Search results for "Molecule-photon collisions"

showing 4 items of 4 documents

Lower Rydberg series of methane: a combined coupled cluster linear response and molecular quantum defect orbital calculation.

2006

Vertical excitation energies as well as related absolute photoabsorption oscillator strength data are very scarce in the literature for methane. In this study, we have characterized the three existing series of low-lying Rydberg states of CH4 by computing coupled cluster linear response (CCLR) vertical excitation energies together with oscillator strengths in the molecular-adapted quantum defect orbital formalism from a distorted Cs geometry selected on the basis of outer valence green function calculations. The present work provides a wide range of data of excitation energies and absolute oscillator strengths which correspond to the Rydberg series converging to the three lower ionization p…

Oscillator strengthIonisation potentialGeneral Physics and AstronomyOrganic compounds ; Rydberg states ; Coupled cluster calculations ; Orbital calculations ; Oscillator strengths ; Photoexcitation ; Molecule-photon collisions ; Molecular configurations ; Ionisation potentialsymbols.namesakeQuantum defectCoupled cluster calculationsOrganic compoundsOscillator strengthsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]PhotoexcitationPhysicsMolecule-photon collisionsValence (chemistry)Rydberg statesMolecular configurationsOrbital calculationsUNESCO::FÍSICA::Química físicaPhotoexcitationCoupled clusterRydberg formulasymbolsIonization energyAtomic physicsExcitationThe Journal of chemical physics
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Nonadiabatic orientation, toroidal current, and induced magnetic field in BeO molecules.

2008

It is predicted that oriented BeO molecules would give rise to unprecedentedly strong, unidirectional electric ring current and an associated magnetic field upon excitation by a right or left circularly polarized laser pulse into the first excited degenerate singlet state. The strong toroidal electric ring current of this state is dominated by the ring current of the 1π± orbital about the molecular axis. Our predictions are based on the analysis of the orbital composition of the states involved and are substantiated by high level electronic structure calculations and wavepacket simulations of the laser-driven orientation and excitation dynamics. Luis.Serrano@uv.es

PhotoexcitationToroidMolecular electronic statesMolecule-photon collisionsMagnetic momentChemistryConfiguration interactionsExcited statesGeneral Physics and AstronomyElectronic structureMolecular orientationMagnetic fieldUNESCO::FÍSICA::Química físicaPhotoexcitationCoupled cluster calculationsBeryllium compoundsExcited stateMagnetic momentsPhysical and Theoretical ChemistryAtomic physics:FÍSICA::Química física [UNESCO]Beryllium compounds ; Configuration interactions ; Coupled cluster calculations ; Excited states ; Magnetic moments ; Molecular electronic states ; Molecular orientation ; Molecule-photon collisions ; PhotoexcitationRing currentExcitationThe Journal of chemical physics
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Raman spectroscopy and crystal-field split rotational states of photoproducts CO and H2 after dissociation of formaldehyde in solid argon

2012

Raman signal is monitored after 248 nm photodissociation of formaldehyde in solid Ar at temperatures of 9–30 K. Rotational transitions J = 2 ← 0 for para-H2 fragments and J = 3 ← 1 for ortho-H2 are observed as sharp peaks at 347.2 cm−1 and 578.3 cm−1, respectively, which both are accompanied by a broader shoulder band that shows a split structure. The rovibrational spectrum of CO fragments has transitions at 2136.5 cm−1, 2138.3 cm−1, 2139.9 cm−1, and 2149 cm−1. To explain the observations, we performed adiabatic rotational potential calculations to simulate the Raman spectrum. The simulations indicate that the splitting of rotational transitions is a site effect, where H2 molecules can resi…

Raman spektroskopiacarbon compoundstranslational statesphotodissociationmatriisi-isolaatiohydrogen neutral moleculesrotational statesrotational-vibrational statesfotodissosiaatiorotaatio-vibraatiotilatmolecule-photon collisionsRaman spectrainterstitialsorgaaniset yhdisteet
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Realization of time-resolved two-vacuum-ultraviolet-photon ionization

2009

International audience; Ultrafast dynamics of excited molecules is studied through time-resolved two-vacuum-ultraviolet (vuv)- photon ionization using a nonlinear volume autocorrelator unit. The two-vuv-photon process is induced by the intense fifth harmonic radiation of a femtosecond Ti:sapphire laser. In a proof-of-principle experiment, ultrafast dynamics of excited ethylene and oxygen molecules are investigated. Molecular decay times are deduced by comparing the experimental data with the results of a numerical model that accounts for the spatial and temporal characteristics of the harmonic field. The present experiments pave a convenient way for time domain investigations in the vuv-xuv s…

spectroscopyattosecondPhoton[ PHYS.PHYS.PHYS-ATOM-PH ] Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]Physics::Opticsphotoionisationnm01 natural sciences7. Clean energyAtmospheric-pressure laser ionization010309 opticsFrequency conversionIonizationhigher order harmonic generation0103 physical sciencesPhysics::Atomic and Molecular Clustersethylenemoleculestwo-photon processesPhysics::Chemical Physics010306 general physicsUltrafast dynamicsPhysics[PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]photodissociationdynamicsVUVAtomic and Molecular Physics and Opticslaser-pulsesVacuum ultravioletExtreme ultravioletmolecule-photon collisionsXUX32.80.Rm 42.65.Re 42.65.KyHHGAtomic physicsultrafast internal-conversionorganic compoundsphysicsRealization (systems)oxygen
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