Search results for " Electron correlation"

showing 8 items of 8 documents

Full configuration interaction calculation of singlet excited states of Be3

2004

The full configuration interaction (FCI) study of the singlets vertical spectrum of the neutral beryllium trimer has been performed using atomic natural orbitals [3s2p1d] basis set. The FCI triangular equilibrium structure of the ground state has been used to calculate the FCI vertical excitation energies up to 4.8 eV. The FCI vertical ionization potential for the same geometry and basis set amounts to 7.6292 eV. The FCI dipole and quadrupole transition moments from the ground state are reported as well. The FCI electric quadrupole moment of the X (3)A(1) (') ground state has been also calculated with the same basis set (Theta(zz)=-2.6461 a.u., Theta(xx)=Theta(yy)=-1/2Theta(zz)). Twelve of …

Atomic clustersElectron correlationsIonisation potentialGeneral Physics and AstronomyFull configuration interactionBeryllium ; Configuration interactions ; Excited states ; Orbital calculations ; Ground states ; Ionisation potential ; Molecular configurations ; Transition moments ; Quadrupole moments ; Molecular moments ; Electron correlations ; Atomic clustersPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Basis setElectronic correlationChemistryConfiguration interactionsExcited statesPhysics::Physics EducationMolecular configurationsTransition momentsUNESCO::FÍSICA::Química físicaOrbital calculationsGround statesDipoleExcited stateQuadrupoleQuadrupole momentsMolecular momentsBerylliumAtomic physicsIonization energyGround stateThe Journal of Chemical Physics
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A computational study of some electric and magnetic properties of gaseous BF3 and BCl3

2005

We present the results of an extended computational study of the electric and magnetic properties connected to Cotton-Mouton birefringences, on the trifluoro- and trichloroborides in the gas phase. The electric dipole polarizabilities, magnetizabilities, quadrupole moments, and higher-order hypersusceptibilities—expressed as quadratic and cubic frequency-dependent response functions—are computed within Hartree-Fock, density-functional, and coupled-cluster response theories employing singly and doubly augmented correlation-consistent basis sets and London orbitals in the magnetic property calculations. The results, which illustrate the capability of time-dependent density-functional theory f…

BirefringenceBirefringenceCondensed matter physicsChemistryElectron correlationsGeneral Physics and AstronomyMagnetic susceptibilityBoron compounds; Polarisability Quadrupole moments ; HF calculations ; Density functional theory ; Coupled cluster calculations ; Electron correlations ; Magnetic anisotropy ; Magnetic susceptibility ; BirefringenceUNESCO::FÍSICA::Química físicaMagnetic susceptibilityMagnetic anisotropyDipoleAtomic orbitalBoron compoundsCoupled cluster calculationsQuadrupolePolarisability Quadrupole momentsDensity functional theoryDensity functional theoryPhysical and Theoretical ChemistryAtomic physicsAnisotropy:FÍSICA::Química física [UNESCO]HF calculationsMagnetic anisotropy
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The chemical bonds in CuH, Cu2, NiH, and Ni2 studied with multiconfigurational second order perturbation theory

1994

The performance of multiconfigurational second order perturbation theory has been analyzed for the description of the bonding in CuH, Cu2, NiH, and Ni2. Large basis sets based on atomic natural orbitals (ANOS) were employed. The effects of enlarging the active space and including the core‐valence correlation contributions have also been analyzed. Spectroscopic constants have been computed for the corresponding ground state. The Ni2 molecule has been found to have a 0+g ground state with a computed dissociation energy of 2.10 eV, exp. 2.09 eV, and a bond distance of 2.23 Å. The dipole moments of NiH and CuH are computed to be 2.34 (exp. 2.4±0.1) and 2.66 D, respectively. pou@uv.es ; merchan@…

Chemical BondsGeneral Physics and AstronomyDissociation EnergyDipole MomentsPerturbation Theory ; Chemical Bonds ; Configuration Interaction ; Copper Hydrides ; Nickel Hydrides ; Copper ; Nickel ; Electron Correlation ; Core Levels ; Dissociation Energy ; Dipole Moments ; Bond Lengths ; Diatomic MoleculesCore LevelsBond LengthsNickelPhysical and Theoretical ChemistryPerturbation theory:FÍSICA::Química física [UNESCO]Nickel HydridesDiatomic MoleculesElectronic correlationChemistryConfiguration interactionBond-dissociation energyDiatomic moleculeUNESCO::FÍSICA::Química físicaBond lengthConfiguration InteractionChemical bondCopper HydridesPerturbation TheoryElectron CorrelationAtomic physicsGround stateCopper
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A CI study of the CuCO and CuCO+ complexes

1987

MO CI calculations are carried out using an optimal space of valence virtual MOs obtained by means of a projection technique, as a linear combination of the AOs which are more occupied in the molecular Fock space. Localization of the occupied MOs and nonvalence virtual MOs is also achieved. The overall procedure is proven to be quite advantageous and well suited to obtain potential energy curves which keep the same physical meaning along the range of distances studied. Using a slightly better than double‐zeta quality basis set, a valence CAS‐CI, and selected CI wave function by the CIPSI algorithm have revealed a possible weak van der Waals interaction for the 2Σ+ state of CuCO, which remai…

General Physics and AstronomyElectronic structureCopper CompoundsMolecular physicsCopper Complexessymbols.namesake:FÍSICA [UNESCO]CarbonylsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Basis setPi backbondingValence (chemistry)Electronic correlationChemistryUNESCO::FÍSICAConfiguration interactionPotential energyUNESCO::FÍSICA::Química físicaConfiguration InteractionValenceElectronic StructuresymbolsElectron CorrelationConfiguration Interaction ; Electron Correlation ; Copper Compounds ; Carbonyls ; Copper Complexes ; Electronic Structure ; Valencevan der Waals forceAtomic physicsThe Journal of Chemical Physics
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Large-scale calculations of excitation energies in coupled cluster theory: The singlet excited states of benzene

1996

Algorithms for calculating singlet excitation energies in the coupled cluster singles and doubles (CCSD) model are discussed and an implementation of an atomic-integral direct algorithm is presented. Each excitation energy is calculated at a cost comparable to that of the CCSD ground-state energy. Singlet excitation energies are calculated for benzene using up to 432 basis functions. Basis-set effects of the order of 0.2 eV are observed when the basis is increased from augmented polarized valence double-zeta (aug-cc-pVDZ) to augmented polarized valence triple-zeta (aug-cc-pVTZ) quality. The correlation problem is examined by performing calculations in the hierarchy of coupled cluster models…

General Physics and AstronomyElectronic structurePhysics and Astronomy (all)Physics::Atomic and Molecular ClustersSinglet statePhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Calculation MethodsValence (chemistry)TripletsElectronic correlationChemistryBenzeneExcited StatesConfiguration interactionUNESCO::FÍSICA::Química físicaConfiguration InteractionCoupled clusterElectronic StructureExcited stateElectron CorrelationBenzene ; Excited States ; Calculation Methods ; Algorithms ; Triplets ; Electronic Structure ; Configuration Interaction ; Correlation Functions ; Electron CorrelationAtomic physicsCorrelation FunctionsExcitationAlgorithms
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Effects of Electron Correlation inside Disordered Crystals

2022

S.P.K. acknowledges support by the National Academy of Sciences of Ukraine (Project No.0116U002067). Calculations were performed using Latvian Super Cluster (LASC), located in the Center of Excellence at Institute of Solid State Physics, the University of Latvia, which is supported by European Union Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-Teaming. Phase two under Grant Agreement No. 739508, project CAMART2.

Inorganic ChemistryNew theoryGeneral Chemical EngineeringElectron correlation:NATURAL SCIENCES::Physics [Research Subject Categories]General Materials ScienceElectron spectrumnew theory; electron correlation; electron spectrum; Hamiltonian of electrons; thermodynamic potentialThermodynamic potentialCondensed Matter PhysicsHamiltonian of electronsCrystals
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Evidence for a different electronic configuration as a primary effect during compression of orthorhombic perovskites: The case of NdM3+ O3 (M=Cr, Ga)

2018

(Mg,Fe)SiO3 perovskite is the most abundant mineral of the Earth's lower mantle, and compounds with the perovskite structure are perhaps the most widely employed ceramics. Hence, they attract both geophysicists and material scientists. Several investigations attempted to predict their structural evolution at high pressure, and recent advancements highlighted that perovskites having ions with the same formal valence at both polyhedral sites (i.e., 3+:3+) define different compressional patterns when transition metal ions (TMI) are involved. In this study, in situ high-pressure synchrotron XRD measurements coupled with ab initio simulations of the electronic population of NdCrO3 perovskite are…

NdCrO3Structural propertiesElectronic Optical and Magnetic MaterialSocio-culturaleNdGaO3Perovskite Elasticity Pressure effect Electron correlation calculation for atoms & ions Structural propertiesPerovskitePressure effectCondensed Matter PhysicscompressionElasticityElectron correlation calculation for atoms &amporthorhombic perovskiteionselectronic configuration
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OpenMolcas: From Source Code to Insight

2019

In this article we describe the OpenMolcas environment and invite the computational chemistry community to collaborate. The open-source project already includes a large number of new developments realized during the transition from the commercial MOLCAS product to the open-source platform. The paper initially describes the technical details of the new software development platform. This is followed by brief presentations of many new methods, implementations, and features of the OpenMolcas program suite. These developments include novel wave function methods such as stochastic complete active space self-consistent field, density matrix renormalization group (DMRG) methods, and hybrid multico…

Wave functionSource codeField (physics)Computer sciencemedia_common.quotation_subjectInterfacesSemiclassical physics010402 general chemistry0601 Biochemistry and Cell Biology01 natural sciencesComputational scienceNOChemical calculationsMathematical methodschemical calculations ; electron correlation ; interfaces ; mathematical methods ; wave function0103 physical sciences0307 Theoretical and Computational ChemistryPhysical and Theoretical ChemistryWave functionWave function Interfaces Chemical calculations Mathematical methods Electron correlationComputingMilieux_MISCELLANEOUSmedia_commonChemical Physics010304 chemical physicsBasis (linear algebra)business.industryDensity matrix renormalization groupElectron correlationSoftware development0803 Computer Software0104 chemical sciencesComputer Science ApplicationsVisualization[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrybusiness
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