Search results for "Vibration"

showing 10 items of 823 documents

The complete basis set Full-CI roto-vibrational spectroscopic constants of AlH, AlH+ and AlH -

2017

The spectroscopic constants of AlH, AlH + and AlH -, as well as their counterparts with H/D isotopic substitution, were obtained at the frozen core Full-CI/CBS limit and corrected for the core-correlation, relativistic and diagonal Born–Oppenheimer contributions, calculated by means of different high-level computational methods. On the basis of the obtained values, some accepted experimental result for these astrochemically relevant species is questioned.

Physical and Theoretical ChemistryAluminum hydrideAstrochemistryRoto-vibrational spectroscopy
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Relaxation processes of point defects in vitreous silica from femtosecond to nanoseconds

2008

We studied ultrafast relaxation of localized excited states at Ge-related oxygen deficient centers in silica using femtosecond transient-absorption spectroscopy. The relaxation dynamics exhibits a biexponential decay, which we ascribe to the departure from the Frank-Condon region of the first excited singlet state in 240 fs, followed by cooling in ∼10 ps. At later times, a nonexponential relaxation spanning up to 40 ns occurs, which is fitted with an inhomogeneous distribution of nonradiative relaxation rates, following a chi-square distribution with one degree of freedom. This reveals several analogies with phenomena such as neutron reactions, quantum dot blinking, or intramolecular vibrat…

Physics and Astronomy (miscellaneous)Chemistrypoint defectSilicaNanosecondExcited state (localized; relaxation processes of point defects in vitreous silica from femtosecond to nanoseconds); Excited singlet state; Localized electronic state; Point defects; Vibrational relaxation (relaxation processes of point defects in vitreous silica from femtosecond to nanoseconds); Optical absorption (transient; relaxation processes of point defects in vitreous silica from femtosecond to nanoseconds)Crystallographic defectSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)ultrafast spectroscopyNuclear magnetic resonanceQuantum dotExcited stateFemtosecondVibrational energy relaxationNeutronrelaxation point defect vitreous silica nanosecondPhysics::Chemical PhysicsAtomic physicsSpectroscopyApplied Physics Letters
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Frequency Range Selection Method for Vibrational Spectra

2018

Theoretical calculations of vibrational properties are widely used to explain and predict experimental spectra. However, with standard quantum chemical methods all molecular motions are considered, which is rather time-consuming for large molecules. Because typically only a specific spectral region is of experimental interest, we propose here an efficient method that allows calculation of only a selected frequency interval. After a computationally cheap low-level estimate of the molecular motions, the computational time is proportional to the number of normal modes needed to describe this frequency range. Results for a medium-sized molecule show a reduction in computational time of up to 1 …

Physics/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energyLetter010304 chemical physics010402 general chemistry01 natural sciencesSpectral line0104 chemical sciencesComputational physicsReduction (complexity)Normal mode0103 physical sciencesRange (statistics)FÍSICO-QUÍMICAMoleculeGeneral Materials ScienceSelection methodSDG 7 - Affordable and Clean EnergyPhysical and Theoretical ChemistryOrder of magnitudeVibrational spectraJournal of Physical Chemistry Letters
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Jet-cooled FTIR spectroscopy and analysis of the C–O stretch fundamental of Ni(CO)4

2008

Rovibrational spectra of the C–O stretch band (ν5) of Ni(CO)4 have been recorded at 0.006 cm− 1 resolution by coupling a low pressure continuous supersonic jet with a high resolution interferometer. The spectrum has been analysed thanks to the STDS software (see http://icb.u-bourgogne.fr/OMR/SMA/SHTDS/) that implements the tensorial formalism developed in the Dijon group for tetrahedral molecules. We obtain a very satisfying simulation thanks to an effective Hamiltonian expanded up to order 3. The asymmetry of the high-J lines is due to a small tetrahedral splitting and is well reproduced. The root mean square deviation is 0.96 × 10− 3 cm− 1. The Coriolis constant is somewhat larger than fo…

Physics010304 chemical physicsDegenerate energy levelsBiophysicsAnalytical chemistryTetrahedral molecular geometry02 engineering and technologyRotational–vibrational spectroscopy021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesSpectral linesymbols.namesake0103 physical sciencessymbolsLevel structurePhysical and Theoretical ChemistryFourier transform infrared spectroscopyAtomic physics0210 nano-technologyHamiltonian (quantum mechanics)Molecular BiologyRoot-mean-square deviationMolecular Physics
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Rovibrational controlled-NOT gates using optimized stimulated Raman adiabatic passage techniques and optimal control theory

2009

Implementation of quantum controlled-NOT (CNOT) gates in realistic molecular systems is studied using stimulated Raman adiabatic passage (STIRAP) techniques optimized in the time domain by genetic algorithms or coupled with optimal control theory. In the first case, with an adiabatic solution (a series of STIRAP processes) as starting point, we optimize in the time domain different parameters of the pulses to obtain a high fidelity in two realistic cases under consideration. A two-qubit CNOT gate constructed from different assignments in rovibrational states is considered in diatomic (NaCs) or polyatomic $({\text{SCCl}}_{2})$ molecules. The difficulty of encoding logical states in pure rota…

Physics010304 chemical physicsField (physics)Stimulated Raman adiabatic passageRotational–vibrational spectroscopyOptimal control01 natural sciencesAtomic and Molecular Physics and OpticsControlled NOT gateQuantum mechanics0103 physical sciencesPhysics::Atomic and Molecular ClustersTime domain010306 general physicsAdiabatic processQuantum computerPhysical Review A
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Rovibrational transitions of H 2 by collision with H + at high temperature

2017

The H+ + H2 reaction is studied by means of both exact and statistical quantum methods. Integral cross-sections for processes initiated with rotationally excited H2(v, j = 1) to produce molecular hydrogen in its rotational ground state are reported up to a value of the collision energy of 3 eV. Rate constants for state-to-state transitions between different H2 rovibrational states are calculated up to 3000 K. Special emphasis is made on ortho/para conversion processes in which the parity j of the H2(j) states changes.

Physics010304 chemical physicsMolecular dataScatteringAstronomy and AstrophysicsRotational–vibrational spectroscopy010402 general chemistryCollisionMolecular processes01 natural sciences0104 chemical sciencesScatteringSpace and Planetary Science0103 physical sciencesAtomic physicsMonthly Notices of the Royal Astronomical Society
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Multiconfigurational Quantum Chemistry Determinations of Absorption Cross Sections (σ) in the Gas Phase and Molar Extinction Coefficients (ε) in Aque…

2021

Theoretical determinations of absorption cross sections (σ) in the gas phase and molar extinction coefficients (e) in condensed phases (water solution, interfaces or surfaces, protein or nucleic acids embeddings, etc.) are of interest when rates of photochemical processes, J = ∫ ϕ(λ) σ(λ) I(λ) dλ, are needed, where ϕ(λ) and I(λ) are the quantum yield of the process and the irradiance of the light source, respectively, as functions of the wavelength λ. Efficient computational strategies based on single-reference quantum-chemistry methods have been developed enabling determinations of line shapes or, in some cases, achieving rovibrational resolution. Developments are however lacking for stron…

Physics010304 chemical physicsRotational–vibrational spectroscopyChromophore01 natural sciencesMolecular physicsQuantum chemistryArticleComputer Science Applications[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryMolecular dynamics13. Climate actionAbsorption bandExcited state0103 physical sciencesPhysical and Theoretical ChemistryAbsorption (chemistry)ComputingMilieux_MISCELLANEOUSSpin-½Journal of Chemical Theory and Computation
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Breakdown of the Reduction of the Rovibrational Hamiltonian: The Case of S18O2F2

2009

Abstract The ground state rotational spectrum of the near-spherical top molecule S18O2F2 (sulfuryl fluoride) has been measured from 50 to 700 GHz. As for the parent isotopologue, S16O2F2 [K. Sarka, J. Demaison, L. Margules, I. Merke, N. Heineking, H. Burger, H. Ruland, J. Mol. Spectrosc. 200 (2000) 55–64], it was necessary to use a non-reduced Hamiltonian in order to obtain a satisfactory fit. It was possible to determine six quartic centrifugal distortion constants (instead of five for a standard asymmetric top) and five sextic constants (one of them not existing in the reduced Hamiltonian) could also be determined. This ground state level has also been analysed thanks to a tensorial forma…

Physics010304 chemical physicsRotational–vibrational spectroscopyProlate spheroid010402 general chemistry01 natural sciencesAtomic and Molecular Physics and OpticsForce field (chemistry)0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrysymbols.namesake[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryQuartic functionQuantum mechanics0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsIsotopologueRotational spectroscopyPhysical and Theoretical ChemistryGround stateHamiltonian (quantum mechanics)SpectroscopyComputingMilieux_MISCELLANEOUS
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Analysis of the rovibrational spectrum of 13CH4 in the Octad range

2013

Abstract We have measured the infrared spectrum of methane 13 CH 4 from 1100 cm −1 (33 THz), below the fundamental range, to about 12 000 cm −1 (360 THz) in the high overtone region at temperatures ranging from 80 K to 300 K by high resolution Fourier transform infrared (FTIR) spectroscopy. With instrumental bandwidths between 0.0027 cm −1 (80 MHz) and 0.01 cm −1 (300 MHz) this provides close to Doppler-limited spectra, using the Zurich prototype spectrometer (ZP2001, Bruker 125HR) combined with a multipath collisional cooling cell. Using perturbation theory and an accurate empirically adjusted potential we have computed ro-vibrational energy levels of 13 CH 4 and 12 CH 4 in the same energy…

Physics010304 chemical physicsSpectrometerInfraredOvertone02 engineering and technologyRotational–vibrational spectroscopy021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesAtomic and Molecular Physics and OpticsSpectral lineComputational physicsRoot mean squaresymbols.namesakeNuclear magnetic resonanceFourier transform0103 physical sciencessymbolsPhysical and Theoretical Chemistry0210 nano-technologySpectroscopySpectroscopyJournal of Molecular Spectroscopy
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Algebraic approach to vibrational spectra of tetrahedral molecules. First order infrared intensity model.

1995

International audience; The algebraic approach we have proposed to describe the vibrational stretching modes of polyatomic molecules (Leroy and Michelot, J. Mol. Spectrosc. 151, 71–96 (1992); Can. J. Phys. 72, 274–289 (1994)) is applied to the silane molecule for up to seven quanta. We then suggest a form of the dipole operator adapted to the (n000) local states by combining the strength of group theory method with the necessity of a compact formulation.

Physics010304 chemical physics[ PHYS.QPHY ] Physics [physics]/Quantum Physics [quant-ph]InfraredOperator (physics)Polyatomic ionVibrational Spectra. Algebraic Approach. Intensity modelTetrahedral molecular geometry010402 general chemistry01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesDipole[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Quantum mechanics0103 physical sciencesMoleculePhysical and Theoretical ChemistryAlgebraic numberAtomic physicsSpectroscopyGroup theory[PHYS.QPHY] Physics [physics]/Quantum Physics [quant-ph]
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