Search results for "Metal ions in aqueous solution"

showing 10 items of 256 documents

Recognition of oxovanadium(V) species and its separation from other metal species through selective complexation by some acyclic ligands

1998

Acyclic molecules possessing –OH (phenoxo and alkoxo type) groups and imine or amine moieties have been developed to sense the specific preference for VO3+ species. These molecules also showed a capability to quantitatively separate oxovanadium(V) species from a reaction mixture containing metal species of V, Mo, U, Fe, and Mn ions in solution. A cascade quantitative separation of VO3+ followed by cis–MoO2+2 followed by trans –UO2+2 species is demonstrated from their mixture. Synthesis and structural details of oxo-species of vanadium molybdenum and uranium are also discussed. Factors influencing the complexation of these molecules towards oxo metal species of V, Mo and U are also addressed.

Absorption SpectraPolyanilineStereochemistryMetal ions in aqueous solutionImineCis-Dioxome(Vi)Vanadiumchemistry.chemical_elementTrans-Dioxoo(Iv)Medicinal chemistryInorganic ChemistryMetalSynthesisTransmetalationchemistry.chemical_compoundOxidationElectronicMaterials ChemistryPolythiophenesMoleculeSelective ComplexationPhysical and Theoretical ChemistryConducting PolymerCis-Dioxov(V)TransmetallationChemistryReactivityChemistryRecognitionMolybdenumvisual_artvisual_art.visual_art_mediumAmine gas treatingCrystallographicPolyhedron
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Structural, magnetic and electronic characterization of an isostructural series of dinuclear complexes of 3d metal ions bridged by tpbd

2013

Abstract Dinuclear complexes of the type [{M(H2O)(phen)}2(μ-tpbd)](ClO4)4 with N,N,N′,N′-Tetrakis-(2-pyridylmethyl)-benzene-1,4-diamine (tpbd) as bridging ligand and M = Mn(II) (1), Fe(II) (2), Co(II) (3), Ni(II) (4), Cu(II) (5), Zn(II) (6) were synthesized, structurally analyzed and their magnetic as well as their electrochemical properties are determined. A ligand-centered one-electron oxidation leads to radical complexes for which the lifetimes are strongly dependent on the coordinated metal ion as followed from time-resolved UV–Vis absorption spectroscopy. In addition to the six homometallic dinuclear complexes, one analog heterometallic Mn(II)/Ni(II) compound (7) of the same constituti…

Absorption spectroscopyChemistryMetal ions in aqueous solutionInorganic chemistryBridging ligandElectrochemistryCharacterization (materials science)Inorganic ChemistryMetalCrystallographyvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryIsostructuralGround statePolyhedron
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Impact of histidine spacing on modified polyhistidine tag – Metal ion interactions

2018

Abstract Histidine rich sequences are chosen both by nature and by molecular biologists due to their high affinity towards metal ions. In this work, we examine the affinity and binding modes of Cu 2+ , Ni 2+ and Zn 2+ towards two histidine tags, the common His 6 -tag (Ac-HHHHHH-NH 2 ) and its modified sequence, which also contains six histidines, but separated with two alanine residues (Ac-HAAHAAHAAHAAHAAHAA-NH 2 ). The spatial separation of histidines has an important impact on its coordination properties. Cu 2+ and Ni 2+ complexes with Ac-HHHHHH-NH 2 are more stable than those with Ac-HAAHAAHAAHAAHAAHAA-NH 2 ; the contrary is observed for Zn 2+ . In a narrow range of pH, Cu 2+ -Ac-HHHHHH-…

Alanine010405 organic chemistryMetal ions in aqueous solutionSequence (biology)010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalCrystallographychemistry.chemical_compoundchemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumOrganic chemistryNarrow rangePhysical and Theoretical ChemistryPolyhistidine-tagHistidineInorganica Chimica Acta
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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
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Interactions of carbon nanotubes with aqueousaquatic media containing organicinorganic contaminants and selected organisms of aquatic ecosystems – A …

2015

Due to their unique molecular architecture translating into numerous every-day applications, carbon nanotubes (CNTs) will be ultimately an increasingly significant environmental contaminant. This work reviews qualitative/quantitative analyses of interactions of various types of CNTs and their chemically modified analogues with aqueous/aquatic media containing organic and inorganic contaminants and selected organisms of aquatic ecosystems. A special emphasis was placed on physicochemical interactions between CNTs as adsorbents of heavy metal cations and aromatic compounds (dyes) with its environmental consequences. The studies revealed CNTs as more powerful adsorbents of aromatic compounds (…

Aquatic OrganismsEnvironmental EngineeringHealth Toxicology and MutagenesisMetal ions in aqueous solutionchemistry.chemical_elementCarbon nanotubeEnvironmentHydrophilizationlaw.inventionAdsorptionlawMetals HeavyAnimalsEnvironmental ChemistryOrganic matterOrganic ChemicalsColoring AgentsEcosystemchemistry.chemical_classificationAqueous solutionNanotubes CarbonChemistryPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollutionDaphniaEnvironmental chemistryAdsorptionEcotoxicityCarbonWater Pollutants ChemicalChemosphere
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Concurrent removal of Cr(III), Cu(II), and Pb(II) ions from water by multifunctional TiO2/Alg/FeNPs beads

2019

Abstract The use of multifunctional materials for water remediation is a modern approach where adsorption phenomena and heterogeneous photocatalysis can be applied for the removal of pollutants. Since the ideal remediation system should be able to remove both organic and inorganic pollutants, a crucial aspect to consider is the knowledge of operational parameters affecting the removal process, especially when heavy metal ions are present in concoction as in real systems. Given the proven efficiency of multifunctional TiO2/Alg/FeNPs magnetic beads for the removal of model organic pollutants, this study investigated the possibility to exploit such system also for the removal of mixed heavy me…

Aqueous solution010405 organic chemistryMetal ions in aqueous solutionInorganic chemistryGroundwater remediationMagnetic nanoparticleAdsorbentPharmaceutical Sciencechemistry.chemical_elementManagement Monitoring Policy and Law010402 general chemistry01 natural sciencesPollution0104 chemical sciencesCatalysisMetalChromiumAdsorptionHeavy metalchemistryvisual_artPhotocatalysisvisual_art.visual_art_mediumEnvironmental ChemistryPhotocatalysis
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A biocompatible ZnNa2-based metal–organic framework with high ibuprofen, nitric oxide and metal uptake capacity

2020

Metal organic frameworks (MOFs) have received significant attention in recent years in the areas of biomedical and environmental applications. Among them, mixed metal MOFs, although promising, are relatively few in number in comparison with their homometallic analogues. The employment of benzophenone-4,4′-dicarboxylic acid (bphdcH2) in mixed metal MOF chemistry provided access to a 3D MOF, [Na2Zn(bphdc)2(DMF)2]n (NUIG1). NUIG1 displays a new topology and is a rare example of a mixed metal MOF based on 1D rod secondary building units. UV-vis, HPLC, TGA, XRPD, solid state NMR and computational studies indicated that NUIG1 exhibits an exceptionally high Ibuprofen (Ibu) and nitric oxide adsorpt…

Aqueous solutionChemistryMetal ions in aqueous solutionInorganic chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMagnetic susceptibility0104 chemical sciencesMetalAdsorptionSolid-state nuclear magnetic resonanceChemistry (miscellaneous)visual_artvisual_art.visual_art_mediumGeneral Materials ScienceMetal-organic framework0210 nano-technologyPowder diffractionMaterials Advances
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Synthesis and characterization of acetazolamide complexes of Ni(II), Cd(II), Hg(II), and Ag(I)

1989

The preparation and characterization of K2Ni2(Acm)3·5H2O, Cd(Acm)·32 H2O, Hg(Acm)·12H2O, Ag2(Acm), and Ag2(Acm)(NH3) complexes are described. The spectral properties suggest that Acm interacts with the metal ions through the doubly deprotonated form as observed in the [Cu(Acm)(NH3)2(OH2)]2·2H2O complex, whose crystalline structure has been previously reported. The crystal field parameters of the Ni(II) complex indicate an octahedral environment for the metal ion in the solid and its aqueous, DMSO, and DMF solutions. UV spectra of all the Acm complexes until now synthesized are discussed.

Aqueous solutionChemistryMetal ions in aqueous solutionSpectral propertiesAnalytical chemistryCrystal structureBiochemistryInorganic ChemistryCrystalMetalCrystallographyDeprotonationOctahedronvisual_artvisual_art.visual_art_mediumJournal of Inorganic Biochemistry
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Electrochemical molecular recognition of silver cation by electropolymerised thieno[3′,4′:5,6][1,4]dithiino[2,3-b]quinoxaline: a joint experimental a…

2000

The novel annelated monomer thieno[3′,4′:5,6][1,4]dithiino[2,3-b]quinoxaline 1 has been electropolymerised on a variety of electrodes, resulting in films which are electroactive in non-aqueous and aqueous solution. The polymer films exhibit a transformation in voltammetric response corresponding to a positive shift in redox potential in the presence of silver cation, the maximum shift being ca. 150 mV in acetonitrile and ca. 400 mV in aqueous LiClO4 solution. Mercury dication demonstrates a similar, but smaller (ca. 130 mV) shift in aqueous solution. Theoretical calculations clearly show the potential of poly(1) as a metal complexation agent. The Ag+ ion coordinates with 1 in two ways: (i) …

Aqueous solutionChemistryMetal ions in aqueous solutionTrimerGeneral ChemistryElectrochemistryDicationchemistry.chemical_compoundCrystallographyQuinoxalineMonomerMaterials ChemistryOrganic chemistryAcetonitrileJournal of Materials Chemistry
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Fabrication of metal nano-structures using anodic alumina membranes grown in phosphoric acid solution: Tailoring template morphology

2007

Abstract The influence of experimental parameters on the morphology of the porous structure and on the formation kinetics has been investigated for anodic alumina membranes (AAM) grown in aqueous H 3 PO 4 at 160 V. It was found that pore aspect ratio and membrane porosity on the solution-side surface are influenced by tensiostatic charge, bath temperature and the presence of Al 3+ ions in solution. Morphological and kinetic data, recorded in different conditions, give useful information on the growth mechanism of pore channels in phosphoric acid solution. Nickel nano-structures have been fabricated using AAM as template. Electroless deposition, performed by adding the reducing agent to a su…

Aqueous solutionMaterials scienceMetal ions in aqueous solutionNanowireGeneral Physics and AstronomyAlumina membraneNanotechnologySurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsNanowirechemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicataMembraneElectrodepositionChemical engineeringchemistryTransition metalNickelNano-PorosityPhosphoric acidApplied Surface Science
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