Search results for "localize"

showing 10 items of 300 documents

Dependence of the Substituent Effect on Solvent Properties

2018

The influence of a solvent on the substituent effect (SE) in 1,4-disubstituted derivatives of benzene (BEN), cyclohexa-1,3-diene (CHD), and bicyclo[2.2.2]octane (BCO) is studied by the use of polarizable continuum model method. In all X–R–Y systems for the functional group Y (NO2, COOH, OH, and NH2), the following substituents X have been chosen: NO2, CHO, H, OH, and NH2. The substituent effect is characterized by the charge of the substituent active region (cSAR(X)), substituent effect stabilization energy (SESE), and substituent constants σ or F descriptors, the functional groups by cSAR(Y), whereas π-electron delocalization of transmitting moieties (BEN and CHD) is characterized by a geo…

Bicyclic molecule010405 organic chemistrySubstituentAromaticity010402 general chemistry01 natural sciencesQuantum chemistryPolarizable continuum model0104 chemical scienceschemistry.chemical_compoundCrystallographyDelocalized electronchemistryFunctional groupPhysical and Theoretical ChemistryOctaneThe Journal of Physical Chemistry A
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Interaction of Au16 Nanocluster with Defects in Supporting Graphite: A Density-Functional Study

2011

Soft-landed adsorption of Au-16 on bilayered graphene is investigated using density functional theory. The orientation of the Au-16 cluster and number of neighboring surface vacancies affect the overall structural and electronic properties of the cluster. The results of the PBE, vdW-DF, and vdW-DF2 exchange-correlation functionals are compared for the cluster-substrate interaction for systems with and without defects. In the presence of defects size two and greater, an Au atom adsorbs into the topmost graphene layer; this strongly influences the binding energy (>3 eV), while inducing substantial bending in the carbon plane and altering electronic properties of the system. Though the T-d-sym…

Binding energyNanotechnology02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionDelocalized electronlawAtomCluster (physics)GraphitePhysical and Theoretical Chemistryta114ChemistryGraphene021001 nanoscience & nanotechnologyElectron localization function0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsJGeneral EnergyChemical physicsddc:540Density functional theory0210 nano-technologyJournal of Physical Chemistry C
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A first-principles DFT study of UN bulk and (001) surface: comparative LCAO and PW calculations.

2008

LCAO and PW DFT calculations of the lattice constant, bulk modulus, cohesive energy, charge distribu- tion, band structure, and DOS for UN single crystal are analyzed. It is demonstrated that a choice of the uranium atom relativistic effective core potentials considerably affects the band structure and magnetic structure at low tem- peratures. All calculations indicate mixed metallic-covalent chemical bonding in UN crystal with U5f states near the Fermi level. On the basis of the experience accumulated in UN bulk simulations, we compare the atomic and elec- tronic structure as well as the formation energy for UN(001) surface calculated on slabs of different thickness using both DFT approach…

Bulk modulusChemistryFermi levelGeneral ChemistryMolecular physicsComputational Mathematicssymbols.namesakeCrystallographyDelocalized electronAtomic orbitalLinear combination of atomic orbitalsAtomsymbolsElectronic band structureBasis setJournal of computational chemistry
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Overview of the JET results

2015

Since the installation of an ITER-like wall, the JET programme has focused on the consolidation of ITER design choices and the preparation for ITER operation, with a specific emphasis given to the bulk tungsten melt experiment, which has been crucial for the final decision on the material choice for the day-one tungsten divertor in ITER. Integrated scenarios have been progressed with the re-establishment of long-pulse, high-confinement H-modes by optimizing the magnetic configuration and the use of ICRH to avoid tungsten impurity accumulation. Stationary discharges with detached divertor conditions and small edge localized modes have been demonstrated by nitrogen seeding. The differences in…

Chemical analysiMagnetic confinementEdge localized modeTokamak:Física [Ciências exactas e naturais]Nuclear engineeringplasma-facing componentsTungsten7. Clean energyiter-like walllaw.inventionheat loadsAlcator C-ModlawPlasma-facing componentalcator C-MODQCPhysicsJet (fluid)Thermally activatedDivertormagnetic confinementMagnetic confinement fusionTokamak deviceerosionCondensed Matter PhysicsChemical erosionPost mortem analysiCondensed Matter Physics; Nuclear and High Energy PhysicsBerylliumAtomic physicstokamaksTokamaksNuclear and High Energy Physicschemistry.chemical_elementImpurity accumulationCondensed Matter PhysicNuclear and High Energy Physics; Condensed Matter PhysicsTungstenFísica Física:Physical sciences [Natural sciences]divertorNuclear fusionNuclear and High Energy PhysicPhysics Physical sciencesGas fuel analysifuel retentionSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)operationOrders of magnitudechemistryJETtransportMagnetic configuration
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The adhesion properties of the Ag/α-Al2O3() interface: an ab initio study

2002

Ab initio computer simulations of the atomic and electronic structure of the Ag/a-Al2O3(0 0 0 1) (corundum) interface have been performed for a periodic two-dimensional slab model using the Hartree–Fock method and a posteriori electron correlation corrections.We have considered both Al- and O-terminated corundum substrate surfaces.The dependence of the adhesion energy on the interfacial distance has been analyzed for the two most favorable Ag adsorption positions over corundum and for two different metal coverages (a 1/3 monolayer (ML) of the Ag(1 1 1) crystallographic plane and a full Ag(1 1 1) monolayer).The two different terminations (Al- and O-) give rise to qualitatively different resu…

ChemistryAb initioCorundumSurfaces and InterfacesElectronic structureengineering.materialCondensed Matter PhysicsSurfaces Coatings and FilmsDelocalized electronCrystallographyPhysisorptionAb initio quantum chemistry methodsMonolayerAtomMaterials ChemistryengineeringSurface Science
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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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Orbiting Orbitals: Visualization of Vi-Bronic Motion at a Conical Intersection

2013

The Jahn-Teller (JT) active unpaired electron of single metalloporphyrin radical anions is imaged through scanning tunneling microscopy. It is demonstrated that the electron is delocalized over the porphyrin macrocycle and its topographic image is determined by vibronic motion: the orbital of the electron adiabatically follows the zero-point pseudorotation of skeletal deformations. Transformation of the polar graphs of the observed images allows visualization of the adiabatic vibrational density to which the electron is coupled. The vibronic potential at the conical intersection is visualized and the half-integer angular momentum characteristic of the Berry phase is revealed in the radial f…

ChemistryElectronConical intersectionlaw.inventionDelocalized electronUnpaired electronGeometric phaseAtomic orbitallawPhysics::Atomic and Molecular ClustersPseudorotationPhysical and Theoretical ChemistryScanning tunneling microscopeAtomic physicsta116The Journal of Physical Chemistry A
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Superradiance and Exciton (De)localization in Light-Harvesting Complex II from Green Plants?

2002

Fluorescence quantum yield and fluorescence lifetime measurements were performed on trimeric light-harvesting complex II (LHCII) from spinach in the temperature range 7−293 K. From the results the radiative rate was calculated, which is related to the amount of delocalization of excitations over different pigments because of intermolecular interactions. The emitting dipole strength of LHCII is very similar to that of unbound Chl a, and it appears to be almost independent of temperature. The apparent increase of the radiative rate upon lowering the temperature can largely be explained by the shrinking of the sample. It is concluded that at all temperatures the amount of exciton delocalizatio…

ChemistryExcitonIntermolecular forceQuantum yieldSuperradianceAtmospheric temperature rangeSurfaces Coatings and FilmsDipoleDelocalized electronChemical physicsMaterials ChemistryRadiative transferPhysical and Theoretical ChemistryAtomic physicsThe Journal of Physical Chemistry B
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N-Methyl-3-methylsulfonyl-N-nitroaniline

2005

In the title compound, C8H10N2O4S, the N—N bond length [1.3488 (18) A] indicates some double-bond character, while the torsion angle between the aromatic ring and the nitramine group [66.3 (2)°] rules out further delocalization in the mol­ecule. The geometry of the methyl­sulfon­yl substituent is quasi-tetra­hedral, as expected. The crystal packing is stabilized by C—H⋯O hydrogen bonds, with the mol­ecules arranged in chains extended along the [101] direction.

ChemistryHydrogen bondStereochemistrySubstituentGeneral ChemistryDihedral angleCondensed Matter PhysicsRing (chemistry)Medicinal chemistryBond lengthDelocalized electronchemistry.chemical_compoundAnilineNitroGeneral Materials ScienceActa Crystallographica Section E Structure Reports Online
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Localized molecular orbitals for excited states of polyenals, polyendials, and polyenones

2003

The work is focused on the generation of localized molecular orbitals for excited states. A recently developed a priori method based in a CAS-SCF–type algorithm is applied. The method generates directly localized orbitals and can be applied to multireference wavefunctions. A detailed description of the performance of the method as well as the locality of the MOs for the example of the singlet nπ* (CO) excited state is given. It is in general possible to obtain local orbitals for the doubly occupied and virtual valence orbitals. The partial delocalization of the π* (CO) orbital is discussed, as is the effect of the use of different CAS spaces. The systems under study are polyenals, polyendia…

ChemistryMolecular orbital theoryLocalized molecular orbitalsCondensed Matter PhysicsAtomic and Molecular Physics and OpticsSlater-type orbitalLinear combination of atomic orbitalsMolecular orbitalValence bond theoryComplete active spacePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsNatural bond orbitalInternational Journal of Quantum Chemistry
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