Search results for "Figura"

showing 10 items of 867 documents

Convergence of coupled cluster perturbation theory.

2016

The convergence of a recently proposed coupled cluster (CC) family of perturbation series [Eriksen, J. J. et al., J. Chem. Phys. 140, 064108 (2014)], in which the energetic difference between two CC models - a low-level parent and a high-level target model - is expanded in orders of the M{\o}ller-Plesset (MP) fluctuation potential, is investigated for four prototypical closed-shell systems (Ne, singlet methylene, distorted HF, and the fluoride anion) in standard and augmented basis sets. In these investigations, energy corrections of the various series have been calculated to high orders and their convergence radii determined by probing for possible front- and back-door intruder states, the…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsFOS: Physical sciencesGeneral Physics and AstronomyPerturbation (astronomy)010402 general chemistry01 natural sciencesFull configuration interaction0104 chemical sciencesIonCoupled clusterPhysics - Chemical Physics0103 physical sciencesSinglet stateStatistical physicsPhysical and Theoretical ChemistryThe Journal of chemical physics
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Incremental Treatments of the Full Configuration Interaction Problem

2020

The recent many-body expanded full configuration interaction (MBE-FCI) method is reviewed by critically assessing its advantages and drawbacks in the context of contemporary near-exact electronic structure theory. Besides providing a succinct summary of the history of MBE-FCI to date within a generalized and unified theoretical setting, its finer algorithmic details are discussed alongside our optimized computational implementation of the theory. A selected few of the most recent applications of MBE-FCI are revisited, before we close by outlining its future research directions as well as its place among modern near-exact wave function-based methods.

Chemical Physics (physics.chem-ph)Theoretical computer science010304 chemical physicsComputer scienceFOS: Physical sciencesContext (language use)010402 general chemistry01 natural sciencesBiochemistryFull configuration interaction0104 chemical sciencesComputer Science ApplicationsComputational MathematicsPhysics - Chemical Physics0103 physical sciencesMaterials ChemistryPhysical and Theoretical Chemistry
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Overview of the JET results

2015

Since the installation of an ITER-like wall, the JET programme has focused on the consolidation of ITER design choices and the preparation for ITER operation, with a specific emphasis given to the bulk tungsten melt experiment, which has been crucial for the final decision on the material choice for the day-one tungsten divertor in ITER. Integrated scenarios have been progressed with the re-establishment of long-pulse, high-confinement H-modes by optimizing the magnetic configuration and the use of ICRH to avoid tungsten impurity accumulation. Stationary discharges with detached divertor conditions and small edge localized modes have been demonstrated by nitrogen seeding. The differences in…

Chemical analysiMagnetic confinementEdge localized modeTokamak:Física [Ciências exactas e naturais]Nuclear engineeringplasma-facing componentsTungsten7. Clean energyiter-like walllaw.inventionheat loadsAlcator C-ModlawPlasma-facing componentalcator C-MODQCPhysicsJet (fluid)Thermally activatedDivertormagnetic confinementMagnetic confinement fusionTokamak deviceerosionCondensed Matter PhysicsChemical erosionPost mortem analysiCondensed Matter Physics; Nuclear and High Energy PhysicsBerylliumAtomic physicstokamaksTokamaksNuclear and High Energy Physicschemistry.chemical_elementImpurity accumulationCondensed Matter PhysicNuclear and High Energy Physics; Condensed Matter PhysicsTungstenFísica Física:Physical sciences [Natural sciences]divertorNuclear fusionNuclear and High Energy PhysicPhysics Physical sciencesGas fuel analysifuel retentionSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)operationOrders of magnitudechemistryJETtransportMagnetic configuration
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An ab initio CI study on the rotational barrier of the allyl anion

1986

All-electron and pseudopotential non-empirical calculations have been performed on C 2v and C s (syn, anti) allyl anion conformations. Using a double-zeta valence-shell basis set within the Epstein-Nesbet definition of the unperturbed Hamiltonian, a value about 19 kcal/mol is found for the barrier to rotation of the allyl anion. This value is the theoretical value obtained with greater accuracy, and the lowest one for the rotational barrier.

ChemistryAb initioConfiguration interactionRotational barrierIonPseudopotentialsymbols.namesakeCrystallographyComputational chemistryPhysics::Atomic and Molecular ClusterssymbolsChiropracticsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Basis setCarbanionTheoretica Chimica Acta
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Synthesis and Isolation of Enantiomerically Enriched Cyclopenta[b]benzofurans Based on Products from Anodic Oxidation of 2,4-Dimethylphenol

2015

The anodic treatment of 2,4-dimethylphenol offers a powerful and direct method for the construction of a dehydrotetramer with four contiguous stereocentres on a multigram scale. The installation of propellanes on this scaffold using enantiomerically pure carbonyl compounds leads to a mixture of diastereomers. This mixture is easily separable using standard chromatography and gives rise to optically pure cyclopenta[b]benzofurans which are important scaffolds in a variety of natural products. The synthesis is easy to perform and allows a reliable access to chiral compounds with very high enantiomeric excess. It was possible to determine the absolute configuration of these compounds by compari…

ChemistryAnodic oxidationOrganic ChemistryVibrational circular dichroismAbsolute configurationDiastereomerOrganic chemistryPhysical and Theoretical ChemistryEnantiomerEnantiomeric excessElectrochemistryChiral resolutionEuropean Journal of Organic Chemistry
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Analytic calculation of the diagonal Born-Oppenheimer correction within configuration-interaction and coupled-cluster theory

2006

Schemes for the analytic calculation of the diagonal Born-Oppenheimer correction (DBOC) are formulated and implemented for use with general single-reference configuration-interaction and coupled-cluster wave function models. Calculations are reported to demonstrate the convergence of the DBOC with respect to electron-correlation treatment and basis set as well as to investigate the size-consistency error in configuration-interaction calculations of the DBOC. The importance of electron-correlation contributions to the DBOC is illustrated in the computation of the corresponding corrections for the reaction energy and activation barrier of the F + H2 --FH + H reaction as well as of the atomiza…

ChemistryComputationDiagonalBorn–Oppenheimer approximationGeneral Physics and AstronomyConfiguration interactionsymbols.namesakeCoupled clusterQuantum electrodynamicsConvergence (routing)symbolsPhysical and Theoretical ChemistryAtomic physicsWave functionBasis setThe Journal of Chemical Physics
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A mutliconfigurational study of low-lying electronic states of KO

1992

Abstract Potential energy curves and spectroscopic parameters of several electronic states of the KO molecule have been calculated using multi-configurational methods. The KO B 2Π state, first time theoretically described, presents a strong avoided crossing with the A 2Π state, and allows for the explanation of the observed fluorescence of the KO molecule. Eleven electronic states have been studied at all the internuclear distances. Effects of complete active space and basis set selections on the results are also analyzed.

ChemistryComputational chemistryAvoided crossingGeneral Physics and AstronomyComplete active spacePhysical and Theoretical ChemistryConfiguration interactionAtomic physicsPotential energyDiatomic moleculeBasis setMolecular electronic transitionDoublet stateChemical Physics
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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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Magnetic exchange interaction in clusters of orbitally degenerate ions. I. Effective Hamiltonian

2001

Abstract A new effective Hamiltonian is reported for the kinetic exchange between two arbitrary terms 2S A +1 Λ A and 2S B +1 Λ B that can be ground or excited in octahedrally coordinated transition metal ions. This Hamiltonian is applicable to both homo- and heterometallic clusters. For the homonuclear cluster the resonance part of the effective Hamiltonian is also presented for the case when one of the ions is excited. The operator part of the exchange Hamiltonian contains symmetry adapted products of the cubic irreducible tensors acting in orbital spaces ΛA and ΛB and scalar product of site spin operators. The parameters of the Hamiltonian are defined by the relevant intercenter transfer…

ChemistryDegenerate energy levelsGeneral Physics and AstronomyHomonuclear moleculesymbols.namesakeOperator (computer programming)Excited statesymbolsCluster (physics)Electron configurationPhysical and Theoretical ChemistryAtomic physicsHamiltonian (quantum mechanics)Ground stateChemical Physics
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Theoretical spectroscopic parameters of the alkali monofluorides LiF, NaF and KF

1992

Abstract Multireference configuration interaction and second-order perturbation theory are used to determine accurate spectroscopic parameters for the ground state of the alkali monofluorides from LiF to KF. Systematic saturation of the spdf subspaces of the atomic basis sets for the electron affinity of fluorine and the ionization potential of the metals have been shown to be more efficient than for the approximate dissociation energies in the molecule. the calculated rotational and vibrational constants and transitions for the three systems show excellent agreement with the expeirmental data.

ChemistryGeneral Physics and AstronomyMultireference configuration interactionConfiguration interactionAlkali metalMolecular physicsDiatomic moleculeBond lengthComputational chemistryPhysics::Atomic and Molecular ClustersRotational spectroscopyPhysics::Chemical PhysicsPhysical and Theoretical ChemistryIonization energyGround stateChemical Physics Letters
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