Search results for "UNESCO::FÍSICA::Química física"

showing 10 items of 81 documents

Ab initio study on the low-lying excited states of retinal

1997

Ab initio results for the electronic spectrum of all-trans-retinal and its truncated model 3-methyl-all-trans (10-s-cis)-2,4,6,8,10-undecapentaen-1-al are presented. The study includes geometry determination of the ground state. Vertical excitation energies have been computed using multiconfigurational second-order perturbation theory through the CASPT2 formalism. The lowest singlet excited state in gas phase is predicted to be of nπ∗ character. The lowest triplet state corresponds, however, to a ππ∗ state. The most intense feature of the spectrum is due to the strongly dipole-allowed ππ∗ transition, in accordance with the observed maximum in the one-photon spectra. The vertical excitation …

PhotochemistryChemistryExcited statesAb initioGeneral Physics and AstronomyPerturbation theoryTriplet stateSpectral lineGround statesUNESCO::FÍSICA::Química físicaAb initio quantum chemistry methodsExcited stateOrganic compoundsSolvent effectsTwo-photon spectraIsomerisationAb initio calculationsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet state:FÍSICA::Química física [UNESCO]Ground stateExcitationOrganic compounds ; Excited states ; Ab initio calculations ; Perturbation theory ; Triplet state ; Solvent effects ; Isomerisation ; Ground states ; Two-photon spectra ; Photochemistry
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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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Excitation levels and magic numbers of small parahydrogen clusters (N⩽40)

2008

The excitation energies of parahydrogen clusters have been systematically calculated by the diffusion Monte Carlo technique in steps of one molecule from 3 to 40 molecules. These clusters possess a very rich spectra, with angular momentum excitations arriving up to L=13 for the heavier ones. No regular pattern can be guessed in terms of the angular momenta and the size of the cluster. Clusters with N=13 and 36 are characterized by a peak in the chemical potential and a large energy gap of the first excited level, which indicate the magical character of these clusters. From the calculated excitation energies the partition function has been obtained, thus allowing for an estimate of thermal e…

PhysicsAngular momentumPartition function (statistical mechanics)Excited statesFOS: Physical sciencesGeneral Physics and AstronomyMonte Carlo methodsSpin isomers of hydrogenMolecular physicsSpectral lineUNESCO::FÍSICA::Química físicaEnergy gapMolecular clustersExcited stateChemical potential ; Energy gap ; Excited states ; Molecular clusters ; Monte Carlo methodsCluster (physics)Diffusion Monte CarloPhysics - Atomic and Molecular ClustersPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Atomic and Molecular Clusters (physics.atm-clus)Chemical potentialExcitationThe Journal of Chemical Physics
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Accurate ab initio density fitting for multiconfigurational self-consistent field methods

2008

Using Cholesky decomposition and density fitting to approximate the electron repulsion integrals, an implementation of the complete active space self-consistent field (CASSCF) method suitable for large-scale applications is presented. Sample calculations on benzene, diaquo-tetra- μ -acetato-dicopper(II), and diuraniumendofullerene demonstrate that the Cholesky and density fitting approximations allow larger basis sets and larger systems to be treated at the CASSCF level of theory with controllable accuracy. While strict error control is an inherent property of the Cholesky approximation, errors arising from the density fitting approach are managed by using a recently proposed class of auxi…

PhysicsBasis (linear algebra)Field (physics)Ab initioGeneral Physics and AstronomyElectronUNESCO::FÍSICA::Química físicaPhysics and Astronomy (all)Ab initio quantum chemistry methodsComputational chemistryOrganic compoundsDensity functional theorySCF calculationsDensity functional theoryComplete active spaceStatistical physicsAb initio calculationsPhysical and Theoretical ChemistryAb initio calculations ; Density functional theory ; Organic compounds ; SCF calculations:FÍSICA::Química física [UNESCO]Cholesky decomposition
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Molecular dynamics simulations of elementary chemical processes in liquid water using combined density functional and molecular mechanics potentials.…

1997

A new approach to carry out molecular dynamics simulations of chemical reactions in solution using combined density functional theory/molecular mechanics potentials is presented. We focus our attention on the analysis of reactive trajectories, dynamic solvent effects and transmission coefficient rather than on the evaluation of free energy which is another important topic that will be examined elsewhere. In a previous paper we have described the generalities of this hybrid molecular dynamics method and it has been employed to investigate low energy barrier proton transfer process in water. The study of processes with activation energies larger than a few kT requires the use of specific tech…

PhysicsChemical processReaction stepMolecular dynamics method ; Chemical reactions ; Solvent effects ; Density functional theory ; WaterWaterGeneral Physics and AstronomyMolecular dynamics methodContext (language use)UNESCO::FÍSICA::Química físicaMolecular dynamicsChemical physicsChemical reactionsQuantum mechanicsSolvent effectsDensity functional theoryDensity functional theoryTransmission coefficientPhysical and Theoretical ChemistrySolvent effects:FÍSICA::Química física [UNESCO]QuantumThe 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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Self‐consistent intermediate Hamiltonians : A coupled cluster type formulation of the singles and doubles configuration interaction matrix dressing

1995

This paper presents a new self‐consistent dressing of a singles and doubles configuration interaction matrix which insures size‐consistency, separability into closed‐shell subsystems if localized molecular orbitals (MOs) are used, and which includes all fourth order corrections. This method yields, among several schemes, a reformulation of the coupled cluster method, including fully the cluster operators of single and double excitations, and partially those of the triples (Bartlett’s algorithm named CCSDT‐1a). Further improvement can be easily included by adding exclusion principle violating corrections. Since it leads to a matrix diagonalization, the method behaves correctly in case of nea…

PhysicsHamiltoniansDiagonalizable matrixGeneral Physics and AstronomyLocalized molecular orbitalsConfiguration interactionMany−Body ProblemUNESCO::FÍSICA::Química físicaMany-body problemSelf−Consistent FieldConfiguration Interactionsymbols.namesakeMatrix (mathematics)Pauli exclusion principleCoupled clusterHamiltonians ; Self−Consistent Field ; Many−Body Problem ; Perturbation Theory ; Configuration Interaction ; AlgorithmsQuantum mechanicssymbolsPerturbation TheoryPerturbation theory (quantum mechanics)Physical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Algorithms
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Configurational entropy of microemulsions : The fundamental length scale

1993

Phenomenological models have been quite successful in characterizing both the various complex phases and the corresponding phase diagrams of microemulsions. In some approaches, e.g., the random mixing model (RMM), the lattice parameter is of the order of the dimension of an oil or water domain and has been used as a length scale for computing a configurational entropy, the so‐called entropy of mixing, of the microemulsion. In the central and material section of this paper (Sec. III), we show that the fundamental length scale for the calculation of the entropy of mixing is of the order of the cube root of the volume per molecule—orders of magnitude smaller than the dimension of such a domain…

PhysicsLength scalePhase StudiesEntropyConfiguration entropyGeneral Physics and AstronomyThermodynamicsEntropy of mixingMicroemulsions ; Entropy ; Phase Diagrams ; Lattice Parameters ; Dispersions ; Phase StudiesUNESCO::FÍSICA::Química físicaPhase spacePhenomenological modelMicroemulsionsLattice ParametersStatistical physicsConfiguration spacePhase DiagramsPhysical and Theoretical ChemistryEntropy (energy dispersal)Dispersions:FÍSICA::Química física [UNESCO]Cube root
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The CC3 model : An iterative coupled cluster approach including connected triples

1997

An alternative derivation of many-body perturbation theory (MBPT) has been given, where a coupled cluster parametrization is used for the wave function and the method of undetermined Lagrange multipliers is applied to set up a variational coupled cluster energy expression. In this variational formulation, the nth-order amplitudes determine the energy to order 2n+1 and the nth-order multipliers determine the energy to order 2n+2. We have developed an iterative approximate coupled cluster singles, doubles, and triples model CC3, where the triples amplitudes are correct through second order and the singles amplitudes are treated without approximations due to the unique role of singles as appro…

PhysicsMany-body problemsIterative methodIterative methodsGeneral Physics and AstronomyRelaxation (iterative method)Function (mathematics)Perturbation theoryFull configuration interactionUNESCO::FÍSICA::Química físicaPhysics and Astronomy (all)Coupled clusterCoupled cluster calculationsPerturbation theory ; Many-body problems ; Coupled cluster calculations ; Iterative methods ; Wave functions ; Variational techniquesComputational chemistryPerturbation theoryPhysical and Theoretical ChemistryPhysics::Chemical PhysicsWave function:FÍSICA::Química física [UNESCO]ParametrizationWave functionsMathematical physicsVariational techniques
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Reduced scaling in electronic structure calculations using Cholesky decompositions

2003

The small numerical rank of the two-electron integral matrix for large molecular systems and large basis sets was demonstrated. Though, the current implementation still requires some improvements on the calculations done in the inner most loop of the decomposition do not exploit the parsity in the Cholesky vectors. With respect to the practical applicability of the presented method an efficient approach to geometrical derivatives was imperative. Such an approach was obtained including certain derivative product functions and decomposing an expanded integral matrix.

PhysicsMolecular electronic statesMolecular electronic states ; Quantum chemistryIntegral matrixGeneral Physics and AstronomyElectronic structureQuantum chemistryUNESCO::FÍSICA::Química físicaPhysics and Astronomy (all)Computational chemistryFock matrixApplied mathematicsDensity fittingPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]ScalingQuantum chemistryCholesky decomposition
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