Search results for " function"

showing 10 items of 9395 documents

Ab initio study of the electronic and atomic structure of the wolframite-type ZnWO4

2009

Abstract Ab initio quantum chemistry calculations of the structural and electronic properties of monoclinic wolframite-type ZnWO 4 crystal have been performed within the periodic linear combination of atomic orbitals (LCAO) method using six different Hamiltonians, based on density functional theory (DFT) and hybrid Hartree-Fock-DFT theory. The obtained results for optimized structural parameters, band gap and partial density of states are compared with available experimental data, and the best agreement is observed for hybrid Hamiltonians. The calculations show that zinc tungstate is a wide band gap material, with the direct gap about 4.6 eV, whose valence band has largely O 2p character, w…

ChemistryBand gapAb initioGeneral ChemistryElectronic structureCondensed Matter PhysicsQuantum chemistryLinear combination of atomic orbitalsAb initio quantum chemistry methodsPhysics::Atomic and Molecular ClustersMaterials ChemistryDensity functional theoryAtomic physicsMonoclinic crystal systemSolid State Communications
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A Comparative Analysis of the Electrophilicity of Organic Molecules between the Computed IPs and EAs and the HOMO and LUMO energies

2007

[EN] The electrophilicity index, omega, of a series of substituted ethylenes used in some relevant organic reactions has been evaluated from the ionization potential JP) and the electron affinity (EA) computed by vertical ionization at the B3LYP/aug-cc-PVTZ level. The corresponding electrophilicity values are well correlated with those obtained from the HOMO and LUMO energies of the neutral molecules. The good linear correlation found between omega(I,A) and omega(H,L)(LBS), and between omega(H,L)(LBS) and omega(H,L)(SBS) allows to confirm the use of the easily available B3LYP/6-31G(*) HOMO and LUMO energies to obtain reasonable values of the global electrophilicity index of organic molecule…

ChemistryBasis-SetsReactivityGeneral Physics and AstronomyScalesOrganic reactionDensity-Functional TheoryComputational chemistryHardnessIonizationElectron affinityElectrophileComputationMoleculeElectron-AffinitiesDensity functional theoryQuantitative characterizationPhysical and Theoretical ChemistryIonization energyHOMO/LUMO
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A hollow tetrahedral cage of hexadecagold dianion provides a robust backbone for a tuneable sub-nanometer oxidation and reduction agent via endohedra…

2007

We show, via density functional theory calculations, that dianionic Au16(2-) cluster has a stable, hollow, Td symmetric cage structure, stabilized by 18 delocalized valence electrons. The cage maintains its robust geometry, with a minor Jahn-Teller deformation, over several charge states (q = -1,0,+1), forming spin doublet, triplet and quadruplet states according to the Hund's rules. Endohedral doping of the Au16 cage by Al or Si yields a geometrically robust, tuneable oxidation and reduction agent. Si@Au16 is a magic species with 20 delocalized electrons. We calculate a significant binding energy for the anionic Si@Au16/O2- complex and show that the adsorbed O2 is activated to a superoxo-s…

ChemistryBinding energyDopingGeneral Physics and AstronomyGeneral MedicineRedoxIonCrystallographyDelocalized electronComputational chemistryChemical physicsTetrahedronCluster (physics)NanometreDensity functional theoryPhysical and Theoretical ChemistryTriplet stateCageValence electronPhysical chemistry chemical physics : PCCP
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Capillary Hysteresis in Nanopores: Theoretical and Experimental Studies of Nitrogen Adsorption on MCM-41

1995

Capillary hysteresis in cylindrical nanopores has been studied using MCM-41 as the prime example of a mesoporous material. These materials, due to their regular pore structure, can be considered to be candidates for reference adsorbents for standardizing adsorption measurements and methods for characterization of porous solids. They provide a unique opportunity for verification of theoretical models employed for predicting phase equilibrium in confined geometry. Three samples with monodisperse pore channels have been synthesized and examined using X-ray diffraction (XRD). Nitrogen adsorption isotherms were modeled using nonlocal density functional theory (NLDFT) in a wide range of pore size…

ChemistryCapillary actionDispersityMineralogyThermodynamicsSurfaces and InterfacesCondensed Matter PhysicsCondensed Matter::Materials ScienceNanoporeHysteresisAdsorptionMetastabilityElectrochemistryGeneral Materials ScienceDensity functional theoryMesoporous materialSpectroscopyLangmuir
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9-Methyl-3-phenyldiazenyl-9H-carbazole: X-ray and DFT-calculated structures

2006

The title compound, C19H15N3, was prepared by condensation of 3-nitroso­carbazole and aniline with subsequent methyl­ation. The structure is built up of stacks of almost planar mol­ecules. Density functional theory (DFT) calculations predict a completely planar conformation, different from that observed in the crystal lattice. HOMA (harmonic oscillator model of aromaticity) indices, calculated for three aromatic rings, demonstrate the small influence of the azo substituent on π electrons in the carbazole system.

ChemistryCarbazoleCondensationSubstituentAromaticityGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundCrystallographyAnilineComputational chemistryDensity functional theoryHarmonic oscillatorActa Crystallographica Section C Crystal Structure Communications
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ChemInform Abstract: Weak Interactions Between Trivalent Pnictogen Centers: Computational Analysis of Bonding in Dimers X3E···EX3(E: Pnictogen, X: Ha…

2009

The nature of weak interactions in dimers X3E···EX3 (E = N−Bi, X = F−I) was investigated by wave function and density functional theory (DFT)-based methods. Out of the 20 systems studied, 10 are found to be bound at the CP-MP2 and LMP2 levels of theory. Detailed partition of the interaction energy into different components revealed that dispersion is the primary force holding the dimers together but there also exists an important ionic component whose contribution increases with increasing halogen size. As expected, standard density functionals fail to describe bonding in the studied systems. However, the performance of DFT methods can be easily improved via empirical dispersion correction …

ChemistryChemical physicsHydrogen bondBinding energyAb initioIonic bondingDensity functional theoryGeneral MedicineInteraction energyDispersion (chemistry)PnictogenChemInform
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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 MRCI PS and CASSCF study of the ground state MgO dissociation energy

1991

Abstract Ab initio calculations at CASSCF and MRCI PS levels are used to determine the dissociation energy for the X 1 Σ + state of MgO, which adiabatically dissociates to the ground state 1 S g of magnesium and to the excited 1 D g state of oxygen, as well as other spectroscopic parameters. Emphasis is placed upon the problem of properly selecting an adequate active space in CASSCF calculations and upon the improvements obtained in MRCI by selecting perturbatively the most important contributions to the total wavefunction and evaluating the remaining ones only by perturbational method. Through a procedure based on stabilizing the computed dissociation energy, values of 3.87 eV (MRCI PS) an…

ChemistryComputational chemistryAb initio quantum chemistry methodsExcited stateAnharmonicityGeneral Physics and AstronomyRotational spectroscopyPhysical and Theoretical ChemistryAtomic physicsWave functionGround stateDiatomic moleculeBond-dissociation energyChemical Physics Letters
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A Density Functional Theory study on gold cyanide interactions: The fundamentals of ore cleaning

2010

We have employed Density Functional Theory calculations to study the adsorption of CN, CN− and KCN on Au(111) and Au(211) surfaces and compare the obtained results to CO. The adsorption of CN, CN−, and KCN are exothermic with respect to the gas-phase moieties, and the adsorption energy increases at steps. Our results show that the binding mechanism of CN− is different from that of CO. The projected LDOS indicates that the bond between the flat surface and CN shows very small overlap between metal and CN states. This overlap increases provided that extra charge is present or low-coordinated Au atoms are available. Charge transfer is analyzed via the Bader method and the Electron Localization…

ChemistryCyanideInorganic chemistrySurfaces and InterfacesCondensed Matter PhysicsElectron localization functionSurfaces Coatings and FilmsMetalchemistry.chemical_compoundElectron transferAdsorptionTransition metalCovalent bondvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical chemistryDensity functional theorySurface Science
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A semi-empirical extrapolation technique for atomic and molecular properties derived from correlated wavefunctions

1976

Abstract A semi-empirical extrapolation technique is suggested for recovering the correlation defect remaining in atomic and molecular properties calculated from highly correlated wavefunctions. These procedures are applied to PNO-CEPA and PNO-IPPA calculations on F, F + , F − , and HF in order to obtain “exact” estimates of the ionization potential, electron affinity, and dissociation energy.

ChemistryElectron affinityExtrapolationGeneral Physics and AstronomyPhysical and Theoretical ChemistryAtomic physicsIonization energyWave functionBond-dissociation energyChemical Physics Letters
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