Search results for "analytical"

showing 10 items of 9586 documents

The identification of vicinally substituted cyclohexane isomers in their mixtures by 1H and 13C NMR spectroscopy.

2000

The radical addition reactions of organobromine compounds, XBr (X = CH2COOMe, PhCH2, CHBr2 and CCl3) with cyclohexene afforded mixtures of cis/trans isomer pairs of 1-X-2-Br-cyclohexanes. In addition to benzyl benzoyloxy derivatives are formed also, when benzoyl peroxide is used as an initiator. Owing to the great difficulties in separating these cis/trans isomer pairs, they are identified directly in their mixtures by NMR spectroscopy. In addition to one-dimensional (ID) 1H, proton decoupled 13C and DEPT-135, also two-dimensional (2D) 13C-13C INADEQUATE as well as 1H-13C HMQC experiments have been used in assigning the signals of each compound in their mixtures. The identification of each …

Addition reactionCarbon IsotopesMagnetic Resonance SpectroscopyCyclohexaneStereochemistryCyclohexeneMolecular ConformationStereoisomerismStereoisomerismBenzoyl peroxideNuclear magnetic resonance spectroscopyTritiumMedicinal chemistryAtomic and Molecular Physics and OpticsAnalytical Chemistrychemistry.chemical_compoundchemistryCyclohexanesmedicineMolecular orbitalInstrumentationSpectroscopyCis–trans isomerismmedicine.drugSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
researchProduct

2014

Carbon-centered radicals represent highly useful reactive intermediates in organic synthesis. Their nucleophilic character is reflected by fast additions to electron deficient C=X double bonds as present in iminium ions or cationic heterocycles. This review covers diverse reactions of preformed or in situ-generated cationic substrates with various types of C-radicals, including alkyl, alkoxyalkyl, trifluoromethyl, aryl, acyl, carbamoyl, and alkoxycarbonyl species. Despite its high reactivity, the strong interaction of the radical’s SOMO with the LUMO of the cation frequently results in a high regioselectivity. Intra- and intermolecular processes such as the Minisci reaction, the Porta react…

Addition reactionChemistryOrganic ChemistryReactive intermediateCationic polymerizationPharmaceutical ScienceIminiumRegioselectivityPhotoredox catalysisPhotochemistryMedicinal chemistryAnalytical ChemistryNucleophileChemistry (miscellaneous)Drug DiscoveryMolecular MedicinePhysical and Theoretical ChemistryMinisci reactionMolecules
researchProduct

Nested MWC model describes hydrolysis of GroEL without assuming negative cooperativity in binding

2002

Folding assistance and ATPase activity of GroEL are based on the existence of different conformations. In order to characterise these conformations, published data on steady state ATPase activity in the absence of GroES were reanalysed simultaneously in terms of the Nested MWC model. This model is a hierarchical extension of the symmetry-model of Monod et al. [J. Mol. Biol. 12 (1965) 88]. An unique set of GroEL specific parameters was obtained. This set was supported by comparison of predictions arising from this set of values with experimental data for hydrolysis of ATP in the presence of ADP and ATPgammaS, binding of ATPgammaS and ADP to GroEL in the absence of ATP, and binding of ATP as …

Adenosine TriphosphatasesModels Molecularchemistry.chemical_classificationChemistryHydrolysisBiophysicsCooperative bindingCooperativityChaperonin 60GroESBiochemistryGroELAnalytical ChemistryAdenosine DiphosphateFolding (chemistry)CrystallographyAdenosine TriphosphateATP hydrolysisCalibrationBiophysicsComputer SimulationNucleotideSteady state (chemistry)Molecular BiologyProtein BindingBiochimica et Biophysica Acta (BBA) - Proteins and Proteomics
researchProduct

Physicochemical characterization of passive films on niobium by admittance and electrochemical impedance spectroscopy studies

2005

An analysis of the electronic properties of amorphous semiconductor-electrolyte junction is reported for thin (D ox < 20 nm) passive film grown on Nb in acidic electrolyte. It will be shown that the theory of amorphous semiconductor-electrolyte junction (a-SC/EI) both in the low band-bending and high band-bending regime is able to explain the admittance data of a-Nb 2 O 5 /El interface in a large range (10 Hz-10 kHz) of frequency and electrode potential values. A modelling of experimental EIS data at different potentials and in the frequency range of 0.1 Hz-100 kHz is presented based on the theory of amorphous semiconductor and compared with the results of the fitting of the admittance data…

AdmittanceChemistryGeneral Chemical EngineeringNiobiumAnalytical chemistrychemistry.chemical_elementphysicochemical characterization; semiconductor-electrolyte junction; electrochemical impedance spectroscopyElectrolyteAmorphous solidDielectric spectroscopysemiconductor-electrolyte junctionelectrochemical impedance spectroscopySettore ING-IND/23 - Chimica Fisica Applicataphysicochemical characterizationElectrochemistryDensity of statesElectrical impedanceElectrode potential
researchProduct

Interpretive search of optimal isocratic and gradient separations in micellar liquid chromatography in extended organic solvent domains

2020

Abstract Micellar liquid chromatography (MLC) is a reversed-phase mode with mobile phases containing an organic solvent and a micellised surfactant. Most procedures developed in MLC are implemented in the isocratic mode, since the general elution problem in chromatography is less troublesome. However, gradient elution may be still useful in MLC to analyse mixtures of compounds within a wide range of polarities, in shorter times. MLC using gradients is attractive to determine by direct injection moderate to low polar compounds in physiological samples. In these analyses, the use of initial micellar conditions (isocratic or gradient) with a fixed amount of surfactant above the critical micell…

Adrenergic beta-Antagonists1-Propanol010402 general chemistry01 natural sciencesBiochemistryMicelleChemistry Techniques AnalyticalAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantHumansMicellesChromatographyElutionChemistryChemical polarity010401 analytical chemistryOrganic ChemistrySodium Dodecyl SulfateGeneral Medicine0104 chemical sciencesSolventMicellar liquid chromatographyCritical micelle concentrationSolventsIndicators and ReagentsAdsorptionChromatography LiquidJournal of Chromatography A
researchProduct

Micellar Liquid Chromatography:  A Worthy Technique for the Determination of β-Antagonists in Urine Samples

1998

Several beta-antagonists (acebutolol, atenolol, celiprolol, labetalol, metoprolol, nadolol, propranolol) were determined in urine samples with fluorometric detection after direct injection, in less than 15 min, with a micellar mobile phase of 0.1 M sodium dodecyl sulfate (SDS), 15% propanol, and 1% triethylamine at pH 3. The limits of detection (38 criterion) were usually between 3 and 30 ng/mL. The addition of propanol and triethylamine and the reduction of the pH of the mobile phase improved the efficiency of the chromatographic peaks that was rather low in pure micellar eluents. The selection of the composition of the mobile phase was easily performed through the use of an interpretive p…

Adrenergic beta-Antagonists1-PropanolHigh-performance liquid chromatographyAnalytical ChemistryPropanolSurface-Active Agentschemistry.chemical_compoundEthylaminesmedicineHumansSodium dodecyl sulfateTriethylamineMicellesDetection limitChromatographySodium Dodecyl SulfateHydrogen-Ion ConcentrationAtenololPropranololAcebutololSpectrometry FluorescenceAtenololchemistryMicellar liquid chromatographyChromatography LiquidMetoprololmedicine.drugAnalytical Chemistry
researchProduct

Performance of amines as silanol suppressors in reversed-phase liquid chromatography

2016

In reversed-phase liquid chromatography, cationic basic compounds yield broad and asymmetrical peaks, as a result of their ionic interaction with the anionic free silanol groups present in the silica-based stationary phases (commonly derivatised with C18 groups). A simple way to improve the peak shape is the addition to the hydro-organic mobile phase of a reagent (usually called additive) with cationic character. This associates with the stationary phase to prevent the access of analytes to the free silanol groups. Cationic additives may interact electrostatically with the anionic silanols. The hydrophobic region of the additive may also associate with the alkyl chains bound to the stationa…

Adrenergic beta-AntagonistsIonic Liquids010402 general chemistry01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundHexylamineEndcappingPhase (matter)BoratesAminesChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryImidazolesCationic polymerizationGeneral MedicineReversed-phase chromatographySilanes0104 chemical sciencesSilanolchemistryIonic liquidPentylamineHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
researchProduct

Magnetic In-Tube Solid Phase Microextraction

2012

We report a new in-tube solid phase microextraction approach named magnetic in-tube solid phase microextraction, magnetic-IT-SPME. Magnetic-IT-SPME has been developed, taking advantage of magnetic microfluidic principles with the aim to improve extraction efficiency of IT-SPME systems. First, a magnetic hybrid material formed by Fe(3)O(4) nanoparticles supported on SiO(2) was synthesized and immobilized in the surface of a bared fused silica capillary column to obtain a magnetic adsorbent extraction phase. The capillary column was placed inside a magnetic coil that allowed the application of a variable magnetic field. Acetylsalicylic acid, acetaminophen, atenolol, diclofenac, and ibuprofen …

AdsorptionChromatographyChemistryElectromagnetic coilPhase (matter)Extraction (chemistry)MicrofluidicsAnalytical chemistrySolid phase extractionSolid-phase microextractionAnalytical ChemistryMagnetic fieldAnalytical Chemistry
researchProduct

Study and Modelling of the Vacuum Swing Adsorption (VSA) Process Employed in the Production of Oxygen

1999

An isothermal and non-equilibrium mathematical model was provided for the multi-component adsorption process. In addition, the software was developed for the VSA-based production of oxygen with the use of a CaX zeolite molecular sieve. The mathematical model and computer software were verified on the basis of experimental data. The study employed a test stand comprising two adsorption columns. The adsorption pressure P A = 150 and 135 kPa and desorption pressure P D = 20 kPa were adopted in the experiments. The tests produced oxygen with the purity of 90–94% O 2 (vol), at an efficiency of 55–73% and productivity of 570–850 kg O 2 per ton per day. The calculation results showed good consiste…

AdsorptionChromatographyChemistryGeneral Chemical EngineeringDiffusionDesorptionAnalytical chemistrySorptionGeneral ChemistryVacuum swing adsorptionMolecular sieveZeoliteIsothermal processChemical Engineering Research and Design
researchProduct

&lt;title&gt;Large-scale computer simulations of metal/oxide interfaces with defects&lt;/title&gt;

2003

Ab initio slab simulations have been performed for silver adhesion to the perfect and defective MgO(001) surfaces. For 1/4 Ag monolayer (ML) coverage of perfect substrate, we observe small silver adhesion energies over both O2- and Mg2+ ions on a regular MgO(001) substrate (0.23 and 0.22 eV per Ag atom, respectively), with negligible interfacial charge transfer towards metal atoms. For larger Ag coverages (beginning with 1/2 ML), silver adsorption over regular O2- ions is much more favorable. We demonstrate that point surface defects on a magnesia surface increase markedly the metal adhesion energy and cause a redistribution of the electron density across the interface. The results for elec…

AdsorptionMaterials sciencePhysisorptionVacancy defectAtomMonolayerBinding energyAnalytical chemistryIonic bondingAtomic physicsIonSPIE Proceedings
researchProduct