Search results for "Oxalates"

showing 10 items of 13 documents

Effect of cooking on oxalate content of pulses using an enzymatic procedure.

2003

An enzymatic method proposed for the determination of oxalate in urine is adapted for the estimation of soluble oxalate content in beans, chickpeas and lentils. Oxalates were extracted in water by refluxing for 2 h. The method is based on the oxidation of oxalate by the oxidase and the determination of the resulting hydrogen peroxide, which in presence of peroxidase, 3-methyl-2 benzotiazinolone and 3-dimethylamino benzoic, gives an indamine compound with an absorption maximum at 590 nm. The linearity (from 0.015 to 0.6 mM) of the method is adequate to the analysis of oxalate contents in pulses, and the inter-day precision of the method expressed as relative standard deviation was good (3.01…

Absorption (pharmacology)chemistry.chemical_classificationOxalatesChromatographyHot TemperaturebiologyChemistryFood HandlingInorganic chemistryRelative standard deviationFabaceaeSoluble oxalateOxalateFood handlingchemistry.chemical_compoundEnzymebiology.proteinHydrogen peroxideMicrowavesNutritive ValueFood SciencePeroxidaseInternational journal of food sciences and nutrition
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Automated pre-column derivatization of amines in biological samples with dansyl chloride and with or without post-column chemiluminescence formation …

1999

On-line automation of two different liquid chromatographic procedures, a pre-column derivatization system and a pre- and post-column system, in order to generate chemiluminescence is reported. Dansyl chloride (Dns-Cl) was used as a pre-column reagent to form fluorophores and bis(2,4,6-trichlorophenyl) oxalate (TCPO) and hydrogen peroxide (H2O2) as a post-column reagent to generate chemiluminescence. This procedure is based on the employment of a primary column packed with C18 material inserted in a multi-dimensional assembly for sample clean-up and derivatization with Dns-Cl. The dansyl derivatives formed are transferred and separated in a LiChrospher 100 RP18 analytical column (125 x 4 mm …

BiochemistryAnalytical Chemistrylaw.inventionMethamphetaminechemistry.chemical_compoundColumn chromatographylawElectrochemistryEnvironmental ChemistryHumansTCPOAminesHydrogen peroxideDerivatizationSpectroscopyChemiluminescenceDansyl CompoundsOxalatesChromatographyChemistryDansyl chlorideAmphetamineReagentLuminescent MeasurementsIndicators and ReagentsQuantitative analysis (chemistry)Chromatography LiquidThe Analyst
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Labeling and preliminary in vivo assessment of niobium-labeled radioactive species: A proof-of-concept study.

2016

Abstract The application of radionuclide-labeled biomolecules such as monoclonal antibodies or antibody fragments for imaging purposes is called immunoscintigraphy . More specifically, when the nuclides used are positron emitters, such as zirconium-89, the technique is referred to as immuno-PET . Currently, there is an urgent need for radionuclides with a half-life which correlates well with the biological kinetics of the biomolecules under question and which can be attached to the proteins by robust labeling chemistry. 90 Nb is a promising candidate for in vivo immuno-PET , due its half-life of 14.6h and low β + energy of E mean =0.35MeV per decay. 95 Nb on the other hand, is a convenient …

Cancer ResearchPathologymedicine.medical_specialtyBiodistributionmedicine.drug_classMetaboliteNiobiumDeferoxamineMonoclonal antibody030218 nuclear medicine & medical imagingImmunoscintigraphy03 medical and health scienceschemistry.chemical_compoundMice0302 clinical medicineChloridesDrug StabilityIn vivomedicineAnimalsRadiology Nuclear Medicine and imagingTissue DistributionRadioisotopesOxalatesChemistryIn vitroBevacizumab030220 oncology & carcinogenesisIsotope LabelingPositron-Emission TomographyBiophysicsMolecular MedicineSpecific activityFemaleEx vivoHalf-LifeNuclear medicine and biology
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Ferromagnetic coupling and magnetic anisotropy in oxalato-bridged trinuclear chromium(iii)-cobalt(ii) complexes with aromatic diimine ligands

2010

Two novel heterotrinuclear chromium(III)-cobalt(II) complexes of formula {[Cr(III)(bpy)(ox)(2)](2)Co(II)(Me(2)bpy)}.2H(2)O (1) and {[Cr(III)(phen)(ox)(2)](2)Co(II)(Me(2)bpy)}.1.5H(2)O (2) [ox = oxalato, bpy = 2,2'-bipyridine, Me(2)bpy = 6,6'-dimethyl-2,2'-bipyridine, and phen = 1,10-phenanthroline] have been synthesized using the "complex-as-ligand/complex-as-metal" strategy. The X-ray crystal structure of 2 consists of neutral oxalato-bridged Cr(III)(2)Co(II) bent entities formed by the coordination of two anionic [Cr(III)(phen)(ox)(2)](-) complexes through one of their oxalato groups toward a cationic cis-[Co(II)(Me(2)bpy)](2+) complex. The three tris(chelated), six-coordinated metal atom…

ChromiumModels MolecularOxalatesMolecular StructureChemistryStereochemistrySupramolecular chemistryStereoisomerismCobaltCrystal structureCrystallography X-RayLigandsMagnetic susceptibilityInorganic ChemistryMagneticsCrystallographyMagnetic anisotropyIntramolecular forceOrganometallic CompoundsAnisotropyAntiferromagnetismMolecular orbitalIminesDiimineDalton Trans.
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Bis(glycylglycinium) oxalate at 100 K.

2003

The structure of the title compound, 2C(4)H(9)N(2)O(3)(+).C(2)O(4)(2-), which has been determined by X-ray diffraction, contains discrete glycylglycine (HGly-Gly)(+) cations in general positions and oxalate anions which lie across centres of inversion. Although the geometry of the (HGly-Gly)(+) cation is not significantly different compared with other structures containing this residue, a few changes in conformation are observed which indicate the presence of molecular interactions. The molecular network in the crystal consists of one nearly linear O-H...O, five N-H...O and two weak C-H.O hydrogen bonds.

GlycylglycineOxalatesbiologyMolecular StructureHydrogen bondStereochemistryGlycylglycineMolecular ConformationHydrogen BondingGeneral MedicineCrystal structureCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyOxalateCrystalCold Temperaturechemistry.chemical_compoundCrystallographychemistryCationsbiology.proteinMoleculeCarboxylateOrganic anionActa crystallographica. Section C, Crystal structure communications
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Insertion of a single-molecule magnet inside a ferromagnetic lattice based on a 3D bimetallic oxalate network: Towards molecular analogues of permane…

2014

The insertion of the single-molecule magnet (SMM) [MnIII(salen) (H2O)]2 2+ (salen2-=N,N-ethylenebis- (salicylideneiminate)) into a ferromagnetic bimetallic oxalate network affords the hybrid compound [MnIII(salen)(H2O)] 2[MnIICrIII(ox)3] 2×(CH3OH)×(CH3CN)2 (1). This cationic Mn2 cluster templates the growth of crystals formed by an unusual achiral 3D oxalate network. The magnetic properties of this hybrid magnet are compared with those of the analogous compounds [Mn III(salen)(H2O)]2[ZnIICr III(ox)3]2×(CH3OH) ×(CH3CN)2 (2) and [InIII(sal 2-trien)][MnIICrIII(ox)3] ×(H2O)0.25×(CH3OH) 0.25×(CH3CN)0.25 (3), which are used as reference compounds. In 2 it has been shown that the magnetic isolatio…

Models MolecularChromium02 engineering and technologyCrystallography X-Ray010402 general chemistry01 natural sciencesCatalysisOxalateMagnetizationParamagnetismchemistry.chemical_compoundFerrimagnetismMagnetic propertiesOrganometallic CompoundsSingle-molecule magnetBimetallic stripCluster compoundsOxalatesManganeseChemistryOrganic ChemistryGeneral ChemistryEthylenediamines021001 nanoscience & nanotechnology0104 chemical sciencesX-ray diffractionCrystallographyFerromagnetismMagnetMagnets0210 nano-technology
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Synyhesis, structure, spectroscopy and redox chemistry of square-planar nickel(II) complexes with tetradentate o-phenylenedioxamidates and related li…

2005

[EN] A series of four-coordinate square-planar nickel(II) complexes of o-phenylenebis(N¿-methyloxamidate) (L1) and related o-phenylene(N¿-methyloxamidate)oxamate (L2) and o-phenylenebis(oxamate) (L3) tetradentate ligands have been synthesized and characterized structurally, spectroscopically and electrochemically. The parent nickel(II)¿L1 complex presents an intense MLCT band in the UV region (¿max = 357 nm) and a distinctive 1 s ¿ 4p CT satellite in the Ni K-edge XANES spectrum (E = 8339.2 eV). These features together with the short Ni¿N(amidate) bond lengths (1.85¿1.93 Å) as revealed by the analysis of the Ni K-edge EXAFS spectrum and confirmed by single-crystal X-ray diffraction are typi…

Models MolecularMagnetic Resonance SpectroscopySpectrophotometry Infraredchemistry.chemical_elementPhenylenediaminesCrystallography X-RayLigandsPhotochemistrySensitivity and SpecificityRedoxlaw.inventionInorganic Chemistrychemistry.chemical_compoundNickellawElectrochemistryOrganometallic CompoundsMoleculeAcetonitrileElectron paramagnetic resonanceOxalatesMolecular StructureExtended X-ray absorption fine structureLigandElectron Spin Resonance SpectroscopySpectrometry X-Ray EmissionStereoisomerismBond lengthNickelCrystallographychemistryFISICA APLICADASpectrophotometry UltravioletOxidation-Reduction
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Molecular and electronic structure of square-planar nickel(ii), nickel(iii) and nickel(iii)π-cation radical complexes with a tetradentate o-phenylene…

2005

The molecular and electronic structures of the electron transfer series of four-coordinate square-planar nickel complexes with the ligand o-phenylenebis(N'-methyloxamidate), [NiL]z (z = 2-, 1-, 0), have been evaluated by DFT and TDDFT calculations, and most of their experimentally available structural and spectroscopic properties (X. Ottenwaelder et al., Dalton Trans., 2005, DOI: 10.1039/b502478a) have been reasonably reproduced at the B3LYP level of theory. The anionic species [NiL]2- and [NiL]- are genuine low-spin nickel II and nickel III complexes with diamagnetic singlet (S = 0) and paramagnetic doublet (S = 1/2) states, respectively. The nickel III complex presents shorter Ni-N(amidat…

OxalatesFree RadicalsMolecular StructureLigandchemistry.chemical_elementElectronsPhenylenediaminesLigandsPhotochemistryInorganic ChemistryParamagnetismElectron transferCrystallographyNickelModels ChemicalchemistryNickelCovalent bondCationsExcited stateOrganometallic CompoundsQuantum TheorySinglet stateGround stateOxidation-ReductionDalton Transactions
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Flow-chemiluminescence: a growing modality of pharmaceutical analysis.

2001

The present article deals with a review of the applications of the chemiluminescence to pharmaceutical analyses by using continuous-flow assemblies. A comprehensive study on the fundamentals of the chemiluminescence is also included.

OxalatesMaterials scienceModality (human–computer interaction)LuminescenceLuminescent MeasurementsMolecular StructureContinuous flowChemistry PharmaceuticalBiophysicsImidazolesOxidation reductionlaw.invention22'-DipyridylChemical engineeringFlow (mathematics)Chemistry (miscellaneous)lawCoordination ComplexesLuminescent MeasurementsAnimalsIndicators and ReagentsLuminolOxidation-ReductionChemiluminescenceFluorescent DyesLuminescence : the journal of biological and chemical luminescence
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Rapid and direct gas chromatographic determination of oxalic acid in urine

1979

The known methods of oxalic acid determination are not suitable for reliable, rapid and economical routine analysis. A rapid gas chromatographic method has been developed which dispenses with separation operations and measures oxalic acid as a diethylester by means of back-flushing, and using malonic acid as an internal standard. One determination can be conducted within 6 to 8 min. and preparation of the specimen takes about the same amount of time. If the gas chromatographic conditions are changed and more time is permitted for analysis, numerous other extractable acidic metabolites can also be determined.

Oxalateschemistry.chemical_compoundChromatography GasChromatographyChemistryUrologyOxalic acidHumansGas chromatographyUrineIn Vitro TechniquesMalonic acidRoutine analysisUrological Research
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