Search results for "spectrum"

showing 10 items of 2043 documents

Studies on coordination compounds vii, chromatographic, thermoanalytical and spectroscopic studies on thermal decomposition of cadmium(II) and lead(I…

1982

On the basis of decomposition temperatures and infrared spectra, cadmium(II) and lead(II) bissalicylaldoximates were considered to havetrans andcis structures, respectively.

chemistry.chemical_classificationCadmiumChemistryThermal decompositionInorganic chemistrychemistry.chemical_elementInfrared spectroscopy010402 general chemistry01 natural sciencesDecomposition010406 physical chemistry0104 chemical sciencesCoordination complexMass spectrumPyrolysisJournal of Thermal Analysis
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Elucidation of structure and microheterogeneity of the polypeptide antibiotics paracelsin and trichotoxin A-50 by fast atom bombardment mass spectrom…

1984

Specific and sensitive procedures have been developed which enabled the structure elucidation of the polypeptide antibiotics (peptaibols), paracelsin isolated from Trichoderma reesei, and of trichotoxin A-50 from Trichoderma viride, by fast atom bombardment and field desorption mass spectrometry. Both peptides were found to exhibit a pronounced microheterogeneity by single and multiple exchange of amino acids. Separation by analytical and semipreparative high-performance liquid chromatography (HPLC) on octadecylsilyl-bonded, reversed-phase columns afforded a series of sequence analogues for each polypeptide. Unequivocal molecular weight and sequence identifications were obtained by positive…

chemistry.chemical_classificationChromatographyChemistryStereochemistryFast atom bombardmentMass spectrometryHigh-performance liquid chromatographyAmino acidchemistry.chemical_compoundField desorptionTrifluoroacetic acidMass spectrumPeptide bondSpectroscopyBiological Mass Spectrometry
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Characterization of commercial synthetic resins by pyrolysis-gas chromatography/mass spectrometry: application to modern art and conservation.

2009

To characterize a set of synthetic resins, a methodology by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) has been developed. The studied reference materials were commercial versions of a wide range of synthetic resins. For each polymer, the pyrolytic and chromatographic conditions were optimized to adequately resolve the fragment mixture in a short time. The proposed analytical method does not require previous treatment of the sample, and due to its high sensitivity, only a small sample quantity in the microgram range can be used. The pyrolysis temperature was found to have little effect on the obtained pyrograms. The summarized data set for the individual polymer materials, es…

chemistry.chemical_classificationChromatographyChromatographySynthetic resinChemistrySpectrometryChromatographic analysisObjectes d'art--Conservació i restauracióPyrolysis-gasPolymerMass spectrometryAnalytical methodSpectrum analysisAnalytical ChemistryCharacterization (materials science)Anàlisi espectralchemistry.chemical_compoundPyrolysis–gas chromatography–mass spectrometryMonomerArt objects--Conservation and restorationPyrolytic carbonCromatografiaSynthetic resinsModern artPyrolysisAnalytical chemistry
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Gaschromatographisch-massenspektrometrische identifizierung der durch umsetzung von aminen mit isocyanaten gebildeten harnstoffderivate

1977

Abstract Gas chromatographic-mass spectrometric identification of urea derivatives formed by the reaction of amines with isocyanates N,N′-Di- and N,N′,N′-trisubstituted ureas constitute suitable derivatives for the gas chromatographic (GC) determination of primary and secondary amines. The GC identification of N- tert. -butyl-,N′,N′-alkyl urea derivatives presented in the first communication has been succesfully confirmed by mass spectrometry (MS) and mass fragmentometry. The reproduced mass spectra of six N- tert. -butyl-,N′,N′-alkyl ureas were interpreted according to the decomposition mechanisms of less complicated alkyl ureas known from the literature. Using combined GC-MS the detection…

chemistry.chemical_classificationDetection limitChromatographyChemistryMass fragmentometryOrganic ChemistryGeneral MedicineMass spectrometryBiochemistryAnalytical ChemistryMass spectrumOrganic chemistryKovats retention indexUrea derivativesAlkylJournal of Chromatography A
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Rapid classification of enzymes in cleaning products by hydrolysis, mass spectrometry and linear discriminant analysis

2008

A method for the rapid classification of proteases, lipases, amylases and cellulases used as enhancers in cleaning products, based on precipitation with acetone, hydrolysis with HCl, dilution of the hydrolysates with ethanol, and direct infusion into the electrospray ion source of an ion-trap mass spectrometer, has been developed. The abundances of the ([M+H]+ ions of the amino acids, from the hydrolysates of both the enzyme industrial concentrates and the detergent bases spiked with them, were used to construct linear discriminant analysis models, capable of distinguishing between the enzyme classes. For this purpose, the variables were normalized as follows: (A) the ion abundance of each …

chemistry.chemical_classificationElectrosprayChromatographybiologyHydrolasesChemistryHydrolysisOrganic ChemistryDiscriminant AnalysisCellulaseMass spectrometryMass SpectrometryHydrolysateIon sourceAnalytical ChemistryAmino acidHydrolysisMass spectrumbiology.proteinSpectroscopyRapid Communications in Mass Spectrometry
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Positive and negative electrospray ionization-collision-induced dissociation of sulfur- containing zwitterionic liquids.

2011

The mass spectrometric properties of several (1,2-dimethyl-1 H-imidazol-3-ium-3-yl)-alkane-1-sulfonates (alkane=ethyl, propyl and butyl) are investigated in this study. These substances, named zwitterionic liquids (ZILs), were synthesized using classical transformations and analyzed in positive and negative electrospray ionization mode using collision-induced dissociation (0–50 eV). We have also performed regioselective deuterium labeling of the alkyl chain of 3-(1,2-dimethyl-1 H-imidazol-3-ium-3-yl)-propane-1-sulfonates. Thus, the mass spectra of isotopically-labeled compounds were used for the confirmation of fragmentation pathways of ZILs. Briefly, the data obtained in this study show t…

chemistry.chemical_classificationElectrosprayCollision-induced dissociationElectrospray ionizationInorganic chemistryGeneral MedicinePhotochemistryAtomic and Molecular Physics and OpticsDissociation (chemistry)chemistry.chemical_compoundSulfonatechemistryFragmentation (mass spectrometry)Mass spectrumSpectroscopyAlkylEuropean journal of mass spectrometry (Chichester, England)
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Peptide–Membrane Interactions Monitored by Fluorescence Lifetime Imaging: A Study Case of Transportan 10

2021

The interest on detailed analysis of peptide-membrane interactions is of great interest in both fundamental and applied sciences as these may relate to both functional and pathogenic events. Such interactions are highly dynamic and spatially heterogeneous, making the investigation of the associated phenomena highly complex. The specific properties of membranes and peptide structural details, together with environmental conditions, may determine different events at the membrane interface, which will drive the fate of the peptide-membrane system. Here, we use an experimental approach based on the combination of spectroscopy and fluorescence microscopy methods to characterize the interactions …

chemistry.chemical_classificationFluorescence-lifetime imaging microscopyChemistryRecombinant Fusion ProteinsSpectrum AnalysisGalaninWasp VenomsPeptideSurfaces and InterfacesCondensed Matter PhysicsFluorescenceArticleMembraneMicroscopy FluorescenceAmphiphileElectrochemistryFluorescence microscopeHigh spatial resolutionBiophysicsPeptide−Membrane Interactions FLIM Transportan 10 PhasorGeneral Materials SciencePeptidesSpectroscopySpectroscopyLangmuir
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On the stability of the 24-meric hemocyanin from Eurypelma californicum.

1998

The stability of the 24-meric hemocyanin from Eurypelma californicum towards various denaturants (GdnHCl, urea, urea derivatives and salts of the Hofmeister series) indicates that the quaternary structure is stabilized by hydrophilic and polar forces. Thus, the interaction between the seven different subunit types of this cheliceratan hemocyanin is comparable with that of the closely related crustacean hemocyanins. In contrast, no significant influence of divalent ions such as Ca2+ and Mg2+ on the stability is observed at pH 8.0 and pH 8.5 but not at pH 7.0. Studies, both in the presence of urea and GdnHCl indicate that the denaturation process consists of a dissociation of the oligomeric s…

chemistry.chemical_classificationHofmeister seriesStereochemistryProtein subunitmedicine.medical_treatmentSpectrum AnalysisBiophysicsHemocyaninBiochemistryDissociation (chemistry)Divalentchemistry.chemical_compoundBiochemistrychemistryStructural BiologyHemocyaninsUreamedicineAnimalsProtein quaternary structureEurypelma californicumMolecular BiologyArthropodsBiochimica et biophysica acta
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Hydrogen-carbon, carbon-carbon double rearrangement induced by proximity effects. 1-formation of methoxybenzyl ions in the electron impact mass spect…

1991

The 75 eV electron impact mass spectra of 1,1-bis(dimethoxyphenyl)methanes bearing o-methoxy groups are dominated by intense peaks corresponding, at least formally, to benzyl ions [(CH3O)2C6H3CH2]+(b). They arise from ions [((CH3O)2C6H3)2CH]+(a), which are in turn formed from molecular ions by loss of an alkyl radical through benzylic cleavage. The analysis of compounds labelled with 2H or 13C at methoxy groups led to the determination of the mechanism. Hydrogen migration, as hydride, followed by electrophilic substitution by the methylene carbon of the phenyl methylene ether cation through a six-centred transition state is responsible for the formation of benzylic ions b.

chemistry.chemical_classificationHydrogenHydridechemistry.chemical_elementEtherPhotochemistryBiochemistryMedicinal chemistrychemistry.chemical_compoundElectrophilic substitutionchemistryMass spectrumMolecular MedicineMethyleneInstrumentationSpectroscopyElectron ionizationAlkylOrganic Mass Spectrometry
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Evaporation of tungsten oxides: A mass-spectrometric study of the vapour contents

1995

Abstract The evaporation of bulk oxides of WO2 and WO3 and oxidised tungsten surfaces (metallic tungsten heated in an oxygen atmosphere) have been studied by the means of mass-spectrometry. The principal constituents of the vapour are found to be molecules of WO2, WO3, W2O6 and W3O9. These results differ from earlier reports, where the presence of molecules smaller than W3O9 in the mass-spectrum was interpreted as an artifact due to electron impact dissociation of larger polymers.

chemistry.chemical_classificationInorganic chemistryAnalytical chemistrychemistry.chemical_elementPolymerTungstenequipment and suppliesCondensed Matter PhysicsMass spectrometryDissociation (chemistry)Surfaces Coatings and FilmsMetalchemistryvisual_artMass spectrumvisual_art.visual_art_mediumMoleculeInstrumentationElectron ionizationVacuum
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