Search results for "Alkene"

showing 10 items of 98 documents

Development of an ICP-IDMS method for accurate routine analyses of toxic heavy metals in polyolefins and comparison with results by TI-IDMS

2000

An inductively coupled plasma isotope dilution mass spectrometric (ICP-IDMS) method was developed as a suitable method - with respect to its sensitivity, precision, accuracy, and time-consumption - for the analysis of toxic heavy metal traces (Pb, Cd, Cr, and Hg) in polyolefins. Results for Pb, Cd, and Cr were compared with those obtained by thermal ionization isotope dilution mass spectrometry (TI-IDMS), which was used as a reference method. Because of its high first ionization potential and its high volatility mercury could not be determined by TI-IDMS. A multi-element spike solution, containing isotopically enriched 206Pb, 116Cd, 53Cr, and 201Hg, was used for the isotope dilution step. D…

Detection limitIsotopeChemistryAnalytical chemistryThermal ionizationchemistry.chemical_elementAlkenesIsotope dilutionMass spectrometrySensitivity and SpecificityBiochemistryHazardous SubstancesMass SpectrometryMercury (element)IsotopesPolyethyleneMetals HeavyInductively coupled plasmaChemical decompositionFresenius' Journal of Analytical Chemistry
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Reactions of Alkenes and Alkynes with an Acyclic Silylene and Heavier Tetrylenes under Ambient Conditions

2014

Cycloaddition reactions of the acyclic silylene Si(SAriPr4)2 (AriPr4 = C6H3-2,6(C6H3-2,6-iPr2)2) with a variety of alkenes and alkynes were investigated. Its reactions with the alkynes phenylacetylene and diphenylacetylene and the diene 2,3-dimethyl-1,3-butadiene yielded silacycles (AriPr4S)2tiebar above startSi(CH═tiebar above endCPh) (1), (AriPr4S)2tiebar above startSi(PhC═tiebar above endCPh) (2), and (AriPr4S)2tiebar above startSiCH2CMeCMetiebar above endCH2 (3) at ambient temperature. The compounds were characterized by X-ray crystallography, 1H, 13C, and 29Si NMR spectroscopy, and IR spectroscopy. No reaction was observed with more substituted alkenes such as propene, (Z)-2-butene, te…

DieneTrimethylsilylacyclic silyleneAlkynealkeenit ja alkyynitPhotochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundraskaammat tetryleenitalkenes and alkynesCyclopenteneambient conditionssykloadditioreaktiotPhysical and Theoretical Chemistryasyklinen silyleeniDiphenylacetyleneta116chemistry.chemical_classificationOrganic ChemistrySilylenecyloaddition reactionsCycloadditionPhenylacetylenechemistrynormaalit ympäristön olosuhteethevier tetrylenes
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Keggin heteropolyacid H3PW12O40 supported on different oxides for catalytic and catalytic photo-assisted propene hydration

2013

Catalytic and catalytic photo-assisted hydration of propene to form 2-propanol in gas–solid regime at atmospheric pressure and 85 1C were carried out by using a heteropolyacid (POM) supported on different oxides. Binary materials were prepared by impregnation of H3PW12O40 on different commercial and home prepared supports (TiO2, SiO2, WO3, ZrO2, ZnO, Al2O3). Some of the composites were active both for catalytic and catalytic photo-assisted reactions. The Keggin type POM was completely and partially degraded, when supported on ZnO and Al2O3, respectively, and these binary solids always resulted as inactive for both catalytic and catalytic photo-assisted reactions. The supported Keggin POM sp…

DiffractionDiffuse reflectance infrared fourier transformAtmospheric pressureSurface PropertiesScanning electron microscopeWaterGeneral Physics and AstronomyOxidesAlkenesPhotochemical ProcessesPhotochemistryCatalysisTungstenCatalysisPropenechemistry.chemical_compoundchemistryPressureSettore CHIM/07 - Fondamenti Chimici Delle Tecnologiesense organsIrradiationKeggin heteropolyacid catalytic propene hydration photo-assisted propene hydrationParticle SizePhysical and Theoretical ChemistryFourier transform infrared spectroscopyPhysical Chemistry Chemical Physics
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Photoluminescence in Carborane–Stilbene Triads : A Structural, Spectroscopic, and Computational Study

2016

A set of triads in which o- and m-carborane clusters are bonded to two stilbene units through Ccluster -CH2 bonds was synthesized, and their structures were confirmed by X-ray diffraction. A study on the influence of the o- and m- isomers on the absorption and photoluminescence properties of the stilbene units in solution revealed no charge-transfer contributions in the lowest excited state, as confirmed by (TD)DFT calculations. The presence of one or two B-I groups in m-carborane derivatives does not affect the emission properties of the stilbenes in solution, probably due to the rather large distance between the iodo substituents and the fluorophore. Nevertheless, a significant redshift o…

DiffractionFluorophorePhotoluminescencecarboranesalkenes010405 organic chemistryOrganic ChemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryExcited statedensity functional calculationsluminescenceCarboraneAbsorption (chemistry)Thin filmLuminescenceta116photophysicsChemistry: A European Journal
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Catalytic Asymmetric Formal [3+2] Cycloaddition of 2-Isocyanatomalonate Esters and Unsaturated Imines: Synthesis of Highly Substituted Chiral γ-Lacta…

2017

[EN] Unlike their isocyano and isothiocyanato analogues, isocyanato esters remain almost unexplored as formal 1,3-dipoles in asymmetric catalytic reactions. The first asymmetric formal [3+2] cycloaddition involving isocyanato esters and electrophilic alkenes is reported. Diisopropyl 2-isocyanatomalonate reacts with a,b-unsaturated N-(o-anisidyl) imines in the presence of a Mg(OTf)2¿BOX complex to give highly substituted chiral pyrrolidinones featuring a conjugate exocyclic double bond with excellent yields and enantiomeric excesses up to 99%. Several transformations of the resulting heterocycles, including the synthesis of a pyroglutamic acid derivative, have been carried out.

Double bondLactamsStereochemistryMolecular ConformationStereoisomerismEnantioselectivityAlkenes010402 general chemistryCrystallography X-Ray01 natural sciencesCatalysisCatàlisiCoordination ComplexesAsymmetric catalysisMagnesiumPyrrolidinoneschemistry.chemical_classificationNucleophilic additionCycloaddition Reaction010405 organic chemistryNitrogen heterocyclesOrganic ChemistryEnantioselective synthesisEstersStereoisomerismGeneral ChemistryCycloadditionMalonates0104 chemical scienceschemistryFISICA APLICADAElectrophileIminesEnantiomerNucleophilic additionQuímica orgànicaIsocyanatesChemistry (Weinheim an der Bergstrasse, Germany)
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The Existence of Nitrate Radicals in Irradiated TiO 2 Aqueous Suspensions in the Presence of Nitrate Ions

2018

Evidence of the existence of nitrate radical in irradiated aqueous TiO2 suspensions in the presence of nitrate ions are reported for the first time. The joint use of UV/Vis and EPR spectroscopy showed that nitrate radicals are formed by hole induced oxidation of nitrate ions. Photocatalytic degradation of a model alkene compound allowed to highlight the presence of an intermediate organic nitrate deriving from nitrate radical attack to the double bond of the substrate. These results not only allow deeper understanding of photocatalytic processes, but open the route to new green photocatalytic syntheses initiated by nitrate radicals and to new insights in the field of atmospheric chemistry.

Double bondRadical010402 general chemistryPhotochemistry01 natural sciencesCatalysisCatalysiCatalysislaw.inventionphotocatalysichemistry.chemical_compoundNitratenitratelawTiO2Electron paramagnetic resonancechemistry.chemical_classificationradicalAqueous solution010405 organic chemistryAlkeneChemistry (all)General MedicineGeneral Chemistrynitrate; photocatalysis; radicals; TiO2; Catalysis; Chemistry (all)radicals0104 chemical scienceschemistryPhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle TecnologiephotocatalysisAngewandte Chemie International Edition
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Experimental and theoretical insights in the alkene-arene intramolecular π-stacking interaction

2016

Chiral acrylic esters derived from biomass were developed as models to have a better insight in the aryl-vinyl π-stacking interactions. Quantum chemical calculations, NMR studies and experimental evidences demonstrated the presence of equilibriums of at least four different conformations: π-stacked and face-to-edge, each of them in an s-cis/s-trans conformation. The results show that the stabilization produced by the π-π interaction makes the π-stacked conformation predominant in solution and this stabilization is slightly affected by the electron density of the aromatic counterpart. Fil: Corne, Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológi…

Electron densityStereochemistryasymmetric synthesisStackingBiomass010402 general chemistry01 natural sciencesFull Research PaperBIOMASS//purl.org/becyt/ford/1 [https]lcsh:QD241-441lcsh:Organic chemistryASYMMETRIC SYNTHESISComputational chemistryCONFORMATIONAL EQUILIBRIUMΠ-STACKING INTERACTION//purl.org/becyt/ford/1.4 [https]conformational equilibriumACRYLIC ESTERSlcsh:Sciencechemistry.chemical_classificationQuantum chemicalbiomass010405 organic chemistryAlkeneacrylic estersOtras Ciencias QuímicasOrganic ChemistryEnantioselective synthesisCiencias Químicasπ-stacking interaction0104 chemical sciencesChemistrychemistryIntramolecular forcelcsh:QCIENCIAS NATURALES Y EXACTAS
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Counterintuitive Mechanisms of the Addition of Hydrogen and Simple Olefins to Heavy Group 13 Alkene Analogues

2013

The mechanism of the reaction of olefins and hydrogen with dimetallenes ArMMAr (Ar = aromatic group; M = Al or Ga) was studied by density functional theory calculations and experimental methods. The digallenes, for which the most experimental data are available, are extensively dissociated to gallanediyl monomers, :GaAr, in hydrocarbon solution, but the calculations and experimental data showed also that they react with simple olefins, such as ethylene, as intact ArGaGaAr dimers via stepwise [2 + 2 + 2] cycloadditions due to their considerably lower activation barriers vis-à-vis the gallanediyl monomers, :GaAr. This pathway was preferred over the [2 + 2] cycloaddition of olefin to monomeric…

EthyleneStereochemistryGalliumAlkenesBiochemistryMedicinal chemistryCatalysisPropenechemistry.chemical_compoundColloid and Surface ChemistryOrganometallic CompoundsSinglet stateta116chemistry.chemical_classificationOlefin fiberDiradicalChemistryAlkeneGeneral ChemistryCycloadditionCyclizationYield (chemistry)Quantum TheoryCyclobutanesAluminumHydrogenJournal of the American Chemical Society
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Amide functionalized aminobisphenolato MoO2 and WO2 complexes: Synthesis, characterization, and alkene epoxidation catalysis

2023

The use of dioxidomolybdenum(vi) and -tungsten(vi) complexes supported by a variety of structurally different tri- and tetradentate aminobisphenolato ligands as pre-catalysts in the epoxidation of alkenes is well established. However, under the widely used standard 1 mol-% catalyst loadings these types of complexes generally show modest activity only. Recently, amide functionalities in the ligand design of various aminomonophenolato MoO2 complexes have been shown to lead to heightened catalytic activity in alkene epoxidation. In this paper we show that similar ligand amide functionalization can lead to significant enhancement in the alkene epoxidation activity of aminobisphenolato MoO2 comp…

Historyhapetusdioxidotungsten(VI)Polymers and PlasticsProcess Chemistry and TechnologyvolframikompleksiyhdisteetIndustrial and Manufacturing Engineeringdioxidomolybdenum(VI)Catalysiskatalyytitalkene epoxidationBusiness and International ManagementalkeenitPhysical and Theoretical Chemistrymolybdeeniaminobisphenolato ligandsMolecular Catalysis
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Identification of highly effective antitrypanosomal compounds in essential oils from the Apiaceae family

2018

The Apiaceae family encompasses aromatic plants of economic importance employed in foodstuffs, beverages, perfumery, pharmaceuticals and cosmetics. Apiaceae are rich sources of essential oils because of the wealth of secretory structures (ducts and vittae) they are endowed with. The Apiaceae essential oils are available on an industrial level because of the wide cultivation and disposability of the bulky material from which they are extracted as well as their relatively cheap price. In the fight against protozoal infections, essential oils may represent new therapeutic options. In the present work, we focused on a panel of nine Apiaceae species (Siler montamon, Sison amomum, Echinophora spi…

Human African trypanosomiasiAlkeneApiaceae; BALB/3T3; Essential oils; Human African trypanosomiasis; Trypanosoma brucei; 3T3 Cells; Alkenes; Animals; Apiaceae; Benzyl Compounds; Cyclohexenes; Dioxolanes; Inhibitory Concentration 50; Mice; Monoterpenes; Oils Volatile; Plant Oils; Pyrogallol; Terpenes; Trypanosoma brucei brucei; Trypanosomiasis; Pollution; Public Health Environmental and Occupational Health; Health Toxicology and MutagenesisHealth Toxicology and Mutagenesis[SDV]Life Sciences [q-bio]VolatileMonoterpeneAllylbenzene DerivativesPlant Oil01 natural sciencesCosmeticsEssential oilTerpenechemistry.chemical_compoundMiceTrypanosoma bruceiBALB/3T3media_commonBicyclic Monoterpenes2. Zero hungerbiologyTraditional medicineChemistryBenzyl CompoundsDioxolanesGeneral Medicine3T3 CellsPollutionHealthEssential oilsTerpeneIdentification (biology)Public HealthDioxolaneCyclohexenesmedia_common.quotation_subjectAcyclic MonoterpenesApiaceae; BALB/3T3; Essential oils; Human African trypanosomiasis; Trypanosoma brucei; 3T3 Cells; Alkenes; Animals; Apiaceae; Benzyl Compounds; Cyclohexenes; Dioxolanes; Inhibitory Concentration 50; Limonene; Mice; Monoterpenes; Oils Volatile; Plant Oils; Pyrogallol; Terpenes; Trypanosoma brucei brucei; TrypanosomiasisTrypanosoma brucei bruceiCyclohexane MonoterpenesTrypanosoma bruceiAlkenesPyrogallolInhibitory Concentration 50TrypanosomiasisBenzyl CompoundsCyclohexenesOils VolatileCyclohexeneAnimalsPlant OilsToxicology and Mutagenesis3T3 CellApiaceaeAnimal010405 organic chemistryTerpenesEnvironmental and Occupational HealthHuman African trypanosomiasisPublic Health Environmental and Occupational Healthbiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistryPyrogallolMonoterpenesCymenesBenzyl CompoundOilsLimoneneApiaceae
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