Search results for "PHOTODISSOCIATION"

showing 10 items of 90 documents

Mechanistic studies on the photogeneration of o- and p-xylylenes from α,α′-dichloroxylenes

1998

Two-colour two-laser techniques have unambiguously proved that photolysis of the o-/p-(chloromethyl)benzyl radical leads to the sequential two-photon generation of o-/pxylylene from α,α'-dichloro-o-/p-xylene. Perez Prieto, Julia, Julia.Perez@uv.es

PhotolysisChemistryUNESCO::QUÍMICAUNESCO::QUÍMICA::Química analíticaPhotodissociationMetals and AlloysXylylenesGeneral ChemistryPhotochemistryPhotogeneration:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBenzyl:QUÍMICA::Química analítica [UNESCO]Materials ChemistryCeramics and CompositesPhotogeneration ; Xylylenes ; Photolysis ; BenzylChemical Communications
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Photodissociation of small group-11 metal cluster ions: Fragmentation pathways and photoabsorption cross sections

2003

Noble metal cluster ions Cu(n)(+), Ag(n)(+) and Au(n)(+) (n = 3-21) have been stored in a Penning trap and photodissociated by low intensity laser pulses of 10 ns at photon energies of 3.49 eV and 4.66 eV. The fragmentation pathways, neutral monomer and dimer evaporation, have been monitored as a function of cluster size, excitation energy and element. It is found that the behavior of the branching ratio between monomer and dimer evaporation as a function of excitation energy depends on the metal under investigation. In particular, the slope of the energy dependence is positive for silver but negative for gold and copper cluster ions. Furthermore, photoabsorption cross sections are determin…

Gold clusterDimerPhotodissociationAnalytical chemistryPenning trapDissociation (chemistry)Ionchemistry.chemical_compoundTransition metalchemistryFragmentation (mass spectrometry)Structural BiologyPhysics::Atomic and Molecular ClustersSpectroscopyJournal of the American Society for Mass Spectrometry
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A novel photochemical 1,4-acyl migration in enol esters. The photolysis of enol acetates of 3-phenylpropiophenones

1987

Abstract Photolysis of the enol acetates 1a,b gives the 1,4-diketones 4a,b by a mechanism involving a primary homolytic carbonyl—oxygen bond cleavage, followed by 1,2-hydrogen shift and in cage recombination.

chemistry.chemical_classificationDiketoneKetoneCarboxylic acidOrganic ChemistryPhotodissociationPhotochemistryBiochemistryEnolHomolysischemistry.chemical_compoundchemistryDrug DiscoveryAliphatic compoundBond cleavageTetrahedron Letters
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Photoinduced molecular rearrangements. Some comments on the ring-photoisomerization of 1,2,4-oxadiazoles into 1,3,4-oxadiazoles

2001

The ring-photoisomerization of 3-amino- and 3-methylamino-5-phenyl-1,2,4-oxadiazoles into the corresponding 2-amino- and 2-methylamino-5-phenyl-1,3,4-oxadiazoles has been reinvestigated by examining the effect of a base on the photoreaction. On irradiating at λ = 254 nm in methanol, yields of the ring-photoisomers were found to be significantly enhanced by the addition of triethylamine (TEA) in the photoreaction medium. By contrast, irradiation of the 3-amino-5-phenyloxadiazole in acetonitrile containing TEA gave an almost complete photoreduction into benzoylguanidine, while few percent of the ring photoisomer were detected. Furthermore, the pyrene-sensitized photolysis of 3-amino-5-phenylo…

chemistry.chemical_classificationchemistry.chemical_compoundBase (chemistry)PhotoisomerizationChemistryOrganic ChemistryPhotodissociationIrradiationMethanolRing (chemistry)PhotochemistryAcetonitrileTriethylamineJournal of Heterocyclic Chemistry
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Shaping of a ground state rotational wavepacket by frequency-chirped pulses

2001

0953-4075; A coherent rotational superposition state is produced in the ground vibronic level of N2 through the interaction of the molecule with the electric field vector of a nonresonant laser pulse. This rotational wavepacket is shaped with a linear frequency chirp of the laser field. The structural shape of the rotational coherences shows a strong dependence with the frequency-chirp amplitude. A comparison with a theoretical model allows the interpretation of the observed effects in terms of dephasing of the wavepacket induced by the laser phase distortion. Application of the presented results to the phase characterization of short XUV pulses is suggested.

CONTROLDephasingPhase (waves)Physics::Opticslaw.inventionCOHERENTSuperposition principleINDUCED POLARIZATION SPECTROSCOPYlawPhysics::Atomic and Molecular ClustersChirpPhysics::Atomic PhysicsFIELDFEMTOSECOND LASER-PULSESINTERFERENCEPhysicsPhase distortionPHOTODISSOCIATIONCondensed Matter PhysicsLaserEVOLUTIONN-2Atomic and Molecular Physics and OpticsAmplitudeAtomic physicsGround stateJournal of Physics B: Atomic, Molecular and Optical Physics
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Measurement report: Photochemical production and loss rates of formaldehyde and ozone across Europe

2021

Various atmospheric sources and sinks regulate the abundance of tropospheric formaldehyde (HCHO), which is an important trace gas impacting the HOx (≡ HO2 + OH) budget and the concentration of ozone (O3). In this study, we present the formation and destruction terms of ambient HCHO and O3 calculated from in situ observations of various atmospheric trace gases measured at three different sites across Europe during summertime. These include a coastal site in Cyprus, in the scope of the Cyprus Photochemistry Experiment (CYPHEX) in 2014, a mountain site in southern Germany, as part of the Hohenpeißenberg Photochemistry Experiment (HOPE) in 2012, and a forested site in Finland, where measurement…

Atmospheric ScienceOzonePhysicsQC1-999PhotodissociationFormaldehydePhotochemistryMethaneTrace gasTropospherechemistry.chemical_compoundChemistrychemistryEnvironmental scienceQD1-999IsopreneNOx
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Soft X-Ray Irradiation of Methanol Ice: Implication for H2CO Formation in Interstellar Regions

2010

We performed 0.3 keV soft X-ray irradiation of a methanol ice at 8 K under ultra-high vacuum conditions. To the best of our knowledge, this is the first time that soft X-rays are used to study photolysis of ice analogs. Despite the low irradiation dose of 10{sup -6} photons molecule{sup -1}, the formation of formaldehyde has been observed. The results of our experiments suggest that X-rays may be a promising candidate to the formation of complex molecules in regions where UV radiation is severely inhibited.

PhysicsPhotodissociationFormaldehydeAstronomy and AstrophysicsRadiationPhotochemistryChemical reactionDecompositionchemistry.chemical_compoundISM: molecules – methods: laboratory – X-rays: ISMSettore FIS/05 - Astronomia E AstrofisicachemistrySpace and Planetary ScienceMoleculeIrradiationMethanolAtomic physics
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The influence of internal degrees of freedom on the unimolecular decay of the molecule–cluster compound Au8+CH3OH

2002

Time-resolved photodissociation measurements of the sequential reaction Au8+CH3OH→Au8+→Au7+ and the direct reaction Au8+→Au7+ have been performed for several excitation energies. The production rates and yields of the final state Au7+ in the sequential process are strongly influenced by the excitation energy deposited into the evaporated methanol molecule during the initial fragmentation step. Both the rate constants and yields can be fitted with a single parameter, the cluster–methanol binding energy.

Reaction rate constantFragmentation (mass spectrometry)ChemistryBinding energyPhotodissociationDegrees of freedom (physics and chemistry)General Physics and AstronomyPhysical chemistryMoleculePhysical and Theoretical ChemistryAtomic physicsExcitationIonThe Journal of Chemical Physics
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Heterocyclic photorearrangements. Photoinduced rearrangement of 3-styryl-1,2,4-oxadiazoles

1990

The photochemical behaviour of 3-styryl-5-phenyl-(5-methyl)-1,2,4-oxadiazoles in methanol at 254 nm has been investigated. A photoinduced rearrangement to the quinoline system has been pointed out and explained as proceeding through an initial photolysis of the ring ON bond, followed by a six membered ring closure reaction involving the styryl moiety.

Intramolecular reactionBicyclic moleculemedicine.drug_classOrganic ChemistryQuinolinePhotodissociationCarboxamideRing (chemistry)PhotochemistryCis trans isomerizationchemistry.chemical_compoundchemistrymedicineMoietyJournal of Heterocyclic Chemistry
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The Role of Excited Oxygen Molecules in the Formation of the Secondary Ozone Layer at 87 to 97 km

2018

The secondary ozone layer is located at elevations of 87 to 97 km in the upper mesosphere – lower thermosphere. It overlaps with the ionospheric D-layer. Daytime intensive UV radiation is dissociating O2 molecules to O atoms and photoexcitating O2 molecules up to 11.07eV level. Ozone photolysis between the wavelengths of 118.7–121.6 nm produces three oxygen atoms from one ozone molecule. Collision reactions of O2(B3 Σu —) and O2(X3 Σg —, υ≥26) with O2(X3 Σg —, υ=0) produce additional oxygen atoms. The number of oxygen atoms is maintained at such a high level that a small but significant ozone concentration survives. UV radiation weakens radically during the night. The number of O atoms show…

secondary ozone zoneOzone010504 meteorology & atmospheric scienceschemistry.chemical_elementEnvironmental Science (miscellaneous)Photochemistry01 natural sciencesOxygenchemistry.chemical_compound0103 physical sciencesOzone layer010303 astronomy & astrophysicsDissociative recombination0105 earth and related environmental sciencesNature and Landscape ConservationO2+ dissociative recombinationEcologyPhotodissociationPollutionchemistryExcited statenightglowsAbsorption (chemistry)Thermospherevibrational and electronical excitation of O2photoexcitation of O2
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