Search results for "PHOTOCHEMICAL"

showing 10 items of 108 documents

Titania Photocatalysts for Selective Oxidations in Water

2011

Heterogeneous photocatalysis by polycrystalline semiconductor oxides is an unconventional technology that has been mainly applied for the degradation of organic and inorganic pollutants in both the vapor and liquid phase. The application of photocatalysis in synthetic routes has also been researched in recent years, demonstrating its viability as an alternative route in organic chemistry. This work illustrates the main findings in the application of heterogeneous photocatalysis to the oxidation of organic compounds dissolved in water, free of any organic co-solvent. Two main aspects of the oxidative process have been studied: the first one is the partial oxidation of various mono-substitute…

TitaniumTiO2 photocatalysis selective oxidationsChemistryGeneral Chemical EngineeringInorganic chemistryWaterPhotochemical ProcessesHeterogeneous catalysisHydrocarbons AromaticCombinatorial chemistryCatalysisWater PurificationGeneral EnergyAlcoholsEnvironmental ChemistryGeneral Materials ScienceSettore CHIM/07 - Fondamenti Chimici Delle TecnologieOxidation-ReductionEnvironmental Restoration and RemediationWater Pollutants ChemicalChemSusChem
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Quasi-isoactinic reactor for photocatalytic kinetics studies

2007

Photochemical reactors characterized by almost uniform values of the local volumetric rate of photon absorption (LVRPA), i.e., quasi-isoactinic photoreactors, are particularly suitable for assessing the influence of radiant field intensity in kinetic studies. In this work, Monte Carlo simulations have been performed to obtain LVRPA values in a flat photoreactor irradiated on both sides. This configuration appears to be particularly suitable for obtaining quasi-isoactinic conditions. The influence of catalyst albedo and scattering phase function is assessed, and the conditions for obtaining iso-actinicity are discussed. Finally, these conditions are related to an easy-to-measure parameter, n…

Work (thermodynamics)Settore ING-IND/26 - Teoria Dello Sviluppo Dei Processi ChimiciGeneral Chemical EngineeringSettore ING-IND/25 - Impianti ChimiciMonte Carlo methodThermodynamicsPhotochemical reactorParticleKinetic energyIndustrial and Manufacturing EngineeringLight scatteringRadiation absorptionOpticsTransmittanceAbsorption (electromagnetic radiation)Heterogeneous photoreactorRadiant fieldChemistrybusiness.industryScatteringWaterGeneral ChemistryPhotocatalysisLight-scatteringAstrophysics::Earth and Planetary AstrophysicsbusinessModel
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Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide

2013

Volatile halogenated organic compounds containing bromine and iodine, which are naturally produced in the ocean, are involved in ozone depletion in both the troposphere and stratosphere. Three prominent compounds transporting large amounts of marine halogens into the atmosphere are bromoform (CHBr3), dibromomethane (CH2Br2) and methyl iodide (CH3I). The input of marine halogens to the stratosphere has been estimated from observations and modelling studies using low-resolution oceanic emission scenarios derived from top-down approaches. In order to improve emission inventory estimates, we calculate data-based high resolution global sea-to-air flux estimates of these compounds from surface ob…

[SDE] Environmental SciencesAtmospheric Science010504 meteorology & atmospheric sciences[SDV]Life Sciences [q-bio]Tropical Tropopause LayerWind-Speed010501 environmental sciencesAtmospheric sciences01 natural sciencesDibromomethaneTroposphereAtmospherelcsh:ChemistryStratospheric Brominechemistry.chemical_compoundFlux (metallurgy)Ocean gyrePhysical Sciences and MathematicsGas-ExchangeOzone Depletion14. Life underwaterEmission inventoryStratosphere0105 earth and related environmental sciencesgeographygeography.geographical_feature_categoryAtlantic-OceanLife SciencesOzone depletionlcsh:QC1-999Halogenated Organic-Compounds[SDV] Life Sciences [q-bio]chemistrylcsh:QD1-99913. Climate actionMarine Boundary-LayerClimatologyPhytoplankton Cultures[SDE]Environmental SciencesPhotochemical Productionlcsh:Physics
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Photochemistry of oxidized Hg(I) and Hg(II) species suggests missing mercury oxidation in the troposphere.

2020

8 pags., 5 figs., 2 tabs.

atmospheric chemistryAtmospheric chemistry010504 meteorology & atmospheric sciencesTropospheric chemistryMercury photoreductionchemistry.chemical_elementatmospheric modelingAtmospheric model010501 environmental sciencesPhotochemistry01 natural sciencesTroposphereMercury oxidationComputer SimulationGas-phase mercury reactivitygas-phase mercury reactivity0105 earth and related environmental sciencesmercury photoreductionThermal oxidationMultidisciplinaryAtmospherePhotodissociationCorrectionMercuryModels TheoreticalPhotochemical Processestropospheric chemistryMercury (element)Atmospheric modelingDeposition (aerosol physics)chemistry13. Climate actionAtmospheric chemistry[CHIM.OTHE]Chemical Sciences/OtherOxidation-ReductionProceedings of the National Academy of Sciences of the United States of America
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New oxygenated eudesmanolides from artemisia herba-alba

1990

Abstract The aerial parts of Artemisia herba-alba Asso subsp.valentina Lam. (Asteraceae) yielded the new eudesmanolides 1-11 and the new sesquiterpene-monoterpene adducts 12-13. The absolute configuration of compound 6 was confirmed with the aid of X-ray diffraction analysis. Some aspects of the thermal and photochemical reactivity of 2,4-cyclohexadienones are discussed.

biologyArtemisia herba-albaStereochemistryChemistryMonoterpeneOrganic ChemistryAbsolute configurationAsteraceaebiology.organism_classificationSesquiterpeneBiochemistrychemistry.chemical_compoundDrug DiscoveryArtemisiaOrganic chemistryPhotochemical reactivityThermal reactionTetrahedron
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Photochemical Functionalization of Allyl Benzoates by C-H Insertion

2013

The photoreactivity of allyl benzoates, containing an electron-rich double bond, has been explored by irradiation at 305 nm in different solvents. Solvent addition products arising from an insertion of the alpha H–C bonds of THF, dioxane, and i-PrOH to the allylic double bond was realized. The observed reactivity depended on reaction conditions and substitution pattern of the substrate. A DFT study on this unusual reaction was performed allowing the formulation of two mechanistic pathways.

chemistry.chemical_classificationAllylic rearrangementDouble bondChemistryOrganic ChemistryMechanistic organic photochemistrySubstrate (chemistry)Organic photochemistryPhotochemical synthesis THF reactivityBiochemistryMedicinal chemistryC-C bond formationDFTBenzoatesSolventDrug DiscoverySurface modificationReactivity (chemistry)C-H insertion
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Synthesis and photophysical properties of hyperbranhced polyfluorenes containing 2,4,6-tris(tiophen-2-yl)-1,3,5-triazine as the core

2011

A series of new hyperbranched polymers containing a 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine core unit and polyfluorene chain arms have been synthesized via Suzuki coupling, and characterized by NMR, IR and GPC. All the polymers exhibit good thermal stability with a high decomposition temperature. By changing the 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine/fluorene ratio the UV-vis absorption and emission spectra can be partially tuned. It has been found that the polymers containing a low ratio of 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine units (P1-P3) have an absorption maximum around 385 nm, localized in the polyfluorene chain, and a shoulder around 425 nm ascribable to a charge transfer stat…

chemistry.chemical_classificationFluorenesMolecular StructureAbsorption spectroscopyPolymersTriazinesGeneral Physics and AstronomyThiophenesPolymerFluorenePhotochemical ProcessesPhotochemistryTwo-photon absorptionchemistry.chemical_compoundPolyfluorenechemistryOrganic chemistryPhysical and Theoretical ChemistryAbsorption (chemistry)HOMO/LUMOta116TriazinePhysical Chemistry Chemical Physics
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Improvement of the mechanical properties of photo-oxidized films after recycling

2002

Mechanical recycling of post-consumer plastics gives rise, in most cases, to secondary materials with mechanical properties worse than those of the reclaimed polymer. This is mostly due to the thermomechanical treatment undergone during the melt reprocessing operations. In this work, low density polyethylene films have been photo-oxidized in artificial accelerated ageing conditions and then the brittle films have been melt reprocessed. It is shown that the secondary material, after reprocessing, shows mechanical properties, in particular elongation at break, better than those of the photo-oxidized films. This behaviour has been attributed to the fact that the melt reprocessing has the effec…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOxidative degradationPolymerCondensed Matter PhysicsMolten stateLow-density polyethyleneBrittlenesschemistryMechanics of MaterialsMaterials ChemistryPhotochemical degradationComposite materialElongationOxygen starvationPolymer Degradation and Stability
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Heterocyclic rearrangements in constrained media. A zeolite-directed photorearrangement of 1,2,4-oxadiazoles

2005

[reaction: see text] The first intrazeolite-photoinduced rearrangement of a five-membered heterocycle is reported. A completely different behavior compared to solution irradiations has been observed. The zeolite's role in directing the photoreaction of 3-phenyl-1,2,4-oxadiazoles toward the formation of the corresponding 1,3,4-oxadiazoles in a ring contraction-ringexpansion route is discussed.

chemistry.chemical_classificationModels MolecularOxadiazolesRING-PHOTOISOMERIZATIONMolecular StructurePHOTOCHEMICAL BEHAVIORChemistryPhotochemistryUltraviolet RaysOrganic ChemistryPATHWAYSSettore CHIM/06 - Chimica OrganicaRing (chemistry)PhotochemistryHeterocyclic compoundCyclizationZeolitesZeolite
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The Quest for Mononuclear Gold(II) and Its Potential Role in Photocatalysis and Drug Action.

2017

The chemistry of gold strongly focuses on the ubiquitous oxidation states +I and +III. The intermediate oxidation state +II is generally avoided in mononuclear gold species. In recent years, gold(II) has been increasingly suggested as a key intermediate in artificial photosynthesis systems, with gold(III) moieties acting as electron acceptors, as well as in gold-catalyzed photoredox catalysis and radical chemistry. This Minireview provides a concise summary of confirmed and characterized mononuclear open-shell gold(II) complexes. Recent findings on structural motifs and reactivity patterns will be discussed. Exciting developments in the fields of photosynthesis, photocatalysis, and potentia…

chemistry.chemical_classificationMolecular Structure010405 organic chemistryChemistryRadicalChemistry PharmaceuticalPhotoredox catalysisElectronsGeneral ChemistryElectron acceptor010402 general chemistryPhotochemical Processes01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesArtificial photosynthesisElectron transferOxidation statePhotocatalysisOrganic chemistryReactivity (chemistry)Organogold CompoundsAngewandte Chemie (International ed. in English)
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