Search results for "Chela"

showing 10 items of 415 documents

Synthesis and X-ray crystal structure of manganese(II) pyridine-2-thiolate

1997

2:1 complexes of pyridine-2(1H)-thione (LH) with manganese(II) were prepared: (LH)2MnCl2, (LH)2MnBr2 and [L2Mn]n. The polymeric chain structure of [L2Mn]n contains a distorted octahedrally coordinated manganese (MnN2S4) with chelating ligands, the N-atoms are in cis positions and the S-atoms of the pyridine-2-thiolates bridging; crystallographic data for [C10H8MnN2S2]n: space group C2/c (monoclinic), and R1 = 0.0571 for 1326 reflexes with Fo4σ(Fo).

Chelating ligandsX-raychemistry.chemical_elementCrystallographic dataCrystal structureManganeseInorganic ChemistryChain structureCrystallographychemistryPyridine-2-thiolateMaterials ChemistryPhysical and Theoretical ChemistryMonoclinic crystal systemInorganica Chimica Acta
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Extraction of uranyl ions from aqueous solutions using silica-gel-bound macrocycles for alpha contaminated waste water treatment

2004

Abstract The efficiency for the extraction of U(VI) of new modified silica gels, namely N-tripropionate (or N-triacetate)-substituted tetraazamacrocycles-bound silica gels, has been studied. The effect of the nature of the ligand, the pH and the temperature was studied both in batch experiments as well as in continuous extraction. These silica gels are good candidates for the extraction of U(VI) when compared to a commercially available acid-type chelating resin. The breakthrough and regeneration tests showed that the total removal of U(VI) from a contaminated solution can be achieved by using a column packed with such tetraazamacrocycles-bound silica gels. Finally, the use of a modified si…

Chelating resinAqueous solutionSilica gelExtraction (chemistry)chemistry.chemical_elementAmericiumUraniumUranylBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryEnvironmental ChemistrySolid phase extractionSpectroscopyNuclear chemistryAnalytica Chimica Acta
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Effect of EDTA and citrate on the functional activity of the first component of complement, C1, and the C1q subcomponent.

1985

The first component of complement, C1, is a calcium-dependent complex of the three distinct subcomponents, C1q, C1r, and C1s. Earlier observations revealed that treatment of C1 with EDTA led to a loss of hemolytic C1 activity even after recalcification. Therefore, it was of interest to study whether EDTA has an additional effect on C1 and its subcomponents, beside its chelating capacity. The chelating effect of EDTA was compared to that of citrate. It was found that treatment of C1 or C1 with EDTA followed by addition of Ca++ led to a loss of hemolytic activity up to 90%, depending on EDTA concentration. Even pretreatment of EDTA with varying amounts of Ca++ did not prevent the inactivation…

Chemical PhenomenaComplement Activating EnzymesMacromolecular SubstancesImmunologyKineticschemistry.chemical_elementCalciumHemolysisDissociation (chemistry)Structure-Activity RelationshipComplement C1medicineImmunology and AllergyStructure–activity relationshipHumansChelationCitratesComplement C1qEdetic AcidComplement C1qHematologymedicine.diseaseHemolysisChemistryKineticsBiochemistrychemistryEdetic AcidCalciumImmunobiology
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cis-Aquabis[bis(diphenylphosphino)ethane-κ2 P,P′]chlororuthenium(II) hexafluorophosphate dichloromethane sesquisolvate hemihydrate

2006

In the title compound, [RuCl(C26H24P)2(H2O)]PF6·1.5CH2Cl2·0.5H2O, the complex RuII cation is in a slightly distorted octahedral environment, chelated by two bis(diphenylphosphino)ethane ligands, with a water molecule and a chloride anion in a mutually cis geometry completing the coordination.

ChemistryHemihydratechemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsHEXAPhosphateMedicinal chemistryChlorideMethaneRutheniumchemistry.chemical_compoundmedicineOrganic chemistryGeneral Materials ScienceChelationmedicine.drugActa Crystallographica Section E Structure Reports Online
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Separation of chelating agents as copper complexes by capillary zone electrophoresis using quaternary ammonium bromides as additives in N-methylforma…

2006

This study presents the use of quaternary ammonium bromides as additives in N-methylformamide (NMF) for the separation and quantification of chelating agents as copper complexes by capillary zone electrophoresis (CZE). The new quaternary ammonium bromides were synthesized in our laboratory and used for the first time for CZE applications performed in NMF media. The methods were developed and optimized for determination of six chelating agents (trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid (CDTA), diethylenetriaminepentaacetic acid (DTPA), ethylenediaminetetraacetic acid (EDTA), N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetic acid (HEDTA), nitrilotriacetic acid (NTA) and trieth…

ChemistryInorganic chemistryNitrilotriacetic acidchemistry.chemical_elementEthylenediaminetetraacetic acidN-MethylformamideBiochemistryCopperAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisBromideEnvironmental ChemistryChelationAmmoniumSpectroscopyAnalytica Chimica Acta
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A 4-tert-butylcalix[4]arene tetrahydroxamate podand based on the 1-oxypiperidine-2-one (1,2-PIPO−) chelate. Self-assembly into a supramolecular ionop…

2014

An octadentate tetrahydroxamic calix[4]arene podand incorporating 1-hydroxypiperidine-2-one (1,2-PIPOH) binding units has been designed as a specific chelator for tetravalent metal cations like Zr4+ or Hf4+. This receptor, which can be considered as the first ever abiotic ligand possessing only cyclic six-membered hydroxamate groups, has been synthesized and characterized in its tetraprotonated form (1H4). Contrary to expectation, however, this new chelator did not form a 1 : 1 complex upon reaction with M(acac)4 (M = Zr and Hf; acac = acetylacetonate), but rather self-assembled into a dimeric species of 2 : 2 stoichiometry. The latter could be characterized in solution by mass spectrometry…

ChemistryLigandStereochemistryGeneral Chemical EngineeringSupramolecular chemistryIonophoreGeneral ChemistryNuclear magnetic resonance spectroscopyAdductMetalvisual_artPolymer chemistryvisual_art.visual_art_mediumChelationStoichiometryRSC Adv.
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Chelating behaviour of diacetylbisbenzoylhydrazone with SnIV, PbII and PbIV

1974

ChemistryPolymer chemistryChelationEducationInorganic and Nuclear Chemistry Letters
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Metal complexes of sulfanilamide derivatives. Crystal structure of [Zn(sulfathiazole)2]·H2O

1993

Abstract The crystal structure of the Zn(sulfathiazole) 2 ·H 2 O complex is reported. The complex crystallizes in the monoclinic space group C 2/ c . The cell dimensions are a = 9.098(3) A, b = 17.871(5) A, c = 14.61(1) A, β = 99.44(6)°, V = 2343(2) A 3 , Z = 4, and D x = 1.68 g/cm 3 . The final conventional R-factor = 0.027 for 2669 “observed” reflections and 191 variables. The Zn ion is surrounded in a regular tetrahedral arrangement by two N amino and two N thiazole atoms pertaining to four sulfathiazole (Hstz) ligands. Each stz anion, acting as a bidentate ligand, chelates to two Zn ions as a bridge through the N thiazole and the N amino atoms. The IR, 13 C NMR in solid state, 1 H NMR, …

ChemistryStereochemistryCrystal structureCarbon-13 NMRBiochemistryInorganic ChemistryMetalCrystallographychemistry.chemical_compoundvisual_artProton NMRvisual_art.visual_art_mediumChelationThiazoleAntibacterial agentMonoclinic crystal systemJournal of Inorganic Biochemistry
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Suppression of pigment interference in the gas chromatographic analysis of proteinaceous binding media in paintings with EDTA.

2004

A method to suppress the interference of pigments in the analysis of proteinaceous media used in paintings is presented in this paper. This method is based on the formation of metallic ion-ethylenediaminetetraacetic acid (EDTA) complexes previous to the derivatisation process, using ethyl chloroformate (ECF), to transform the amino acids in N(O,S)-ethoxycarbonyl (EOC) ethyl esters. Test specimens, containing different proteinaceous media such as albumin, porcine gelatine and casein mixed with lead white, chalk, verdigris and raw Sienna have been prepared for carrying out this study. Different pH conditions have been probed for the different pigments studied. Values of peak area ratio of ami…

ChromatographyChromatography GasChemistryOrganic ChemistryProteinsGeneral MedicineAnimal gluePigments BiologicalHydrogen-Ion ConcentrationBiochemistryAnalytical Chemistrychemistry.chemical_compoundPigmentCaseinvisual_artvisual_art.visual_art_mediumChelationEthyl chloroformatePaintingsGas chromatographyDerivatizationEdetic AcidVerdigrisJournal of chromatography. A
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Determination of alternative and conventional chelating agents as copper(II) complexes by capillary zone electrophoresis—The first use of didecyldime…

2006

Abstract A capillary zone electrophoresis (CZE) method for analyzing 11 chelating agents [β-alaninediacetic acid (β-ADA), trans-1,2-diaminocyclohexane- N , N , N ′, N ′-tetraacetic acid (CDTA), diethylenetriaminepentaacetic acid (DTPA), ethylenediaminetetraacetic acid (EDTA), N -(2-hydroxyethyl)ethylenediamine- N , N ′, N ′-triacetic acid (HEDTA), N -(2-hydroxyethyl)iminodiacetic acid (HEIDA), iminodiacetic acid (IDA), methylglycinediacetic acid (MGDA), nitrilotriacetic acid (NTA), 1,3-diaminopropane- N , N , N ′, N ′-tetraacetic acid (PDTA) and triethylenetetraaminehexaacetic acid (TTHA)] as negatively charged copper(II) complexes has been established. Both conventional and alternative che…

ChromatographyIminodiacetic acidPentetic acidNitrilotriacetic acidElectrophoresis CapillaryEthylenediamineEthylenediaminetetraacetic acidHydrogen-Ion ConcentrationBiochemistryOrganophosphatesAnalytical ChemistryQuaternary Ammonium Compoundschemistry.chemical_compoundCapillary electrophoresischemistryReagentEnvironmental ChemistryIndicators and ReagentsChelationCopperSoftwareSpectroscopyChelating AgentsAnalytica Chimica Acta
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