Search results for "Spectroscopy"

showing 10 items of 10293 documents

Tin(IV) catalyzed D-galacturonic acid anomerization

2008

A comparative kinetic study of anomerization between the four main forms (alpha/beta-pyranosides and alpha/beta-furanosides) of D-galacturonic acid (GalAH(2), 1) and tin(IV) complexed D-galacturonate ([Sn(CH(3))(2)(GalA)(H(2)O)(2)], 2) in D(2)O, is reported. Important differences are shown by pD vs. mutarotation rate profiles of 1 and 2. Coordination, in fact, causes: i) a spectacular increase of the rate due to kinetic template assistance of the carboxylic tail holding the metal in close proximity to the reactive centre and ii) a change in the dependence of the rate on the pD. Entropic and enthalpic factors contribute to the huge activation energy decrease in 2. Anomerization rates of the …

AnomerMagnetic Resonance SpectroscopyRotationStereochemistrychemistry.chemical_elementMedicinal chemistryMutarotationCatalysisCatalysiskinetic template effectInorganic Chemistrychemistry.chemical_compoundReaction rate constantNMR spectroscopyNucleophilegalacturonic acidanomerizationTin(IV)/ NMR kinetic / Galacturonic / 119SnHexuronic AcidsTin CompoundsStereoisomerismRing sizeKineticschemistryNMR spectroscopy; kinetic template effect; galacturonic acid; Tin(IV) catalysis; anomerizationTinTin(IV) catalysisD-Galacturonic acid
researchProduct

Synthesis, characterization and the first crystal structure of the Zn(II) complex of 4,6-O-ethylidine-N-(2-hydroxybenzylidene)-β-D-glucopyranosylamine

2001

4,6-O-Ethylidine-N-(2-hydroxybenzylidene)-β-D-glucopyranosylamine (H3L1) and N-(5-bromo-2-hydroxybenzylidene-4,6-O-ethylidine-β-D-glucopyranosylamine (H3L2) molecules possessing a–C-1–N=C(H)–moiety for metal-ion binding were synthesized by condensing the 4,6–O–ethylidene–β–D–glucopyranosylamine with salicylaldehyde or 5–bromosalicylaldehyde. Complexes of these ligands with Zn(II) were isolated and characterized using elemental analysis, FTIR, UV–Vis absorption, NMR spectroscopic and FAB mass spectrometric techniques. The structure of the Zn(II) complex derived from H3L1 was established for the first time by a single-crystal X-ray diffraction study. The anomeric nature of the saccharide moie…

AnomerMagnetic Resonance SpectroscopyStereochemistrySynthesis (Chemical)Crystal structureCrystallography X-RayLigandsBiochemistryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundX-Ray DiffractionOrganometallic CompoundsMoietyMoleculeFourier transform infrared spectroscopyGlucosamineMolecular StructureLigandChemistryOrganic ChemistryGeneral MedicineCrystallographyZincSalicylaldehydeProton NMRCrystal StructureSpectrophotometry UltravioletComplexationIndraStra Global
researchProduct

Synthesis, characterization and X-ray structure of glycosyl-1,2-isoxazoles and glycosyl-1,2-isoxazolines prepared via 1,3-dipolar cycloaddition

2013

Abstract A convenient preparative method of a series of glycosyl-1,2-isoxazoles ( 6–11 ) and glycosyl-1,2-isoxazolines ( 15–20 ) by a simple and efficient 1,3-dipolar cycloaddition of a series of aryl nitrile oxide, generated in situ from aryl oximes ( 4–5 ), with a variety of O -propargyl glycosyles ( 1 – 3 ) or O -allyl glycosyles ( 12–14 ) respectively, is reported. The carbohydrate-containing 1,2-isoxazoles and 1,2-isoxazolines compounds were isolated in excellent yields (81–91%) and they were fully characterized by 1 H, 13 C NMR and mass spectrometry. The relative stereochemistry of the glycosyl-1,2-isoxazole 10 was confirmed by single crystal X-ray analysis. The molecular structure of…

AnomerNitrileChemistryStereochemistryArylOrganic ChemistryAcetalCycloadditionAnalytical ChemistryInorganic Chemistrychemistry.chemical_compound13-Dipolar cycloadditionPropargylGlycosylSpectroscopyJournal of Molecular Structure
researchProduct

Interaction of metal ions with D-glucobenzothiazoline: isolation and characterization of the resultant products

2002

Six different metal-ion complexes of D-glucobenzothiazoline were synthesized and characterized by analytical and spectral techniques. Formation of different types of species (ML and ML2) were observed with Cu2+, Ag+, Cd2+, Hg2+, and Zn2+ ions. Existence of an anomeric mixture in the case of the Cu2+ complex is identified from the EPR spectra, and the results were further supported by the simulated spectra. The structures were proposed based on different studies.

AnomerSilverStereochemistryMetal ions in aqueous solutionSynthesis (Chemical)BiochemistrySpectral lineAnalytical ChemistryD-glucobenzothiazolinelaw.inventionIonlawGlucobenzothiazolineBenzothiazolesElectron paramagnetic resonanceMercury (Metal)ChemistrySpectrum AnalysisOrganic ChemistrySpectrum AnalyzersElectron Spin Resonance SpectroscopyGeneral MedicineMercuryCharacterization (materials science)ThiazolesZincGlucoseMetalsPhysical chemistryStructure (Composition)CopperCadmiumIndraStra Global
researchProduct

Inhibitoren der Korrosion (11). Nachweis der auf Eisengrenzflächen gebildeten Sekundärinhibitoren durch UV-Absorptions- und Fluoreszenzspektroskopie

1972

Aus Triphenylbenzylphosphoniumchlorid bildet sich in saurer Losung auf der Eisenoberflache eine Schicht, die aufgrund der UV-Reflexionsspektroskopie mit Triphenylphosphin identisch sein durfte. Auch das Mono- und Bis-Phosphoniumsalz wird an der Eisengrenzflache reduktiv abgebaut; die dabei entstehenden Anthracenderivate werden auf dieselbe Weise identifiziert. Es handelt sich um Methylanthracen. Die zur weiteren Aufgliederung der Reaktionsprodukte vorgenommene dunnschicht-chromatografische Auftrennung (Untersuchung des Extrakts in Cyclohexanol und Methanol) ergibt kein sich deutlich unterscheidenden Fluoreszenzspektren. Identification, by UV absorption and fluorescence spectroscopy, of the …

AnthraceneMechanical EngineeringMetals and AlloysCyclohexanolGeneral MedicineChlorideFluorescence spectroscopyThin-layer chromatographySurfaces Coatings and Filmschemistry.chemical_compoundchemistryMechanics of MaterialsPolymer chemistryMaterials ChemistrymedicineEnvironmental ChemistryMethanolSpectroscopyPhosphinemedicine.drugMaterials and Corrosion/Werkstoffe und Korrosion
researchProduct

Radioactively labelled epoxides. part V. Tritium labelled K-region oxides and trans-dihydrodiols of pyrene, benzo[a]pyrene and dibenz[a, h]anthracene

1987

Tritium labelled K-region oxides of pyrene, benzo[a]pyrene and dibenz[a,h]anthracene have been prepared by cyclization of the corresponding trans-dihydrodiols which were obtained by reduction of K-region quinones with sodium borotritide in the presence of oxygen. This synthetic pathway not only yields two metabolically important radioactively labelled derivatives of polycyclic aromatic hydrocarbons in a simple and efficient manner, but also requires a rather inexpensive source of tritium.

AnthraceneOrganic Chemistrychemistry.chemical_elementBiochemistryMedicinal chemistryOxygenAnalytical Chemistrychemistry.chemical_compoundchemistryBenzo(a)pyreneDrug Discoverypolycyclic compoundsDibenz(ah)anthracenePyreneOrganic chemistryRadiology Nuclear Medicine and imagingTritiumSpectroscopySodium borotritideJournal of Labelled Compounds and Radiopharmaceuticals
researchProduct

Anthracene Fluorescence Quenching by a Tetrakis (Ketocarboxamide) Cavitand

2014

Quenching of both fluorescence lifetime and fluorescence intensity of anthracene was investigated in the presence of a newly derived tetrakis (ketocarboxamide) cavitand at various concentrations. Time-correlated single photon counting method was applied for the lifetime measurements. A clear correlation between the fluorescence lifetime of anthracene as a function of cavitand concentration in dimethylformamide solution was observed. The bimolecular collisional quenching constant was derived from the decrease of lifetime. Fluorescence intensity was measured in the emission wavelength region around 400 nm as a result of excitation at 280 nm. Effective quenching was observed in the presence of…

AnthraceneQuenching (fluorescence)Article SubjectChemistryAnalytical chemistryCavitandPhotochemistryseoksetFluorescenceAtomic and Molecular Physics and OpticsPhoton countingcarbon-tetrachlorideAnalytical Chemistrychemistry.chemical_compoundWavelengthlcsh:QC350-467Dimethylformamideta116stern-volmer plotslcsh:Optics. LightSpectroscopyExcitationJournal of Spectroscopy
researchProduct

The different redox-activity of dianthrylbenzene and dianthrylbiphenyl

1989

Abstract The reduction of dianthrylbenzene and dianthrylbiphenyl to stable tetraanion salts is described by NMR spectroscopy and cyclic voltammetry. The significantly different Coulomb interactions between the anthracene units are compared with those in dianthrylalkanes.

Anthracenechemistry.chemical_compoundchemistryOrganic ChemistryDrug DiscoveryInorganic chemistryNuclear magnetic resonance spectroscopyCyclic voltammetryBiochemistryRedox ActivityTetrahedron Letters
researchProduct

Atomic fluorescence determination of total and inorganic arsenic species in beer

2001

A simple and nearly direct procedure has been developed for the determination of As in beers, based on hydride generation and atomic fluorescence detection. Using 2 mol l−1 HCl with a carrier flow of 6 ml min−1, 3% m/v NaBH4 with a flow of 1.3 ml min−1, a reaction coil of 200 cm and an argon flow of 400 ml min−1, total arsenic in beer could be determined in samples diluted 1∶10 with a final concentration of 2 mol l−1 HCl, 1% m/v KI and 0.08% v/v of an antifoam agent. For the estimation of AsIII and AsV concentrations in beer samples, the difference between the analytical sensitivities of the fluorescence signals obtained for As hydride, without and with previous treatment of samples with KI…

Antifoam agentDetection limitAtomic fluorescenceAshingInorganic arsenicChemistryHydrideAnalytical chemistrychemistry.chemical_elementFluorescenceSpectroscopyArsenicAnalytical ChemistryJ. Anal. At. Spectrom.
researchProduct

A New Phenanthrene Glycoside and Other Constituents from Dioscorea opposita

2005

Phytochemical investigation of the rhizome of Dioscorea opposita has led to the isolation of a new phenanthrene glycoside, 3,4,6-trihydroxyphenanthrene-3-O-beta-D-glucopyranoside (1), and five known compounds, soyacerebroside I (2), adenosine (3), beta-sitosterol (4), palmitic acid (5) and palmitoyloleoylphosphatidylcholine (6). Their structures were determined by spectroscopic methods, including 1D- and 2D-NMR. Compounds 1-6 exhibited no antifungal activity against the human pathogenic yeasts Candida albicans, C. glabrata and C. tropicalis.

Antifungal AgentsMagnetic Resonance SpectroscopyDioscoreaceaeMicrobial Sensitivity TestsPalmitic acidchemistry.chemical_compoundDrug DiscoverymedicineGlycosidesCandida albicansCandidachemistry.chemical_classificationMolecular StructureTraditional medicinebiologyDioscoreaPlant ExtractsGlycosideGeneral ChemistryGeneral MedicinePhenanthrenesPhenanthrenebiology.organism_classificationAdenosineRhizomechemistryBiochemistryPhytochemicalDioscoreaRhizomemedicine.drugChemical and Pharmaceutical Bulletin
researchProduct