Search results for "Deriva"

showing 10 items of 1423 documents

Synthesis of borylindenides; structure of [Li(N,N′,N″-Me3-1,3,5-C3H6N3)][1-C9H6{B(NMe2)2}]

1998

Abstract Borylation of lithium indenide (LiInd) affords indenylboranes. With BCl(NMe2)2 the primary allylic 1-indenyl derivative IndB(NMe2)2 (1) readily rearranges to the more stable vinylic bis(dimethylamino)(3-indenyl)borane 1′. With BCl(OCMe2)2 the (1-indenyl)-1,3,2-dioxaborolane IndB(OCMe2)2 (2) is obtained. Both indenylboranes 1′ and 2 readily undergo metalation when treated with lithium amides such as LiTMP or LDA to give 1-borylindenides Li[C9H6B(NMe2)2] [Li(3)] and Li[C9H6B(OCMe2)2] [Li(5)] in high yields. In the systems 1′/LiInd and 2/LiInd metalation equilibria are established with equlibrium constants K≈1 (1'/LiInd) and K≈1.4 (2/LiInd). The structure of the solvate [Li(TMHT)][1-C…

Allylic rearrangementMetalationOrganic Chemistrychemistry.chemical_elementCrystal structureBoraneBiochemistryBorylationInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryLithiumPhysical and Theoretical ChemistryDerivative (chemistry)Journal of Organometallic Chemistry
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A Quantitative Estimate of Ascorbic and Isoascorbic Acid by High Performance Liquid Chromatography: Application to Citric Juices

1993

Abstract The present report deals with the optimization and verification of a simple HPLC isocratic method useful for determining ascorbic and isoascorbic acids in standard solutions and fruit juices. Sample preparation is minimal and docs not require derivatization. The method uses an octadecyl reversed phase, a mobile phase which contains cetyltrimethyl ammonium bromide 0.05M as the ionic pair and potassium dihydrogen phosphate as a buffer, at pH=4.5, and 4-hydro-xyacetanilide as internal standard. The proposed method makes it possible to quantify ascorbic and isoascorbic acid in less than 13 minutes, with precision (C. V. 3.5%) and accuracy (recover' of 98%).

Ammonium bromidechemistry.chemical_compoundChromatographychemistryPotassiumIon chromatographyMolecular Medicinechemistry.chemical_elementSample preparationStandard solutionDerivatizationAscorbic acidHigh-performance liquid chromatographyJournal of Liquid Chromatography
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Stimulated emission and optical properties of pyranyliden fragment containing compounds in PVK matrix

2017

This work has been supported by National Research program “Multifunctional materials and composites, photonics and nanotechnology (IMIS2)”. Financial support provided by Scientific Research Project for Students and Young Researchers No. SJZ2015/12 realised at the Institute of Solid State Physics, University of Latvia is greatly acknowledged.

Amplified spontaneous emissionPhotoluminescenceMaterials scienceQuantum yieldElectron donor02 engineering and technologyPhotochemistry01 natural sciences010309 opticschemistry.chemical_compound0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]Stimulated emissionElectrical and Electronic EngineeringAmplified spontaneous emissionGlass forming low molecular weight compoundsDCMLaser dyeDye laser021001 nanoscience & nanotechnologyThreshold energyAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialschemistryPyranyliden derivatives0210 nano-technologyMethyl group
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Application of solid-phase microextraction combined with derivatization to the determination of amphetamines by liquid chromatography

2004

This work evaluates the utility of solid-phase microextraction (SPME) in the analysis of amphetamines by liquid chromatography (LC) after chemical derivatization of the analytes. Two approaches have been tested and compared, SPME followed by on-fiber derivatization of the extracted amphetamines, and solution derivatization followed by SPME of the derivatives formed. Both methods have been applied to measure amphetamine (AP), methamphetamine (MA), and 3,4-methylenedioxymethamphetamine (MDMA), using the fluorogenic reagent 9-fluorenylmethyl chloroformate (FMOC) and carbowax-templated resin (CW-TR)-coated fibers. Data on the application of the proposed methods for the analysis of different kin…

AnalyteAqueous solutionChromatographyChemistryMicrochemistryAmphetaminesExtraction (chemistry)BiophysicsReproducibility of ResultsCell BiologyChloroformateSolid-phase microextractionSensitivity and SpecificityBiochemistryMatrix (chemical analysis)chemistry.chemical_compoundReference ValuesReagentDerivatizationMolecular BiologyChromatography High Pressure LiquidAnalytical Biochemistry
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On-Line Derivatization into Precolumns for the Determination of Drugs by Liquid Chromatography and Column Switching:  Determination of Amphetamines i…

1996

A chromatographic system for the on-line derivatization of drugs using column switching is described. The system uses a 20 mm × 2.1 mm i.d. precolumn packed with a unmodified ODS stationary phase. This column is used for sample cleanup and enrichment of the analytes. Next, the trapped analytes are derivatized by injection of the derivatization reagent into the precolumn. Finally, the derivatives are transferred to the analytical column for their separation under reversed-phase conditions. The influence of several parameters such as the reaction time, the amount of derivatization reagent, or the system design has been studied using some amphetamines as model compounds and three derivatizatio…

AnalyteChromatographyAmphetaminesUrineChloroformateMethamphetamineAnalytical ChemistrySubstance Abuse Detectionchemistry.chemical_compoundColumn chromatographychemistryReagentIndicators and ReagentsColumn switchingDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidAnalytical Chemistry
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o-Phthalaldehyde–N-acetylcysteine polyamine derivatives: formation and stability in solution and in C18 supports

2001

A comparative study of different derivatization procedures has been performed in order to improve the stability of the reaction products o-phthalaldehyde-N-acetylcysteine (OPA-NAC) polyamines. Procedures such as solution derivatization, solution derivatization followed by retention on a packing support, derivatization on different packing supports and on-column derivatization, have been optimized and compared. The degradation rate constant (k) of the derivative was dependent on the procedure used and on the analyte. For the spermine (the most unstable isoindol tested) k was 8 +/- 2 x 10(-2) min(-1) in solution versus 7.7 +/- 1.1 x 10(-4) min(-1) on the (C18) solid support. The results obtai…

AnalyteChromatographyChemistryElutionGeneral ChemistryStandard solutionSensitivity and SpecificityAcetylcysteineMatrix (chemical analysis)O-Phthalaldehydechemistry.chemical_compoundDrug StabilityReagentPolyaminesSpectrophotometry UltravioletSolid phase extractionDerivatizationChromatography High Pressure Liquido-PhthalaldehydeJournal of Chromatography B: Biomedical Sciences and Applications
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Determination of aliphatic amines in water by liquid chromatography using solid-phase extraction cartridges for preconcentration and derivatization

2001

Bond Elut C18 solid-phase extraction cartridges were used for preconcentration and pre-column derivatization with 3,5-dinitrobenzoyl chloride (DNB) of aliphatic amines in water. Conditions for analyte preconcentration and derivatization (including the volume of sample, concentration of reagent, time of reaction and pH) were investigated, using ethylamine, isopropylamine and dimethylamine as model compounds. On the basis of these studies, a rapid and sensitive method for the determination of aliphatic amines in water is presented. The analytes are retained and purified on the cartridges and then derivatized and desorbed by drawing in succession the DNB solution and acetonitrile. The collecte…

AnalyteChromatographyElutionReproducibility of ResultsBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryElectrochemistryHumansEnvironmental ChemistrySolid phase extractionIsopropylamineAminesEthylamineDerivatizationAliphatic compoundDimethylamineWater Pollutants ChemicalSpectroscopyChromatography LiquidThe Analyst
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Enhancement of retention predictions in reversed-phase liquid chromatography using reference compounds

2004

Abstract The use of reference compounds to correct errors associated with the preparation of mobile phase is studied, in order to enhance modelling of retention for optimisation purposes in reversed-phase liquid chromatography. The method fits individual retention models for a set of reference compounds, which are present in all injections. In second step, mobile-phase composition is corrected for each chromatogram, according to the fitted models of the reference compounds. The enhanced precision provided by the large number of replicates for the reference compounds is partially propagated to the retention models of the analytes. The approach is assayed in the separation of amino acids, aft…

AnalyteChromatographyIsoindolesChemistryAnalytical chemistryReversed-phase chromatographyBiochemistryAnalytical Chemistrychemistry.chemical_compoundReagentPhase (matter)Environmental ChemistryDerivatizationAcetonitrileSpectroscopyPhthalaldehydeAnalytica Chimica Acta
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Application of solid-phase microextraction combined with derivatization to the enantiomeric determination of amphetamines.

2005

Abstract The utility of combining chiral derivatization and solid-phase microextraction (SPME) for the enantiomeric analysis of primary amphetamines by liquid chromatography has been investigated. Different derivatization/extraction strategies have been evaluated and compared using the chiral reagent o -phthaldialdehyde (OPA)– N -acetyl- l -cysteine (NAC) and fibres with a Carbowax-templated resin coating. Amphetamine, norephedrine and 3,4-methylenedioxyamphetamine (MDA) were used as model compounds. On the basis of the results obtained, a new method is presented based on the derivatization of the analytes in solution followed by SPME of the OPA–NAC derivatives formed. The proposed conditio…

AnalyteClinical BiochemistryPhenylpropanolaminePharmaceutical ScienceSolid-phase microextractionAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryHumansDerivatizationSpectroscopyChromatography High Pressure LiquidAqueous solutionChromatographyExtraction (chemistry)AmphetaminesReproducibility of ResultsStereoisomerismSolutionsSpectrometry FluorescencechemistryReagentCentral Nervous System StimulantsIndicators and ReagentsEnantiomerQuantitative analysis (chemistry)Journal of pharmaceutical and biomedical analysis
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One-Pot Analysis: a New Integrated Methodology for Determination of TAG and FA Determination through LC/MS and in-silico Saponification

2017

Vegetable oils differ significantly for their lipid profile and are mainly constituted by triacylglycerols (TAGs). These are esters formed bonding glycerol to three fatty acids (FAs). To the best of our knowledge, FA and TAG profiles in oils and fats are obtained using at least two different experimental techniques. In particular, FA determination requires elaborated procedures for sample preparation and analyte derivatization. In this work, we propose a one-pot analysis able to determine both TAG and FA contents of edible oils, using experimental data obtained from a simple liquid chromatography/mass spectrometry determination of TAGs. This experimental procedure is followed by an in silic…

AnalyteMass spectrometryTriacylglycerol01 natural sciencesApplied Microbiology and BiotechnologyAnalytical Chemistrychemistry.chemical_compound0404 agricultural biotechnologyLiquid chromatography–mass spectrometryGlycerolSample preparationFood scienceSafety Risk Reliability and QualityDerivatizationChromatography010401 analytical chemistry04 agricultural and veterinary sciencesFatty acid040401 food scienceFAME0104 chemical sciencesLipid profileVegetable oilBlood chemistrychemistryIn silico saponificationSafety ResearchSaponificationFood ScienceFood Analytical Methods
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