Search results for " Density Functional Theory."

showing 10 items of 106 documents

A Molecular Electron Density Theory Study of the Reactivity of Azomethine Imine in [3+2] Cycloaddition Reactions

2017

The electronic structure and the participation of the simplest azomethine imine (AI) in [3+2] cycloaddition (32CA) reactions have been analysed within the Molecular Electron Density Theory (MEDT) using DFT calculations at the MPWB1K/6-311G(d) level. Electron localisation function (ELF) topological analysis reveals that AI has a pseudoradical structure, while the conceptual DFT reactivity indices characterise this TAC as a moderate electrophile and a good nucleophile. The non-polar 32CA reaction of AI with ethylene takes place through a one-step mechanism with low activation energy, 5.3 kcal/mol-1. A bonding evolution theory (BET) study indicates that this reaction takes place through a non-…

Models MolecularThiosemicarbazones[3+2] cycloaddition reactionsImineMolecular Conformationmolecular mechanismsazomethine iminePharmaceutical ScienceElectronsElectronic structureActivation energy010402 general chemistry01 natural sciencesArticlebonding evolution theoryAnalytical Chemistrychemistry.chemical_compoundNucleophileComputational chemistryDrug Discoveryconceptual density functional theoryMoleculeReactivity (chemistry)organic_chemistryelectron densityPhysical and Theoretical Chemistryazomethine imine; [3+2] cycloaddition reactions; molecular electron density theory; conceptual density functional theory; electron localisation function; bonding evolution theory; electron density; molecular mechanisms; chemical reactivityCycloaddition ReactionMolecular Structure010405 organic chemistrymolecular electron density theoryOrganic ChemistryCycloaddition0104 chemical scienceschemistryChemistry (miscellaneous)ElectrophileQuantum TheoryThermodynamicsMolecular MedicineDensity functional theoryImineselectron localisation functionAzo Compoundschemical reactivityMolecules; Volume 22; Issue 5; Pages: 750
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Optical Properties of Monolayer-Protected Aluminum Clusters: Time-Dependent Density Functional Theory Study

2015

We examine the electronic and optical properties of experimentally known monolayer-protected aluminum clusters Al4(C5H5)4, Al50(C5Me5)12, and Al69(N(SiMe3)2)183– using time-dependent density functional theory. By comparing Al4(C5H5)4 and the theoretical Al4(N(SiMe3)2)4 cluster, we observe significant changes in the optical absorption spectra caused by different hybridization between metal core and ligands. Using these initial observations, we explain the calculated spectra of Al50(C5Me5)12 and Al69(N(SiMe3)2)183–. Al50(C5Me5)12 shows a structured spectrum with clear regions of low-intensity core-to-core transitions followed by high-intensity ligand-to-core transitions due to its high symmet…

ta114Chemistrychemistry.chemical_elementTime-dependent density functional theorySpectral lineSymmetry (physics)3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsaluminum clustersMetalCrystallographytime-dependent density functional theoryGeneral EnergyAluminiumvisual_artMonolayervisual_art.visual_art_mediumCluster (physics)Density functional theoryPhysical and Theoretical Chemistryta116Journal of Physical Chemistry C
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Multiconfigurational second-order perturbation study of the decomposition of the radical anion of nitromethane

2004

The doublet potential energy surfaces involved in the decomposition of the nitromethane radical anion (CH(3)NO(2) (-)) have been studied by using the multistate extension of the multiconfigurational second-order perturbation method (MS-CASPT2) in conjunction with large atomic natural orbital-type basis sets. A very low energy barrier is found for the decomposition reaction: CH(3)NO(2) (-)--[CH(3)NO(2)](-)--CH(3)+NO(2) (-). No evidence has been obtained on the existence of an isomerization channel leading to the initial formation of the methylnitrite anion (CH(3)ONO(-)) which, in a subsequent reaction, would yield nitric oxide (NO). In contrast, it is suggested that NO is formed through the …

Potential Energy SurfacesNitromethaneOrganic CompoundsGeneral Physics and AstronomyOrganic Compounds ; Negative Ions ; Potential Energy Surfaces ; Dissociation ; Ion-Molecule Reactions ; Perturbation Theory ; Density Functional Theory ; SCF CalculationsSCF CalculationsPotential energyDissociation (chemistry)UNESCO::FÍSICA::Química físicaIonIon-Molecule Reactionschemistry.chemical_compoundchemistryComputational chemistryPerturbation TheoryNegative IonsDensity functional theorySymmetry breakingPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]IsomerizationDissociationDensity Functional TheoryChemical decompositionThe Journal of Chemical Physics
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Nuclear Energy Density Optimization: UNEDF2

2014

The parameters of the UNEDF2 nuclear energy density functional (EDF) model were obtained in an optimization to experimental data consisting of nuclear binding energies, proton radii, odd-even mass staggering data, fission-isomer excitation energies, and single particle energies. In addition to parameter optimization, sensitivity analysis was done to obtain parameter uncertainties and correlations. The resulting UNEDF2 is an all-around EDF. However, the sensitivity analysis also demonstrated that the limits of current Skyrme-like EDFs have been reached and that novel approaches are called for.

Physics[PHYS.NUCL] Physics [physics]/Nuclear Theory [nucl-th]skyrme energy densityNuclear Theory[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]ta114nuclear density functional theoryNuclear TheoryFOS: Physical sciencesLibrary scienceOak Ridge National Laboratory7. Clean energyNuclear Theory (nucl-th)Nuclear physicsEnergy densityNational laboratoryComputer Science::Operating SystemsNuclear theory
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Time-dependent density-functional theory of strong-field ionization of atoms by soft x rays

2014

Under the terms of the Creative Commons Attribution License 3.0 (CC-BY).-- et al.

PhysicsXrayAtomic Physics (physics.atom-ph)FOS: Physical sciencesSoft X-raysTime-dependent density functional theoryRate equationLaserAtomic and Molecular Physics and OpticsSettore FIS/03 - Fisica Della MateriaPhysics - Atomic Physics3. Good healthlaw.inventionlawIonizationPhysics::Atomic and Molecular ClustersDensity functional theoryPhysics - Atomic and Molecular ClustersAtomic physicsPhysics::Chemical PhysicsAdiabatic processWave functionAtomic and Molecular Clusters (physics.atm-clus)
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The first example of cofacial bis(dipyrrins)

2016

International audience; Two series of cofacial bis(dipyrrins) were prepared and their photophysical properties as well as their bimolecular fluorescence quenching with C-60 were investigated. DFT and TDDFT computations were also performed as a modeling tool to address the nature of the fluorescence state and the possible inter-chromophore interactions. Clearly, there is no evidence for such interactions and the bimolecular quenching of fluorescence, in comparison with mono-dipyrrins, indicates that C-60-bis(dipyrrin) contacts occur from the outside of the "mouth" of the cofacial structure.

010402 general chemistryPhotochemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysisTransition metalexcitation-energiesmolecular-orbital methodsorganometallic compoundsMaterials Chemistry[CHIM]Chemical Sciencessinglet energy transfersdensity-functional theoryvalence basis-setsGroup 2 organometallic chemistryQuenching (fluorescence)010405 organic chemistryChemistryGeneral ChemistryTime-dependent density functional theorytransition-metalsFluorescence0104 chemical scienceslight-harvesting systems2nd-row elementsDensity functional theoryextended basis-sets
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Precision measurement of the magnetic octupole moment in 45Sc as a test for state-of-the-art atomic- and nuclear-structure theory

2020

We report on measurements of the hyperfine $A, B$ and $C$-constants of the $3d4s^2 ~^2D_{5/2}$ and $3d4s^2 ~^2D_{3/2}$ atomic states in $^{45}$Sc. High-precision atomic calculations of the hyperfine fields of these states and second-order corrections are performed, and are used to extract $C_{5/2}=-0.06(6)$ kHz and $C_{3/2}=+0.04(3)$ kHz from the data. These results are one order of magnitude more precise than the available literature. From the combined analysis of both atomic states, we infer the nuclear magnetic octupole moment $\Omega = -0.07(53) \mu_N b$, including experimental and atomic structure-related uncertainties. With a single valence proton outside of a magic calcium core, scan…

Nuclear and High Energy PhysicsoctupoleNuclear Theorynuclear density functional theory010308 nuclear & particles physicsPhysicsQC1-999tiheysfunktionaaliteoriaFOS: Physical sciences01 natural sciencesNuclear Theory (nucl-th)0103 physical sciencesnuclear structurePhysics::Atomic Physicsoktupooli ydinrakenneNuclear Experiment (nucl-ex)010306 general physicsydinfysiikkaNuclear Experiment
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Isospin-symmetry breaking in masses of ≃ Nuclei

2018

Effects of the isospin-symmetry breaking (ISB) beyond mean-field Coulomb terms are systematically studied in nuclear masses near the N=Z line. The Coulomb exchange contributions are calculated exactly. We use extended Skyrme energy density functionals (EDFs) with proton–neutron-mixed densities, to which we add new terms breaking the isospin symmetry. Two parameters associated with the new terms are determined by fitting mirror and triplet displacement energies (MDEs and TDEs) of isospin multiplets. The new EDFs reproduce MDEs for the T=12 doublets and T=1 triplets, and TDEs for the T=1 triplets. Relative strengths of the obtained isospin-symmetry-breaking terms are not consistent with the d…

Nuclear and High Energy PhysicsParticle physicsprotonitNuclear TheoryTriplet displacement energy (TDE)01 natural sciencesComputer Science::Digital LibrariesDisplacement (vector)Energy density functional (EDF)Proton–neutron mixingproton–neutron mixingnuclear physicstiheysmirror displacement energy (MDE)0103 physical sciencesCoulombSymmetry breaking010306 general physicsnuclear density functional theory (DFT)density functional theoryLine (formation)Physicsdensityenergiata114protons010308 nuclear & particles physicsScatteringtiheysfunktionaaliteorianeutronsneutronitenergy density functional (EDF)lcsh:QC1-999Symmetry (physics)Isospin symmetry breaking (ISB)Isospintriplet displacement energy (TDE)isospin symmetry breaking (ISB)ydinfysiikkaMirror displacement energy (MDE)Parametrizationlcsh:PhysicsenergyPhysics Letters
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Correlation effects in bistability at the nanoscale: Steady state and beyond

2012

The possibility of finding multistability in the density and current of an interacting nanoscale junction coupled to semi-infinite leads is studied at various levels of approximation. The system is driven out of equilibrium by an external bias and the nonequilibrium properties are determined by real-time propagation using both time-dependent density functional theory (TDDFT) and many-body perturbation theory (MBPT). In TDDFT the exchange-correlation effects are described within a recently proposed adiabatic local density approximation (ALDA). In MBPT the electron-electron interaction is incorporated in a many-body self-energy which is then approximated at the Hartree-Fock (HF), second-Born,…

PhysicsSteady state (electronics)ta114Condensed Matter - Mesoscale and Nanoscale PhysicsBistabilityTime evolutionFOS: Physical sciences02 engineering and technologyTime-dependent density functional theory021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesSettore FIS/03 - Fisica della MateriaElectronic Optical and Magnetic MaterialsQuantum mechanicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)0103 physical sciencesDensity functional theoryPerturbation theoryLocal-density approximation010306 general physics0210 nano-technologyMultistabilityPhysical Review B
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Kohn-Sham Decomposition in Real-Time Time-Dependent Density-Functional Theory An Efficient Tool for Analyzing Plasmonic Excitations

2017

The real-time-propagation formulation of time-dependent density-functional theory (RT-TDDFT) is an efficient method for modeling the optical response of molecules and nanoparticles. Compared to the widely adopted linear-response TDDFT approaches based on, e.g., the Casida equations, RT-TDDFT appears, however, lacking efficient analysis methods. This applies in particular to a decomposition of the response in the basis of the underlying single-electron states. In this work, we overcome this limitation by developing an analysis method for obtaining the Kohn-Sham electron-hole decomposition in RT-TDDFT. We demonstrate the equivalence between the developed method and the Casida approach by a be…

plasmonic excitationsTheoretical computer scienceKohn-Sham decompositionComputer scienceta221Kohn–Sham equationsFOS: Physical sciencesPhysics::Optics02 engineering and technology01 natural sciencesPhysics - Chemical Physics0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)Decomposition (computer science)Physics::Atomic and Molecular ClustersStatistical physicsPhysical and Theoretical ChemistryPhysics::Chemical Physics010306 general physicsta116PlasmonEigenvalues and eigenvectorsChemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale Physicsta114tiheysfunktionaaliteoriaMaterials Science (cond-mat.mtrl-sci)Time-dependent density functional theory16. Peace & justice021001 nanoscience & nanotechnologyComputer Science ApplicationsplasmonitBenzene derivativesnanohiukkaset0210 nano-technologyJOURNAL OF CHEMICAL THEORY AND COMPUTATION
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