Search results for "Vibrational spectroscopy"

showing 10 items of 85 documents

High-resolution rovibrational spectroscopy of c-C3H2+: The ν7 C–H antisymmetric stretching band

2020

Abstract The ν 7 antisymmetric C–H stretching fundamental of c- C 3 H 2 + has been characterized in a cryogenic 22-pole ion trap by a novel type of action spectroscopy, in which the rovibrational excitation of c- C 3 H 2 + is detected as a slowing down of the low-temperature reaction c- C 3 H 2 +  + H2 → C 3 H 3 + + H. Ninety-one rovibrational transitions with partly resolved fine structure doublets were measured in high resolution. Supported by high-level quantum chemical calculations, spectroscopic parameters were determined by fitting the observed lines with an effective Hamiltonian for an asymmetric rotor in a doublet electronic ground state, X ˜ A 1 2 , yielding a band origin at 3113.6…

010405 organic chemistryAntisymmetric relationChemistryOrganic ChemistryRotational–vibrational spectroscopy010402 general chemistry01 natural sciencesMolecular physics0104 chemical sciencesAnalytical ChemistryInorganic Chemistrysymbols.namesakesymbolsMoleculeIon trapGround stateHamiltonian (quantum mechanics)SpectroscopySpectroscopyExcitationJournal of Molecular Structure
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The MIRS computer package for modeling the rovibrational spectra of polyatomic molecules

2003

International audience; The MIRS spectroscopic software for the modeling of ro-vibrational spectra of polyatomic molecules is presented. It is designed for the global treatment of complex band systems of molecules to take full account of symmetry properties. It includes e cient algorithms based on the irreducible tensor formalism. Predictions and simultaneous data fi tting (positions and intensities) are implemented as well as advanced options related to group theory algebra. Illustrative examples on CH3D, CH4, CH3Cl and PH3 are reported and the present status of data available is given. It is written in C++ for standard PC computer operating under Windows. The full package including on-lin…

010504 meteorology & atmospheric sciences01 natural sciencesSpectral lineSoftwareComputer package0103 physical sciencesMoleculeSpectroscopy0105 earth and related environmental sciencesPhysics[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]RadiationSpectroscopic database010304 chemical physicsbusiness.industryPolyatomic ionRotational–vibrational spectroscopyMolecular spectroscopyAtmospheric applicationsAtomic and Molecular Physics and OpticsComputational physics[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Rotation vibrationCurve fittingbusinessInfraredGroup theorySoftware
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The high overtone and combination levels of SF6 revisited at Doppler-limited resolution: A global effective rovibrational model for highly excited vi…

2017

Abstract Sulfur hexafluoride is an important prototypal molecule for modeling highly excited vibrational energy flow and multi quanta absorption processes in hexafluoride molecules of technological importance. It is also a strong greenhouse gas of anthropogenic origin. This heavy species, however, features many hot bands at room temperature (at which only 30% of the molecules lie in the ground vibrational state), especially those originating from the lowest, v 6 =1 vibrational state. Using a cryogenic long path cell with variable optical path length and temperatures regulated between 120 and 163 K, coupled to Synchrotron Radiation and a high resolution interferometer, Doppler-limited spectr…

010504 meteorology & atmospheric sciencesOvertoneInfrared spectroscopylow temperature01 natural sciences7. Clean energyHot bandSpectral linechemistry.chemical_compoundHexafluorideFar infraredhot bandRotation-vibration spectroscopy of SF 60103 physical sciencesSpectroscopy0105 earth and related environmental sciencesPhysics[PHYS]Physics [physics]Radiation[ PHYS ] Physics [physics]010304 chemical physicsRotational–vibrational spectroscopyAtomic and Molecular Physics and Opticschemistry13. Climate actiongreenhouse gasExcited stateinfrared absorptionAtomic physicstensorial formalismLong path cell
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High-resolution spectroscopy and analysis of the V2 + V3 combination band of SF6 in a supersonic jet expansion

2013

International audience; Sulphur hexafluoride is a very strong greenhouse gas whose concentration is increasing in the atmosphere. It is detected through infrared absorption spectroscopy in the strong ν3 fundamental region. Due to the existence of low-lying vibrational states of this molecule, however, many hot bands arise at room temperature and those are still not known. We present here a contribution to the elucidation of this hot band structure, by analysing the ν2 + ν3 combination band. We use a supersonic jet expansion high-resolution spectrum at a rotational temperature of ca. 25 K that was recorded thanks to the Jet-AILES setup at the Source Optimisée de Lumière d'Energie Intermédiai…

010504 meteorology & atmospheric sciencessupersonic jet expansionBiophysicsInfrared spectroscopy7. Clean energy01 natural sciencesHot bandlaw.inventionsymbols.namesake[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]law0103 physical sciencesSupersonic speedPhysical and Theoretical ChemistrySpectroscopy[ PHYS.PHYS.PHYS-ATM-PH ] Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]Molecular BiologyComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciences[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]010304 chemical physicssulphur hexafluorideChemistry[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]Rotational temperatureRotational–vibrational spectroscopyCondensed Matter PhysicsSynchrotron[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]13. Climate actiongreenhouse gassymbolsinfrared absorption[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physicsHamiltonian (quantum mechanics)tensorial formalism
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Challenges in clinical analysis by infrared spectroscopy

2014

En els últims anys, el desenvolupament de metodologies d’anàlisi clínic basades en espectroscòpia infraroja (IR) s’ha convertit en un camp molt actiu d’investigació. Millores en la instrumentació i en el processament de les dades han contribuït a que l’espectroscòpia IR s’utilitze per a obtindré informació de la composició de fluids i teixits biològics. Aquesta tesis consolida aquesta tècnica com una eina versàtil en el desenvolupament de metodologies per a extraure una gran quantitat d’informació en un ampli espectre de mostres mitjançant instrumentació senzilla, ràpida i econòmica. Tot i que la tècnica té problemes de sensibilitat i selectivitat, els resultats obtinguts en aquesta Tesi de…

:QUÍMICA::Química analítica::Análisis bioquímico [UNESCO]UNESCO::QUÍMICA::Química analítica::Espectroscopía de infrarrojosdiagnosisinfrared:MATEMÁTICAS::Estadística::Análisis multivariante [UNESCO]UNESCO::MATEMÁTICAS::Estadística::Análisis multivarianteclinical analysisUNESCO::QUÍMICA::Química analítica::Análisis bioquímicochemometrics:QUÍMICA::Química analítica::Espectroscopía de infrarrojos [UNESCO]vibrational spectroscopy
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The vibrational levels of methane obtained from analyses of high-resolution spectra

2006

International audience; Methane and its tetrahedral isotopologues are spherical-top molecules whose high-resolution rovibrational spectra can only be analyzed in detail, thanks to sophisticated symmetry-adapted tensorial models. However, the effective Hamiltonian parameters of such models do not give direct access to the positions of the vibrational sublevels. In this paper, we present a calculation of the vibrational level positions for 12CH4, 13CH4, 12CD4 and 13CD4 performed using the effective Hamiltonian parameters obtained through recent analyses. We also include the results of a re-analysis of the octad system of 12CH4 performed with a higher order of the development which slightly im…

Absorption spectroscopy01 natural sciencesSpectral lineMethanesymbols.namesakechemistry.chemical_compoundvibrational levels and sublevels0103 physical sciencesIsotopologuepolyads010303 astronomy & astrophysicsSpectroscopyPhysics[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Radiation010304 chemical physicsmethanepotential surfaceRotational–vibrational spectroscopyAtomic and Molecular Physics and OpticsMathematical Operatorschemistry[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]TetrahedronsymbolsAtomic physicsHamiltonian (quantum mechanics)tensorial formalism
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High resolution Fourier transform infrared spectroscopy and analysis of the ν 6 band of jet-cooled Mo(CO) 6

2000

Abstract Rovibrational FTIR spectra of Mo(CO) 6 have been recorded in supersonic argon expansions at 0.004 cm −1 resolution. Rotational constants have been determined for the ν 6 fundamental band of Mo( 12 CO) 6 and for the parallel band of the symmetric top isotopomer Mo( 13 CO)( 12 CO) 5 . From these results, a precise estimate of the Coriolis parameter for the ν 6 band of the main isotopomer Mo( 12 CO) 6 is derived, necessary for the analysis of the ν 6 spectrum. The observation of an octahedral splitting clearly resolved for the highest J-lines in the R branch prompted the use of a specific treatment based on the tensorial formalism developed by J.P. Champion, M. Loete, G. Pierre (Spher…

ArgonOrganic ChemistryAnalytical chemistrychemistry.chemical_elementRotational–vibrational spectroscopySpectral lineAnalytical ChemistryIsotopomersInorganic ChemistryInterstellar mediumchemistryFourier transform infrared spectroscopySpectroscopyMolecular beamSpectroscopyJournal of Molecular Structure
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Optical Shielding of Destructive Chemical Reactions between Ultracold Ground-State NaRb Molecules

2020

Polar quantum gases represent promising platforms for studying many-body physics and strongly correlated systems with possible applications e.g. in quantum simulation or quantum computation. Due to their large permanent electric dipole moment polar molecules in electric field exhibit strong long-range anisotropic dipole-dipole interactions (DDIs). The creation and trapping of ultracold dipolar diatomic molecules of various species are feasible in many experimental groups nowadays. However long time trapping is still a challenge even in the case of the so called nonreactive molecules which are supposed to be immune against inelastic collisions in their absolute ground state [1] . Various hyp…

Atomic Physics (physics.atom-ph)Inelastic collisionGeneral Physics and AstronomyFOS: Physical sciencesQuantum simulator01 natural sciences7. Clean energyMolecular physicslaw.inventionPhysics - Atomic Physics[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]law0103 physical sciencesMoleculeSpontaneous emissionPhysics::Atomic Physics010306 general physicsComputingMilieux_MISCELLANEOUSPhysics[PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]Rotational–vibrational spectroscopyLaserDiatomic moleculeDipoleElectric dipole momentQuantum Gases (cond-mat.quant-gas)Excited stateAtom optics[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physicsCondensed Matter - Quantum GasesGround state
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Vibronic Relaxation Pathways in Molecular Spin Qubit Na9[Ho(W5O18)2]·35H2O under Pressure

2023

In order to explore how spectral sparsity and vibronic decoherence pathways can be controlled in a model qubit system with atomic clock transitions, we combined diamond anvil cell techniques with synchrotron-based far infrared spectroscopy and first-principles calculations to reveal the vibrational response of Na9[Ho(W5O18)2]·35H2O under compression. Because the hole in the phonon density of states acts to reduce the overlap between the phonons and f manifold excitations in this system, we postulated that pressure might move the HoO4 rocking, bending, and asymmetric stretching modes that couple with the MJ = ±5, ±2, and ±7 levels out of resonance, reducing their …

Chemistry (miscellaneous)strategies to minimize decoherenceMaterials Chemistryspin qubithigh pressure vibrational spectroscopyQuímicaVibracióvibronic couplingElectronic Optical and Magnetic MaterialsMagnetochemistry
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Collisional shifting and broadening coefficients for the rovibrational anisotropic lines of the ν1/2ν2 fermi dyad in CO2 gas studied by stimulated Ra…

1998

High-resolution stimulated Raman spectroscopy was applied to the study of collisional broadening and shifting for rovibrational anisotropic Raman lines of the Fermi dyad of molecular carbon dioxide. The O(J) lines of the ν1 band and the S(J) lines of the 2ν2 band were recorded at 295 K. The pressure-induced line shifts were obtained and compared with the overall shift of the high-density Raman Q-branch. A rotational quantum number dependence of the rovibrational line broadening coefficients was observed. The experimental line broadening coefficients were used in order to check the ability of two theoretical methods (random phase approximation and sum rule) for calculating the line broadenin…

ChemistryAnalytical chemistryRotational–vibrational spectroscopyQuantum numbersymbols.namesakesymbolsGeneral Materials ScienceCoherent anti-Stokes Raman spectroscopyAtomic physicsSpectroscopyRaman spectroscopySpectroscopyRaman scatteringDoppler broadeningLine (formation)Journal of Raman Spectroscopy
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