Search results for "Spectroscopy"

showing 10 items of 10293 documents

Application of molecularly imprinted polymers in analytical chiral separations and analysis

2018

Over the last two decades the process of development and application of a new types of molecular imprinted polymer (MIP) sorbents in the field of analytical chemistry have been widely described in the literature. One of the new trends in analytical chemistry practice is the use of new types of MIP sorbents as specific sorption materials constituting the stationary phase in advanced separation techniques. The following review paper contains comprehensive information about the application of a specific and well defined MIP sorbents (with the data base in the paper about the reagents used in MIP preparation process) as stationary phases in separation techniques including high performance liqui…

Capillary electrochromatographychiral separationMaterials sciencehigh performance liquid chromatography010401 analytical chemistryMolecularly imprinted polymerEnantioselective synthesisNanotechnologySorptionenantiomers02 engineering and technologycapillary electrochromatography021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryStationary phasemolecularly imprinted polymers0210 nano-technologySpectroscopyTrac-Trends in Analytical Chemistry
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Phase diagram of polymer blends in confined geometry

2001

Within self-consistent field theory we study the phase behavior of a symmetrical binary AB polymer blend confined into a thin film. The film surfaces interact with the monomers via short range potentials. One surface attracts the A component and the corresponding smei-infinite system exhibits a first order wetting transition. The surface interaction of the opposite surface is varied as to study the crossover from capillary condensation for symmetric surfaces fields to the interface localization/delocalization transition for antisymmetric surface fields. In the former case the phase diagram has a single critical point close to the bulk critical point. In the latter case the phase diagram exh…

Capillary waveMaterials scienceCapillary condensationCondensed matter physicsStatistical Mechanics (cond-mat.stat-mech)FOS: Physical sciencesFísicaCondensed Matter - Soft Condensed MatterCondensed Matter PhysicsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsTricritical pointWetting transitionCritical point (thermodynamics)Polymer blendsMaterials ChemistrySoft Condensed Matter (cond-mat.soft)Ising modelPhysical and Theoretical ChemistryCritical exponentConfined geometrySpectroscopyCondensed Matter - Statistical MechanicsPhase diagram
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Drying enhances immunoactivity of spent brewer's yeast cell wall β-D-glucans.

2015

Due to immunological activity, microbial cell wall polysaccharides are defined as 'biological response modifiers' (BRM). Cell walls of spent brewer's yeast also have some BRM activity. However, up to date there is no consensus on the use of spent brewer's yeast D-glucan as specific BRM in humans or animals. The aim of this paper is to demonstrate the potential of spent brewer's yeast β-D-glucans as BRM, and drying as an efficient pretreatment to increase β-D-glucan's immunogenic activity. Our results revealed that drying does not change spent brewer's yeast biomass carbohydrate content as well as the chemical structure of purified β-D-glucan. However, drying increased purified β-D-glucan TN…

Carbohydrate contentbeta-GlucansChemical structureBioengineeringSaccharomyces cerevisiaeBiologyPolysaccharideApplied Microbiology and BiotechnologyCell wallchemistry.chemical_compoundCell WallSpectroscopy Fourier Transform InfraredAnimalsDesiccationCells Culturedchemistry.chemical_classificationMice Inbred ICRExtraction (chemistry)Fungal PolysaccharidesGeneral MedicineYeastPleurancarbohydrates (lipids)stomatognathic diseaseschemistryBiochemistryYeast biomassMacrophages PeritonealBiotechnologyJournal of biotechnology
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Evaluation of nutritional parameters in infant formulas and powdered milk by Raman spectroscopy

2007

It has been made a critical evaluation of the application of near infrared Fourier transform-Raman spectroscopy for the simultaneous determination of the most important nutritional parameters such as energetic value, carbohydrate, protein and fat contents of infant formula and powdered milk samples based on the use of partial least squares (PLS) regression analysis. A highly heterogeneous population of 23 samples, covering a wide range of infant food formula and powdered milk, were obtained from the Spanish market. Raman spectra, obtained by excitation with a Nd:YAG laser at 1064 nm, show no disturbing fluorescence effects; therefore sample spectra can be recorded without any previous prepa…

CarbohydratesFluorescence spectrometryAnalytical chemistrySample (statistics)Spectrum Analysis RamanBiochemistryFourier transform spectroscopyAnalytical ChemistryFatsSet (abstract data type)Partial least squares regressionCalibrationAnimalsHumansEnvironmental ChemistrySpectroscopyChemistryInfant NewbornInfantProteinsReplicateInfant FormulaMilkInfant formulaFoodCalibrationFood AnalysisAnalytica Chimica Acta
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Thermodynamic analysis of binding between drugs and glycosaminoglycans by isothermal titration calorimetry and fluorescence spectroscopy

2007

The thermodynamics of the interaction of positively charged drug molecules with negatively charged glycosaminoglycans (GAGs) is investigated by isothermal titration calorimetry (ITC) and fluorescence spectroscopy. The drugs considered are propranolol hydrochloride, tacrine, and aminacrine, and the polymers used as model GAGs are dextran sulfate, chondroitin sulfate, and hyaluronic acid. The ITC results show that the interaction between drugs and GAGs is via direct binding and that GAGs bind to drugs at one set of sites. Large negative values of heat capacity change (DeltaC(p)) are observed upon binding of GAGs to drugs. Such negative DeltaC(p) is not expected for purely electrostatic intera…

CarbohydratesFluorescence spectrometryPharmaceutical ScienceCalorimetryCalorimetryFluorescence spectroscopychemistry.chemical_compoundChondroitin sulfateHyaluronic AcidFluorescent DyesGlycosaminoglycansLiaisonChemistryChondroitin SulfatesTemperatureProteinsMembranes ArtificialIsothermal titration calorimetryHydrogen-Ion ConcentrationPropranololAminacrineSpectrometry FluorescenceMembranePharmaceutical PreparationsBiochemistryDrug deliveryTacrineBiophysicsThermodynamicsIndicators and ReagentsEuropean Journal of Pharmaceutical Sciences
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1H, 13C and 15N NMR spectral characterization of twenty-seven 1,2-diaryl-(4E)-arylidene-2-imidazolin-5-ones.

2006

1H, 13C and 15N NMR chemical shifts and couplings nJ(H,C) in DMSO-d6 at 30 °C have been determined for 1,2-diaryl-(4E)-arylidene-2-imidazolin-5-one derivatives 1–27. Their chemical shift assignments are based on PFG DQF 1H,1H COSY, PFG 1H,13C HMQC as well as PFG 1H,13C and 1H,15N HMBC experiments. For compounds 1–10 including aryl fluorine substituent(s) also the couplings nJ(F,C) (n = 1 − 4) are reported. Copyright © 2006 John Wiley & Sons, Ltd.

Carbon IsotopesMagnetic Resonance SpectroscopyMolecular StructureNitrogen IsotopesStereochemistryArylChemical shiftSubstituentchemistry.chemical_elementGeneral ChemistryCarbon-13 NMRchemistry.chemical_compoundchemistryProton NMRFluorineGeneral Materials ScienceImidazolinesHydrogenMagnetic resonance in chemistry : MRC
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Complete 1H and 13C NMR assignments of clerodane diterpenoids of Salvia splendens.

2006

Unambiguous and complete assignments of 1H and 13C NMR chemical shifts for five clerodane diterpenes, four of them isolated from Salvia splendens (salviarin, splendidin and splenolides A and B) and one obtained by acetylation of splenolide A, are presented. The assignments are based on 2D shift-correlated [1H,1H–COSY, 1H,13C-gHSQC–1J(C,H) and 1H,13C-gHMBC-nJ(C,H) (n = 2 and 3)] and nuclear Overhauser effect (NOE) experiments. The conformation of the rings of these compounds is supported by the 3J(H,H) values and NOE results. Copyright © 2006 John Wiley & Sons, Ltd.

Carbon IsotopesMagnetic Resonance SpectroscopybiologyStereochemistryChemistryChemical shiftAcetylationGeneral ChemistryNuclear Overhauser effectCarbon-13 NMRSalviabiology.organism_classificationDiterpenes ClerodaneUnambiguous and complete assignments of 1H and 13C NMR chemical shifts for five clerodane diterpenes four of them isolated from Salvia splendens (salviarin splendidin and splenolides A and B) and one obtained by acetylation of splenolide A are presented. The assignments are based on 2D shiftcorrelated [1H1H–COSY 1H13C-gHSQC–1J(CH) and 1H13C-gHMBC-nJ(CH) (n = 2 and 3)] and nuclear Overhauser effect (NOE) experiments. The conformation of the rings of these compounds is supported by the 3J(HH) values and NOE results. Copyright  2006 John Wiley & Sons LtdClerodane DiterpenesProton NMRGeneral Materials ScienceSalviaHydrogenMagnetic resonance in chemistry : MRC
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Reversible coordination of dioxygen by tripodal tetraamine copper complexes incorporated in a porous silica framework.

2010

The present study reports the synthesis and rational design of porous structured materials by using a templating method. A tetraethoxysilylated tripodal tetraamine (TREN) was covalently incorporated in a silica framework with a double imprint: A surfactant template and a metal ion imprint. The presence of a cationic surfactant (CTAB) endowed the material with a high porosity, and the tripodal or square-pyramidal topology of the ligand was preserved thanks to the use of the silylated Cu(II) complex. After removal of the surfactant and de-metalation, the incorporated tetraamine was quantitatively complexed by CuCl(2) and the material has shown after thermal activation that a reversible bindin…

Carbon MonoxideSilicon dioxideLigandNitrogenMetal ions in aqueous solutionOrganic ChemistryInorganic chemistryCationic polymerizationElectron Spin Resonance Spectroscopychemistry.chemical_elementGeneral ChemistrySilicon DioxideCopperCatalysisAdductOxygenchemistry.chemical_compoundchemistryCoordination ComplexesTripodal ligandPolymer chemistryReactivity (chemistry)AminesPorosityCopperChemistry (Weinheim an der Bergstrasse, Germany)
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Sensor Properties of Pristine and Functionalized Carbon Nanohorns

2016

Nanodispersions of pristine single-wall carbon nanohorns (i.e., p-SWCNHs) and oxidized-SWCNHs (i.e.; o-SWCNHs) were used to modify screen printed electrode (SPE). p-SWCNHs and o-SWCNHs were fully characterized by using several analytical techniques, as: HR-TEM (High Resolution-Transmission Electron Microscopy), FE-SEM/EDX (Field Emission-Scanning Electron Microscopy/Energy Dispersive X-ray Analysis), Raman spectroscopy, thermogravimetric analysis, differential thermal analysis (DTA), and the Brunauer-Emmett-Teller (BET) method. The chemically modified SPEs were also characterized with Cyclic Voltammetry (CV), using several different electro-active targets. In all cases, p-SWCNHs showed bett…

Carbon NanohornThermogravimetric analysisScreen Printed ElectrodesMaterials scienceAnalytical chemistrychemistry.chemical_element02 engineering and technologyGlassy carbon010402 general chemistryElectrochemistry01 natural sciencesCarbon NanohornsAnalytical Chemistrysymbols.namesakeDifferential thermal analysisElectrochemistrySettore CHIM/01 - Chimica AnaliticaSingle-WallCarbon Nanohorns; Screen Printed Electrodes; Single-Wall; Analytical Chemistry; ElectrochemistryScreen Printed Electrode021001 nanoscience & nanotechnology0104 chemical scienceschemistryElectrodesymbolsCyclic voltammetry0210 nano-technologyRaman spectroscopyCarbonElectroanalysis
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Studies on ultramicro- and trace analysis of organic substances

1965

Summary For the determination of about 1 μg hydrogen in nonvolatile organic compounds 10–40 μg of the substance are burnt at > 1000°C in a slow stream of oxygen. The water generated is converted to H 2 S by reaction with carbon disulfide in a flow of nitrogen at 500°C catalyzed by α-Al 2 O 3 . The hydrogen sulfide is argentimetrically titrated by a potentiometric method. The standard deviation of the method is ± 10 ng H. There are no interferences by N, S, and the halogens.

Carbon disulfideHydrogenHydrogen sulfideInorganic chemistrychemistry.chemical_elementNitrogenOxygenAnalytical ChemistryCatalysischemistry.chemical_compoundchemistryHalogenElectroanalytical methodSpectroscopyMicrochemical Journal
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