Search results for " clusters"

showing 10 items of 1091 documents

Rovibrational structure of the Ar–CO complex based on a novel three-dimensional ab initio potential

2002

The first three-dimensional ab initio intermolecular potential energy surface of the Ar–CO van der Waals complex is calculated using the coupled cluster singles and doubles including connected triples model and the augmented correlation-consistent polarized valence quadruple zeta (aug-cc-pVQZ) basis set extended with a (3s3p2d1f1g) set of midbond functions. The three-dimensional surface is averaged over the three lowest vibrational states of CO. Rovibrational energies are calculated up to 50 cm−1 above the ground state, thus enabling comprehensive comparison between theory and available experimental data as well as providing detailed guidance for future spectroscopic investigations of highe…

Potential Energy SurfacesCoupled Cluster CalculationsAb initioGeneral Physics and AstronomyPhysics and Astronomy (all)symbols.namesakeAb initio quantum chemistry methodsQuasimoleculesPhysics::Atomic and Molecular ClustersVibrational StatesPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryArgon:FÍSICA::Química física [UNESCO]Rotational-Vibrational StatesBasis setValence (chemistry)ChemistryRotational–vibrational spectroscopyCarbon CompoundsUNESCO::FÍSICA::Química físicaCoupled clustersymbolsArgon ; Carbon Compounds ; Quasimolecules ; Rotational-Vibrational States ; Potential Energy Surfaces ; Ab Initio Calculations ; Intermolecular Mechanics ; Coupled Cluster Calculations ; Vibrational StatesIntermolecular Mechanicsvan der Waals forceAtomic physicsGround stateAb Initio Calculations
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Study of the benzene⋅N2 intermolecular potential-energy surface

2003

The intermolecular potential-energy surface pertaining to the interaction between benzene and N2 is investigated theoretically and experimentally. Accurate intermolecular interaction energies are evaluated for the benzene–N2 van der Waals complex using the coupled cluster singles and doubles including connected triples [CCSD(T)] method and the aug-cc-pVDZ basis set extended with a set of 3s3p2d1f1g midbond functions. After fitting the energies to an analytic function, the intermolecular Schrödinger equation is solved to yield energies, rotational constants, and Raman-scattering coefficients for the lowest intermolecular levels of several benzene–N2 isotopomers. Experimentally, intermolecula…

Potential Energy SurfacesCoupled Cluster CalculationsNitrogenBinding energyGeneral Physics and AstronomyPotential Energy Functionssymbols.namesakePhysics and Astronomy (all)IsomerismQuasimoleculesRotational IsomerismPhysics::Atomic and Molecular ClustersQuantum-mechanical explanation of intermolecular interactionsRotational StatesPhysical and Theoretical ChemistryPhysics::Chemical Physics:FÍSICA::Química física [UNESCO]Basis setSchrodinger EquationChemistryOrganic CompoundsIsotope EffectsIntermolecular forceStimulated Raman ScatteringUNESCO::FÍSICA::Química físicaCoupled clustersymbolsAtomic physicsvan der Waals forceOrganic Compounds ; Nitrogen ; Quasimolecules ; Potential Energy Surfaces ; Potential Energy Functions ; Coupled Cluster Calculations ; Rotational States ; Isomerism ; Isotope Effects ; Stimulated Raman Scattering ; Rotational Isomerism ; Schrodinger EquationRaman spectroscopyRaman scattering
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Computational and experimental investigation of intermolecular states and forces in the benzene-helium van der Waals complex

2003

A study of the intermolecular potential-energy surface (IPS) and the intermolecular states of the perprotonated and perdeuterated benzene–He complex is reported. From a fit to ab initio data computed within the coupled cluster singles and doubles including connected triples model for 280 interaction geometries, an analytic IPS including two- to four-body atom–atom terms is obtained. This IPS, and two other Lennard-Jones atom–atom surfaces from the literature, are each employed in dynamically exact (within the rigid-monomer approximation) calculations of J = 0 intermolecular states of the isotopomers. Rotational constants and Raman-scattering coefficients for intermolecular vibrational trans…

Potential Energy SurfacesCoupled Cluster CalculationsRaman SpectraHelium Neutral AtomsOrganic Compounds ; Helium Neutral Atoms ; Intermolecular Mechanics ; Quasimolecules ; Potential Energy Surfaces ; Ab Initio Calculations ; Coupled Cluster Calculations ; Lennard-Jones Potential ; Isotope Effects ; Isomerism ; Rotational States ; Raman SpectraAb initioGeneral Physics and AstronomyIsotopomerssymbols.namesakePhysics and Astronomy (all)IsomerismAb initio quantum chemistry methodsQuasimoleculesKinetic isotope effectPhysics::Atomic and Molecular ClustersRotational StatesPhysics::Atomic PhysicsLennard-Jones PotentialPhysics::Chemical PhysicsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]ChemistryOrganic CompoundsIsotope EffectsIntermolecular forceUNESCO::FÍSICA::Química físicaCoupled clusterLennard-Jones potentialsymbolsIntermolecular MechanicsAtomic physicsvan der Waals forceAb Initio Calculations
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Influence of structure on the polarizability of hydrated methane sulfonic acid clusters

2015

Abstract: The relationship between polarizability and structure is investigated in methane sulfonic acid (MSA) and in 36 hydrated MSA clusters. The polarizabilities are calculated at B3LYP and MP2 level and further partitioned into molecular contributions using classic and iterative Hirshfeld methods. The differences in the two approaches for partitioning of polarizabilities are thoroughly analyzed. The polarizabilities of the molecules are found to be influenced in a systematic way by the hydrogen bond network in the clusters, proton transfer between MSA and water molecules, and weak interactions between water molecules and the methyl group of MSA.

ProtonChemistryHydrogen bondPhysicsQuantitative Biology::GenomicsComputer Science Applicationschemistry.chemical_compoundQuantitative Biology::Quantitative MethodsChemistryComputational chemistryPolarizabilityMethane sulfonic acidPhysics::Atomic and Molecular ClustersMoleculePhysics::Atomic PhysicsPhysical and Theoretical ChemistryPhysics::Chemical PhysicsMethyl groupJournal of chemical theory and computation
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Ab initio limits of atomic nuclei

2019

We predict the limits of existence of atomic nuclei, the proton and neutron drip lines, from the light through medium-mass regions. Starting from a chiral two- and three-nucleon interaction with good saturation properties, we use the valence-space in-medium similarity renormalization group to calculate ground-state and separation energies from helium to iron, nearly 700 isotopes in total. We use the available experimental data to quantify the theoretical uncertainties for our ab initio calculations towards the drip lines. Where the drip lines are known experimentally, our predictions are consistent within the estimated uncertainty. For the neutron-rich sodium to chromium isotopes, we provid…

ProtonNuclear TheoryNuclear TheoryAb initioGeneral Physics and Astronomychemistry.chemical_elementFOS: Physical sciences01 natural sciences7. Clean energyNuclear Theory (nucl-th)0103 physical sciencesPhysics::Atomic and Molecular ClustersNeutronNuclear drip linePhysics::Atomic PhysicsNuclear Experiment (nucl-ex)010306 general physicsNuclear ExperimentNuclear ExperimentHeliumPhysicsIsotopeStarke Wechselwirkung und exotische Kerne – Abteilung BlaumRenormalization groupchemistryAtomic nucleusAtomic physics
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ChemInform Abstract: 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.

PseudopotentialCrystallographysymbols.namesakeChemistryPhysics::Atomic and Molecular ClustersAb initiosymbolsGeneral MedicinePhysics::Chemical PhysicsHamiltonian (quantum mechanics)Rotational barrierBasis setIonChemischer Informationsdienst
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Why benchmark-quality computations are needed to reproduce 1-adamantyl cation NMR chemical shifts accurately.

2011

While the experimental (1)H NMR chemical shiftsof the 1-adamantyl cation can be computed within reasonably small error bounds, the usual Hartree-Fock and density functional quantum-chemical computations, as well as those based on rather elaborate second-order Møller-Plesset perturbation theory, fail to reproduce its experimental (13)C NMR chemical shifts satisfactorily. This also is true even if the NMR shielding calculations treat electron correlation adequately by the coupled-cluster singles and doubles model augmented by a perturbative correction for triple excitations (i.e., at the CCSD(T) level) with quadruple-ζ basis sets. We demonstrate that good agreement can be achieved if highly a…

Quality (physics)Electronic correlationBasis (linear algebra)Computational chemistryChemistryComputationChemical shiftPhysics::Atomic and Molecular ClustersProton NMRPerturbation theory (quantum mechanics)Physical and Theoretical ChemistryCarbon-13 NMRComputational physicsThe journal of physical chemistry. A
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A theoretical study of solvent effects on the conformational equilibria of neutral glycine in aqueous solution

2003

Abstract In this work conformational equilibrium of neutral glycine in solution is systematically investigated by using DFT and MP2 methods combined with solvent continuum models. A systematic exploration of the potential energy surface and full geometry optimizations for several conformers have been carried out in the gas phase and aqueous solution at the MP2/6-31+G** and B3LYP/6-31+G** levels. Zero-point and thermal contributions to the free energy have been obtained at the B3LYP level. Both theoretical levels lead to very similar results, in geometrical and energetic terms, both in the gas phase and in solution. Solvent effects play an important role on the conformational equilibria of n…

Quantitative Biology::BiomoleculesAqueous solutionChemistryCondensed Matter PhysicsBiochemistryTautomerSolventEnergy minimumComputational chemistryPotential energy surfaceThermalPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistrySolvent effectsConformational isomerismJournal of Molecular Structure: THEOCHEM
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Difficulties of density functional theory in predicting the torsional potential of 2,2?-bithiophene

1998

The internal rotation of 2,2′-bithiophene was investigated within the density functional theory (DFT) approach. Fully optimized DFT torsional potentials are compared with Moller–Plesset (MP2) results which predict a fourfold potential with s-cis- and s-trans-gauche minima. DFT calculations fail in describing the energetics of the internal rotation because they favor planar vs. perpendicular conformers. Gradient-corrected functionals provide torsional potentials where the gauche minima have almost vanished and the s-ciss-trans interconversion barriers are twice as high as the barriers obtained at the MP2 level. The use of local functionals augments the shortcomings of the DFT approach. The g…

Quantitative Biology::BiomoleculesChemistryInternal rotationCondensed Matter PhysicsMolecular physicsAtomic and Molecular Physics and OpticsMaxima and minimasymbols.namesakePlanarFourier transformComputational chemistryPhysics::Atomic and Molecular ClustersPerpendicularsymbolsDensity functional theoryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryTorsional potentialConformational isomerismInternational Journal of Quantum Chemistry
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Structure and Matrix Isolation Infrared Spectrum of Formyl Fluoride Dimer:  Blue-Shift of the C−H Stretching Frequency

2006

Infrared spectroscopy (IR) of formyl fluoride (HCOF) dimer is studied in low-temperature argon and krypton matrixes. New IR absorptions, ca. 17 cm(-1) blue shifted from the monomer C-H stretching fundamental, are assigned to the HCOF dimer. The MP2/6-311++G calculations were utilized to define structures and harmonic frequencies of various HCOF dimers. Among the four optimized structures, the dimer having two C-H...O hydrogen bonds possesses strongest intermolecular bonding. The calculated harmonic frequencies of this dimer structure are shifted from the monomer similarly as observed in the experiment. Thus, we suggest that the experimentally observed blue shifted C-H bands belong to the di…

Quantitative Biology::BiomoleculesFormatesSpectrophotometry InfraredHydrogen bondInfraredDimerKryptonIntermolecular forceMatrix isolationchemistry.chemical_elementInfrared spectroscopyPhotochemistrySensitivity and SpecificityFluoridesCrystallographychemistry.chemical_compoundModels ChemicalchemistryPhysics::Atomic and Molecular ClustersQuantum TheoryComputer SimulationPhysical and Theoretical ChemistryDimerizationFormyl fluorideThe Journal of Physical Chemistry A
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