Search results for "Spectroscopy"

showing 10 items of 10293 documents

Enhancement of sensitivity in high-resolution stimulated Raman spectroscopy of gases: Applicaion to the 2ν2 (1285 cm−1) band of CO2

1990

The application of a multiple-pass gas cell to quasi-cw stimulated Raman scattering is demonstrated to be a powerful method for significantly increasing the sensitivity. As a consequence, such a device offers the possibility of working in the 0.1–1 Torr pressure range for weak bands. As a striking example, experimental results are given for the 2ν2 band of CO2 at 1285 cm−1. The band is almost completely resolved with a very good signal-to-noise ratio. The Raman frequencies and the collisional broadening coefficients are determined as a function of quantum number J. Moreover, the possibility of auto-stimulated Raman effect on CO2 at moderate pressure via the sharp ν1 band (1388 cm−1) is demo…

chemistry.chemical_classificationChemistryTriatomic moleculeAnalytical chemistryQuantum numberMolecular physicssymbols.namesakeTorrsymbolsGeneral Materials ScienceCoherent anti-Stokes Raman spectroscopyRaman spectroscopySpectroscopyInorganic compoundSpectroscopyRaman scatteringJournal of Raman Spectroscopy
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Stabilization of polynuclear plutonium(IV) species by humic acid

2014

Abstract Although the formation of tetravalent plutonium (Pu(IV)) polymers with natural organic matter was previously observed by spectroscopy, there is no quantitative evidence of such reaction in batch experiments. In the present study, Pu(IV) interaction with humic acid (HA) was investigated at pH 1.8, 2.5 and 3, as a function of HA concentration and for Pu total concentration equal to 6 × 10−8 M. The finally measured Pu(IV) concentrations ([Pu(IV)]eq) are below Pu(IV) solubility limit. Pu(IV)–HA interaction can be explained by the complexation of Pu(IV) monomers by HA up to [Pu(IV)]eq ∼ 10−8 M. However, the slope of the log–log Pu(IV)–HA binding isotherm changes from ∼0.7 to ∼3.5 for hi…

chemistry.chemical_classificationChemistrychemistry.chemical_elementPlutoniumchemistry.chemical_compoundHydrolysisMonomerTetramerGeochemistry and PetrologyHumic acidSolubilitySpectroscopyStoichiometryNuclear chemistryGeochimica et Cosmochimica Acta
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Water-induced local ordering of chitosan polymer chains in thin layer films

2015

International audience; Carbon-13 NMR (CP-MAS and FSLG 1H–13C HETCOR) have been applied to chitosan salt films synthesized in acetic acid and exposed to different relative humidity environments (32% or 75%) at 20 °C for 1 month. It gives insight in the relationship between structure and functional properties according to the hydration level of this biomaterial as a film. The acetate ions trapped in the chitosan act as structuring agents between chitosan chains for the low hydration state. But, increasing the moisture content induces spontaneous removal of acetic acid and a subsequent modification in the film structure, with an increase in local ordering. HETCOR experiments also showed a mul…

chemistry.chemical_classificationChitosanMagnetic Resonance SpectroscopyPolymers and PlasticsPolymersOrganic ChemistryActive packagingBiomaterialWaterStructureGlycosidic bondPolymerControlled releaseNMRChitosanAcetic acidchemistry.chemical_compoundchemistryPolymer chemistryMaterials Chemistry[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyMultiplicity (chemistry)Polymer[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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Near infrared dyes by combination of squaraine and ferrocene chromophores

2000

Abstract Squaraines represent a class of compounds which attracts a lot of attention in materials science. A synthetic sequence for the preparation of the symmetrical squaraines 12a , b , which contain ferrocene units as electron donors, is described. The compounds exhibit, in dichloromethane or chloroform, two intense absorption bands. One of them is located at 641/650 nm—a normal region for squaraines; however, the other band is strongly shifted to long wavelengths and has its maximum at 921/961 nm. Alkyl sidechains enhance the solubility of 12a , b , which represent a new type of NIR dyes.

chemistry.chemical_classificationChloroformOrganic ChemistryNear-infrared spectroscopyChromophorePhotochemistryBiochemistrychemistry.chemical_compoundchemistryFerroceneDrug DiscoveryAbsorption (chemistry)SolubilityAlkylDichloromethaneTetrahedron Letters
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Interaction of aminomethylated resorcinarenes with rhodamine B

2009

The interaction of aminomethylated resorcinarenes with a red xanthene dye, rhodamine B, was investigated in chloroform, methanol and chloroform–methanol solutions using UV-vis, NMR and fluorescence spectroscopy. Aminomethylated resorcinarenes 1 and 2 shift the rhodamine B equilibrium from the zwitterion to the lactone form unlike reference compounds 3 and 4, which do not contain tertiary amino groups at the upper rim, giving an example of how supramolecular hosts can influence the equilibrium of rhodamine B isomers.

chemistry.chemical_classificationChloroformSupramolecular chemistryGeneral ChemistryPhotochemistryCatalysisFluorescence spectroscopychemistry.chemical_compoundchemistryXanthene dyeZwitterionMaterials ChemistryRhodamine BMethanolLactoneNew Journal of Chemistry
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Modelling retention and peak shape of small polar solutes analysed by nano-HPLC using methacrylate-based monolithic columns.

2019

Abstract The development of methacrylate-based monolithic columns was studied for the separation of pharmaceutical hydrophilic compounds in nano-liquid chromatography. The selected polymerisation mixture consisted of 7.5% hexyl methacrylate, 4.5% methacrylic acid and 18.0% ethylene dimethacrylate (w/w), in a binary porogenic solvent (35:35 w/w 1-propanol/1,4-butanediol). The polymer synthesised with this mixture has a good permeability, not excessive back-pressure, and reasonable retention times for polar and non-polar solutes. Monolithic columns (12 cm total capillary length, 100 μm i.d.), prepared with this mixture, were able to produce hydrogen bonding and electrostatic interactions, giv…

chemistry.chemical_classificationChromatography010401 analytical chemistry02 engineering and technologyPolymer021001 nanoscience & nanotechnologyMethacrylate01 natural sciencesBiochemistryHigh-performance liquid chromatography0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundchemistryMethacrylic acidEnvironmental ChemistryAlkylbenzenesParticle size0210 nano-technologySelectivitySpectroscopyAnalytica chimica acta
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Spectrophotometric Determination of Cystine with O-Phthalaldehyde in the Absence of Thiol

1988

Abstract A spectrophotometric method for the determination of cystine with o-phthalaldehyde (OPA) in the absence of thiol is described. When cystine is heated at 60[ddot]C for 30 min in a low excess of OPA (pH 9.5), a very stable derivative with 1:2 stoichiometry (cystine:OPA) and an absorption maximum at 335 nm (E = 4600) is formed. At pH < 1 the derivative is protonated (protonation constants: log K1 = 5.88 and log K2 = 3.70 at I = 0.1 and 20[ddot]C) and another absorption band at 440 nm (E = 3800) appears, which allows the determination of cystine in the presence of other amino acids.

chemistry.chemical_classificationChromatographyBiochemistry (medical)Clinical BiochemistryCystineProtonationBiochemistryAnalytical ChemistryAmino acidchemistry.chemical_compoundO-PhthalaldehydechemistryElectrochemistryThiolAbsorption (chemistry)SpectroscopyDerivative (chemistry)StoichiometryNuclear chemistryAnalytical Letters
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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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Chiral separation of ephedrines by liquid chromatography using β-cyclodextrins

2001

β-cyclodextrins (β-CDs) have been evaluated as chiral recognition agents for the enantioseparation of ephedrines by liquid chromatography (LC). The compounds tested were norephedrine, ephedrine, pseudoephedrine, N-methylephedrine and N-methylpseuoephedrine. Two possibilities have been investigated, the employment of a chiral stationary phase consisting of immobilized β-cyclodextrin, and the addition of the chiral selector to the mobile phase. In the latter approach the following chiral agents have been assayed, native β-cyclodextrin (β-CD), methyl-β-cyclodextrin (M-β-CD), carboxyethyl-β-cyclodextrin (CE-β-CD), carboxymethyl-β-cyclodextrin (CM-β-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD)…

chemistry.chemical_classificationChromatographyCyclodextrinBiochemistryAnalytical ChemistryNasal decongestantChiral column chromatographySolventchemistryIonic strengthmedicineEnvironmental ChemistryEphedrineEnantiomerChiral derivatizing agentSpectroscopymedicine.drugAnalytica Chimica Acta
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Thermodynamic Properties of Sodium n-Alkanecarboxylates in Water and in Water + Cyclodextrins Mixtures

1998

Densities and heat capacities of water−substrate, water−cyclodextrin, and water−substrate−cyclodextrin systems were determined at 298 K. The substrates studied are sodium n-alkanecarboxylates (CnCOONa) (from sodium acetate to sodium decanoate) and the cyclodextrins are hydroxypropyl-α-cyclodextrin (HP-α-CD), hydroxypropyl-β-cyclodextrin, (HP-β-CD), hydroxypropyl-γ-cyclodextrin (HP-γ-CD) and β-cyclodextrin (β-CD). The apparent molar volumes and heat capacities of CnCOONa in water were calculated as functions of concentration. The standard partial molar properties agree with those obtained by using the additivity rule. HP-β-CD essentially does not affect the thermodynamic properties of C1COON…

chemistry.chemical_classificationChromatographyCyclodextrinSodiumInorganic chemistrySubstrate (chemistry)chemistry.chemical_elementPartial molar propertySurfaces and InterfacesCondensed Matter PhysicsHeat capacitychemistry.chemical_compoundMolar volumechemistryElectrochemistryGeneral Materials ScienceSodium acetateSpectroscopyEquilibrium constantLangmuir
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