Search results for "hydride"

showing 10 items of 322 documents

Investigation into the reaction of (t-BuC5H4)2Nb(η2-Te2)H with CH3Li: Hydride abstraction versus telluride methylation

2007

Abstract The reaction of [ Cp 2 ′ Nb ( Te 2 ) H ] ( 1 ) (Cp′ =  t -BuC 5 H 4 ) with CH 3 Li in THF was examined by variable temperature 1 H NMR, ESR and mass spectroscopic means. From these methods it is evident that the diamagnetic compounds [ Cp 2 ′ NbH 2 ( TeCH 3 ) ] ( 2 ) and [ Cp 2 ′ Nb ( Te ) CH 3 ] ( 3 ) as well as the paramagnetic compound [ Cp 2 ′ Nb ( TeCH 3 ) 2 ] ( 4 ) form simultaneously. In the subsequent reaction of the intermediate solution with [Co 2 (CO) 8 ] compound 4 was consumed and the compound [ Cp 2 ′ Nb ( μ - TeCH 3 ) 2 Co(CO) 2 ] ( 5 ) formed in good yield. Complex 5 was characterized by IR and variable temperature 1 H NMR spectroscopies. Electrochemical two-electro…

Analytical chemistrychemistry.chemical_element010402 general chemistryElectrochemistry01 natural sciencesInorganic ChemistryParamagnetismchemistry.chemical_compoundcarbonyl ligandsTelluridetelluriumMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS010405 organic chemistryHydride[ CHIM.COOR ] Chemical Sciences/Coordination chemistrycobalt0104 chemical sciencesCrystallographychemistryelectrochemistryYield (chemistry)Proton NMRTelluriumniobiumCobalt
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Determination of fatty alcohol ethoxylates and alkylether sulfates by anionic exchange separation, derivatization with a cyclic anhydride and liquid …

2011

A method for the separation, characterization and determination of fatty alcohol ethoxylates (FAE) and alkylether sulfates (AES) in industrial and environmental samples is described. Separation of the two surfactant classes was achieved in a 50:50 methanol-water medium by retaining AES on a strong anionic exchanger (SAX) whereas most FAE were eluted. After washing the SAX cartridges to remove cations, the residual hydrophobic FAE were eluted by increasing methanol to 80%. Finally, AES were eluted using 80:20 and 95:5 methanol-concentrated aqueous HCl mixtures. Methanol and water were removed from the FAE and AES fractions, and the residues were dissolved in 1,4-dioxane. In this medium, este…

AnionsEthylene OxideFatty alcoholBiochemistryAnalytical ChemistryDioxanesSurface-Active Agentschemistry.chemical_compoundAcetic acidSeawaterDerivatizationChromatography High Pressure LiquidPhthalic anhydrideAqueous solutionChromatographyEsterificationSulfatesElutionOrganic ChemistryExtraction (chemistry)General MedicineChromatography Ion ExchangechemistryMethanolFatty AlcoholsDibenzoxepinsJournal of Chromatography A
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Experimental and Theoretical Studies of Nonclassical d 0 Cyclopentadienyl Polyhydride Complexes of Molybdenum and Tungsten

1998

Low-temperature protonation of compounds Cp{sup *}MH{sub 5}(PMe{sub 3}) (M = Mo, 1; W, 2) by HBF{sub 4}{center_dot}Et{sub 2}O in CD{sub 2}Cl{sub 2} or CDFCl{sub 2} affords the thermally unstable hexahydride derivatives [Cp{sup *}MH{sub 6}(PMe{sub 3})]{sup +} (M = Mo, 3; W, 4). The corresponding protonation of 1- and 2-d{sup 5} affords 3- and 4-d{sup 5}, respectively. The {Delta}{delta} on going from H{sub 6} to HD{sub 5} is small for both compounds, but positive for 3 and negative for 4, and no isotopic perturbation of resonance (IPR) is observed. The T{sub 1min} at 400 MHz for [Cp{sup *}MH{sub 6}(PMe{sub 3})]{sup +} apparently doubles on going from Mo to W (52 ms for 3 and approximately 10…

AnionsReaction mechanismschemistry.chemical_elementProtonation010402 general chemistryLigands01 natural sciencesInorganic ChemistryCyclopentadienyl complexChemical structureMathematical methodsComputational chemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryHydrideOrganic Chemistry3. Good health0104 chemical sciencesCrystallographychemistryChemical bondMolybdenumPotential energy surfaceDihydrogen complex
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Determination of non-ionic and anionic surfactants in industrial products by separation on a weak ion-exchanger, derivatization and liquid chromatogr…

2013

Abstract A method for the determination of priority surfactants, including fatty alcohol ethoxylates (FAE), alkylether sulfates (AES) and linear alkylbenzene sulfonates (LAS) is described. The samples were diluted with 50% methanol at pH 4 prior to solid-phase extraction on a weak anionic exchanger (WAX). The AES and LAS surfactant classes were retained, whereas the non-ionic components, including most FAE oligomers were eluted. After washing the WAX cartridge to remove cations, the remaining hydrophobic FAE oligomers were eluted using hot 80% methanol at pH 4 (at ca. 50 °C). These two eluates were combined to constitute the non-ionic fraction. Then, AES and LAS were eluted using 80% MeOH w…

AnionsWaxPhthalic anhydrideChromatographyEsterificationLinear alkylbenzeneElutionOrganic ChemistryExtraction (chemistry)Fatty alcoholGeneral MedicineHydrogen-Ion ConcentrationChromatography Ion ExchangeBiochemistryAnalytical ChemistrySurface-Active Agentschemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumMethanolDerivatizationChromatography High Pressure LiquidJournal of Chromatography A
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Atomic fluorescence determination of total and inorganic arsenic species in beer

2001

A simple and nearly direct procedure has been developed for the determination of As in beers, based on hydride generation and atomic fluorescence detection. Using 2 mol l−1 HCl with a carrier flow of 6 ml min−1, 3% m/v NaBH4 with a flow of 1.3 ml min−1, a reaction coil of 200 cm and an argon flow of 400 ml min−1, total arsenic in beer could be determined in samples diluted 1∶10 with a final concentration of 2 mol l−1 HCl, 1% m/v KI and 0.08% v/v of an antifoam agent. For the estimation of AsIII and AsV concentrations in beer samples, the difference between the analytical sensitivities of the fluorescence signals obtained for As hydride, without and with previous treatment of samples with KI…

Antifoam agentDetection limitAtomic fluorescenceAshingInorganic arsenicChemistryHydrideAnalytical chemistrychemistry.chemical_elementFluorescenceSpectroscopyArsenicAnalytical ChemistryJ. Anal. At. Spectrom.
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Determination of antimony in drinking waters by an inexpensive, reproducible hydride generator for atomic spectroscopy.

1991

A method for determining antimony in drinking waters is described. In order to prevent a substantial error caused by the different oxidation states of antimony, Sb(V) is reduced to Sb(III) with potassium iodide-ascorbic acid. Covalent hydride is generated with a home made device by adding NaBH4. The hydride is then atomized in a flame-heated silica tube and atomic absorption is measured spectrophotometrically. The optimal conditions for this determination are discussed and interference effects are described. Results obtained by determining linearity range (0-200 ng), detection (LOD) and quantitation (LOQ) limits (LOD = 0.347 ng/ml, LOQ = 1.158 ng/ml), precision (instrumental CV 4.08% and me…

Antimonymedicine.diagnostic_testHydridePotassiumSpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementReproducibility of ResultsOxidation reductionAtomic spectroscopyHydrogen-Ion Concentrationlaw.inventionKineticschemistryAntimonylawPredictive Value of TestsWater SupplySpectrophotometryCalibrationCalibrationmedicineAtomic absorption spectroscopyOxidation-ReductionFood ScienceDie Nahrung
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A convenient route for the preparation of the monohydride catalyst trans-[RuCl(H)(dppe)2] (dppe=Ph2PCH2CH2PPh2): improved synthesis and crystal struc…

2013

Abstract A novel and improved room temperature synthesis of the monohydride catalyst trans-[RuCl(H)(dppe)2] complex (1, dppe (1,2-bis(diphenylphosphino)ethane) = Ph2PCH2CH2PPh2) proceeds through oxidation of methanol (the solvent) by the pentacoordinated cis-[RuCl(dppe)2][PF6] complex and t-BuOK as the base is described. Compound 1 was fully characterized by NMR (1H, 13C, 31P), ESI-MS(TOF +), FTIR and elemental analysis. The X-ray structure of 1 was reported for the first time and unambiguously confirms the trans-configuration of the complex.

Base (chemistry)chemistry.chemical_elementHomogeneous catalysisCrystal structure.PhotochemistryMedicinal chemistryRutheniumCatalysisInorganic Chemistrychemistry.chemical_compoundFaculdade de Ciências Exatas e da EngenhariaMaterials ChemistryPhysical and Theoretical ChemistryFourier transform infrared spectroscopyta116Syntethic methdoschemistry.chemical_classificationChemistryHydridesHomogeneous catalisysX-ray crystal structureRutheniumSolventMethanolHydrogenation
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Cycloaddition reactions of 3-vinylthiophen

1987

Abstract Cycloaddition reactions between 3-vinylthiophen and the dienophiles maleic anhydride, methyl acrylate, dimethyl acetylene - dicarboxylate, and methyl propiolate give products including methyl benzo[b]thiophen-7-carboxylate (11) and its dihydroderivative (10), the 6,7-dicarboxylic acid (3), its dimethyl ester (7) and dihydroester (6); the naphtho[a,b]dithiophen (14), and the novel ethano bridged benzo[b]thiophen (15).

Bicyclic moleculeMethyl propiolateOrganic ChemistryMaleic anhydrideNuclear magnetic resonance spectroscopyBiochemistryMedicinal chemistryDimethyl esterCycloadditionchemistry.chemical_compoundAcetylenechemistryDrug DiscoveryOrganic chemistryMethyl acrylateTetrahedron
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Hemoglobin loaded polymeric nanoparticles: preparation and characterizations.

2011

In the present work polymeric nanoparticles based on Poly (maleic anhydride-alt-butyl vinyl ether) 5% grafted with m-PEG (2000) and 95% grafted with 2-methoxyethanol (VAM41-PEG) were loaded with human hemoglobin (Hb) and characterized from a physicochemical point of view. The assessment of structural and functional features of the loaded Hb was performed and the effect of the introduction of different reducing agents as aimed at minimizing Hb oxidation during the nanoparticles formulation process, was also investigated. Nanoparticles possessing an average diameter of 138 ± 10 nm and physicochemical features suitable for this kind of application were successfully obtained. Although the oxida…

Biocompatible polymerVinyl CompoundsInjectable systemsBiocompatibilityReducing agentPharmaceutical ScienceNanoparticleBiocompatible MaterialsPolymeric nanoparticlePolyethylene Glycolschemistry.chemical_compoundHemoglobinsBlood SubstitutesPolymer chemistrymedicineHumansMicroparticleParticle SizeMaleic AnhydridesDrug CarriersBlood substituteMaleic anhydrideVinyl etherSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)chemistryChemical engineeringNanoparticlesEthylene GlycolsDrug carrierEthylene glycolmedicine.drugEthersEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
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Electronic aspects of the hydride transfer mechanism. Ab initio analytical gradient studies of the cyclopropenyl‐cation/lithium hydride model reactan…

1985

The electronic mechanisms of a model hydride transfer reaction are theoretically studied with ab inito RHF and UHF SCF MO procedures at the 4‐31G basis set level and analytical gradient methods. The model system describes the reduction of cyclopropenyl cation to cyclopropene by the oxidation of lithium hydride to lithium cation. The molecular fragments corresponding to the asymptotic reactive channels characterizing the stepwise mechanisms currently discussed in the literature have been characterized. The binding energy between the fragments is estimated within a simple electrostatic approximate scheme. The results show that a hydride‐ion mechanism is a likely pathway for this particular sy…

Biological MaterialsAb initioGeneral Physics and Astronomychemistry.chemical_elementchemistry.chemical_compoundElectron transferAb initio quantum chemistry methodsComputational chemistry:FÍSICA [UNESCO]CationsRedox ProcessPhysical and Theoretical ChemistryTriplet stateCycloalkenes:FÍSICA::Química física [UNESCO]HydrideUNESCO::FÍSICAChemical ReactionsUNESCO::FÍSICA::Química físicachemistryLithium hydrideChemical physicsLithium HydridesAb Initio Calculations ; Chemical Reactions ; Cycloalkenes ; Cations ; Lithium Hydrides ; Redox Process ; Biological MaterialsLithiumLithium CationAb Initio Calculations
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