Search results for "Configuration interactions"

showing 6 items of 6 documents

Computation of conical intersections by using perturbation techniques

2005

Multiconfigurational second-order perturbation theory, both in its single-state multiconfigurational second-order perturbation theory (CASPT2) and multistate (MS-CASPT2) formulations, is used to search for minima on the crossing seams between different potential energy hypersurfaces of electronic states in several molecular systems. The performance of the procedures is tested and discussed, focusing on the problem of the nonorthogonality of the single-state perturbative solutions. In different cases the obtained structures and energy differences are compared with available complete active space self-consistent field and multireference configuration interaction solutions. Calculations on dif…

Potential Energy SurfacesConfiguration Interactions ; Perturbation Theory ; Potential Energy Surfaces ; Molecular Electronic States ; SCF Calculations ; Lithium Compounds ; Organic Compounds ; Wave FunctionsOrganic CompoundsChemistryComputationUNESCO::FÍSICAConfiguration InteractionsGeneral Physics and AstronomyMultireference configuration interactionConical surfaceSCF CalculationsPotential energyWave FunctionsMaxima and minima:FÍSICA [UNESCO]Molecular Electronic StatesQuantum mechanicsPerturbation TheoryLithium CompoundsStatistical physicsComplete active spacePerturbation theory (quantum mechanics)Physical and Theoretical ChemistryWave functionThe Journal of Chemical Physics
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Size-consistent self-consistent configuration interaction from a complete active space : Excited states

1998

The self-consistent size consistent on a complete active space singly and doubly configuration interaction (SC)2CAS-SDCI method is applied to excited states. The (SC)2 correction is performed on a closed shell state, and the excited states are obtained by diagonalization of the dressed matrix. A theoretical justification of the transferability of the improvement concerning the dressing state to all roots of the matrix is presented. The method is tested by three tests on the spectrum of small molecules. sanchezm@uv.es ; nebot@uv.es

PhysicsConfiguration interactionsSpectrum (functional analysis)Excited statesGeneral Physics and AstronomyMultireference configuration interactionState (functional analysis)Configuration interactionExcited states ; Configuration interactionsUNESCO::FÍSICA::Química físicaMatrix (mathematics)Excited stateComplete active spacePhysical and Theoretical ChemistryAtomic physics:FÍSICA::Química física [UNESCO]Open shell
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Detection of the Lowest-Lying Odd-Parity Atomic Levels in Actinium

2020

Two lowest-energy odd-parity atomic levels of actinium, 7s27pP21/2o, 7s27pP23/2o, were observed via two-step resonant laser-ionization spectroscopy and their respective energies were measured to be 7477.36(4) and 12 276.59(2) cm-1. The lifetimes of these states were determined as 668(11) and 255(7) ns, respectively. In addition, we observed the effect of the hyperfine structure on the line for the transition to P23/2o. These properties were calculated using a hybrid approach that combines configuration interaction and coupled-cluster methods, in good agreement with the experiment. The data are of relevance for understanding the complex atomic spectra of actinides and for developing efficien…

FUNDAMENTAL PHYSICSGeneral Physics and Astronomychemistry.chemical_elementHYPERFINE STRUCTURE01 natural sciences7. Clean energyATOMIC SPECTROSCOPYLASER IONIZATION SPECTROSCOPYATOMSCOMPLEX ATOMIC SPECTRALaser coolingIonization0103 physical sciences010306 general physicsSpectroscopyNUMERICAL METHODSHyperfine structurePhysicsHYBRID APPROACHATOM LASERSActinideConfiguration interactionCOUPLED-CLUSTER METHODSACTINIUMMEDICAL ISOTOPE PRODUCTIONActiniumchemistryLASER COOLINGIONIZATIONProduction (computer science)Atomic physicsCONFIGURATION INTERACTIONS
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Full configuration interaction calculation of BeH adiabatic states.

2008

An all-electron full configuration interaction (FCI) calculation of the adiabatic potential energy curves of some of the lower states of BeH molecule is presented. A moderately large ANO basis set of atomic natural orbitals (ANO) augmented with Rydberg functions has been used in order to describe the valence and Rydberg states and their interactions. The Rydberg set of ANOs has been placed on the Be at all bond distances. So, the basis set can be described as 4s3p2d1f3s2p1d(BeH)+4s4p2d(Be). The dipole moments of several states and transition dipole strengths from the ground state are also reported as a function of the R(Be-H) distance. The position and the number of states involved in sever…

ChemistryConfiguration interactionsGeneral Physics and AstronomyBond lengthsBeryllium compounds ; Bond lengths ; Configuration interactions ; Ground states ; Molecular moments ; Potential energy surfaces ; Rydberg states ; Vibrational statesRydberg statesPotential energyFull configuration interactionGround statesUNESCO::FÍSICA::Química físicaDipolesymbols.namesakeAtomic orbitalBeryllium compoundsPotential energy surfacesRydberg formulasymbolsMolecular momentsVibrational statesPhysical and Theoretical ChemistryAtomic physicsGround stateAdiabatic process:FÍSICA::Química física [UNESCO]Basis setThe Journal of chemical physics
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Nonadiabatic orientation, toroidal current, and induced magnetic field in BeO molecules.

2008

It is predicted that oriented BeO molecules would give rise to unprecedentedly strong, unidirectional electric ring current and an associated magnetic field upon excitation by a right or left circularly polarized laser pulse into the first excited degenerate singlet state. The strong toroidal electric ring current of this state is dominated by the ring current of the 1π± orbital about the molecular axis. Our predictions are based on the analysis of the orbital composition of the states involved and are substantiated by high level electronic structure calculations and wavepacket simulations of the laser-driven orientation and excitation dynamics. Luis.Serrano@uv.es

PhotoexcitationToroidMolecular electronic statesMolecule-photon collisionsMagnetic momentChemistryConfiguration interactionsExcited statesGeneral Physics and AstronomyElectronic structureMolecular orientationMagnetic fieldUNESCO::FÍSICA::Química físicaPhotoexcitationCoupled cluster calculationsBeryllium compoundsExcited stateMagnetic momentsPhysical and Theoretical ChemistryAtomic physics:FÍSICA::Química física [UNESCO]Beryllium compounds ; Configuration interactions ; Coupled cluster calculations ; Excited states ; Magnetic moments ; Molecular electronic states ; Molecular orientation ; Molecule-photon collisions ; PhotoexcitationRing currentExcitationThe Journal of chemical physics
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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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