Search results for "resolution."

showing 10 items of 1825 documents

Monolayer Structure of Arachidic Acid on Graphite

2010

The self-assembly of arachidic acid (C(19)H(39)COOH) at the liquid solid interface between 1-phenyloctane (C(6)H(5)(CH(2))(7)CH(3)) and highly oriented pyrolytic graphite (HOPG) is studied by scanning tunneling microscopy (STM) to identify the structure of the monomolecular film. We observe the formation of highly ordered domains with molecules oriented in three different orientations compatible with the symmetry of the HOPG substrate, a spontaneous enantiomeric separation of the pro-chiral molecules, and reveal structural details with submolecular resolution. To determine the surface unit cell with an intrinsic calibration to the substrate atomic structure, the intermolecular distance is p…

Resolution (electron density)Substrate (electronics)530Surfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionCrystallographychemistry.chemical_compoundGeneral EnergyHighly oriented pyrolytic graphitechemistrylawMonolayerArachidic acidMoleculeGraphitePhysical and Theoretical ChemistryScanning tunneling microscope
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Enantioresolution in electrokinetic chromatography-complete filling technique using sulfated gamma-cyclodextrin. Software-free topological anticipati…

2016

Few papers have tried to predict the resolution ability of chiral selectors in capillary electrophoresis for the separation of the enantiomers of chiral compounds. In a previous work, we have used molecular information available on-line to establish enantioresolution levels of basic compounds using highly sulfated β-CD (HS-β-CD) as chiral selector in electrokinetic chromatography-complete filling technique (EKC-CFT). The present study is a continuation of this previous work, introducing some novelties. In this work, the ability of sulfated γ-cyclodextrin (S-γ-CD) as chiral selector in EKC-CFT is modelled for the first time. Thirty-three structurally unrelated cationic and neutral compounds …

Resolution (mass spectrometry)02 engineering and technologyTopology01 natural sciencesBiochemistryAnalytical ChemistryElectrokinetic phenomenaCapillary electrophoresisCationsMoleculeLeast-Squares AnalysisPesticidesTopology (chemistry)Chromatography Micellar Electrokinetic CapillaryChromatographyChemistry010401 analytical chemistryOrganic ChemistryCationic polymerizationDiscriminant AnalysisStereoisomerismGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesPharmaceutical PreparationsAsymmetric carbonIndicators and ReagentsEnantiomer0210 nano-technologySoftwaregamma-CyclodextrinsJournal of Chromatography A
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Use of triacylglycerol profiles established by high performance liquid chromatography with ultraviolet–visible detection to predict the botanical ori…

2011

A method for the determination of triacylglycerols (TAGs) in vegetable oils from different botanical origins by HPLC with UV–vis detection has been developed. Using a core-shell particle packed column (C18, 2.6 micron), TAG separation was optimized in terms of mobile phase composition and column temperature. Using isocratic elution with acetonitrile/n-pentanol at 10 °C, excellent efficiency with good resolution between most of the TAG peak pairs, within a total analysis time of 15 min, was achieved. Using mass spectrometry detection, a total of 15 peaks, which were common to oils of six different botanical origins (corn, extra virgin olive, grapeseed, hazelnut, peanut and soybean) were iden…

Resolution (mass spectrometry)Analytical chemistrymedicine.disease_causeMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistrySpectrophotometrymedicinePlant OilsChromatography High Pressure LiquidTriglyceridesPacked bedBOTANICAL ORIGINIsocratic elutionChromatographymedicine.diagnostic_testChemistryOrganic ChemistryDiscriminant Analysisfood and beveragesGeneral MedicineTRIACYLGLYCEROLSLINEAR DISCRIMINANT ANALYSISPhase compositionSpectrophotometry UltravioletHPLCVEGETABLE OILSUltravioletJournal of Chromatography A
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Rugged Large Volume Injection for Sensitive Capillary LC-MS Environmental Monitoring

2017

A rugged and high throughput capillary column (cLC) LC-MS switching platform using large volume injection and on-line automatic filtration and filter back-flush (AFFL) solid phase extraction (SPE) for analysis of environmental water samples with minimal sample preparation is presented. Although narrow columns and on-line sample preparation are used in the platform, high ruggedness is achieved e.g. injection of 100 non-filtrated water samples would did not result in a pressure rise/clogging of the SPE/capillary columns (inner diameter 300 µm). In addition, satisfactory retention time stability and chromatographic resolution were also features of the system. The potential of the platform for …

Resolution (mass spectrometry)Capillary actionAnalytical chemistry02 engineering and technologycapillary LC01 natural scienceslaw.inventionlcsh:ChemistrylawLiquid chromatography–mass spectrometrySample preparationSolid phase extractionon-line solid phase extractionFiltrationOriginal ResearchDetection limitChromatographyChemistry010401 analytical chemistryGeneral ChemistryRepeatability021001 nanoscience & nanotechnology0104 chemical sciencespharmaceutical productsChemistrylcsh:QD1-999column switchinglarge volume injection0210 nano-technologyFrontiers in Chemistry
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High pressure liquid chromatography resolution of racemic mixtures of chiral tricarbonyl arene chromium(0) and cyclopentadienyl-titanium(IV) complexes

1998

Abstract Enantiomers of chiral tricarbonyl arene chromium(0) and cyclopentadienyl-titanium(IV) complexes have been separated by high pressure liquid chromatography employing a Chiralcel OD (Daicel) column, eluting with hexane/2-propanol mixtures. The capacity factors ( k ) and selectivity factors ( α ) concerning the separation of these compounds have been determined. The resolution of tricarbonyl( η 6 -methyl o -acetylbenzoate)chromium ( IV ), was carried out on semipreparative scale: a comparison of the CD spectra of the enantiomers IVa and IVb with that reported in the literature for a similar complex allowed to establish the absolute configuration [( 1R )] for the most retained enantiom…

Resolution (mass spectrometry)ChemistryAbsolute configurationchemistry.chemical_elementMedicinal chemistryHigh-performance liquid chromatographyInorganic ChemistryHexanechemistry.chemical_compoundChromiumCyclopentadienyl complexMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryEnantiomerSelectivityInorganica Chimica Acta
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Lineshapes and optical selectivity in high-resolution double-resonance ionization mass spectrometry

1999

Abstract Lineshapes expected in high-resolution double-resonance ionization spectroscopy are calculated using the density matrix formalism, integrated over experimentally realistic conditions including atomic velocity and angular distributions as well as laser intensity profiles. The results of these calculations are compared with experimental measurements on the system 4s2 1S0 → 4s4p 1P1 → 4s4d 1D1 → ion for calcium. The measurements of lineshape, with a dynamic range of >106, reveal and confirm subtle effects predicted by theory. These include the shape, position and intensity of the laser-induced structure in the spectra and the simultaneous presence of coherent and incoherent excitation…

Resolution (mass spectrometry)ChemistryAnalytical chemistryMass spectrometryMolecular physicsAtomic and Molecular Physics and OpticsSpectral lineAnalytical ChemistryIonIonizationMass spectrumPhysics::Atomic PhysicsSpectroscopyInstrumentationSpectroscopyExcitationSpectrochimica Acta Part B: Atomic Spectroscopy
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A PLE-based resolution of cocaine, pseudococaine, and 6- and 7-methoxylated cocaine analogues

1996

Abstract The enzymatic hydrolysis of racemic cocaine and cocaine analogues using pig liver esterase (PLE) is shown to afford a practical means for achieving their chemical resolution. This reaction was found to proceed not only with good enantioselectivity, but with an interesting chemoselectivity as well.

Resolution (mass spectrometry)ChemistryOrganic ChemistryClinical BiochemistryPharmaceutical ScienceBiochemistryEsterasePseudococaineEnzymatic hydrolysisDrug DiscoveryMolecular MedicineOrganic chemistryChemoselectivityMolecular BiologyPig liverBioorganic & Medicinal Chemistry Letters
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Spectrophotometric analysis of mixtures of two components with extensively or completely overlapping spectra by the H-point standard additions method

1990

This paper discusses the requirements and scope of application of the H-Point Standard Additions Method (HPSAM) for resolving binary mixtures. Various mixtures of dyes with extensively or completely overlapping spectra were assayed with accurate, precise results. The method thus developed was also applied to the spectrophotometric resolution of binary mixtures of phenol and o-cresol, the absorption bands of which lie in similar positions and feature similar absorptivities.

Resolution (mass spectrometry)ChemistryStandard additionAnalytical chemistryBinary numberPoint (geometry)Absorption (chemistry)Mass spectrometryBiochemistrySpectral lineAnalytical ChemistryFresenius' Journal of Analytical Chemistry
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Optimization of a LC method for the enantioseparation of a non-competitive glutamate receptor antagonist, by experimental design methodology

2006

Abstract The aim of this work was to obtain the direct optical resolution of a new glutamate receptor antagonist (( p -chloro)1-aryl-6,7,-dimethoxy-1,2,3,4-tetrahydroisoquinoline, PS3), by liquid chromatography on Chiralcel ® OD column. A response surface methodology (RSM) was employed to optimize the enantiomeric separation of the racemate with the lowest number of experiments; in particular, a face-centred design (FCD) was applied to evaluate the influence of critical parameters on the experimental response. Furthermore, in order to find the best compromise between several responses, a multicriteria decision-making approach, the Derringer's desirability function, was successful to simulta…

Resolution (mass spectrometry)Clinical BiochemistryAnalytical chemistryPharmaceutical ScienceChiral liquid chromatography Enantioresolution Chiralcel® OD Tetrahydroisoquinoline derivative Face-centred design Desirability functionHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundTetrahydroisoquinolinesDrug DiscoveryGlutamate receptor antagonistResponse surface methodologySpectroscopyChiral liquid chromatographyChromatographyMolecular StructureAntagonistChiralcel® ODStereoisomerismTetrahydroisoquinoline derivativeDesirability functionFace-centred designHexanechemistryModels ChemicalDesirability functionEnantiomerEnantioresolutionExcitatory Amino Acid AntagonistsChromatography Liquid
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Potential of human serum albumin as chiral selector of basic drugs in affinity electrokinetic chromatography-partial filling technique

2006

The enantiomeric resolution of compounds using HSA by means of affinity EKC (AEKC)-partial filling technique is the result of a delicate balance between different experimental variables such as protein concentration, running pH (background electrophoretic buffer (BGE), protein, and compound solutions), and plug length. In this paper, the possibility of using HSA as chiral selector for enantioseparation of 28 basic drugs using this methodology is studied. The effect of the physicochemical parameters, the structural properties of compounds, and compound-HSA protein binding percentages over their chiral resolution with HSA is outlined. Based on the results obtained, a decision tree is proposed…

Resolution (mass spectrometry)Clinical BiochemistryPlasma protein bindingBuffersBiochemistryChromatography AffinityAnalytical ChemistryElectrokinetic phenomenaMolar volumemedicineHumansSerum AlbuminChromatography Micellar Electrokinetic CapillaryChromatographyMolecular StructureChemistryStereoisomerismHydrogen-Ion ConcentrationHuman serum albuminChiral resolutionbody regionsElectrophoresisPharmaceutical Preparationsembryonic structuresEnantiomerHydrophobic and Hydrophilic Interactionsmedicine.drugELECTROPHORESIS
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