Search results for "AROMA"

showing 10 items of 1006 documents

Tandem Reactions of 1,2,4-Oxadiazoles with Allylamines

2011

A reaction of 3-chloro-1,2,4-oxadiazoles with allylamine and diallylamine has been investigated. 3,3a,4,5-Tetrahydroisoxazolo[3,4-d]pyrimidines are produced through a tandem ANRORC/[3 + 2]cycloaddition pathway consisting of the addition of allylamine to the 1,2,4-oxadiazole, followed by ring opening, nitrone formation, and finally cycloaddition. 3-N-Allylamino-1,2,4-oxadiazoles were also obtained as minor products through a classical SNAr. Conversely, a reaction with diallylamine produces 3-N,N-diallylamino-1,2,4-oxadiazole and imidazoline through tandem SNAr/aziridination and nucleophilic ring opening.

chemistry.chemical_classificationOxadiazolesMolecular StructureTandemChemistryOrganic ChemistryImidazoline receptorStereoisomerismSettore CHIM/06 - Chimica OrganicaRing (chemistry)BiochemistryMedicinal chemistryCycloadditionAllylamineAllylamineNitronechemistry.chemical_compoundANRORC Oxadiazoles cycloadditionsPyrimidinesNucleophileCyclizationNucleophilic aromatic substitutionPhysical and Theoretical Chemistry
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Oxygen-containing polycyclic aromatic hydrocarbons (OPAHs) in urban soils of Bratislava, Slovakia: patterns, relation to PAHs and vertical distributi…

2011

Abstract We determined concentrations, sources, and vertical distribution of OPAHs and PAHs in soils of Bratislava. The ∑14 OPAHs concentrations in surface soil horizons ranged 88–2692 ng g−1 and those of ∑34 PAHs 842–244,870 ng g−1. The concentrations of the ∑9 carbonyl-OPAHs (r = 0.92, p = 0.0001) and the ∑5 hydroxyl-OPAHs (r = 0.73, p = 0.01) correlated significantly with ∑34 PAHs concentrations indicating the close association of OPAHs with parent-PAHs. OPAHs were quantitatively dominated by 9-fluorenone, 9,10-anthraquinone, 1-indanone and benzo[a]anthracene-7,12-dione. At several sites, individual carbonyl-OPAHs had higher concentrations than parent PAHs. The concentration ratios of se…

chemistry.chemical_classificationPersistent organic pollutantSlovakiaOpahbiologyChemistryHealth Toxicology and MutagenesisGeneral MedicineToxicologybiology.organism_classificationPollutionSoilHydrocarbonEnvironmental chemistrySoil waterSoil horizonSoil PollutantsVolatile organic compoundLeaching (agriculture)Polycyclic Aromatic HydrocarbonsSubsoilUrban RenewalEnvironmental MonitoringEnvironmental pollution (Barking, Essex : 1987)
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Photoelectrocatalytic selective oxidation of 4-methoxybenzyl alcohol in water by TiO2 supported on titanium anodes

2013

The photoelectrocatalytic partial oxidation of 4-methoxybenzyl alcohol in aqueous solution irradiated by near-UV light was carried out in a three-electrode batch reactor. TiO2 films were either deposited by dip-coating of a TiO2 sol onto a Ti foil and subsequent calcination or generated on Ti plates by thermal oxidation in air at 400-700 degrees C. The effects of the anode preparation method and bias potential values on conversion and selectivity to the corresponding aldehyde were investigated. The photoelectrocatalytic results were compared with the photocatalytic and electrocatalytic ones. The results indicated that no reaction occurred during the electrocatalytic experiments, whereas the…

chemistry.chemical_classificationPhotoelectrocatalysis Titanium TiO2/Ti 4-Methoxybenzaldehyde Aromatic alcohols Green synthesisProcess Chemistry and TechnologyInorganic chemistryAlcoholAldehydeCatalysislaw.inventionchemistry.chemical_compoundchemistrylawBenzyl alcoholSaturated calomel electrodePhotocatalysisCalcinationReactivity (chemistry)Partial oxidationGeneral Environmental Science
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Chemical speciation of polycyclic aromatic hydrocarbons in sediments: partitioning and extraction of humic substances.

2010

The primary objective of this study was to examine the chemical speciation of polycyclic aromatic hydrocarbons (PAHs) found in sediments endowed with different characteristics. To achieve this purpose and because the nature of the sediments influences the distribution of PAHs, we have analyzed four different types of sediments. To study the role of organic matter in the sequestration of PAHs, we fractionated humic substances into humic acids and humin–mineral fractions. After their separation and purification, the humic components were examined for their sorptive reactivity by extracting them with organic solvents; these extracts were subsequently subjected to GC/MS analysis. Our results sh…

chemistry.chemical_classificationPollutionPersistent organic pollutantGeologic Sedimentsmedia_common.quotation_subjectExtraction (chemistry)Solid Phase ExtractionSedimentFraction (chemistry)PAHsChemical speciationHumicSandy and muddy sedimentsAquatic ScienceChemical FractionationOceanographyPollutionSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliGas Chromatography-Mass SpectrometrySpeciationHydrocarbonchemistryEnvironmental chemistryOrganic matterPolycyclic Aromatic HydrocarbonsHumic Substancesmedia_commonEnvironmental MonitoringMarine pollution bulletin
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Polycyclic Aromatic Hydrocarbons in Sediments of Marine Coastal Lagoons in Messina, Italy: Extraction and GC/MS Analysis, Distribution and Sources

2004

The content of 21 polycyclic aromatic hydrocarbons (PAHs) has been determined in 16 samples of sediments collected from Ganzirri and Faro marine coastal lagoons in Messina (Italy). Analysis was performed by gas chromatography/mass spectrometry (GC/MS) in selected ion monitoring (SIM) mode. The total concentration of polycyclic aromatic hydrocarbons (PAHs) ranged from 74 to 5755 ...g/Kg of dry matrix. The resulting distributions and molecular ratios of specific compounds have been discussed in terms of sampling location and origin of organic matter. The results obtained show that levels of contamination are not homogeneous throughout the stations, while the relative distributions of PAH are…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryExtraction (chemistry)ContaminationMass spectrometrypolycyclic aromatic hydrocarbons sediments organic matter content coastal marine lagoonsSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliMatrix (chemical analysis)Environmental chemistryMaterials ChemistrySettore CHIM/01 - Chimica AnaliticaSelected ion monitoringOrganic matterGas chromatographyGas chromatography–mass spectrometryPolycyclic Aromatic Compounds
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Influence of preparation conditions of nano-crystalline ceria catalysts on the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon

2007

Abstract Nano-crystalline ceria catalysts prepared by homogeneous precipitation with urea were tested for the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon (PAH). Systematic variation of preparation conditions, including calcination temperature, calcination time and aging time, resulted in differences in surface area, reducibility, morphology and crystallite size of the CeO 2 catalyst and hence differences in catalytic performance. A combination of high surface area, small crystallite size and high oxygen defect concentration was found to favor the efficiency of the ceria catalysts for the total oxidation of naphthalene. Optimum preparation conditions for this stud…

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryPolycyclic aromatic hydrocarbonHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundHydrocarbonCatalytic oxidationchemistrylawCalcinationCrystalliteGeneral Environmental ScienceNaphthaleneApplied Catalysis B: Environmental
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UV-B-Induced acute toxicity of pyrene to the waterflea Daphnia magna in natural freshwaters.

1999

Abstract The effects of various water characteristics in natural freshwaters on the acute toxicity of one polycyclic aromatic hydrocarbon (PAH), pyrene, to a pelagic invertebrate Daphnia magna was studied under ultraviolet B (UV-B) radiation and in the dark. Pyrene was photoactivated and was more toxic to D. magna in the presence of UV-B radiation. Dissolved organic material (DOM), measured as dissolved organic carbon (DOC), significantly reduced the photoenhanced toxicity of pyrene. Under UV-B radiation the EC50 values were lower and in relation to the amount of DOM, ranging from 3.0 to 30.0 μg/L pyrene, whereas in the dark they were between 29.2 and 54.8 μg/L and not related to the amount…

chemistry.chemical_classificationPyrenesbiologyDose-Response Relationship DrugUltraviolet RaysHealth Toxicology and MutagenesisDaphnia magnaPublic Health Environmental and Occupational HealthPolycyclic aromatic hydrocarbonFresh WaterGeneral Medicinebiology.organism_classificationPollutionAcute toxicitychemistry.chemical_compoundchemistryCladoceraDaphniaEnvironmental chemistryDissolved organic carbonToxicityPyreneAnimalsOrganic matterOrganic ChemicalsEcotoxicology and environmental safety
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Biopartitioning micellar chromatography: An alternative high-throughput method for assessing the ecotoxicity of anilines and phenols

2007

An investigation of the use of the chromatographic retention (log k) as an in vitro approach for modelling the toxicity to Fathead Minnows of anilines and phenols is developed. A data set of 65 compounds with available experimental toxicity data was used. Log k data at three pH values were used for the compounds classification and two groups or 'MODEs' were identified. For one 'MODE' a quantitative retention-activity relationship (QRAR) model was calculated. Finally, it was used to estimate the toxicity to Fathead minnows of anilines and phenols for which experimental data are not available. These estimations were compared to those obtained from another toxicity (to Tetrahymena pyriformis) …

chemistry.chemical_classificationQuantitative structure–activity relationshipAniline CompoundsChromatographyToxicity dataTetrahymena pyriformisClinical BiochemistryCyprinidaeQuantitative Structure-Activity RelationshipAromatic amineExperimental dataCell BiologyGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundPhenolschemistryTetrahymena pyriformisToxicityAnimalsSpectrophotometry UltravioletPhenolsEcotoxicityChromatography Micellar Electrokinetic CapillaryJournal of Chromatography B
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Nanostructured rutile TiO2 for selective photocatalytic oxidation of aromatic alcohols to aldehydes in water

2008

WOS: 000253100100022

chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaChemistryGeneral ChemistryBiochemistryAldehydeCatalysisCrystallinityColloid and Surface ChemistryTiO2 Rutile Selectice photocatalytic oxidation Aromatic Alcohol Aromatic AldehydesRutilePhotocatalysisOrganic chemistrySelectivity
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Watching the photo-oxidation of a single aromatic hydrocarbon molecule

2001

International audience; The photooxidation of single dye molecules (see scheme) can be followed by confocal fluorescence microscopy. The self-sensitized reaction with singlet oxygen leads to a suite of products, which may be differentiated spectrally. Tentative structures for certain photoproducts have been obtained from quantum-chemical calculations.

chemistry.chemical_classificationSingle-molecule spectroscopyphotochemistryChemistrySinglet oxygenConfocalGeneral ChemistryPhotochemistryCatalysisFluorescence spectroscopySingle Molecule Spectroscopychemistry.chemical_compoundbiological sciencesFluorescence microscopeMolecule[CHIM]Chemical SciencesPhysics::Chemical PhysicsAromatic hydrocarbonFluorescence spectroscopy
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