Search results for "init"

showing 10 items of 6629 documents

Hartree–Fock study of adhesion and charge redistribution on the Ag/MgO(0 0 1) interface

2001

Abstract Ab initio study of the Ag/MgO(0 0 1) interfaces based on a quantitative analysis of the bonding in the interfacial region is provided in the framework of Hartree–Fock approach. We are describing the way interfacial electronic and other properties evolve as a function of metal coverage. General conclusion that could be drawn from our calculations is that chemical bond formation is not important for the Ag/MgO(0 0 1) perfect interface. Physisorption of Ag atoms over surface O 2− ions associated with atomic polarization and charge redistribution in the metal planes are the dominant effects. The adhesion energy is enhanced by the interaction of the substrate Mg 2+ ions with the surplus…

ChemistryHartree–Fock methodAb initioSurfaces and InterfacesElectronic structureCondensed Matter PhysicsSurfaces Coatings and FilmsIonChemical bondPhysisorptionAb initio quantum chemistry methodsChemical physicsMonolayerMaterials ChemistryPhysical chemistrySurface Science
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Solute-induced Water Structure: Computer Simulation on a Model System

1988

Abstract Two series of Monte Carlo simulations have been carried out on a system consisting of 125 water molecules, one of which is kept fixed to simulate a water molecule whose mobility is restricted by a solute. The results are checked against similar simulations without restrictions, used as a control, and they show how the blocked molecule helps increase both the structural order and the connectivity of the hydrogen bond network. Cooperativity originating from proton polarizability of H-bonds and/or from many-body terms of interaction potentials cannot be involved since we use a rigid water model and ab initio pair potentials. The present findings are interpreted as indicative of a moti…

ChemistryHydrogen bondGeneral Chemical EngineeringMonte Carlo methodAb initioCooperativityGeneral ChemistryCondensed Matter PhysicsChemical physicsComputational chemistryPolarizabilityModeling and SimulationWater modelDynamic Monte Carlo methodMoleculeGeneral Materials ScienceInformation SystemsMolecular Simulation
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An ab Initio MO Study of Silver Triflate Complexation in [2.2.1]Cyclophane π-Prismands

2002

Ab initio Hartree-Fock and DFT MO calculations have been used to study the conformations of six [2.2.1]cyclophane π-prismands and the formation of their π-complexes with silver triflate (AgSO 3 CF 3 ). The lowest energy cyclophane conformations and their silver triflate π-complexes have been calculated with HF/3-21G* and B3LYP/3-21G* levels of theory. The nature of bonding in silver triflate π-complexes has been studied with natural bond orbital analysis (NBO). Energies of the calculated cyclophanes and complexes, together with the formation energies of those complexes, have also been discussed. The results have been compared to available X-ray crystal structures and also to results of the …

ChemistryHydrogen bondLigandOrganic ChemistryAb initioPhotochemistryIonInorganic ChemistryCrystallographychemistry.chemical_compoundAb initio quantum chemistry methodsPhysical and Theoretical ChemistryTrifluoromethanesulfonateCyclophaneNatural bond orbitalOrganometallics
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Structural and electronic contributions to hyperpolarizability in methyl p-hydroxy benzoate

2006

Abstract The single crystals of methyl p-hydroxy benzoate (MPHB) are grown from methanol solution by a low temperature solution growth technique. The SHG efficiency is tested using Q-switched Nd:YAG laser of wavelength λ at 1064 nm, which is approximately 1.2 times that of urea. Vibrational spectral analysis using NIR-FT Raman and FT-IR spectra is carried out to understand the structural and electronic contributions to hyperpolarizability in MPHB. The DFT computations are also performed at B3LYP/6-311G(d,p) level to derive equilibrium geometry, vibrational wavenumbers and intensities. The results of ab initio calculations at HF/6-311G(d,p) level show that the vibrational contribution for th…

ChemistryHydrogen bondOrganic ChemistryIntermolecular forceAnalytical chemistryHyperpolarizabilityAcceptorAnalytical ChemistryInorganic Chemistrysymbols.namesakeAb initio quantum chemistry methodsIntramolecular forcesymbolsElectronic effectPhysical chemistryRaman spectroscopySpectroscopyJournal of Molecular Structure
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Raman spectroscopy of acetic acid monomer and dimers isolated in solid argon

2011

Acetic acid (AA) monomer and its dimers were studied by means of Raman spectroscopy combined with the matrix isolation technique. All fundamental bands of CH3COOH monomer were identified, including the CH3 torsional mode. Additionally, three overtone or combination modes were observed as a result of their enhanced intensities by Fermi resonance (FR). Twenty bands of the cyclic dimer (C2h) were identified and assigned, among which appear all intermolecular modes. Bands due to two different higher energy forms of the dimer were also identified. The experimental assignments are supported by ab initio calculations. Copyright © 2011 John Wiley & Sons, Ltd.

ChemistryHydrogen bondOvertoneDimerMatrix isolationPhotochemistryCrystallographychemistry.chemical_compoundsymbols.namesakeMonomerAb initio quantum chemistry methodssymbolsGeneral Materials ScienceFermi resonanceRaman spectroscopyta116SpectroscopyJournal of Raman Scpectroscopy
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First principles slab calculations of the regular Cu/MgO(001) interface

2004

Ab initio slab calculations are performed for the copper adhesion over magnesium ions on the perfect MgO(0 0 1) surface with 1/4 monolayer (ML), two types of 1/2 ML and 1 ML substrate coverages. Results of our calculations are compared with various experimental and theoretical data. Both small atomic polarization and charge redistribution give the dominant contributions to the physisorption bonding on a regular Cu/MgO(0 0 1) interface.

ChemistryInorganic chemistryAb initiochemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsMolecular physicsCopperSurfaces Coatings and FilmsPhysisorptionTransition metalAb initio quantum chemistry methodsMonolayerMaterials ChemistrySlabMagnesium ionSurface Science
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Influence of layer structure preservation on the catalytic properties of the pillared zeolite MCM-36

2010

MCM-36 is a catalytically active material made by swelling and subsequent pillaring of a layered zeolite precursor, MCM-22(P). However, the swelling procedures lead to significant destruction of layer structure and alteration of framework silicon/aluminum (Si/Al) ratio, which are likely to influence the acidity and catalytic activity of the final materials. We report a milder swelling and pillaring process to prevent such structural destruction. The resulting pillared materials show higher crystallinity and improved retention of the zeolitic layer structure when compared to the ones prepared by the previously reported methods involving more aggressive treatments. Implications of such struct…

ChemistryInorganic chemistryXyleneAlkylationMolecular sieveHeterogeneous catalysisCatalysisCatalysisCrystallinitychemistry.chemical_compoundmedicinePhysical and Theoretical ChemistrySwellingmedicine.symptomZeoliteJournal of Catalysis
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The Nature of Transannular Interactions in E4N4 and E82+ (E = S, Se)

2015

The electronic structures of tetrachalcogen tetranitrides, E4N4, and octachalcogen dications, E8(2+), and the nature of their intramolecular E···E interactions (E = S, Se) was studied with high-level theoretical methods. The results reveal that the singlet ground states of both systems have a surprisingly large correlation contribution which functions to weaken and therefore lengthen the cross-ring E-E bond. The observed correlation effects are primarily static in E4N4, whereas in E8(2+) the dynamic part largely governs the total correlation contribution. The presented description of bonding is the first that gives an all-inclusive picture of the origin of cross-ring interactions in E4N4 an…

ChemistryIntermolecular forceAb initioElectronic structureConfiguration interactionComputer Science ApplicationsChemical physicsQuantum mechanicsIntramolecular forceSinglet statePhysical and Theoretical ChemistryPerturbation theoryWave functionta116Journal of Chemical Theory and Computation
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Theoretical Study of the Twisted Intramolecular Charge Transfer in 1-Phenylpyrrole

2000

Ab initio results for the electronic spectra of 1-phenylpyrrole are presented. Vertical, emission, and nonvertical excitation energies have been computed using multiconfigurational second-order per...

ChemistryIntramolecular forceAb initioCharge (physics)Physics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsExcitationSpectral lineThe Journal of Physical Chemistry A
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Sicilian bottled natural waters: Major and trace inorganic components

2013

Sixteen bottled waters of various Sicilian brands, 11 natural mineral waters and five normal drinking waters, were analyzed for major and trace inorganic components by ion chromatography (IC) and inductively coupled plasma-mass spectrometry (ICP-MS), respectively. The bottled waters represent a variety of water types with significantly different compositions in terms of salinity, major components and trace elements. Chemically, they range from Ca–HCO3 and Ca–SO4 to Na–HCO3 types. Total dissolved solids ranges from 54 to 433 mg/L, total hardness from 25 to 238 mg/L CaCO3, and measured Na content from 5.7 to 57 mg/L. According to total dissolved ions, all the bottled waters were classified as…

ChemistryIon chromatographyBottled waterMass spectrometryTotal dissolved solidsPollutionSettore GEO/08 - Geochimica E VulcanologiaSalinityNutrientGeochemistry and PetrologyEnvironmental chemistryEnvironmental ChemistryWater qualitybottled natural waters major and trace elements municipal watersChemical compositionApplied Geochemistry
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