Search results for "potential energy"

showing 10 items of 274 documents

Theoretical study of the NH tautomerism in free base porphyrin

1997

Abstract The NH tautomerism of free base porphyrin is investigated at the semiempirical spin-unrestricted AM1 (UAM1) and ab initio RHF/3-21G levels. The UAM1 method provides delocalized geometries for all stationary structures without imposing any symmetry constraint. RHF/3-21G geometry optimizations have to be performed under symmetry restrictions to ensure that realistic delocalized structures are obtained. Both the semiempirical and the ab initio calculations predict that the interconversion between trans tautomers proceeds in an asynchronous two-step process via intermediate cis tautomers. The cis tautomers are characterized as minima in the potential energy surface and are 8–10 kcal m…

Ab initioFree baseActivation energyCondensed Matter PhysicsBiochemistryPorphyrinTautomerchemistry.chemical_compoundDelocalized electronchemistryComputational chemistryAb initio quantum chemistry methodsPotential energy surfacePhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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Ab Initio Study on the Mechanism of the Reactions of the Nitrate Radical with Haloalkenes:  1,2-Dichloroethene, 1,1-Dichloroethene, Trichloroethene, …

2000

A general mechanism for the reactions of the NO3 radical with 1,2-dichloroethene, 1,1-dichloroethene, trichloroethene, and tetrachloroethene is proposed from ab initio DFT calculations. The calculated mechanism shows three main parallel reaction pathways. For the systems where the two carbon atoms are differently substituted, the study includes both the attacks with Markownikoff and contra-Markownikoff orientation. The first reaction pathway leads to the formation of an epoxide along with the NO2 radical, the second one to the formation of carbonyl compounds, and the third one leads, through the cleavage of the C−C bond, to the formation of carbonyl compounds with a lower number of carbon a…

Ab initiochemistry.chemical_elementEpoxidePhotochemistry12-Dichloroethene11-Dichloroethenechemistry.chemical_compoundchemistryComputational chemistryPotential energy surfaceDensity functional theoryPhysical and Theoretical ChemistryCarbonBasis setThe Journal of Physical Chemistry A
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Conformational studies into N-methylation of alanine diamide models: A quantitative approach

2006

Abstract A systematic theoretical analysis was performed on N -acetyl- l -alanine N ′-methylamide (Ac- l -Ala-NHMe) and the analogues methylated on the N-terminus (Ac- l -(Me)Ala-NHMe), C-terminus (Ac- l -Ala-NMe 2 ), and both N/C-termini (Ac- l -(Me)Ala-NMe 2 ), to evaluate the influence of methylation of the amide group on the conformational properties of the affected residues. The ϕ , ψ potential energy surfaces were calculated at the B3LYP/6-31+G**//HF/3-21G level of theory with inclusion of the solvent (water) effect (SCRF method). The conformers localised were fully optimised at the B3LYP/6-31+G** in vacuo. The accessible areas of the potential energy surfaces; the number of conformer…

AlanineHydrogen bondStereochemistryCondensed Matter PhysicsBiochemistrySolventchemistry.chemical_compoundchemistryAmidePotential energy surfacePeptide bondMoleculePhysical and Theoretical ChemistryConformational isomerismJournal of Molecular Structure: THEOCHEM
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The Ã 1Au state and the T2 potential surface of acetylene: Implications for triplet perturbations in the fluorescence spectra of the à state

1996

The cis–trans isomerization reaction on the T2 surface of acetylene and the lowest excited singlet state of acetylene, A 1Au, are investigated by ab initio electronic structure theory. We report optimized geometries, dipole moments, and harmonic vibrational frequencies of stationary points and adiabatic energy differences between them using basis sets as large as triple‐ζ plus double polarization with higher angular momentum functions, TZ(2df,2pd), and theoretical methods up to coupled‐cluster singles and doubles with a perturbative triples correction [CCSD(T)] and the equation‐of‐motion coupled‐cluster method (EOM‐CCSD). Our theoretical predictions should aid the interpretation of observat…

Angular momentumZeeman effectChemistryAb initioGeneral Physics and AstronomyElectronic structureQuantum chemistryPotential energyDipolesymbols.namesakechemistry.chemical_compoundAcetylenePhysics::Atomic and Molecular ClusterssymbolsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsThe Journal of Chemical Physics
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Experimental and Theoretical Studies of Nonclassical d 0 Cyclopentadienyl Polyhydride Complexes of Molybdenum and Tungsten

1998

Low-temperature protonation of compounds Cp{sup *}MH{sub 5}(PMe{sub 3}) (M = Mo, 1; W, 2) by HBF{sub 4}{center_dot}Et{sub 2}O in CD{sub 2}Cl{sub 2} or CDFCl{sub 2} affords the thermally unstable hexahydride derivatives [Cp{sup *}MH{sub 6}(PMe{sub 3})]{sup +} (M = Mo, 3; W, 4). The corresponding protonation of 1- and 2-d{sup 5} affords 3- and 4-d{sup 5}, respectively. The {Delta}{delta} on going from H{sub 6} to HD{sub 5} is small for both compounds, but positive for 3 and negative for 4, and no isotopic perturbation of resonance (IPR) is observed. The T{sub 1min} at 400 MHz for [Cp{sup *}MH{sub 6}(PMe{sub 3})]{sup +} apparently doubles on going from Mo to W (52 ms for 3 and approximately 10…

AnionsReaction mechanismschemistry.chemical_elementProtonation010402 general chemistryLigands01 natural sciencesInorganic ChemistryCyclopentadienyl complexChemical structureMathematical methodsComputational chemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryHydrideOrganic Chemistry3. Good health0104 chemical sciencesCrystallographychemistryChemical bondMolybdenumPotential energy surfaceDihydrogen complex
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Gradient elasticity and nonstandard boundary conditions

2003

Abstract Gradient elasticity for a second gradient model is addressed within a suitable thermodynamic framework apt to account for nonlocality. The pertinent thermodynamic restrictions upon the gradient constitutive equations are derived, which are shown to include, besides the field (differential) stress–strain laws, a set of nonstandard boundary conditions. Consistently with the latter thermodynamic requirements, a surface layer with membrane stresses is envisioned in the strained body, which together with the above nonstandard boundary conditions make the body constitutively insulated (i.e. no long distance energy flows out of the boundary surface due to nonlocality). The total strain en…

Applied MathematicsMechanical EngineeringConstitutive equationGeometryMechanicsEquilibrium equationCondensed Matter PhysicsTotal strainMinimum total potential energy principleQuantum nonlocalityMechanics of MaterialsModeling and SimulationGeneral Materials ScienceBoundary value problemSurface layerElasticity (economics)MathematicsInternational Journal of Solids and Structures
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Temperature at Small Scales: A Lower Limit for a Thermodynamic Description

2011

We analyze the concept of equilibrium temperature in a set of interacting argon atoms, confined in a nanostructure, a zeolite with an intricate distribution of channels through which the atoms may move. The temperature is computed following two procedures: by averaging over the kinetic energy of the particles and over the forces acting on them. It is shown that for external surfaces and for regions which do not fall under the whole pattern of potential energy distribution, smaller than a quarter of a crystal unit cell, both temperatures, kinetic and configurational, show significant differences. The configurational temperature accounts for the different interactions on the particles in the …

ArgonNanostructureMean kinetic temperatureThermodynamic equilibriumchemistry.chemical_elementThermodynamicsKinetic energyPotential energySurfaces Coatings and FilmsCrystalchemistryNano-Materials ChemistryPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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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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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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Argon broadening of the 13CO R(0) and R(7) transitions in the fundamental band at temperatures between 80 and 297K: comparison between experiment and…

2003

We present measurements of Ar-broadening parameters for the R(0) and R(7) lines in the fundamental band of13CO at eight temperatures from 80 to 297 K. The broadening parameters are determined by simultaneous least-squares fitting of spectra recorded using a frequency stabilized diode laser spectrometer. The comparison of the broadening parameter values for R(7) derived at room temperature and different pressures from different line profiles shows that an empirical line profile, which takes into account narrowing effects (Dicke narrowing and absorber speed dependence) but neglects any correlation between collisions, is able to describe the observed lines with constant values of the narrowing…

Atomic and Molecular Physics and OpticArgonMaterials sciencebusiness.industryTunable diode laserAb initiochemistry.chemical_elementAtomic and Molecular Physics and OpticsSpectral lineOpticschemistryPotential energy surfaceLow temperatureLine broadeningPhysical and Theoretical ChemistryAtomic physicsCarbon monoxideSpectroscopyHomogeneous broadeningbusinessSpectroscopyLine (formation)Doppler broadeningJournal of Molecular Spectroscopy
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