bulk crystals

1998

Abstract This paper focuses on photoluminescence (PL) and selective photoluminescence (SPL) of ZnTe bulk crystals grown by the cold traveling heater method. The crystals exhibit a PL response with a much more intense excitonic zone than the one due to free-to-bound and donor–acceptor bands, denoting a good sample quality. In particular, we have investigated the Y 1 and Y 2 peaks which, in epitaxial layers, have usually been associated with structural defects. On bulk samples they have not been detected so far because of different masked mechanisms. SPL measurements show that the electrons are the most likely involved carriers for this emission. Additionally, the analysis of the PL variation…

Range (particle radiation)Materials sciencePhotoluminescencebusiness.industryMineralogyActivation energyElectronCondensed Matter PhysicsEpitaxyMolecular physicsInorganic ChemistrySemiconductorMaterials ChemistryRadiative transferbusinessLuminescenceJournal of Crystal Growth
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Temperature dependent photoluminescence of photocatalytically active titania nanopowders

2007

Abstract Temperature photoluminescence (PL) in the sub-ambient range has been developed as a tool for characterizing photocatalytic materials. The use of well-characterized TiO2 nanoparticles with calibrated particle sizes allowed to face the temperature dependent PL results with the photocatalytic activity and several important physico-chemical parameters. In the relaxation of the photoexcited electron/hole pairs, the transfer towards surface sites is in competition with radiative and non-radiative recombinations. Temperature dependent PL appears thus to be a very sensitive technique to study the efficiency of the electron or the hole trapping at the surface of titania nanoparticles where …

Range (particle radiation)PhotoluminescenceQuenching (fluorescence)Materials scienceNanoparticle02 engineering and technologyGeneral ChemistryActivation energyElectron010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry7. Clean energy01 natural sciencesCatalysis0104 chemical sciencesChemical physicsPhotocatalysisParticle0210 nano-technology
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Analysis of small-angle scattering patterns from a commercial Al-Li alloy by means of a model incorporating a repulsive step potential

1992

Abstract Small-angle X-ray scattering measurements are reported for a commercial Al-8·49%Li-51% Cu (atomic composition) alloy solution treated at 520°C and thermally aged for several times at several temperatures. Data have been analysed by means of a model of ellipsoidal precipitate particles previously proposed by some of us and by a modification of this model where, in the interparticle interference term, allowance is made for interactions between the precipitate particles at longer range than previously. This was achieved by the introduction, in addition to the hard-sphere interaction potential, of a potential step. Our fits indicate that the precipitate particles interact through a rep…

Range (particle radiation)ScatteringChemistryGeneral Chemical EngineeringAlloyGeneral Physics and AstronomyThermodynamicsActivation energyengineering.materialThermal diffusivitySolution of Schrödinger equation for a step potentialCrystallographyengineeringParticleSmall-angle scatteringPhilosophical Magazine B
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Evidences of cannabinoids-induced modulation of paroxysmal events in an experimental model of partial epilepsy in the rat

2010

Different studies have been shown a clear anticonvulsant activity exerted by cannabinoids (CB) through the CB1 receptor activation. The purpose of this study was to evaluate, in an in vivo experimental model of temporal lobe epilepsy (maximal dentate gyrus activation - MDA) in the rat, the protective effect of (R)-(+)-[2,3-Dihydro-5-methyl-3-(4-morpholinylmethyl) pyrrolo[1,2,3-de]-1,4-benzoxazin-6-Yl]-1-naphthalenylmethanone (WIN 55,212-2, CB agonist) alone or in combination with N-(piperidin-1-yl)-5-(4-iodophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide (AM251, selective CB1 antagonist). Pre-treatment with AM251 (1 mg kg-1, 30 min interval) dramatically reduced the signif…

Rat Maximal dentate activation Epilepsy Control CannabinoidsSettore BIO/09 - Fisiologia
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Effcts of Dextran Sulphate (Dxs) on Lymphocyte Localization in Complement-Deficient Mice: Evidence that the Fifth Component of Complement is not Impl…

1984

AbstractThe effects of subcutaneously or intraperitoneally administered dextran sulphate (DXS) (5nmg/kg) on the subseguent 1 h localization of intravenously injected radiolabelled lymph node cells was investigated in complement deficient mice which lack C5.DXS proved to be equally as potent in depressing cell localizzation in deficient as compared to normal mice. These findings. indicate that the terminal complement components are not, essential for DXS activity.

RatónLymphocyteImmunologyCellCell CommunicationBiologyToxicologyMicechemistry.chemical_compoundCell MovementmedicineAnimalsLymphocytesComplement ActivationLymph nodePharmacologyComplement component 5Dextran SulfateComplement C5DextransBiological activityMolecular biologymedicine.anatomical_structureDextranMechanism of actionchemistryImmunologyFemaleLymph Nodesmedicine.symptomJournal of Immunopharmacology
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Reversible complexation of ethylene by a silylene under ambient conditions.

2014

Treatment of toluene solutions of the silylenes Si(SArMe6)2 (ArMe6 = C6H3-2,6(C6H2-2,4,6-Me3)2, 1) or Si(SArPri4)2 (ArPri4 = C6H3-2,6(C6H3-2,6-Pri2)2, 2) with excess ethylene gas affords the siliranes (ArMe6S)2tiebar above startSiCH2tiebar above endCH2 (3) or (ArPri4S)2tiebar above startSiCH2tiebar above endCH2 (4). Silirane 4 evolves ethylene spontaneously at room temperature in toluene solution. A Van’t Hoff analysis by variable-temperature 1H NMR spectroscopy showed that ΔGassn = −24.9(2.5) kJ mol–1 for 4. A computational study of the reaction mechanism using a model silylene Si(SPh)2 (Ph = C6H5) was in harmony with the Van’t Hoff analysis, yielding ΔGassn = −24 kJ mol–1 and an activatio…

Reaction mechanism1h nmr spectroscopyEthyleneChemistrySilyleneGeneral ChemistryActivation energymetallylene-isocyanide complexesPhotochemistryBiochemistryTolueneCatalysischemistry.chemical_compoundbonding analysisColloid and Surface Chemistrysitoutuminen (toiminta)ta116metallyleeni-isosyanidi -kompleksitJournal of the American Chemical Society
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Benzyl alcohol to benzaldehyde oxidation on MnOx clusters: Unraveling atomistic features

2021

Abstract The catalytic oxidation of benzyl alcohol with O 2 is a promising option for the production of benzaldehyde, from both environmental and economical viewpoints. In particular, highly dispersed MnO x systems feature good activity and selectivity in a wide range of temperatures, although deactivation phenomena by over-oxidation and/or poisoning of active sites are generally recorded. On this account, a density functional theory study was performed on cluster-sized catalyst models, namely Mn 4 O 8 and over-oxygenated Mn 4 O 9 fragments, to predict the reactivity pattern of MnO x catalysts in the selective aerobic oxidation of benzyl alcohol. Several pathways concur to determine the who…

Reaction mechanismCatalyst deactivationReaction mechanismsProcess Chemistry and TechnologyMnOx based catalystsPhotochemistryDFTCatalysisCatalysisBenzaldehydechemistry.chemical_compoundchemistryCatalytic oxidationBenzyl alcoholAlcohol oxidationCatalyst deactivation; DFT; MnO; x; based catalysts; Oxidative dehydrogenation; Reaction mechanismsReactivity (chemistry)Physical and Theoretical ChemistryOxidative dehydrogenationSettore CHIM/02 - Chimica FisicaBenzoic acidMolecular Catalysis
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From CO2 to dimethyl carbonate with dialkyldimethoxystannanes: the key role of monomeric species.

2011

International audience; The formation of dimethyl carbonate (DMC) from CO(2) and methanol with the dimer [n-Bu(2)Sn(OCH(3))(2)](2) was investigated by experimental kinetics in support of DFT calculations. Under the reaction conditions (357-423 K, 10-20 MPa), identical initial rates are observed with three different reacting mixtures, CO(2)/toluene, supercritical CO(2), and CO(2)/methanol, and are consistent with the formation of monomeric di-n-butyltin(iv) species. An intramolecular mechanism is, therefore, proposed with an Arrhenius activation energy amounting to 104 ± 10 kJ mol(-1) for DMC synthesis. DFT calculations on the [(CH(3))(2)Sn(OCH(3))(2)](2)/CO(2) system show that the exothermi…

Reaction mechanismDimerInorganic chemistryGeneral Physics and AstronomyCATALYSTSActivation energy010402 general chemistry01 natural sciencesMedicinal chemistryHOMOGENEOUS HYDROGENATIONCatalysischemistry.chemical_compoundsymbols.namesake[CHIM.ANAL]Chemical Sciences/Analytical chemistryReactivity (chemistry)Physical and Theoretical ChemistryCOORDINATION CHEMISTRYCOPOLYMERIZATIONCHALLENGES010405 organic chemistryOXIDEREACTIVITY0104 chemical sciencesGibbs free energy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryIntramolecular force[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbols[ CHIM.ANAL ] Chemical Sciences/Analytical chemistryMETAL-COMPLEXESDimethyl carbonateEPOXIDESDIOXIDE
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Regulatory effects of polyamines on membrane-bound acetylcholinesterase

1974

The effects of putrescene, spermidine and spermine on membrane-bound acetylcholinesterase from human erythrocyte ‘ghosts’ and the solubilized enzyme of the electric organ of the electric eel were studied by kinetic methods. Measurements were made by using a photometric method which made it possible to record the enzyme reaction in the steady-state phase. Substrate-concentration-dependent activation and inhibition of acetylcholinesterase by polyamines is similar to that by Na+, K+, Ca2+, Mg2+ and certain quaternary and bisquaternary amines. The kinetics suggest an allosteric reaction mechanism. On the basis of the kinetic results a role for the polyamines as modulators of synaptic acetylchol…

Reaction mechanismErythrocytesSpermidineKineticsAllosteric regulationSpermineBiochemistrychemistry.chemical_compoundAllosteric RegulationPolyaminesPutrescineAnimalsHumansMolecular Biologychemistry.chemical_classificationElectric OrganbiologyCellular Interactions and Control ProcessesCell MembraneCell Biologybiology.organism_classificationAcetylcholinesteraseElectric eelEnzyme ActivationSpermidineKineticsEnzymechemistryBiochemistryElectrophorusAcetylcholinesteraseSpermineCholinesterase InhibitorsBiochemical Journal
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