Search results for "transition"

showing 10 items of 3988 documents

Application of SQMFF Vibrational Calculations to Transition States:  DFT and ab Initio Study of the Kinetics of Methyl Azide and Ethyl Azide Thermoly…

1998

DFT including nonlocal corrections and ab initio calculations at MP2 and MP4 levels of theory have been performed in order to provide information concerning the mechanism of the rate limiting step of the thermal decomposition of methyl azide and ethyl azide. The chemically interesting points of the ground-state potential energy surface have been fully optimized, and a detailed normal-mode analysis for the reagents and the transition states is presented. The well-established scaled quantum mechanical force field method has been used to obtain reliable vibrational frequencies for these molecular structures. The force fields of transition states have been modified by using the scale factors co…

Arrhenius equationAb initioThermodynamicsTransition statesymbols.namesakeTransition state theorychemistry.chemical_compoundchemistryAb initio quantum chemistry methodsComputational chemistryPotential energy surfacesymbolsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryGround stateMethyl azideThe Journal of Physical Chemistry A
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Determination of the glass transition temperature of poly(cyclohexyl acrylate) from oxygen permeability measurements

1993

Abstract The glass transition temperature ( T g ) of poly(cyclohexyl acrylate) (PCA) has been obtained from measurements of the oxygen permeability ( P = 0.60 barrers, T g = 23.5 ± 2.0°C) using a potentiostatic electrochemical sensor, and from the oxygen diffusion coefficient ( D = 0.12 × 10 −8 cm 2 s −1 , T g = 24.0 ± 1.8°C) by the time-lag method. A T g of 25 ± 1°C was found by differential scanning calorimetry and a T g of 25.0 ± 3.5°C was obtained from the specific volume by dilatometry. The fractional free volume ( v f ) at T g is 0.020 ± 0.002, which is slightly below (∼ 20%) most glassy polymers. A linear correlation has been observed between ln D and the reciprocal of v f , which su…

Arrhenius equationAcrylatePolymers and PlasticsDiffusionOrganic ChemistryAnalytical chemistrychemistry.chemical_elementActivation energyOxygensymbols.namesakeOxygen permeabilitychemistry.chemical_compoundDifferential scanning calorimetrychemistryPolymer chemistryMaterials ChemistrysymbolsGlass transitionPolymer
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Role of vitreous matrix on the optical activity of Ge-doped silica

2003

Abstract We report an experimental study on the relationship between the optical activity of Ge-oxygen deficient centers and dynamic properties and conformational heterogeneity of vitreous matrix in silica. We focus our attention on the absorption band at ∼5.2 eV (B 2β ) and on the two related emissions at ∼4.2 eV (α E ) and at ∼3.1 eV (β). From the temperature dependence of B 2β band we estimate a mean energy value of 26 meV for local vibrational modes coupled to the electronic transition, suggesting that the chromophore and its surrounding have access to low frequency dynamics. From the thermal behavior of the two emissions we distinguish the two competitive relaxation processes from the …

Arrhenius equationChemistryRelaxation (NMR)General ChemistryActivation energyChromophoreCondensed Matter PhysicsMolecular physicsMolecular electronic transitionsymbols.namesakeNuclear magnetic resonanceAbsorption bandExcited statesymbolsGeneral Materials ScienceTriplet stateJournal of Physics and Chemistry of Solids
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A theory ofnonverticaltriplet energy transfer in terms of accurate potential energy surfaces: The transfer reaction from π,π* triplet donors to 1,3,5…

2004

Triplet energy transfer (TET) from aromatic donors to 1,3,5,7-cyclooctatetraene (COT) is an extreme case of "nonvertical" behavior, where the transfer rate for low-energy donors is considerably faster than that predicted for a thermally activated (Arrhenius) process. To explain the anomalous TET of COT and other molecules, a new theoretical model based on transition state theory for nonadiabatic processes is proposed here, which makes use of the adiabatic potential energy surfaces (PES) of reactants and products, as computed from high-level quantum mechanical methods, and a nonadiabatic transfer rate constant. It is shown that the rate of transfer depends on a geometrical distortion paramet…

Arrhenius equationGeneral Physics and AstronomyTriplet stateMolecular configurationsAcceptorPotential energyGround statesUNESCO::FÍSICA::Química físicaCyclooctatetraenechemistry.chemical_compoundsymbols.namesakeTransition state theoryOrganic compounds ; Potential energy surfaces ; Triplet state ; Ground states ; Molecular configurationschemistryPotential energy surfacesOrganic compoundssymbolsMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryTriplet stateAtomic physics:FÍSICA::Química física [UNESCO]Adiabatic processThe Journal of Chemical Physics
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Solidification behavior of the theta system 2-propanol/poly(n-butyl methacrylate) I. Influences of thermoreversible gelation on stationary flow

1994

Zero shear viscosities, η0, were determined by means of a magnetoviscometer for melts of poly(n-butyl methacrylate) (M = 8.7 to 450 kg/mol, T =53.5 to 200°C) and for concentrated solutions of the highest molecular weight sample in isopropanol (T = 34.8 to 131.5 °C). Master curves can be constructed in both cases if the reference temperature is set proportional to the gelation temperature of the particular fluid. Special intersegmental interactions (eventually leading to thermoreversible gelation) can above all be felt in η0 (T) and in M c , the critical molecular weight determined in plots of log η0 vs. log M. As the temperature is lowered, the behavior changes from WLF to Arrhenius, and M …

Arrhenius equationMaterials scienceTheta solventThermodynamicsCondensed Matter PhysicsMethacrylatePoly n-butyl methacrylatePropanolShear (sheet metal)symbols.namesakechemistry.chemical_compoundchemistryPolymer chemistrysymbolsStationary flowGeneral Materials ScienceGlass transitionRheologica Acta
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Dynamics of spin state conversion processes in the solid state

1989

High spin (HS) ⇌ low spin (LS) conversions in transition metal complexes are nonradiative transitions between spin states. In this contribution, we present a study of the temperature and pressure dependence of the HS ⇌ LS intersystem crossing dynamics. For some iron(II) spin-crossover complexes, the rate constants were determined by line shape analysis of57Fe Mossbauer spectra. Their temperature dependence is described by an Arrhenius equation, their pressure dependence is interpreted within absolute rate theory. HS → LS conversion rates at low temperatures were determined from the relaxation of light-induced formation of HS states, monitored by optical spectroscopy. Deviations from a simpl…

Arrhenius equationNuclear and High Energy PhysicsSpin statesChemistryThermodynamicsCondensed Matter PhysicsAtomic and Molecular Physics and Opticssymbols.namesakeReaction rate constantIntersystem crossingTransition metalComputational chemistrysymbolsPhysical and Theoretical ChemistrySpectroscopyQuantum tunnellingShape analysis (digital geometry)Hyperfine Interactions
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Dipolar and orientational glass formation in two-dimensional films of CO mixtures

2002

Heat-capacity and dielectric measurements have been performed to study orientational and dipolar order and disorder phenomena in submonolayer films of CO and binary mixtures of CO physisorbed on graphite and boron nitride (BN). With both methods transitions to quadrupolar and dipolar ordered low-temperature phases have been found for pure CO. Calorimetric measurements revealed that the dipolar transition of CO on graphite belongs to the universality class of the two-dimensional (2D) Ising model. It will be shown that in dilute mixtures of CO with CH 4 molecules a dramatic suppression of this phase transition occurs. This effect turned out to be much stronger than that previously observed in…

Arrhenius equationPhase transitionCondensed matter physicsChemistryDielectricCondensed Matter PhysicsElectronic Optical and Magnetic Materialssymbols.namesakechemistry.chemical_compoundBoron nitrideImpurityChemical physicsMaterials ChemistryCeramics and CompositessymbolsIsing modelGraphiteOrientational glassJournal of Non-Crystalline Solids
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Memory effects and coverage dependence of surface diffusion in a model adsorption system

1999

We study the coverage dependence of surface diffusion coefficients for a strongly interacting adsorption system O/W(110) via Monte Carlo simulations of a lattice-gas model. In particular, we consider the nature and emergence of memory effects as contained in the corresponding correlation factors in tracer and collective diffusion. We show that memory effects can be very pronounced deep inside the ordered phases and in regions close to first and second order phase transition boundaries. Particular attention is paid to the details of the time dependence of memory effects. The memory effect in tracer diffusion is found to decay following a power law after an initial transient period. This beha…

Arrhenius equationPhysicsSurface diffusionPhase transitionCondensed matter physicsPhysicsMonte Carlo method02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesPower lawMonte Carlo simulationslattice-gas modelsymbols.namesakeExponential growth0103 physical sciencessymbolssurface diffusion coefficientsDiffusion (business)Exponential decay010306 general physics0210 nano-technologyadsorption systemsPhysical Review B
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Fragmentation of polycarbonate macroinitiators in solution and in the bulk state

1990

The diphenylethane initiator 3,4-diethyl-3,4-(p-methoxyphenyl)-hexane (T–OCH3) was synthesized. By cocondensation of bisphenol A or C and the bisphenol derivative (“T”) of T–OCH3 with phosgene, polycarbonate macroinitiators PC(TxA1-x) and PC(TxC1-x) with different compositions x were made. The thermal fragmentation of T–OCH3 and the copolycarbonates was investigated with and without a radical scavenger both in solution and in the bulk state. The primary dissociation of T–OCH3 is a monomolecular Arrhenius process with a characteristic temperature of T* (τ = 1h) = 140°C (τ: average life time of the intact molecule). When the radicals are not intercepted, the dissociation is excessively revert…

Arrhenius equationPolymers and PlasticsChemistryRadicalActivation energyCondensed Matter PhysicsDissociation (chemistry)symbols.namesakeFragmentation (mass spectrometry)visual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumsymbolsPhysical and Theoretical ChemistryPolycarbonateRadical disproportionationGlass transitionJournal of Polymer Science Part B: Polymer Physics
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Global exponential stability of delayed Markovian jump fuzzy cellular neural networks with generally incomplete transition probability

2014

The problem of global exponential stability in mean square of delayed Markovian jump fuzzy cellular neural networks (DMJFCNNs) with generally uncertain transition rates (GUTRs) is investigated in this paper. In this GUTR neural network model, each transition rate can be completely unknown or only its estimate value is known. This new uncertain model is more general than the existing ones. By constructing suitable Lyapunov functionals, several sufficient conditions on the exponential stability in mean square of its equilibrium solution are derived in terms of linear matrix inequalities (LMIs). Finally, a numerical example is presented to illustrate the effectiveness and efficiency of our res…

Artificial neural networkMarkov chainCognitive NeuroscienceTransition rate matrixMarkov ChainsMarkovian jumpLyapunov functionalExponential stabilityArtificial IntelligenceControl theoryFuzzy cellular neural networksApplied mathematicsNeural Networks ComputerEquilibrium solutionAlgorithmsMathematicsNeural Networks
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