Search results for "Clusters"

showing 10 items of 1274 documents

Valence bands of poly(methylmethacrylate) and photoion emission in vacuum ultraviolet region

1992

Photoion and photoelectron yields were measured for poly(methylmethacrylate) in the photon energy region of 8–40 eV using synchrotron radiation. Further, the valence‐band structure was investigated with ultraviolet photoelectron spectra and valence effective Hamiltonian calculations. A significant difference was observed between the photon energy dependencies of photoion and photoelectron yields. The threshold energy for photoion emission was found to be 10.5 eV, while that for photoelectron emission was 8.5 eV, indicating holes created near the valence‐band top do not contribute to the ion emission. At the higher‐energy region, the ion emission efficiency was found to be enhanced in the ph…

PmmaValence BandsAstrophysics::High Energy Astrophysical PhenomenaGeneral Physics and AstronomySynchrotron radiationPhotoelectron photoion coincidence spectroscopyAstrophysics::Cosmology and Extragalactic AstrophysicsPhoton energymedicine.disease_causeSpectral lineX-ray photoelectron spectroscopyEv Range 10−100:FÍSICA [UNESCO]medicinePmma ; Ion Emission ; Electron Emission ; Photoelectron Spectroscopy ; Ev Range 10−100 ; Valence Bands ; Band StructurePhysics::Atomic and Molecular ClustersIon EmissionPhysics::Atomic PhysicsElectron EmissionBand StructureAstrophysics::Galaxy AstrophysicsValence (chemistry)ChemistryPhotoelectron SpectroscopyUNESCO::FÍSICAThreshold energyAtomic physicsUltraviolet
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Local properties of quantum chemical systems: the LoProp approach.

2004

A new method is presented, which makes it possible to partition molecular properties like multipole moments and polarizabilities, into atomic and interatomic contributions. The method requires a subdivision of the atomic basis set into occupied and virtual basis functions for each atom in the molecular system. The localization procedure is organized into a series of orthogonalizations of the original basis set, which will have as a final result a localized orthonormal basis set. The new localization procedure is demonstrated to be stable with various basis sets, and to provide physically meaningful localized properties. Transferability of the methyl properties for the alkane series and of t…

Polarisabilitybusiness.industryChemistryGeneral Physics and AstronomyBasis functionQuantum chemistryQuantum mechanicsddc:540Theoretical chemistryPhysics::Atomic and Molecular ClustersPartition (number theory)Molecular momentsOrthonormal basisStatistical physicsSet theoryPhysical and Theoretical ChemistrybusinessMultipole expansionQuantum chemistryBasis setSubdivisionThe Journal of chemical physics
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Laboratory Studies of Scattering Properties of Polluted Cloud Droplets: Implications for FSSP Measurements

2008

Abstract Laboratory experiments were conducted in the Mainz vertical wind tunnel to study the effects of pollutants dissolved or suspended in cloud droplets on the droplet size measurements of a Forward Scattering Spectrometer Probe (FSSP). The FSSP is a widely used instrument to derive microphysical properties of atmospheric clouds. Individual droplets of different well-defined sizes were freely falling at their terminal velocities in the wind tunnel while the intensity of radiation emitted by the He–Ne laser of the FSSP and scattered by the droplets was measured. For this purpose, the FSSP was adapted and mounted to the wind tunnel. The intensity of radiation scattered by the droplets in …

Pollutantendocrine systemAtmospheric ScienceAmmonium sulfateMaterials scienceSpectrometerbusiness.industryScatteringForward scattertechnology industry and agricultureAnalytical chemistryOcean EngineeringRadiationcomplex mixtureseye diseasesPhysics::Fluid Dynamicschemistry.chemical_compoundOpticschemistryPhysics::Atomic and Molecular ClustersbusinessRadiant intensityPhysics::Atmospheric and Oceanic PhysicsWind tunnelJournal of Atmospheric and Oceanic Technology
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Resonant laser ionization of polonium at rilis-isolde for the study of ground- and isomer-state properties

2008

Three new ionization schemes for polonium have been tested with the resonant ionization laser ion source (RILIS) during the on-line production of 196Po in a UCx target at ISOLDE. The saturation of the atomic transitions has been observed and the yields of the isotope chain 193–198,200,202,204Po have been measured. This development provides the necessary groundwork for performing in-source resonant ionization spectroscopy on the neutron-deficient polonium isotopes (Z = 84). ispartof: Nuclear Instruments & Methods in Physics Research B vol:266 issue:19 pages:4403-4406 ispartof: location:FRANCE, Deauville status: published

PoloniumNuclear and High Energy Physicschemistry.chemical_element[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]7. Clean energy01 natural scienceslaw.inventionlawIonization0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics::Atomic Physics010306 general physicsSpectroscopyNuclear ExperimentInstrumentationPoloniumIsotope010308 nuclear & particles physicsOptical transitionSaturationLaserIon sourcechemistryOptical transitionProduction yieldLaser ionizationAlpha decay[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physics
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Ultra-small gold nanoclusters assembled on plasma polymer-modified zeolites: a multifunctional nanohybrid with anti-haemorrhagic and anti-inflammator…

2021

Refereed/Peer-reviewed Hemostatic agents are pivotal for managing clinical and traumatic bleeding during emergency and domestic circumstances. Herein, a novel functional hybrid nanocomposite material consisting of plasma polymer-modified zeolite 13X and ultra-small gold nanoclusters (AuNCs) was fabricated as an efficient hemostatic agent. The surface of zeolite 13X was functionalised with amine groups which served as binding sites for carboxylate terminated AuNCs. Protein corona studies revealed the enhanced adsorption of two proteins, namely, coagulation factors and plasminogen as a result of AuNCs immobilization on the zeolite surface. The immune response studies showed that the hybrid na…

PolymersAnti-Inflammatory AgentsProtein CoronaHemorrhagezeolites02 engineering and technology010402 general chemistry01 natural sciencesNanoclustersAdsorptionprotein coronaHumansGeneral Materials ScienceZeoliteHemostatic AgentNanocompositebiologyChemistry021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceshemostatic agentsbiology.proteinZeolitesAmine gas treatingVitronectinGold0210 nano-technology
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Torsional effects on the molecular polarizabilities of the benzothiazole (A)-benzobisthiazole (B) oligomer A-B13-A

1996

Abstract We outline a method for the calculation of multipole moments and molecular dipole-dipole ( ), dipole-quadrupole ( ), and quadrupole-quadrupole ( ) polarizabilities, which we have successfully applied to benzothiazole (A)-benzobisthiazole (B) oligomer A-B13-A. Three model rotational isomers have been characterized: (1) the fully planar (000) rotational isomer; (2) a conformation with each unit rotated 10° in the alternate direction (+−+), and (3) a rotational isomer with each unit rotated 10° in the same direction (+++). The dipole moment, μ , is smaller for isomers 000 and +−+ than for isomer +++. The calculation of , , and has been performed by use of the interacting induced dipol…

PolymersChemistryStatic ElectricityMolecular ConformationBiophysicsBiochemistryOligomerThiazolesCrystallographychemistry.chemical_compoundDipoleModels ChemicalSolubilityBenzothiazoleComputational chemistryComputer GraphicsPhysics::Atomic and Molecular ClustersPolarComputer SimulationBenzothiazolesPhysics::Chemical PhysicsSolubilityAnisotropyMultipole expansionOrder of magnitudeJournal of Molecular Graphics
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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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