Search results for "Acetone"

showing 10 items of 350 documents

Volatile constituents of the aerial parts of white salsify (Tragopogon porrifolius L., Asteraceae).

2010

Tragopogon porrifolius L. grows as a vegetable in southern Italy and all parts of it are edible. In the present study the volatile components of the aerial part are described. Gas chromatography and gas chromatography-mass spectrometry analysis showed the presence of 38 components in all. On the whole, the volatile fraction was constituted mainly by carbonylic compounds (24.6%), phenols (21.5%) and fatty acids and esters (19.7%). The most abundant compounds were 4-vinyl guaiacol (19.0%), hexadecanoic acid (17.9%), hexahydrofarnesylacetone (15.8%) and hentriacontane (10.7%).

Chromatography GasPalmitic AcidPlant ScienceAsteraceaeBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryTragopogonPalmitic acidchemistry.chemical_compoundBotanyPhenolsHentriacontaneTragopogon porrifolius Asteraceae white salsify Volatile constituents 4-vinyl guaiacol hexadecanoic acid hexahydrofarnesylacetonebiologyTerpenesOrganic ChemistryGuaiacolSettore CHIM/06 - Chimica OrganicaAsteraceaePlant Components Aerialbiology.organism_classificationchemistryGuaiacolGas chromatographyGas chromatography–mass spectrometryVolatilizationNatural product research
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Processing of Generator-Produced 68Ga for Medical Application

2007

The (68)Ge/(68)Ga generator provides an excellent source of positron-emitting (68)Ga. However, newly available "ionic" (68)Ge/(68)Ga radionuclide generators are not necessarily optimized for the synthesis of (68)Ga-labeled radiopharmaceuticals. The eluates have rather large volumes, a high concentration of H(+) (pH of 1), a breakthrough of (68)Ge, increasing with time or frequency of use, and impurities such as stable Zn(II) generated by the decay of (68)Ga, Ti(IV) as a constituent of the column material, and Fe(III) as a general impurity.We have developed an efficient route for the processing of generator-derived (68)Ga eluates, including the labeling and purification of biomolecules. Prec…

ChromatographyAqueous solutionElutionIon chromatographyGallium RadioisotopesFraction (chemistry)Hydrochloric acidEquipment DesignReference StandardsEquipment Failure Analysischemistry.chemical_compoundColumn chromatographychemistryGermanyIsotope LabelingAcetoneRadiology Nuclear Medicine and imagingRadionuclide GeneratorJournal of Nuclear Medicine
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Large scale fractionation of pullulan and dextran

2006

Abstract A recently developed large scale fractionation technique named continuous spin fractionation (CSF) was applied to fractionate pullulan and dextran. 450 g of pullulan with a broad molecular weight distribution were fractionated using water as solvent and acetone as precipitant. In this study, we have in five CSF runs prepared three fractions with apparent M ¯ w * values ranging from 17.6 to 413 kg mol−1. Seventy grams of dextran were fractionated with a mixed solvent of water plus methanol. Five fractionation steps resulted in four samples with M ¯ w values between 4.36 and 18.2 kg mol−1.

ChromatographyPolymers and PlasticsOrganic ChemistryPullulanFractionationSolventchemistry.chemical_compoundDextranchemistryPhysical separationMaterials ChemistryAcetoneMolar mass distributionMethanolCarbohydrate Polymers
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Thin-layer chromatography of chlorinated anisoles and veratroles

1989

The thin-layer chromatography of chlorinated anisoles (methoxybenzenes) and veratroles (1,2-dimethoxybenzenes) has been examined on silica gel G60 and RP-18 thin-layer plates. More than fifty solvent systems were screened and some of them recommended for particular separations. Acetone was shown to be suitable for group separation of both chlorinated anisoles and veratroles on a silica gel G60 stationary phase having a very narrow range of RF values. On the other hand, benzene, dichloromethane and the various mixtures of light petroleum (b.p. 40–60°C) and a more polar eluent (such as diethyl ether, acetone or ethyl acetate) were recommended for separation of certain individual isomers. The …

ChromatographySilica gelOrganic ChemistryClinical BiochemistryEthyl acetateReversed-phase chromatographyBiochemistryThin-layer chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographychemistryAcetoneDiethyl etherDichloromethaneChromatographia
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Synthesis and characterization of vanadyl(IV) complexes of Schiff bases derived from anthranilic acid and salicylaldehyde (or its derivatives) or ace…

1997

Anhydrous, dimeric vanadyl(IV) complexes of Schiff bases derived from [1+1] condensation of salicylaldehyde (or its derivatives) and anthranilic acid, have been synthesized from CH3CN and were characterized by elemental analysis, FTIR, EPR, absorption, TGA, cyclic voltammetry and room temperature magnetic susceptibility measurements. These complexes were found to be oxidized by air in polar solvents like MeOH and DMF to V-V products. The E(1/2) values were found to be around 660 mV indicating that the carboxylate group favours vanadyl(IV) binding when compared to the alkoxo-bound vanadium complexes. Oxidative instability of these complexes are dependent on the substituent on the salicylalde…

Coordination sphereAcetylacetoneDimeric Vanadyl(Iv)Inorganic chemistryDecavanadateVanadiumchemistry.chemical_elementRedoxSingle Crystal X-RayInorganic Chemistrychemistry.chemical_compoundOxidationPyridinePolymer chemistryMaterials ChemistryAnthranilic acidPhysical and Theoretical ChemistrySchiff BasesSchiff baseReactivityVanadiumBindingMononuclear Octahedral Vo3+chemistrySalicylaldehydeDecavanadatesPyridiniumOxidative InstabilityOxovanadium(Iv)Polyhedron
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The chemistry of acetone at extreme conditions by density functional molecular dynamics simulations

2011

Density functional molecular dynamics simulations have been performed in the NVT ensemble (moles (N), volume (V) and temperature (T)) on a system formed by ten acetone molecules at a temperature of 2000 K and density ρ = 1.322 g cm(-3). These conditions resemble closely those realized at the interface of an acetone vapor bubble in the early stages of supercompression experiments and result in an average pressure of 5 GPa. Two relevant reactive events occur during the simulation: the condensation of two acetone molecules to give hexane-2,5-dione and dihydrogen and the isomerization to the enolic propen-2-ol form. The mechanisms of these events are discussed in detail.

DFT molecular dynamicsCondensationTemperatureacetoneGeneral Physics and AstronomyThermodynamicsMolecular Dynamics SimulationMolecular dynamicschemistry.chemical_compoundchemistryVolume (thermodynamics)extreme conditionPressureAcetoneQuantum TheoryPhysical chemistryVapor bubbleMoleculeDensity functional theoryPhysical and Theoretical ChemistryIsomerizationThe Journal of Chemical Physics
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New insights into the reactivity of the tantalocene hydride Cp′2TaH3 (Cp′=η5-tBuC5H4). Synthesis and characterisation of cationic Ta(V) complexes wit…

2002

Abstract Reaction of various neutral LXH bidentate ligands (2-aminobenzoic acid, acetylacetone, dibenzoylmethan and 2-aminobenzenethiol) with [Cp′2TaH2]+, obtained in situ from Cp′2TaH3 treated with triphenylmethan cation, affords after dihydrogen elimination the corresponding cationic species [Cp′2Ta(H)(LX)]+ in BF4 or PF6 salts. Complexes [Cp′2TaH(η2-O2CC6H4-o-NH2O,O′)]PF6 (3), {Cp′2Ta[η2-OC(Me)CHC(Me)OO,O′]}BF4 (4a), {Cp′2TaH[η2-OC(Ph)CHC(Ph)OO,O′]}BF4 (4b) and [Cp′2TaH(η2-SC6H4-o-NH2S,N)]PF6 (5) are characterised by analytical and spectroscopic methods. With thiopyridine, the kinetic (6) and the thermodynamic (6′) isomers [Cp′2TaH(η2-2-SC5H4NS,N)]PF6 are identified. Crystal struc…

DenticityChelating ligandsStereochemistryHydrideAcetylacetoneOrganic ChemistryCationic polymerizationCrystal structureBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryJournal of Organometallic Chemistry
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Mono- and Binuclear Copper(II) and Nickel(II) Complexes with the 3,6-Bis(picolylamino)-1,2,4,5-Tetrazine Ligand

2021

Four new compounds of formulas [Cu(hfac)2(L)] (1), [Ni(hfac)2(L)] (2), [{Cu(hfac)2}2(µ-L)]·2CH3OH (3) and [{Ni(hfac)2}2(µ-L)]·2CH3CN (4) [Hhfac = hexafluoroacetylacetone and L = 3,6-bis(picolylamino)-1,2,4,5-tetrazine] have been prepared and their structures determined by X-ray diffraction on single crystals. Compounds 1 and 2 are isostructural mononuclear complexes where the metal ions [copper(II) (1) and nickel(II) (2)] are six-coordinated in distorted octahedral MN2O4 surroundings which are built by two bidentate hfac ligands plus another bidentate L molecule. This last ligand coordinates to the metal ions through the nitrogen atoms of the picolylamine fragment. Compounds 3 and 4 are cen…

DenticityMaterials science42Pharmaceutical Sciencechemistry.chemical_element5-tetrazinecrystal structure determination010402 general chemistry01 natural sciencesO.ArticleAnalytical ChemistryM.lcsh:QD241-441Julvechemistry.chemical_compoundTetrazinenickelStetsiukN 1lcsh:Organic chemistryA.Drug DiscoveryLloret[CHIM]Chemical SciencesPhysical and Theoretical ChemistryIsostructural1245-tetrazine010405 organic chemistryLigandHexafluoroacetylacetoneOrganic ChemistryMagnetic susceptibility0104 chemical sciencesNickelCrystallographyAvarvarichemistryChemistry (miscellaneous)F.Intramolecular forcecopperMolecular Medicinemagnetic propertiesnitrogen ligandsEl-Ghayoury
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Designing dicyanamide bridged 1D molecular architecture from a mononuclear copper(II) Schiff base precursor: Syntheses, structural variations and mag…

2009

International audience; A new tridentate N2O donor Schiff base ligand [(C6H5C(OH)CHC(CH3)NCH2C5H4N)LH] was obtained by 1:1 condensation of benzoylacetone with 2-picolylamine and has been used to synthesise a mononuclear [CuLCl] (1) and an end-to-end dicyanamide bridged polynuclear {[Cu2(μ-L)2(μ2-1,5-(CN)2N)]ClO4}n (2) copper(II) complexes. The ligand, 1 and 2 were clearly characterised by elemental analysis, FT-IR, 1H NMR, UV–Vis spectral studies, electrochemical studies and in addition single crystal X-ray diffraction studies were performed for 1 and 2. The Schiff base ligand [LH] shows a significant variation in its coordination behaviour with copper(II) ion in absence and in presence of …

DenticityStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesInorganic ChemistrySchiff basechemistry.chemical_compoundDeprotonationDicyanamide bridged polymerMagnetic properties[CHIM.CRIS]Chemical Sciences/CristallographyMaterials Chemistry[CHIM]Chemical SciencesPhysical and Theoretical ChemistryDicyanamideSchiff base010405 organic chemistryLigandMagnetic susceptibilityCopper0104 chemical sciencesCrystallography[CHIM.POLY]Chemical Sciences/PolymerschemistryMononuclear precursorProton NMRCopper(II) complexes2-Picolylamine and benzoylacetonePolyhedron
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On-line analysis of carbonyl compounds with derivatization in aqueous extracts of atmospheric particulate PM10 by in-tube solid-phase microextraction…

2011

Abstract A new device for carbonyl compounds based on coupling on-line and miniaturizing both, sample pretreatment and chromatographic separation, is reported. Two capillary columns, a GC capillary column (95% methyl–5% phenyl substituted backbone, 70 cm × 0.32 mm i.d., 3 μm film thickness) in the injection valve for in-tube solid-phase microextraction (IT-SPME) and a Zorbax SB C18 (150 mm × 0.5 mm i.d., 5 μm particle diameter) LC capillary column were employed. Different combinations of IT-SPME and derivatization using 2,4-dinitrophenylhydrazine (DNPH) were examined for mixtures containing 15 carbonyl compounds (aliphatic, aromatic and unsaturated aldehydes and ketones). A screening analys…

Detection limitAldehydesAqueous solutionChromatographyCapillary actionOrganic ChemistryReproducibility of ResultsGeneral MedicineParticulatesReference StandardsSolid-phase microextractionBiochemistrySensitivity and SpecificityAnalytical ChemistryAcetonechemistry.chemical_compoundchemistryCapillary columnTube (fluid conveyance)Particulate MatterParticle SizeDerivatizationSolid Phase MicroextractionChromatography LiquidJournal of chromatography. A
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