Search results for " function"

showing 10 items of 9395 documents

Towards multifunctional magnetic systems through molecular-programmed self assembly of Re(IV) metalloligands

2015

Abstract The molecular-programmed approach based on the use as ligands of tailor-made metalloligands containing stable six-coordinate rhenium(IV) as paramagnetic centres is presented in this review article. A relatively large amount of spin density is covalent-delocalized away from the rhenium to the peripheral atoms of the ligands in the case of the Re(IV) metalloligands, as shown by polarized neutron diffraction experiments and density functional theory calculations. This feature accounts for the significant through space-magnetic interactions that occur in most of its mononuclear species and more interestingly it also explains the strengthening of the magnetic interactions in the heterom…

ChemistryStereochemistryPolyatomic ionchemistry.chemical_elementBridging ligandRheniumInorganic Chemistrychemistry.chemical_compoundParamagnetismCrystallographyCyclamMaterials ChemistryMoleculeDensity functional theorySelf-assemblyPhysical and Theoretical ChemistryCoordination Chemistry Reviews
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A 58-electron superatom-complex model for the magic phosphine-protected gold clusters (Schmid-gold, Nanogold®) of 1.4-nm dimension

2011

We have re-investigated the structural identity of the famous gold-phosphine-halide Au:PR3:X compound having 55–69 gold atoms and core size of 1.4 nm (similar to “Schmid gold” or Nanogold®) from the viewpoint of the Superatom-Complex (SAC) model for ligand protected metal clusters, and in consideration of the ligand-adatom groups observed previously for the structurally known 39-atom cluster [Au39(PR3)14Cl6]−1. Density functional theory is used to define the formation energy of various compositions and structures, enabling a comparison of the stability of different cluster-sizes. In agreement with the SAC model, we find a strong correlation between optimal energy and delocalized electron sh…

ChemistrySuperatomShell (structure)Electron shell02 engineering and technologyGeneral ChemistryElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesIonDelocalized electronCrystallographyComputational chemistryCluster (physics)Density functional theory0210 nano-technologyChemical Science
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Electromechanical Properties of Ba(1–x)SrxTiO3 Perovskite Solid Solutions from First-Principles Calculations

2017

Many thanks to M. Maček-Kržmanc, R. A. Evarestov, D. Gryaznov and D. Fuks for fruitful discussions. This study was supported by the ERA-NET HarvEnPiez project.

ChemistryThermodynamics02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesPiezoelectricityFerroelectricityHybrid functionalTetragonal crystal systemComputational chemistryLinear combination of atomic orbitalsPhase (matter)0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]Physical and Theoretical Chemistry010306 general physics0210 nano-technologyPerovskite (structure)Solid solution
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Vibrational analysis of the electronic spectrum of ethylene based onab initio SCF-CI calculations

1972

Ab initio calculations for CH2 twisting and CC stretching vibrational wavefunctions and energy levels are reported for various electronic states of ethylene C2H4. Electronic transition moments between these states are also obtained to allow a calculation of the oscillator strengths for vibrational transitions involved in various electronic band systems; from this study it is concluded that thevertical electronic energy differenceΔE e may differ significantly from the energy of the absorption maximumΔE max with which it is often equated. In particular it is found in the case of theπ→π * singlet-singlet excitation of ethylene that theΔE e value overestimates the most probable vibrational tran…

ChemistryTransition dipole momentAb initioMolecular electronic transitionsymbols.namesakeAb initio quantum chemistry methodsRydberg formulasymbolsChiropracticsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsAbsorption (electromagnetic radiation)Wave functionExcitationTheoretica Chimica Acta
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Anharmonic vibrational frequency calculations for solvated molecules in the B3LYP Kohn–Sham basis set limit

2012

Abstract The solvent dependence of harmonic and anharmonic vibrational wavenumbers of water, formaldehyde and formamide was studied using the B3LYP method. The results obtained with the hierarchy of Jensen's polarization-consistent basis sets were fitted with two-parameter formula toward the B3LYP Kohn–Sham complete basis set (CBS) limit. Anharmonic corrections have been obtained by a second order perturbation treatment (VPT2) and vibrational configuration interaction (VCI) method. The solvent environment was treated according to the self-consistent reaction field polarizable continuum model (SCRF PCM) approach.

ChemistryVibrational partition functionMolecular vibrationAnharmonicityPhysics::Atomic and Molecular ClustersKohn–Sham equationsPhysics::Chemical PhysicsSolvent effectsConfiguration interactionAtomic physicsPolarizable continuum modelSpectroscopyBasis setVibrational Spectroscopy
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Cluster-model density functional study of a W–Cu(100) STM junction

1999

Abstract In this article, we investigate the electronic properties of different clusters modelling a tungsten tip, the Cu(1 0 0) surface and interacting W–Cu(1 0 0) systems in STM configuration. Electronic structure calculations are carried out within the LDA approximation of the Density Functional Theory (DFT). Both integrated (densities of states) and local properties (electronic density and electrostatic potential) are considered. The study is performed for top and hollow surface sites and two different tip–sample separations.

Chemistrychemistry.chemical_elementHeterojunctionGeneral ChemistryElectronic structureTungstenCondensed Matter PhysicsMolecular physicsTransition metalComputational chemistryDensity of statesCluster (physics)General Materials ScienceDensity functional theoryElectronic densityJournal of Physics and Chemistry of Solids
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Thiolate Adsorption on Au(hkl) and Equilibrium Shape of Large Thiolate-covered Gold Nanoparticles

2013

The adsorption of thiolates on Au surfaces employing density-functional-theory calculations has been studied. The dissociative chemisorption of dimethyl disulfide (CH3S−SCH3) on 14 different Au(hkl) is used as a model system. We discuss trends on adsorption energies, bond lengths, and bond angles as the surface structure changes, considering every possible Au(hkl) with h, k, l ≤ 3 plus the kinked Au(421). Methanethiolate (CH3S-) prefers adsorption on bridge sites on all surfaces considered; hollow and on top sites are highly unfavourable. The interface tensions for Au(hkl)-thiolate interfaces is determined at low coverage. Using the interface tensions in a Wulff construction method, we cons…

ChemistrytiheysfunktionaaliteoriaGeneral Physics and AstronomyNanoparticleDissociation (chemistry)kultaBond lengthCrystallographyMolecular geometryAdsorptionChemisorptionDensity functional theoryGoldPhysical and Theoretical ChemistryWulff constructionta116density functional theory
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Dyes That Bear Thiazolylazo Groups as Chromogenic Chemosensors for Metal Cations

2011

A family of dyes (L 1-L 6) that contain a thiazolylazo group as signalling subunit and several macrocyclic cavities with different ring sizes and type and number of heteroatoms as binding sites has been synthesized and characterized. Solutions of L 1-L 6 in acetonitrile show broad and structureless absorption bands in the 554-577 nm range with typicalmolar absorption coefficients that range from 20000 to 32000 M -1 cm -1. A detailed protonation study was carried out with solutions of L 1, L 2 and L 5 in acetonitrile. Addition of one equivalent of protons to L 1 and L 2 resulted in the development of a new band at 425 and 370 nm, respectively, which was ascribed to protonation in the aniline…

ChemosensorsHeteroatomQUIMICA INORGANICAProtonationMercuryCation sensorsPhotochemistryInorganic ChemistryMetalchemistry.chemical_compoundAzodyesDensity functional calculationsQUIMICA ORGANICAchemistryLeadAbsorption bandvisual_artBathochromic shiftQUIMICA ANALITICAvisual_art.visual_art_mediumMoietyDensity functional theoryAcetonitrileDyes
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Large hiatal hernia at chest radiography in a woman with cardiorespiratory symptoms

2012

Hiatal hernia (HH) is a frequent entity. Rarely, it may exert a wide spectrum of clinical presentations mimicking acute cardiovascular events such as angina-like chest pain until manifestations of cardiac compression that can include postprandial syncope, exercise intolerance, respiratory function, recurrent acute heart failure, and hemodynamic collapse. A 69-year-old woman presented to the emergency department complaining of fatigue on exertion, cough, and episodes of restrosternal pain with less than 1 hour of duration. Her medical history only included some episodes of bronchitis and no history of hypertension. The 12-lead electrocardiogram demonstrated sinus rhythm with right bundle-bra…

Chest Painmedicine.medical_specialtyBundle-Branch BlockChest painHiatal herniaElectrocardiographymedicine.arteryInternal medicinemedicineHumansRespiratory functionSinus rhythmmedicine.diagnostic_testbusiness.industryGeneral Medicinemedicine.diseaseRadiographyHernia HiatalHeart failurePulmonary arteryEmergency MedicineCardiologyFemaleRadiologymedicine.symptomTransthoracic echocardiogramEmergency Service HospitalbusinessElectrocardiographyThe American Journal of Emergency Medicine
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Process-independent strong running coupling

2016

We unify two widely different approaches to understanding the infrared behaviour of quantum chromodynamics (QCD), one essentially phenomenological, based on data, and the other computational, realised via quantum field equations in the continuum theory. Using the latter, we explain and calculate a process-independent running-coupling for QCD, a new type of effective charge that is an analogue of the Gell-Mann--Low effective coupling in quantum electrodynamics. The result is almost identical to the process-dependent effective charge defined via the Bjorken sum rule, which provides one of the most basic constraints on our knowledge of nucleon spin structure. This reveals the Bjorken sum to be…

Chiral perturbation theoryNuclear TheoryFOS: Physical sciences01 natural sciencesEffective nuclear chargeNuclear Theory (nucl-th)High Energy Physics - LatticeHigh Energy Physics - Phenomenology (hep-ph)Quantum mechanics0103 physical sciencesBeta function (physics)Quantum field theoryNuclear Experiment (nucl-ex)010306 general physicsNuclear ExperimentPhysicsCoupling constantQuantum chromodynamics010308 nuclear & particles physicsHigh Energy Physics - Lattice (hep-lat)High Energy Physics::PhenomenologyHigh Energy Physics - PhenomenologySum rule in quantum mechanicsUltraviolet fixed pointProcess-independentRunning coupling
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