Search results for "Calculation"

showing 10 items of 594 documents

Towards an accurate molecular orbital theory for excited states : Ethene, butadiene, and hexatriene

1993

A newly proposed quantum chemical approach for ab initio calculations of electronic spectra of molecular systems is applied to the molecules ethene, trans‐1,3‐butadiene, and trans‐trans‐1,3,5‐hexatriene. The method has the aim of being accurate to better than 0.5 eV for excitation energies and is expected to provide structural and physical data for the excited states with good reliability. The approach is based on the complete active space (CAS) SCF method, which gives a proper description of the major features in the electronic structure of the excited state, independent of its complexity, accounts for all near degeneracy effects, and includes full orbital relaxation. Remaining dynamic ele…

ErrorsGeneral Physics and AstronomyPolyenesElectronic structuresymbols.namesakeRydberg StatesAb initio quantum chemistry methodsComputational chemistrySinglet statePhysical and Theoretical ChemistryTriplet state:FÍSICA::Química física [UNESCO]AccuracyExcitationCalculation MethodsButadieneTripletsChemistryMolecular orbital theoryScf CalculationsExcited StatesCalculation Methods ; Quantum Chemistry ; Ab Initio Calculations ; Electron Spectra ; Butadiene ; Accuracy ; Scf Calculations ; Triplets ; Rydberg States ; Excitation ; Errors ; Polyenes ; Excited StatesQuantum ChemistryUNESCO::FÍSICA::Química físicaElectron SpectraExcited stateRydberg formulasymbolsRydberg stateAtomic physicsAb Initio Calculations
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Benefits of Integrating an Explicit Self-Efficacy Intervention With Calculation Strategy Training for Low-Performing Elementary Students

2021

This study examined the malleability of math self-efficacy (SE) among children with poor calculation fluency via an intervention that targeted four sources of SE (mastery experiences, vicarious experiences, social persuasions, and emotional and physiological states). The effect of pure strategy training was contrasted with an intervention that integrated strategy training and explicit SE support. Moreover, the changes in SE source experiences and their relation with math SE, as well as the relation between math-SE profiles and calculation fluency development, were examined. In a quasi-experimental design, 60 Finnish children with calculation fluency problems in Grades 2 to 4 participated in…

minäpystyvyyseducationalakoululaisetinterventiotutkimusbehavioral disciplines and activitiesBF1-990low performancemathmatemaattiset taidotPsychologysources of self-efficacyself-efficacycalculation fluencyinterventionOriginal ResearchFrontiers in Psychology
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Adducts of free-base meso-tetraarylporphyrins with trihaloacetic acids: Structure and photostability

2020

Abstract Four diverse meso-tetraarylporphyrins in the form of diprotonated adducts with trifluoro-, trichloro-, tribromoacetic acids and acetic acid were investigated in benzene solution. Despite similar structural distortion of the chromophore system due to protonation, the respective adducts demonstrated different photostability when exposed to UV irradiation. The trifluoro- and trichloroacetic adducts, and the acetic acid one, showed some common features both molecular and in the mechanism of photodegradation. However, the tribromo-derivative decayed according to a different kinetic scheme, revealing a considerable impact of the bromine atoms upon the pyrrole units of the porphyrin macro…

Meso-tetraarylporphyrinsSinglet oxygenGeneral Chemical EngineeringGeneral Physics and AstronomyFree baseProtonation02 engineering and technologyGeneral ChemistryChromophore010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryDFT calculations01 natural sciencesPorphyrinTrihaloacetic acids0104 chemical sciencesAdductPorphyrin protonationchemistry.chemical_compoundAcetic acidchemistry0210 nano-technologyPhotodegradationPyrroleJournal of Photochemistry and Photobiology A-Chemistry
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Inclusive B-meson production at small p_T in the general-mass variable-flavor-number scheme

2015

We calculate the cross section for the inclusive production of B mesons in pp and ppbar collisions at next-to-leading order in the general-mass variable-flavor-number scheme and show that a suitable choice of factorization scales leads to a smooth transition to the fixed-flavor-number scheme. Our numerical results are in good agreement with data from the Tevatron and LHC experiments at small and at large transverse momenta.

Particle physicsPhysics and Astronomy (miscellaneous)TevatronFOS: Physical scienceslow [transverse momentum]01 natural sciencesCross section (physics)High Energy Physics - Phenomenology (hep-ph)Factorization0103 physical sciencesscattering [p p]Order (group theory)B mesonddc:530Batavia TEVATRON Collinclusive production [B]factorization [scale]010306 general physicsnumerical calculationsNuclear ExperimentEngineering (miscellaneous)Variable (mathematics)PhysicsLarge Hadron Colliderscattering [anti-p p]higher-order [correction]010308 nuclear & particles physicsHigh Energy Physics::Phenomenologycalculated [total cross section]Transverse planeHigh Energy Physics - PhenomenologyCERN LHC Coll[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph]High Energy Physics::Experiment1 [higher-order]correction [total cross section]
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Evidence of oblate-prolate shape coexistence in the strongly-deformed nucleus 119Cs

2021

International audience; Prolate-oblate shape coexistence close to the ground state in the strongly-deformed proton-rich A≈120 nuclei is reported for the first time. One of the four reported bands in 119Cs, built on a 11/2− state at 670 keV, consists of nearly degenerate signature partners, and has properties which unequivocally indicate the strongly-coupled πh11/2[505]11/2− configuration associated with oblate shape. Together with the decoupled πh11/2[541]3/2− band built on the 11/2− prolate state at 110 keV, for which a half-life of T1/2=55(5)μs has been measured, the new bands bring evidence of shape coexistence at low spin in the proton-rich strongly deformed A≈120 nuclei, a phenomenon p…

58Ni(64Zn3p)119CsNuclear reactionNuclear and High Energy PhysicsQC1-999Nuclear TheoryModel calculation-coincidences[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]01 natural sciencesMolecular physicsMeasured γγγ-coincidencescesium0103 physical sciencesmedicineNuclear reaction:58Ni(64Zn3p)119CsZnCovariant transformationCs010306 general physicsSpin (physics)Ni(PhysicsLinear polarization010308 nuclear & particles physicsLinear polarizationPhysicsDegenerate energy levels3p)Oblate-prolate coexistenceNuclear reactionmedicine.anatomical_structureNuclear reaction:Angular correlationsDensity functional theoryydinfysiikkaGround stateMeasuredNucleusPhysics Letters B
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Azoxybenzene rearrangement catalyzed by solid acids

2008

Abstract For the first time, the potential of acidic cation-exchange resin (sulfonated polystyrene) to catalyze the Wallach rearrangement of azoxybenzene into 4-hydroxyazobenzene has been proved. This finding reveals an alternative reaction path possible in a heterogeneous process using solid acids and may help to clear some doubts concerning the rearrangement mechanism postulated so far. The resin-induced reaction was found to proceed exclusively in a non-polar medium. Reasonable yield was obtained particularly in isooctane due to favorable distribution of azoxybenzene throughout the resin's matrix. On the contrary, the HY type zeolite did not activate the rearrangement, most probably beca…

Steric effectsHeterogeneous catalysisZeoliteAzo compoundProcess Chemistry and TechnologyDFT calculationsWallach rearrangementHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundchemistryComputational chemistryYield (chemistry)Azoxybenzene rearrangementPolymer chemistryPolystyrenePhysical and Theoretical ChemistryZeoliteSulfonated polystyrene resinJournal of Molecular Catalysis A: Chemical
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DFT and experimental studies on structure and spectroscopic parameters of 3,6-diiodo-9-ethyl-9H-carbazole

2015

The first report on crystal and molecular structure of 3,6-diiodo-9-ethyl-9H-carbazole is presented. Experimental room-temperature X-ray and 13C chemical shift studies were supported by advanced theoretical calculations using density functional theory (DFT). The 13C nuclear magnetic shieldings were predicted at the non-relativistic and relativistic level of theory using the zeroth-order regular approximation (ZORA). Theoretical relativistic calculations of chemical shifts of carbons C3 and C6, directly bonded to iodine atoms, produced a reasonable agreement with experiment (initial deviation from experiment of 44.3 dropped to 4.25 ppm). The changes in ring aromatic character via simple harm…

Relativistic Effects3Simple harmonic motionDFT calculations010402 general chemistryRing (chemistry)13C NMR spectra01 natural sciencesMolecular physicsChemical shift indexCrystalZORA6-diiodo-9-ethyl-9H-carbazoleComputational chemistrycarbazoleFaculty of ScienceMolecule/dk/atira/pure/core/keywords/TheFacultyOfSciencePhysical and Theoretical Chemistry010405 organic chemistryChemistryChemical shiftAromaticityQuantum ChemistryCondensed Matter Physicscomputational chemistry0104 chemical sciencesZORA GIAO NMR calculationsNMR spectrocopyDensity functional theoryX-ray structureNMR; chemical shiftStructural Chemistry
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Controlled time integration for the numerical simulation of meteor radar reflections

2016

We model meteoroids entering the Earth[U+05F3]s atmosphere as objects surrounded by non-magnetized plasma, and consider efficient numerical simulation of radar reflections from meteors in the time domain. Instead of the widely used finite difference time domain method (FDTD), we use more generalized finite differences by applying the discrete exterior calculus (DEC) and non-uniform leapfrog-style time discretization. The computational domain is presented by convex polyhedral elements. The convergence of the time integration is accelerated by the exact controllability method. The numerical experiments show that our code is efficiently parallelized. The DEC approach is compared to the volume …

010504 meteorology & atmospheric sciencesComputer scienceMETEORPLASMATIC OBJECTSRADAR REFLECTIONS01 natural sciencesplasmatic objectslaw.inventionINTEGRAL EQUATIONSlawRadar010303 astronomy & astrophysicsSpectroscopyEARTH ATMOSPHEREvolume integral equationRadiationPLASMANUMERICAL MODELSMathematical analysisFinite differenceNUMERICAL METHODMETEORSAtomic and Molecular Physics and OpticsCALCULATIONSControllabilityDISCRETE EXTERIOR CALCULUSAstrophysics::Earth and Planetary AstrophysicsMAGNETOPLASMADiscretizationRADAR REFLECTIONTIME DOMAIN ANALYSISVOLUME INTEGRAL EQUATIONdiscrete exterior calculusELECTROMAGNETIC SCATTERINGOpticsFINITE DIFFERENCE TIME DOMAIN METHOD0103 physical sciencesSCATTERINGTime domainmeteorsNUMERICAL METHODS0105 earth and related environmental sciencesta113ta114Computer simulationbusiness.industryta111Finite-difference time-domain methodRADARDiscrete exterior calculuselectromagnetic scatteringradar reflectionsELECTROMAGNETIC METHODmeteoritbusinessJournal of Quantitative Spectroscopy and Radiative Transfer
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Computation of conical intersections by using perturbation techniques

2005

Multiconfigurational second-order perturbation theory, both in its single-state multiconfigurational second-order perturbation theory (CASPT2) and multistate (MS-CASPT2) formulations, is used to search for minima on the crossing seams between different potential energy hypersurfaces of electronic states in several molecular systems. The performance of the procedures is tested and discussed, focusing on the problem of the nonorthogonality of the single-state perturbative solutions. In different cases the obtained structures and energy differences are compared with available complete active space self-consistent field and multireference configuration interaction solutions. Calculations on dif…

Potential Energy SurfacesConfiguration Interactions ; Perturbation Theory ; Potential Energy Surfaces ; Molecular Electronic States ; SCF Calculations ; Lithium Compounds ; Organic Compounds ; Wave FunctionsOrganic CompoundsChemistryComputationUNESCO::FÍSICAConfiguration InteractionsGeneral Physics and AstronomyMultireference configuration interactionConical surfaceSCF CalculationsPotential energyWave FunctionsMaxima and minima:FÍSICA [UNESCO]Molecular Electronic StatesQuantum mechanicsPerturbation TheoryLithium CompoundsStatistical physicsComplete active spacePerturbation theory (quantum mechanics)Physical and Theoretical ChemistryWave functionThe Journal of Chemical Physics
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Beyond ideal two-dimensional metals: Edges, vacancies, and polarizabilities

2018

Recent experimental discoveries of graphene-stabilized patches of two-dimensional (2D) metals have motivated also their computational studies. However, so far the studies have been restricted to ideal and infinite 2D metallic monolayers, which is insufficient because in reality the properties of such metallic patches are governed by microstructures pervaded by edges, defects, and several types of perturbations. Here we use density-functional theory to calculate edge and vacancy formation energies of hexagonal and square lattices of 45 elemental 2D metals. We find that the edge and vacancy formation energies are strongly correlated and decrease with increasing Wigner-Seitz radii, analogously…

Work (thermodynamics)Materials scienceCoordination numberFOS: Physical sciences02 engineering and technologyEdge (geometry)010402 general chemistry01 natural sciencesSquare (algebra)polarisaatioMetalnanorakenteetnanocrystalsVacancy defectMesoscale and Nanoscale Physics (cond-mat.mes-hall)charge polarizationcrystal defectspoint defectsIdeal (ring theory)Condensed matter physicsta114Condensed Matter - Mesoscale and Nanoscale Physicsline defectsviat021001 nanoscience & nanotechnologyvacancies0104 chemical sciencesBond lengthvisual_artfirst-principles calculationsvisual_art.visual_art_medium0210 nano-technology
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