Search results for "anharmonicity"

showing 10 items of 118 documents

Density functional theory (DFT) prediction of structural and spectroscopic parameters of cytosine using harmonic and anharmonic approximations

2015

The applicability of popular and efficient B3LYP hybrid density functional and medium-size Pople-type basis set in combination with computationally expensive anharmonic model to obtain more accurate theoretical structure, vibrational frequencies and GIAO NMR parameters of cytosine was tested. We report on prediction of cytosine equilibrium (R e ) and rovibrationally averaged (R v ) structures and vibrational frequencies in the gas phase and DMSO solution using density functional theory combined with 6-311++G** basis set. The harmonic and anharmonic vibrational frequencies (using second-order vibrational perturbation theory, VPT2) were critically discussed. In comparison with initial harmoni…

ProtonBasis (linear algebra)Anharmonicityharmonic versus anharmonic frequenciesCondensed Matter PhysicsDFTMolecular physicschemistry.chemical_compoundGIAO NMRchemistryComputational chemistryHarmonicDensity functional theorystructurePhysics::Chemical PhysicsPhysical and Theoretical ChemistryPerturbation theorycytosineCytosineBasis setStructural Chemistry
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Analytic evaluation of the dipole Hessian matrix in coupled-cluster theory

2013

The general theory required for the calculation of analytic third energy derivatives at the coupled-cluster level of theory is presented and connected to preceding special formulations for hyperpolarizabilities and polarizability gradients. Based on our theory, we have implemented a scheme for calculating the dipole Hessian matrix in a fully analytical manner within the coupled-cluster singles and doubles approximation. The dipole Hessian matrix is the second geometrical derivative of the dipole moment and thus a third derivative of the energy. It plays a crucial role in IR spectroscopy when taking into account anharmonic effects and is also essential for computing vibrational corrections t…

Hessian matrixChemistryAnharmonicityGeneral Physics and AstronomyVDP::Mathematics and natural science: 400::Chemistry: 440::Theoretical chemistry quantum chemistry: 444Third derivativeMoment (mathematics)symbols.namesakeDipoleCoupled clusterClassical mechanicsPolarizabilityQuantum mechanicssymbolsNumerical differentiationPhysical and Theoretical ChemistryVDP::Matematikk og Naturvitenskap: 400::Kjemi: 440::Teoretisk kjemi kvantekjemi: 444
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A MRCI PS and CASSCF study of the ground state MgO dissociation energy

1991

Abstract Ab initio calculations at CASSCF and MRCI PS levels are used to determine the dissociation energy for the X 1 Σ + state of MgO, which adiabatically dissociates to the ground state 1 S g of magnesium and to the excited 1 D g state of oxygen, as well as other spectroscopic parameters. Emphasis is placed upon the problem of properly selecting an adequate active space in CASSCF calculations and upon the improvements obtained in MRCI by selecting perturbatively the most important contributions to the total wavefunction and evaluating the remaining ones only by perturbational method. Through a procedure based on stabilizing the computed dissociation energy, values of 3.87 eV (MRCI PS) an…

ChemistryComputational chemistryAb initio quantum chemistry methodsExcited stateAnharmonicityGeneral Physics and AstronomyRotational spectroscopyPhysical and Theoretical ChemistryAtomic physicsWave functionGround stateDiatomic moleculeBond-dissociation energyChemical Physics Letters
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Phase transition systematics in BiVO4 by means of high-pressure–high-temperature Raman experiments

2018

We report here high-pressure--high-temperature Raman experiments performed on ${\text{BiVO}}_{4}$. We characterized the fergusonite and scheelite phases (powder and single crystal samples) and the zircon polymorph (nanopowder). The experimental results are supported by ab initio calculations, which, in addition, provide the vibrational patterns. The temperature and pressure behavior of the fergusonite lattice modes reflects the distortions associated with the ferroelastic instability. The linear coefficients of the zircon phase are in sharp contrast to the behavior observed in the fergusonite phase. The boundary of the fergusonite-to-scheelite second-order phase transition is given by ${T}_…

Phase transitionMaterials scienceScatteringAnharmonicity02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyFergusonite01 natural sciences0104 chemical sciencesCrystallographysymbols.namesakeAb initio quantum chemistry methodsLattice (order)symbols0210 nano-technologyRaman spectroscopySingle crystalPhysical Review B
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Protein dynamics: conformational disorder, vibrational coupling and anharmonicity in deoxy-hemoglobin and myoglobin.

1993

In this work we study the temperature dependence of the Soret band lineshape of deoxymyoglobin and deoxyhemoglobin, in the range 300-20 K. To fit the measured spectra we use an approach originally proposed by Champion and coworkers (Srajer et al. 1986; Srajer and Champion 1991). The band profile is modelled as a Voigt function that accounts for the coupling with low frequency vibrational modes, whereas the coupling with high frequency modes is responsible for the vibronic structure of the spectra. Moreover, owing to the position of the iron atom out of the mean heme plane, inhomogeneous broadening brings about a non-Gaussian distribution of 0-0 electronic transition frequencies. The reporte…

Voigt profileChemical PhenomenaChemistry PhysicalMyoglobinProtein ConformationProtein dynamicsAnharmonicityBiophysicsTemperatureDynamic properties Heme proteins Optical spectroscopyGeneral MedicineMolecular physicsMolecular electronic transitionSpectral linechemistry.chemical_compoundHemoglobinsNuclear magnetic resonanceMyoglobinchemistrySpectrophotometryMolecular vibrationAnimalsThermodynamicsRotational–vibrational couplingEuropean biophysics journal : EBJ
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Berry Phase and Parametric Harmonic Oscillator

2001

Our concern in this section is once more with the time-dependent harmonic oscillator with Lagrangian $$\displaystyle{ L = \frac{1} {2}\dot{x}^{2} -\frac{1} {2}\omega ^{2}(t)x^{2}\;. }$$ To present a coherent picture of the whole problem, let us briefly review some of the results of Chap. 21. There we found the propagation function

Section (fiber bundle)PhysicsVackář oscillatorGeometric phaseQuantum mechanicsAnharmonicityFunction (mathematics)Parametric oscillatorOmegaHarmonic oscillator
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Estimation of formamide harmonic and anharmonic modes in the Kohn-Sham limit using the polarization consistent basis sets.

2010

Formamide harmonic and anharmonic frequencies of fundamental vibrations in the gas phase and in several solvents were successfully estimated in the B3LYP Kohn-Sham complete basis set limit (KS CBS). CBS results were obtained by extrapolating a power function (two-parameter formula) to the results calculated with polarization-consistent basis sets. Anharmonic corrections using the second order perturbation treatment (PT2) and hybrid B3LYP functional combined with polarization consistent pc-n (n = 0, 1, 2, 3, 4) and several Pople’s basis sets were analyzed for all fundamental formamide vibrational modes in the gas phase and solution. Solvent effects were modeled within a PCM method. The anhar…

FormamideAcetonitrilesMolecular ConformationAnharmonic vibrationSolvent effectMolecular physicsCatalysisInorganic ChemistryAcetonechemistry.chemical_compoundComputational chemistryScissoringHexanesComputer SimulationDimethyl SulfoxideHarmonic vibrationPhysical and Theoretical ChemistryPhysics::Chemical PhysicsCarbon TetrachlorideBasis setQuantitative Biology::BiomoleculesOriginal PaperFormamidesOrganic ChemistryAnharmonicityWaterComplete basis set limitFormamideComputer Science ApplicationsComputational Theory and MathematicschemistryModels ChemicalMolecular vibrationHarmonicSolventsThermodynamicsFermi resonanceChloroformGasesSolvent effectsJournal of molecular modeling
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The Equilibrium Structure of Benzene

2000

The re structure of benzene is revised on the basis of high-level quantum chemical calculations at the CCSD(T)/cc-pVQZ level as well a reanalysis of the experimental rotational constants using computed vibrational corrections. A least-squares fit to empirically determined Be constants yields re(CC) = 1.3914 ± 0.0010 A and re(CH) = 1.0802 ± 0.0020 A; the latter distance is significantly shorter than the best previous estimate based on experimental data. Comparison of computed rg and rz distances with experiment as well as considerations of bond lengthening due to anharmonicity are consistent with the estimated re distance, indicating that the recommended structural parameters are very accura…

Quantum chemicalchemistry.chemical_compoundchemistryBasis (linear algebra)AnharmonicityStructure (category theory)ThermodynamicsPhysical and Theoretical ChemistryBenzeneThe Journal of Physical Chemistry A
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Inelastic neutron scattering study of proton dynamics in Ca(OH)2 at 20 K

1995

Abstract Inelastic neutron scattering (INS) spectra of Ca(OH) 2 at 20 K are presented from 30 to 4000 cm −1 for a powder sample, from 30 to 12000 cm −1 for an oriented single-crystal. INS band splitting due to the lattice density-of-states is observed. Polarization effects reveal the orientation of atomic displacements for each mode and a new band assignment scheme is proposed. For the single-crystal, the v OH mode and overtones are observed. This oscillator shows only moderate anharmonicity. Spectrum simulation reveals that INS spectral intensities are not consistent with simple normal coordinates and harmonic force-fields for Ca(OH) 2 entities. A new dynamical model is proposed, including…

010304 chemical physicsInfraredChemistryAnharmonicityGeneral Physics and Astronomy02 engineering and technology021001 nanoscience & nanotechnologyPolarization (waves)01 natural sciencesMolecular physicsSpectral lineInelastic neutron scatteringsymbols.namesakeCrystallographyLattice (order)0103 physical sciencessymbolsNormal coordinates[CHIM]Chemical SciencesPhysical and Theoretical Chemistry0210 nano-technologyRaman spectroscopyComputingMilieux_MISCELLANEOUS
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Theoretical investigation of the potential energy surface of the van der Waals complex CH4-N-2

2009

International audience; The interaction potential energy surface of the van der Waals CH4-N-2 complex has been calculated for a broad range of intermolecular separations and configurations in the approximation of rigid interacting molecules at the CCSD(T) and MP2 levels of theory using the correlation consistent aug-cc-pVTZ basis set. The BSSE correction was taken into account for all the calculations. The most stable configurations of the complex were found. Binding energies were calculated in the CBS limit with accounting for the molecular deformations. The harmonic and anharmonic fundamental vibrational frequencies and rotational constants for the ground and first excited vibrational sta…

010304 chemical physicsChemistryBinding energyIntermolecular forceAnharmonicityVan der Waals surfaceGeneral Physics and Astronomy010402 general chemistry01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistrysymbols.namesakeLennard-Jones potentialExcited state0103 physical sciencesPotential energy surface[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsPhysics::Atomic and Molecular ClustersPhysical and Theoretical Chemistryvan der Waals forceAtomic physicsPhysics::Chemical Physics
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