Search results for " correlation"

showing 10 items of 1380 documents

Electron correlation effects on the calculated 13C NMR spectra of vinyl cations

1997

Abstract A study of calculated 13C NMR chemical shifts in vinyl cations is presented. The sensitivity of predicted isotropic shifts to correlation, basis set and geometry effects is explored. In order to obtain accurate estimates that are reasonably well converged with respect to further improvements in theory, it appears that the CCSD(T) method must be used with a basis of triple-zeta plus polarization quality on the carbon atoms. Second-order many-body perturbation theory performs adequately for all carbons except for that bearing the formal positive charge, while the self-consistent field approximation cannot be relied upon to predict even the correct qualitative ordering in the spectrum…

Electronic correlationChemistryChemical shiftIsotropyExtrapolationCarbon-13 NMRCondensed Matter PhysicsBiochemistryMolecular physicsSpectral lineComputational chemistryAdditive functionPhysical and Theoretical ChemistryBasis setJournal of Molecular Structure: THEOCHEM
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Quantitative prediction of gas-phase F19 nuclear magnetic shielding constants

2008

Benchmark calculations of (19)F nuclear magnetic shielding constants are presented for a set of 28 molecules. Near-quantitative accuracy (ca. 2 ppm deviation from experiment) is achieved if (1) electron correlation is adequately treated by employing the coupled-cluster singles and doubles (CCSD) model augmented by a perturbative correction for triple excitations [CCSD(T)], (2) large (uncontracted) basis sets are used, (3) gauge-including atomic orbitals are used to ensure gauge-origin independence, (4) calculations are performed at accurate equilibrium geometries [obtained from CCSD(T)/cc-pVTZ calculations correlating all electrons], and (5) vibrational averaging and temperature corrections…

Electronic correlationChemistryGeneral Physics and AstronomyElectronStandard deviationAtomic orbitalElectromagnetic shieldingPhysics::Atomic and Molecular ClustersDensity functional theoryPerturbation theory (quantum mechanics)Physics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsIndependence (probability theory)The Journal of Chemical Physics
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Perturbative treatment of triple excitations in internally contracted multireference coupled cluster theory.

2012

Internally contracted multireference coupled cluster (ic-MRCC) methods with perturbative treatment of triple excitations are formulated based on Dyall's definition of a zeroth-order Hamiltonian. The iterative models ic-MRCCSDT-1, ic-MRCC3, and their variants ic-MRCCSD(T), ic-MRCC(3) which determine the energy correction from triples by a non-iterative step are consistent in the single-reference limit with CCSDT-1a, CC3, CCSD(T), and CC(3), respectively. Numerical tests on the potential energy surfaces of BeH(2), H(2)O, and N(2) as well as on the structure and harmonic vibrational frequencies of the ozone molecule show that these methods account very well for higher order correlation effects…

Electronic correlationChemistryGeneral Physics and AstronomyEnergy minimizationPotential energyMolecular physicssymbols.namesakeCoupled clusterMolecular vibrationHarmonicsymbolsPerturbation theory (quantum mechanics)Physical and Theoretical ChemistryAtomic physicsHamiltonian (quantum mechanics)The Journal of chemical physics
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A two-scale approach to electron correlation in multiconfigurational perturbation theory.

2014

We present a new approach for the calculation of dynamic electron correlation effects in large molecular systems using multiconfigurational second-order perturbation theory (CASPT2). The method is restricted to cases where partitioning of the molecular system into an active site and an environment is meaningful. Only dynamic correlation effects derived from orbitals extending over the active site are included at the CASPT2 level of theory, whereas the correlation effects of the environment are retrieved at lower computational costs. For sufficiently large systems, the small errors introduced by this approximation are contrasted by the substantial savings in both storage and computational de…

Electronic correlationChemistryScale (descriptive set theory)General ChemistryMolecular systemsWhole systemsCorrelationComputational Mathematicscaspt2Atomic orbitalmultiscaleExcited stateStatistical physicsPerturbation theoryAtomic physicsJournal of computational chemistry
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1H nmr chemical shifts of [14]annulenes and their dianion salts

1987

Abstract The bridged (14]annulene 2 was reduced into its dianion and the structure of the dianion salt was proven by chemical and spectroscopic means. The 1H NMR spectroscopic properties of 2 are similar to those of the structurally related bridged [14]annulene 1 , whereas the corresponding dianions 2 2- and 1 2- are strikingly different. The geometries of 1 and 2 and their dianions were studied by means of a modified π-SCF force field approach. Almost planar perimeters without significant bond length alternation are obtained for the neutral annulenes 1 and 2 , whereas their dianions are characterized by structures with reduced symmetry. The 1H chemical shifts of the bridged [14]annulenes a…

Electronic correlationChemistryStereochemistryChemical shiftOrganic ChemistryCharge densityNuclear magnetic resonance spectroscopyAnnuleneConjugated systemBiochemistryCrystallographyDrug DiscoveryProton NMRMoleculeTetrahedron
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First-principles calculations for SrTiO3() surface structure

2002

As a continuation of our recent abinitio calculations of SrTiO 3(1 0 0) surface relaxation for the two different terminations (SrO and TiO2) [Phys. Rev. B 64 (2001) 23417], we analyze here their electronic structures (band structure, density of states, and the electronic density redistribution with emphasis on the covalency effects). We compare results of abinitio Hartree–Fock method with electron correlation corrections and density functional theory with different exchange-correlation functionals, including hybrid (B3PW, B3LYP) exchange techniques. Our results are also compared with previous abinitio plane-wave local density approximation calculations and experiments when availab le. Consi…

Electronic correlationChemistrySurfaces and InterfacesElectronic structureCondensed Matter PhysicsMolecular physicsSurfaces Coatings and FilmsAb initio quantum chemistry methodsComputational chemistryMaterials ChemistryDensity of statesDensity functional theoryLocal-density approximationElectronic band structureElectronic densitySurface Science
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The extended CC2 model ECC2

2013

We present a size-extensive extension to the CC2 model that avoids the complications with quasi-degeneracies that are present in the CC2 model and related perturbation theory-based approaches. The formulation also provides a consistent model for treating different parts of a molecular system at different levels of electron correlation. Such a subsystem approach leads to large reductions in the computational requirements without compromising the accuracy. In this initial study, we focus on static molecular properties. © 2013 Copyright Taylor and Francis Group, LLC.

Electronic correlationComputer scienceECC2BiophysicsExtension (predicate logic)Condensed Matter Physicelectron correlationCondensed Matter PhysicsCoupled clusterBiophysiccoupled clusterStatistical physicsAtomic physicsPerturbation theoryPhysical and Theoretical ChemistryFocus (optics)Molecular Biologysubsystem
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Quantitative prediction of gas-phase N15 and P31 nuclear magnetic shielding constants

2010

High-level ab initio benchmark calculations of the (15)N and (31)P NMR chemical shielding constants for a representative set of molecules are presented. The computations have been carried out at the Hartree-Fock self-consistent field (HF-SCF), density functional theory (DFT) (B-P86 and B3-LYP), second-order Moller-Plesset perturbation theory (MP2), coupled cluster singles and doubles (CCSD), and CCSD augmented by a perturbative treatment of triple excitations [CCSD(T)] level of theory using basis sets of triple zeta quality or better. The influence of the geometry, the treatment of electron correlation, as well as basis set and zero-point vibrational effects on the shielding constants are d…

Electronic correlationField (physics)ChemistryAb initioGeneral Physics and AstronomyCoupled clusterAb initio quantum chemistry methodsElectromagnetic shieldingPhysics::Atomic and Molecular ClustersDensity functional theoryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsBasis setThe Journal of Chemical Physics
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Ab initio calculations of zero-field splitting parameters in linear polyacenes

2003

Abstract The results of ab initio calculations of zero-field splitting (ZFS) parameters are presented for the linear polyacenes from benzene to pentacene. We show how the electron spin–spin (SS) parameters can be efficiently obtained from restricted high-spin open-shell wave functions (ROHF), and present calculations of these, comparing with the results of a recent multi-configurational self-consistent field approach. The SS parameters are obtained from electron SS coupling strengths evaluated as expectation values over the wave functions and from state-to-state spin–orbit (SO) interactions. The results for the two lowest triplet states of naphthalene demonstrate that excellent values can b…

Electronic correlationField (physics)Condensed matter physicsChemistryGeneral Physics and AstronomyZero field splittingMolecular physicsAb initio quantum chemistry methodsSinglet statePhysics::Chemical PhysicsPhysical and Theoretical ChemistryTriplet stateWave functionSpin (physics)Chemical Physics
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Structural and vibrational study of the tautomerism of histamine free-base in solution.

2003

Infrared and Raman spectroscopy in H(2)O and D(2)O and quantum Density Functional calculations were used to determine the structure of histamine free-base in aqueous solution. A quantum mechanical study of the tautomeric equilibrium of histamine free-base in solution was performed at the 6-311G level. Electronic correlation energies were included by using the hybrid functional B3LYP. The solvent was simulated as a continuum characterized by a dielectric constant, and the quantum system (solute) was placed in an ellipsoidal cavity. Solute-solvent electrostatic interaction was calculated by means a multipolar moment expansion introduced in the Hamiltonian. Four relevant histamine conformation…

Electronic correlationMolecular StructureChemistryInfrared spectroscopyGeneral ChemistrySpectrum Analysis RamanBiochemistryMolecular physicsPotential energyCatalysisHybrid functionalSolutionssymbols.namesakeColloid and Surface ChemistryNormal modeComputational chemistryMolecular vibrationSpectroscopy Fourier Transform InfraredsymbolsQuantum TheoryThermodynamicsRaman spectroscopyConformational isomerismHistamineJournal of the American Chemical Society
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