Search results for "diatomic molecule"

showing 10 items of 86 documents

Molecular equilibrium structures from experimental rotational constants and calculated vibration–rotation interaction constants

2002

A detailed study is carried out of the accuracy of molecular equilibrium geometries obtained from least-squares fits involving experimental rotational constants B(0) and sums of ab initio vibration-rotation interaction constants alpha(r)(B). The vibration-rotation interaction constants have been calculated for 18 single-configuration dominated molecules containing hydrogen and first-row atoms at various standard levels of ab initio theory. Comparisons with the experimental data and tests for the internal consistency of the calculations show that the equilibrium structures generated using Hartree-Fock vibration-rotation interaction constants have an accuracy similar to that obtained by a dir…

FREQUENCIESChemistryGAUSSIAN-BASIS SETSAb initioGeneral Physics and AstronomyDiatomic moleculeSTATEBORONBond lengthVibrationHOFMETHANEMolecular geometryCCSD(T) 2ND DERIVATIVESAb initio quantum chemistry methodsACIDWAVE-FUNCTIONSPhysics::Atomic and Molecular ClustersMoleculeQUARTIC FORCE-FIELDPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsRotation (mathematics)The Journal of Chemical Physics
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Quantum-chemical calculation of Born–Oppenheimer breakdown parameters to rotational constants

2010

The paper describes how Born–Oppenheimer breakdown parameters for the rotational constants of diatomic molecules can be determined via quantum-chemical computations. The deviations from the Born–Oppenheimer equilibrium values are accounted for by considering the adiabatic correction to the equilibrium bond distances, the electronic contribution to the rotational constant via the rotational g tensor, and the so-called Dunham correction, which can be computed directly from a polynomial expansion of the potential curve around the equilibrium distance. Calculations for HCl, SiS, and HF demonstrate the accuracy that can be achieved in the theoretical treatment of the considered Born–Oppenheimer …

Field (physics)ChemistryBiophysicsBorn–Oppenheimer approximationRotational transitionRotational temperatureCondensed Matter PhysicsDiatomic moleculesymbols.namesakesymbolsRotational spectroscopyPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsRotational partition functionAdiabatic processMolecular BiologyMolecular Physics
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Levels of self-consistency in the GW approximation

2009

We perform $GW$ calculations on atoms and diatomic molecules at different levels of self-consistency and investigate the effects of self-consistency on total energies, ionization potentials and on particle number conservation. We further propose a partially self-consistent $GW$ scheme in which we keep the correlation part of the self-energy fixed within the self-consistency cycle. This approximation is compared to the fully self-consistent $GW$ results and to the $G W_0$ and the $G_0W_0$ approximations. Total energies, ionization potentials and two-electron removal energies obtained with our partially self-consistent $GW$ approximation are in excellent agreement with fully self-consistent $…

GW approximationSelf consistencyGeneral Physics and AstronomyFOS: Physical sciencesELECTRON-GASGreen's function methodsATOMSMOLECULESQuality (physics)IonizationPhysics - Chemical Physicsionisation potentialWAVE-FUNCTIONSKOOPMANS THEOREMPhysical and Theoretical ChemistryfysiikkaPhysicsChemical Physics (physics.chem-ph)total energyNONEQUILIBRIUM PROCESSESDiatomic moleculeTRANSPORTCondensed Matter - Other Condensed MatterYield (chemistry)GROUND-STATECORRELATION ENERGIESIonization energyAtomic physicsEXTENSIONOther Condensed Matter (cond-mat.other)
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Nonadiabatic transitions between lambda-doubling states in the capture of a diatomic molecule by an ion

2008

The low-energy capture of a dipolar diatomic molecule in an adiabatically isolated electronic state with a good quantum number Hund’s coupling case a by an ion occurs adiabatically with respect to rotational transitions of the diatom. However, the capture dynamics may be nonadiabatic with respect to transitions between the pair of the -doubling states belonging to the same value of the intrinsic angular momentum j. In this work, nonadiabatic transition probabilities are calculated which define the -doubling j-specific capture rate coefficients. It is shown that the transition from linear to quadratic Stark effect in the ion-dipole interaction, which damps the T �1/2 divergence of the captur…

IonsAngular momentumTime FactorsRotationChemistryStatic ElectricityGeneral Physics and AstronomyElectronsElectronDiatomic moleculeIonGood quantum numbersymbols.namesakeDipoleStark effectsymbolsQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryAtomic physicsAdiabatic processAlgorithmsThe Journal of Chemical Physics
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Calculated line broadening parameters for methane perturbed by diatomic molecules

2013

International audience; We report semiclassical line broadening calculations for methane perturbed by diatomic molecules: nitrogen, N2, oxygen, O2 and hydrogen, H2, at room temperature. For this, we have developed a symmetrized version of the Robert and Bonamy theory. The interaction potential was built from electrostatic (octopole and hexadecapole for methane, quadrupole for the diatomic molecules) and atom-atom contributions. The relative (classical) trajectories of the molecules were computed in the frame of the usual parabolic model, through analytical formula. High orders of developments had to be used for the short range molecular interactions in the case of N2 and O2. For H2, a lower…

Line broadening coefficients010504 meteorology & atmospheric sciencesHydrogen[ PHYS.QPHY ] Physics [physics]/Quantum Physics [quant-ph]Nitrogenchemistry.chemical_elementInfrared spectroscopySemiclassical physics02 engineering and technology7. Clean energy01 natural sciencesMethanechemistry.chemical_compound[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Diatomic moleculesMoleculePhysical and Theoretical ChemistryInfrared spectroscopySpectroscopy0105 earth and related environmental sciencesLine (formation)Physics021001 nanoscience & nanotechnologyDiatomic moleculeAtomic and Molecular Physics and OpticsOxygenchemistryQuadrupoleAtomic physics0210 nano-technologyMethaneHydrogen
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Dual-broadband rotational CARS modelling of nitrogen at pressures up to 9 MPa. II. Rotational Raman line widths

2002

International audience; Rotational coherent anti-Stokes Raman spectroscopy (CARS) is a well-established spectroscopic technique for thermometry at pre-combustion temperatures an atmospheric pressure. However, at pressures of several MPa, a previous investigation revealed large discrepancies between experimental data and the theoretical model. A re-evaluation has been made of these data (at room temperature and in the range 1.5-9 MPa) with two improvements to the spectral code. The first is the inclusion of an inter-branch interference effect, which is described in detail in Paper I. The second is the use of experimental S-1-branch Raman line widths measured at 295 K, with a temperature depe…

Materials sciencePhysics and Astronomy (miscellaneous)General Physics and AstronomyRotational transitionchemistry.chemical_element02 engineering and technology01 natural sciencesMolecular physicsQ-BRANCH010309 opticsRaman linesymbols.namesakeNuclear magnetic resonanceMaschinenbau0103 physical sciencesBroadbandSCATTERING THERMOMETRYSPECTRAQuantum optics[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics][ PHYS.PHYS.PHYS-OPTICS ] Physics [physics]/Physics [physics]/Optics [physics.optics]Atmospheric pressureRANGEGeneral Engineering021001 nanoscience & nanotechnologyNitrogenDiatomic moleculeSPECTROSCOPY CARSN-2COchemistrysymbolsHIGH-TEMPERATURELINEWIDTHS0210 nano-technologyRaman spectroscopyCOEFFICIENTS
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Molecular electric quadrupole moments calculated with matrix dressed SDCI

2002

Abstract We have calculated the molecular electric quadrupole moment (MEQM) for the set of molecules N 2 , C 2 H 2 , CO, CO 2 , CS 2 , HF, and BH. We have used SR-SDCI and (SC) 2 -SR-SDCI methods and we have compared our results with high-level theoretical ones, including FCI values for HF and BH, and with experimental values. The calculated MEQM provides a test of the effect that the energy converged (SC) 2 dressing method brings to the SDCI wavefunctions. The results suggest that the (SC) 2 -SR-SDCI method can be a cost-effective and quite accurate method for the calculation of post-SCF effects on electric quadrupole moments.

Matrix (mathematics)ChemistryComputational chemistryTriatomic moleculeQuadrupoleGeneral Physics and AstronomyDressing methodMoleculePhysical and Theoretical ChemistryAtomic physicsConfiguration interactionWave functionDiatomic moleculeChemical Physics Letters
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Actinide and lanthanide molecules to search for strong CP-violation

2020

The existence of the fundamental CP-violating interactions inside the nucleus leads to the existence of the nuclear Schiff moment. The Schiff moment potential corresponds to the electric field localized inside the nucleus and directed along its spin. This field can interact with electrons of an atom and induce the permanent electric dipole moment (EDM) of the whole system. The Schiff moment and corresponding electric field are enhanced in the nuclei with the octupole deformation leading to the enhanced atomic EDM. There is also a few-order enhancement of the T,P-violating effects in molecules due to the existence of energetically close levels of opposite parity. We study the Schiff moment e…

Nuclear TheoryAtomic Physics (physics.atom-ph)HadronNuclear TheoryGeneral Physics and AstronomyFOS: Physical sciencesElectron01 natural sciencesPhysics - Atomic PhysicsNuclear Theory (nucl-th)High Energy Physics - Phenomenology (hep-ph)Electric fieldPhysics - Chemical Physics0103 physical sciencesPhysics::Atomic PhysicsPhysical and Theoretical Chemistry010306 general physicsNuclear ExperimentPhysicsChemical Physics (physics.chem-ph)010308 nuclear & particles physicsDiatomic moleculeFundamental interactionElectric dipole momentHigh Energy Physics - PhenomenologyDiamagnetismCP violationAtomic physics
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Theoretical simulations of the radiation-induced defect processes in insulating materials

1994

Abstract The results of two basic kinds of computer simulations of radiation-induced processes in insulating materials, one based on quantum-mechanical and pair-potential (atomistic) approaches, and the other a phenomenological theory of diffusion-controlled reactions, are presented. It is shown that, by combining different techniques (atom-atom potentials and semi-empirical quantum chemical methods) the optimized geometry and the electronic structure of a family of hole centres in crystalline corundum (α-Al2O3) could be found. Their energetics are analyzed; V2−, V−V−Mg hole centres all have a common basic element, namely the diatomic molecule O23−, which is responsible for their similar ab…

Nuclear and High Energy PhysicsChemistryCorundumActivation energyElectronic structureengineering.materialAlkali metalPolaronDiatomic moleculeCovalent bondengineeringAtomic physicsAbsorption (electromagnetic radiation)InstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Comparison of full-configuration interaction and coupled-cluster harmonic and fundamental frequencies for BH and HF

2001

The harmonic and fundamental frequencies are calculated for the potential-energy curves of BH and HF using the full-configuration interaction model and two hierarchies of coupled-cluster wavefunction models. The anharmonic contributions are also obtained using second-order vibrational perturbation theory. A consistent and systematic improvement is seen for both the harmonic and anharmonic contributions when increasing the level of the correlation treatment. The changes are largest for the harmonic contributions. This is also the case when including valence or diffuse functions in the basis set. Second-order perturbation theory gives a good approximation to the anharmonic contribution and in…

Nuclear magnetic resonanceCoupled clusterChemistryQuantum mechanicsAnharmonicityHarmonicGeneral Physics and AstronomyPhysical and Theoretical ChemistryConfiguration interactionWave functionFull configuration interactionDiatomic moleculeBasis setChemical Physics Letters
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