Search results for "Molecular spectroscopy"

showing 10 items of 27 documents

Introduction to the special issue on molecular spectroscopy, atmospheric composition and climate change

2018

International audience

010304 chemical physicsClimate changeMolecular spectroscopy010402 general chemistryAtmospheric sciences01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryAtmospheric composition13. Climate action0103 physical sciencesEnvironmental sciencePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSSpectroscopyJournal of Molecular Spectroscopy
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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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Spectroscopic tools for remote sensing of greenhouse gases CH4, CF4 and SF6

2003

International audience; Highly symmetrical molecules such as CH4, CF4 or SF6 are known to be atmospheric pollutants and greenhouse gases. High-resolution spectroscopy in the infrared is particularly suitable for the monitoring of gas concentration and radiative transfers in the earth's atmosphere. This technique requires extensive theoretical studies for the modeling of the spectra of such molecules (positions, intensities and shapes of absorption lines). Here, we have developed powerful tools for the analysis and the simulation of absorption spectra of highly symmetrical molecules. These tools have been implemented in the spherical top data system (STDS) and highly-spherical top data syste…

010504 meteorology & atmospheric sciencesAbsorption spectroscopy[ PHYS.QPHY ] Physics [physics]/Quantum Physics [quant-ph]Infrared01 natural sciencesSpectral lineAtmosphereSoftware[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]0103 physical sciencesRadiative transferEnvironmental ChemistryClimate changeSpectroscopy0105 earth and related environmental sciencesRemote sensingCH4010304 chemical physicsbusiness.industryChemistryCF4Molecular spectroscopyGreenhouse gases13. Climate actionGreenhouse gasbusinessSimulationSF6
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The 2009 Edition of the GEISA Spectroscopic Database

2011

The updated 2009 edition of the spectroscopic database GEISA (Gestion et Etude des Informations Spectroscopiques Atmosphériques; Management and Study of Atmospheric Spectroscopic Information) is described in this paper. GEISA is a computer-accessible system comprising three independent sub-databases devoted, respectively, to: line parameters, infrared and ultraviolet/visible absorption cross-sections, microphysical and optical properties of atmospheric aerosols. In this edition, 50 molecules are involved in the line parameters sub-database, including 111 isotopologues, for a total of 3,807,997 entries, in the spectral range from 10-6 to 35,877.031cm-1.The successful performances of the new …

010504 meteorology & atmospheric sciencesMeteorologyTélédétectionPhysique atomique et moléculaireMolecular spectroscopyInfrared atmospheric sounding interferometercomputer.software_genre01 natural sciencesLine parametersAtmospheric radiative transfer0103 physical sciences010303 astronomy & astrophysicsSpectroscopy0105 earth and related environmental sciencesRemote sensingWeb site[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]RadiationSpectroscopic database[ PHYS.PHYS.PHYS-OPTICS ] Physics [physics]/Physics [physics]/Optics [physics.optics]DatabaseGEISAOptically activeAtmospheric aerosolsMolecular spectroscopyAtomic and Molecular Physics and Optics[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryOn boardSpectroscopie [électromagnétisme optique acoustique][ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryEarth's and planetary atmospheresEnvironmental scienceAtmospheric absorptionAtmospheric absorptionCross-sectionscomputer
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Non-chromatographic speciation

2010

We evaluate the main strategies for screening trace-element species in most types of sample to establish their strengths and weaknesses, as they offer fast, sensitive and cheaper alternatives to classical methods involving chromatography. We consider the principles of non-chromatographic speciation analysis, based on the different behaviors of chemical species before measurement by atomic and molecular spectrometry and electroanalytical methods, so as to give an update on the literature in this field of research.

Alternative methodsChemical speciesChromatographyChemistryGenetic algorithmElectroanalytical methodAtomic spectroscopyMolecular spectroscopyInductively coupled plasma mass spectrometrySpectroscopyAnalytical ChemistryTrAC Trends in Analytical Chemistry
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Syntheses and Structures of a Series of Acyclic Diaminocarbene Palladium(II) Complexes Derived from 3,4-Diaryl-1H-pyrrol-2,5-diimines and Bisisocyani…

2018

Reactions of 3,4-diaryl-1H-pyrrol-2,5-diimines with various bisisocyanide palladium(II) complexes were studied. The coupling proceeds with one isocyanide ligand to accomplish the acyclic diaminocarbene complexes. The structure of generated diaminocarbene complexes depends on bulkiness of isocyanide ligand in the bisisocyanide complexes of palladium(II). The imino-group of 3,4-diaryl-1H-pyrrol-2,5-diimine reacts with one isocyanide ligand of cis-[PdCl2(CN–R)2] (R = i-Pr, Cy, t-Bu, Bn), and the nitrogen atom of the pyrrole ring is coordinated to the palladium center as the second isocyanide ligand remains intact. In the case of cis-[PdCl2(CN–R)2] (R = 2-acyloxyphenyl, 2-sulfonyloxyphenyl), on…

Coordination sphere010405 organic chemistryChemistryLigandIsocyanideOrganic Chemistrychemistry.chemical_elementMolecular spectroscopy010402 general chemistryRing (chemistry)01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundPolymer chemistryPhysical and Theoretical ChemistryCyclic voltammetryPyrrolePalladiumOrganometallics
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High-resolution infrared spectroscopy of the CH2 = CD2 molecule

2018

In this thesis we have considered spectra of the CH2=CD2 molecule. In the experimental part we recorded high-resolution (~ 0.0025 cm-1) infrared spectra and made full assignment of the recorded transitions. We were able to assign for the first time a lot of transitions to the weak combinations υ4+υ10, υ4+υ7 and 2υ10 overtone; forbidden due to the symmetry υ4, υ7+υ10, υ8+υ10; «hot» υ7+υ10–υ10 and υ8+υ10–υ10 bands. More than 7000 previously unknown transitions were assigned to the fundamental bands υ2, υ3, υ6, υ7, υ8, υ10, υ12 and 2υ7 overtone. On the base of operator perturbation theory and the symmetry properties of the studied molecule, we constructed an effective Hamiltonian and then fitt…

EthyleneResonant interactions[PHYS.PHYS]Physics [physics]/Physics [physics]Spectroscopie moléculaire à haute résolution[PHYS.PHYS] Physics [physics]/Physics [physics]Interactions résonantesHigh resolution molecular spectroscopy
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Twentieth colloquium on high resolution molecular spectroscopy - Dijon, 3 to 7 September 2007 - Foreword

2008

International audience

Materials science010304 chemical physicsBiophysicsAnalytical chemistryHigh resolutionMolecular spectroscopy010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryPhysical and Theoretical ChemistryMolecular BiologyComputingMilieux_MISCELLANEOUS
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First High-Resolution Raman Spectrum and Analysis of the ν5 Bending Fundamental of SF6

2002

Abstract The high-resolution Raman spectrum of the Q , R , and S branches of the ν 5 bending fundamental of SF 6 has been recorded at a temperature of 195 K (dry ice) and a pressure of 39 mbar. This is the first study ever performed of a ν 5 band of an XY 6 molecule. It has been analyzed thanks to the HTDS software ( http://www.u-bourgogne.fr/LPUB/shTDS.html ) developed in Dijon. This contribution should be of help in understanding the role hot bands in the strong absorbing ν 3 region.

Materials scienceHigh resolutionBendingMolecular spectroscopyAtomic and Molecular Physics and OpticsSulfur hexafluoridesymbols.namesakechemistry.chemical_compoundNuclear magnetic resonancechemistrysymbolsMoleculePhysical and Theoretical ChemistryAtomic physicsRaman spectroscopySpectroscopyJournal of Molecular Spectroscopy
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Multiple Decay Mechanisms and 2D-UV Spectroscopic Fingerprints of Singlet Excited Solvated Adenine-Uracil Monophosphate

2016

The decay channels of singlet excited adenine uracil monophosphate (ApU) in water are studied with CASPT2//CASSCF:MM potential energy calculations and simulation of the 2D-UV spectroscopic fingerprints with the aim of elucidating the role of the different electronic states of the stacked conformer in the excited state dynamics. The adenine 1La state can decay without a barrier to a conical intersection with the ground state. In contrast, the adenine 1Lb and uracil S(U) states have minima that are separated from the intersections by sizeable barriers. Depending on the backbone conformation, the CT state can undergo inter-base hydrogen transfer and decay to the ground state through a conical …

Models Molecularmolecular electronicsChemistry MultidisciplinaryMolecular electronicsphotophysic2-DIMENSIONAL ELECTRONIC SPECTROSCOPYSTATE DYNAMICSBASE-STACKINGPhotochemistry01 natural sciences[CHIM] Chemical SciencesNUCLEIC-ACIDSQuímica quànticaEspectrofotometriaConformational isomerismComputingMilieux_MISCELLANEOUSphotophysics010304 chemical physicsFull PaperHydrogen bondChemistryChemistry (all)Full PapersMolecular spectroscopy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryChemistryFOURIER-TRANSFORM SPECTROSCOPYSpectrophotometryExcited statePhysical Sciences1ST-PRINCIPLES SIMULATION03 Chemical SciencesGround stateUridine MonophosphateQuantum chemistryEspectroscòpia molecularmolecular electronic010402 general chemistryMolecular physicsCatalysisUltraviolet visible spectroscopy0103 physical sciencesPhotophysics | Hot Paper[CHIM]Chemical SciencesSinglet stateUV/Vis spectroscopyULTRAFAST INTERNAL-CONVERSIONSpectroscopyLIGHT-HARVESTING COMPLEXab initio calculationScience & Technologyab initio calculationsOrganic ChemistryGeneral ChemistryDNAConical intersectionDNA FingerprintingAdenosine Monophosphate0104 chemical sciences[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryAB-INITIO SIMULATIONSElectrònica molecularMOLECULAR-DYNAMICSSpectrophotometry Ultraviolet
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