Search results for "citation"

showing 10 items of 1710 documents

A theoretical study of the electronic spectrum of biphenyl

1995

Abstract The electronic spectrum of biphenyl in the energy range up to 6.0 eV has been studied using multiconfigurational second-order perturbation theory (CASPT2) and a basis set of ANO type, including polarization functions on all carbon atoms. The calculated spectrum gives conclusive assignments to all valence excited singlet states and the low-lying triplet states. The change of the torsional angle between the two benzene rings in the different excited states is shown to be of considerable importance and explains the different excitation energies observed in the gas phase as compared to solution or crystalline biphenyl at low temperatures. The intense transition to the 1 1B1u state is m…

BiphenylValence (chemistry)General Physics and AstronomyPolarization (waves)symbols.namesakechemistry.chemical_compoundchemistryExcited stateRydberg formulasymbolsPhysical and Theoretical ChemistryAtomic physicsBenzeneExcitationBasis setChemical Physics Letters
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Vers le contrôle de l'alignement et de l'orientation : théorie et expérience

2010

This thesis is about the control and characterisation of the alignment and orientation of molecules by ultra short laser pulses on a theoretical and experimental approach. Alignment corresponds to a symmetric angular distribution of the molecular axis peaked along the laser field axis, whereas orientation provides an asymmetric distribution favouring one spatial direction. Orientation by sudden two-colour (2+1) pulses is studied extensively for the non resonant case and conditions required for achieving significant orientation are explored. A second two-colour scheme, where the second harmonic is in quasi resonance with a vibrational level of the molecule, is also presented and discussed. T…

BiréfringenceChamp bi couleurNO moleculeMolécule N2Impulsions laser ultracourtesUltra short laserSingle-shot detection[PHYS.COND.CM-GEN] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]PolarizabilityExcitation rovibrationnelleN2 moleculeMoment angulaireBirefringenceOrientation moléculaireMolecular alignmentRotational wave packetAlignement moléculaireAngular momentum[ PHYS.COND.CM-GEN ] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]CO2 moleculeMolecular orientationPhase controlTwo-colour fieldPolarisabilitéHyperpolarizability[PHYS.COND.CM-GEN]Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]Molécule NOHyperpolarisabilitéRovibrational excitationPaquet d'ondes rotationnellesControl cohérentCoherent controlMolécule CO2Interférences
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Dipole moments of 4′-aminoflavonols determined using electro-optical absorption measurements or molecular Stark-effect spectroscopy

2002

The electro-optical absorption measurements (EOAM) were used to measure the dipole moments of the normal form of 4 � -(methoxy)-3hydroxyflavone (FOM), 4 � -(dimethylamino)-3-hydroxyflavone (FME), and 4 � -N-(15-azacrown-5)-3-hydroxyflavone (FCR). For these probes the excited state intramolecular proton transfer (ESIPT) takes place. For comparison, the dipole moments of 4 � -(dimethylamino)-3methoxyflavone (FME3ME), for which ESIPT is lacking, were measured. In the case of FCR, FME, and FME3ME the equilibrated ground (µg) and excited Franck–Condon state (µ FC ) electrical dipole moments are parallel to each other and also parallel to the transition dipole moment. The electrical dipole moment…

Bond dipole momentChemistryGeneral Chemical EngineeringTransition dipole momentGeneral Physics and AstronomyGeneral Chemistrysymbols.namesakeDipoleNuclear magnetic resonanceStark effectExcited statesymbolsAtomic physicsGround stateSpectroscopyExcitationJournal of Photochemistry and Photobiology A: Chemistry
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A comparison of excited state properties for iterative approximate triples linear response coupled cluster methods

2001

Abstract A computational study of the potential energy curves of the 1 Π state of BH, 1 Π state of CH + , 1 Σ u and 1 Π u states of C 2 , 1 Π state of CO, and 1 Π g and 1 Σ − u states of N 2 is carried out with the CC3 and CCSDT-3 corrections to EOMEE-CCSD. Good agreement in structure, vibrational frequencies, and excitation energies of these iterative triples-corrected methods with respect to experiment is found for most of these examples. However, deficiencies in the approximate treatment of triples is evident for BH and CH + .

Bond lengthCoupled clusterChemistryComputational chemistryExcited stateStructure (category theory)General Physics and AstronomyState (functional analysis)Physical and Theoretical ChemistryAtomic physicsDiatomic moleculePotential energyExcitationChemical Physics Letters
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Evidence for long-lived, optically generated quenchers of excitons in single-walled carbon nanotubes.

2011

The nonlinear dependence of near-infrared photoluminescence (PL) emission on excitation intensity has been measured for individual nanotubes representing six different (n,m) species. Significant deviations from linearity are observed for intensities as low as ~100 W/cm(2), and an approximate inverse correlation is found between nonlinearity and PL action cross section (brightness). A model in which all PL nonlinearity arises from exciton-exciton annihilation is insufficient to account for the experimental data using realistic parameters. It is proposed that additional nonlinear quenching arises from photoinduced quenching states or species with longer lifetimes than emissive excitons. Evide…

BrightnessPhotoluminescenceLightExcitonBioengineeringCarbon nanotubelaw.inventionAbsorptionCondensed Matter::Materials SciencelawMetastabilityScattering RadiationGeneral Materials ScienceComputer SimulationParticle SizeQuenching (fluorescence)AnnihilationChemistryNanotubes CarbonMechanical EngineeringGeneral ChemistryCondensed Matter PhysicsRefractometryModels ChemicalAtomic physicsExcitationNano letters
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Deformation and mixing of coexisting shapes in neutron-deficient polonium isotopes

2015

Coulomb-excitation experiments are performed with postaccelerated beams of neutron-deficient Po196,198,200,202 isotopes at the REX-ISOLDE facility. A set of matrix elements, coupling the low-lying states in these isotopes, is extracted. In the two heaviest isotopes, Po200,202, the transitional and diagonal matrix elements of the 2+1 state are determined. In Po196,198 multistep Coulomb excitation is observed, populating the 4+1,0+2, and 2+2 states. The experimental results are compared to the results from the measurement of mean-square charge radii in polonium isotopes, confirming the onset of deformation from Po196 onwards. Three model descriptions are used to compare to the data. Calculati…

CHARGE RADIINuclear and High Energy PhysicsTRANSITION-PROBABILITYchemistry.chemical_elementCoulomb excitation[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]7. Clean energy01 natural sciences114 Physical sciencessymbols.namesakeMatrix (mathematics)NUCLEAR-DATA SHEETSCOULOMB-EXCITATION0103 physical sciencesSTATE PROPERTIESNuclear Physics - ExperimentNeutronfysiikka010306 general physicsEVEN-EVEN NUCLIDESMixing (physics)isotopesPoloniumINTRUDER STATESGAMMA-RAY SPECTROSCOPYPhysicsSPIN STATESisotoopitPO ISOTOPESIsotopeta114010308 nuclear & particles physicsBohr modelchemistryPhysics and AstronomysymbolsAtomic physicsInteracting boson modelphysicspolonium25.70.De 23.20.Js 25.60.−t 27.80.+w
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Tuning Azoheteroarene Photoswitch Performance through Heteroaryl Design

2017

International audience; Photoswitchable compounds, which can be reversibly switched between two isomers by light, continue to attract significant attention for a wide array of applications. Azoheteroarenes represent a relatively new but understudied type of photoswitch, where one of the aryl rings from the conventional azobenzene class has been replaced with a five-membered heteroaromatic ring. Initial studies have suggested the azoheteroarenes – the arylazopyrazoles in particular – to have excellent photoswitching properties (quantitative switching and long Z isomer half-life). Here we present a systematic computational and experimental study to elucidate the origin of the long thermal hal…

CHEMICAL-REACTIONSMOLECULAR SWITCHESFUNCTIONAL RESPONSE THEORYChemistry Multidisciplinary010402 general chemistryRing (chemistry)Photochemistry01 natural sciencesBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryAZO-COMPOUNDSPHOTOISOMERIZATION[CHIM]Chemical SciencesTO-TRANS ISOMERIZATIONAZOBENZENEScience & TechnologyPhotoswitch010405 organic chemistryArylSOLAR THERMAL STORAGEGeneral ChemistryCombinatorial chemistry0104 chemical sciencesChemistrychemistryAzobenzenePhysical SciencesEXCITATION-ENERGIESVISIBLE-LIGHT03 Chemical Sciences
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The diffusion and influence of theoretical models of information behaviour : the case of Savolainen's ELIS model

2020

PurposeTo ascertain the diffusion and influence of Savolainen's ELIS model and its use as a theoretical and/or methodological basis for research.Design/methodology/approachA context citation analysis was made of the work where this researcher published his model. Analysis covered the year of publication, the type of work and the subject matter of the citing documents concerned. In-context citations were analysed for their frequency in each citing text, style, location and content cited.FindingsThe ELIS model received 18.5 cites/year. 20.2 per cent of them corresponded to papers published in journals in other areas, mainly computer science. The average of cites per paper was 1.8; 64.5 percen…

CITES05 social sciencesTheoretical modelsContext (language use)Ciències de la informacióLibrary and Information Sciences050905 science studiesPopularityStyle (sociolinguistics)InvestigacióCitation analysisInformació Teoria de la0509 other social sciencesSocial scienceParagraph050904 information & library sciencesSentenceInformation Systems
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Molecular orbital studies on the mechanism of catalytic isomerization of xylenes II. The photochemical process

1981

Abstract The feasibility of an intermediate step in the mechanism of photochemical isomerization of xylenes in acidic media is explored by using CNDO molecular orbital methods. Along the reaction path from 2,6-dimethylbenzenium ion to dimethylbicyclo[3.1.0]hexenyl cation, the energy surfaces for this intermediate step have been drawn both for the first singlet S1 and triplet T1 excited states. The energies of these excited states have been calculated by adding to the ground-state energy calculated by CNDO/2 method the excitation energy calculated by CNDO/S-CI method. An optimization of the saddle point energy is achieved by introducing the angle between methyl groups and the ring plane as a…

CNDO/2ChemistryExcited stateMolecular orbitalSinglet statePhysical and Theoretical ChemistryPhotochemistryGround stateIsomerizationCatalysisExcitationIonJournal of Catalysis
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Cadmium clusters in CdI2layered crystals: the influence on the optical properties

2007

The influence of overstoichiometric Cd i atoms on the optical properties of cadmium iodide layered crystals has been investigated. The results of optical absorption, luminescence, and luminescence excitation studies of CdI 2 crystals with controlled deviation from stoichiometric composition allow observing correlations between the Cd i concentration and features in absorption and emission spectra up to concentrations of 10 18 cm -3 . At higher concentrations the overstoichiometric cadmium atoms form clusters, which were observed using scanning electron microscopy. The extinction spectra of (CdI i ) n clusters are calculated in the frame of Mie theory and are found to correlate with the opti…

CadmiumScanning electron microscopeMie scatteringAnalytical chemistrychemistry.chemical_elementCondensed Matter Physicschemistry.chemical_compoundCadmium iodidechemistryGeneral Materials ScienceEmission spectrumAbsorption (chemistry)LuminescenceExcitationJournal of Physics: Condensed Matter
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