Search results for "anharmonicity"

showing 10 items of 118 documents

Vibrational spectra and force constants of symmetric tops

1983

The infrared spectrum of H3SiI in the 800–1050 cm-1 region has been recorded with a resolution of 0·04 cm-1 and rotationally analysed. Features related to the Fermi resonance between v 5 and v 3 + v 6 and to the Coriolis x, y resonance between v 2 and v 5 have been explained, and a set of vibration-rotation parameters for the three bands has been determined by least-squares calculations, σ(J, K) = 9·4 × 10-3 cm-1. The Fermi resonance matrix element |W 356| is found to be 3·7859(7) cm-1 and the vibrational frequencies are v 2 0 = 904·551(1), v 5 0 = 941·0746(8) and (v 3 + v 6)0 = 953·688(3) cm-1. The anharmonicity constant, x 36 = -1·745(9) cm-1, has been determined. Comparison is made with …

Force constantInfraredChemistryAnharmonicityResolution (electron density)BiophysicsAnalytical chemistryResonanceCondensed Matter PhysicsMatrix elementFermi resonancePhysical and Theoretical ChemistryAtomic physicsMolecular BiologyVibrational spectraMolecular Physics
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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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Dynamics of myoglobin in confinement: An elastic and quasi-elastic neutron scattering study

2008

In order to clarify the role of hard confinement on protein dynamics, elastic and quasi-elastic neutron scattering experiments have been performed on ferric horse myoglobin in two different systems: the protein embedded in a porous silica matrix, and the corresponding hydrated protein powder. Elastic data have been analysed using two different models (dynamical heterogeneity and anharmonic double-well potential) that take into account deviations of elastic intensity from Gaussian behaviour. The profile of quasi-elastic spectra has been approximated by a combination of Lorentzian and Gaussian components. Comparison between the data relative to the two different samples indicates that geometr…

GLASS-TRANSITIONGaussianGeneral Physics and AstronomyHydrationNeutron scatteringSol–gelMYELIN BASIC-PROTEINMolecular physicsSpectral linesymbols.namesakechemistry.chemical_compoundDynamical heterogeneityPhysical and Theoretical ChemistryPorosityHEMOGLOBINSOLVENTQuantitative Biology::BiomoleculesProtein dynamicsAnharmonicitySolvent dynamicCrystallographyMyoglobinchemistrysymbolsProtein dynamicSilica hydrogels
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Thermal broadening of the Soret band in heme complexes and in heme-proteins: role of iron dynamics

1994

We report the thermal broadening of the Soret band in heme-CO, heme-OH and protoporphyrin IX in the temperature range 300-20 K. For protoporphyrin IX the temperature dependent Gaussian line broadening follows the behavior predicted by the harmonic approximation in the entire temperature range investigated. In contrast, for heme-CO and heme-OH the harmonic behavior is obeyed only up to about 180 K and an anomalous line broadening increase is observed at higher temperatures. This effect is attributed to the onset of anharmonic motions of the iron atom with respect to the porphyrin plane. Comparison with previously reported analogous data for heme proteins enables us to suggest that the onset …

HemeproteinsHot TemperatureHemeproteinIronBiophysicsProtoporphyrinsHemePhotochemistryMolecular physicsHemoglobinschemistry.chemical_compoundAtomAnimalsHemeProtoporphyrin IXMyoglobinProtein dynamicsAnharmonicityGeneral MedicineAtmospheric temperature rangePorphyrinCarboxyhemoglobinchemistrySpectrophotometryThermodynamicsCattleEuropean Biophysics Journal
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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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Anharmonicity modeling in hydrogen bonded solvent dimers

2021

Abstract Harmonic and anharmonic frequencies of dimers and mixed dimers of water, methanol and benzene were computed and the results were critically analysed to investigate the anharmonicity of the normal mode vibrations within density functional theory (DFT) with empirically included Grimme correction for dispersion (D3). From several options, the B3LYP-D3/6-31++G* level of theory was selected as a good compromise between accuracy and calculation speed, suitable for future modeling of larger solvent clusters. The obtained raw harmonic and anharmonic second-order perturbation theory of vibrational frequencies (VPT2) were additionally scaled using a two-range procedure (below and above 2000 …

Hydrogenchemistry.chemical_element02 engineering and technology010402 general chemistryDFT01 natural sciencesMolecular physicsQuality (physics)Normal modePhysics::Atomic and Molecular ClustersMaterials ChemistryVPT2Physics::Chemical PhysicsPhysical and Theoretical ChemistryPerturbation theorySpectroscopyPhysicsAnharmonicity021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and OpticsFrequency scaling0104 chemical sciencesElectronic Optical and Magnetic MaterialsVibrationchemistrySolvent dimersHarmonicH-BondingDensity functional theoryAnharmonic vibrational frequencies0210 nano-technologyJournal of Molecular Liquids
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On the electronic coupling of the C=O stretching vibrations in Cl(2)Pt(malonate)(-).

2001

Ab initio calculations on the complex Cl(2)Pt(malonate)(-) have been performed to estimate the magnitude and the source of the splitting between the symmetric and antisymmetric C=O stretches. It is shown that a large part of the splitting can result from pure electronic coupling mediated via the pi-structure of the ligand. Calculations have also been performed on the free ligand malonate(-) and the neutral malonaldehyde that show decreasing electronic coupling, which is consistent with the decreasing resonance stabilization. A simple effective C=O interaction potential has been produced for Cl(2)Pt(malonate)(-) that is used to estimate the electronic splitting of the 1600 cm(-1) IR band to …

Inorganic ChemistryVibrationCouplingchemistry.chemical_compoundCrystallographyInteraction potentialMalonatechemistryLigandAb initio quantum chemistry methodsAnharmonicityPhysical and Theoretical ChemistryPhotochemistryInorganic chemistry
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Lagrangian dynamics and possible isochronous behavior in several classes of non-linear second order oscillators via the use of Jacobi last multiplier

2015

Abstract In this paper, we employ the technique of Jacobi Last Multiplier (JLM) to derive Lagrangians for several important and topical classes of non-linear second-order oscillators, including systems with variable and parametric dissipation, a generalized anharmonic oscillator, and a generalized Lane–Emden equation. For several of these systems, it is very difficult to obtain the Lagrangians directly, i.e., by solving the inverse problem of matching the Euler–Lagrange equations to the actual oscillator equation. In order to facilitate the derivation of exact solutions, and also investigate possible isochronous behavior in the analyzed systems, we next invoke some recent theoretical result…

Isochronous dynamicConservation lawApplied MathematicsMechanical EngineeringMathematical analysisAnharmonicityIsotonic potentialJacobi Last Multiplier (JLM)Simple harmonic motionInverse problemMultiplier (Fourier analysis)Nonlinear systemsymbols.namesakeSimple harmonic oscillatorMechanics of MaterialssymbolsNoether's theoremSettore MAT/07 - Fisica MatematicaLagrangianConservation lawsVariable (mathematics)MathematicsInternational Journal of Non-Linear Mechanics
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The equilibrium structure and fundamental vibrational frequencies of dioxirane

1998

Complete sets of quadratic and cubic force constants calculated for four isotopomers of dioxirane (CH2OO) are used to estimate vibration-rotation interaction contributions to observed values of rotational constants (B″), thereby yielding empirical estimates of the corresponding equilibrium values (Be). At the highest levels of theory, least-squares refinements of atomic coordinates to both the empirical Be values and the associated isotope shifts yield consistent sets of structural parameters. Recommended values are re(CO)=1.3846±0.0005 A; re(OO)=1.5133±0.0005 A; re(CH)=1.0853±0.0015 A and θe(HCH)=117.03±0.20°. Semidiagonal quartic force constants (in the normal coordinate representation) a…

IsotopeInfraredAnharmonicityGeneral Physics and AstronomyThermodynamicsIsotopomerschemistry.chemical_compoundQuadratic equationDioxiranechemistryComputational chemistryQuartic functionPhysical and Theoretical ChemistryRepresentation (mathematics)The Journal of Chemical Physics
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Predicting the structure and vibrational frequencies of ethylene using harmonic and anharmonic approaches at the Kohn–Sham complete basis set limit

2016

In this work, regular convergence patterns of the structural, harmonic, and VPT2-calculated anharmonic vibrational parameters of ethylene towards the Kohn–Sham complete basis set (KS CBS) limit are demonstrated for the first time. The performance of the VPT2 scheme implemented using density functional theory (DFT-BLYP and DFT-B3LYP) in combination with two Pople basis sets (6-311++G** and 6-311++G(3df,2pd)), the polarization-consistent basis sets pc-n, aug-pc-n, and pcseg-n (n = 0, 1, 2, 3, 4), and the correlation-consistent basis sets cc-pVXZ and aug-cc-pVXZ (X = D, T, Q, 5, 6) was tested. The BLYP-calculated harmonic frequencies were found to be markedly closer than the B3LYP-calculated h…

Kohn–Sham equationsAnharmonic vibrationPolarization-consistent basis sets010402 general chemistry01 natural sciencesDFTSTO-nG basis setsCatalysisCBSInorganic ChemistryEthyleneQuantum mechanicsCorrelation-consistent basis sets0103 physical sciencesLimit (mathematics)Physical and Theoretical ChemistryVPT2Basis setPhysicsOriginal Paper010304 chemical physicsBasis (linear algebra)AnharmonicityOrganic Chemistry0104 chemical sciencesComputer Science ApplicationsComputational Theory and MathematicsHarmonicDensity functional theoryJournal of Molecular Modeling
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