Search results for "metal ions"

showing 10 items of 282 documents

Triplet of cysteines – Coordinational riddle?

2020

Polythiol binding of metal ions plays crucial role in the proper functioning of cysteine-rich proteins that are responsible for metal homeostasis and defending processes against metal toxicity (including heavy metals detoxification). The coordination properties of cysteine residues involved in specific sequencional patterns in proteins (like those present in e.g. metallothioneins) are interesting not only from a chemical point of view but may also lead to a better understanding of the purpose and allocation of metal ions in various biomolecules. In this study, the interaction of Zn2+, Cd2+ and Ni2+ ions with four peptides containing cysteine triplet motif were studied by potentiometric and …

StereochemistryMetal ions in aqueous solutionMetal toxicity010402 general chemistry01 natural sciencesBiochemistryInorganic ChemistryMetalResidue (chemistry)chemistry.chemical_compoundCoordination ComplexesNickelAmideHumansCysteinechemistry.chemical_classification010405 organic chemistryBiomoleculePeptide Fragments0104 chemical sciencesZincchemistryvisual_artThiolvisual_art.visual_art_mediumMetallothioneinCadmiumCysteineJournal of Inorganic Biochemistry
researchProduct

Unusual binding ability of α,β-dehydrodipeptides towards metal ions

1994

Abstract Ni II , Zn II and Co II complexes of α,β-dehydro-dipeptides (containing Gly, Leu, Ala, Val or Phe residues) were studied by potentiometric and spectroscopic methods. Deprotonation and coordination of amide nitrogens occurred in all cases around the physiological pH range. The dipeptides with composition of Xaa-Δ-Ala formed octahedral species, while Gly-Δ-Xaa (Xaa = Leu or Phe) formed square planar bis complexes with Ni II .

StereochemistryMetal ions in aqueous solutionPotentiometric titrationbody regionsInorganic Chemistrychemistry.chemical_compoundBinding abilityDeprotonationTermészettudományokchemistryOctahedronAmideMaterials ChemistryPh rangePhysical and Theoretical ChemistryKémiai tudományokPolyhedron
researchProduct

A novel polynitrile ligand with different coordination modes: Synthesis, structure and magnetic properties of the series [M(tcnoprOH)2(H2O)2] (M=Mn, …

2008

International audience; A novel polynitrile ligand (tcnoprOH− = [(NC)2CC(OCH2CH2CH2OH)C(CN)2]−) with up to five potentially coordinating groups has been synthesized in a one-pot reaction from a cyclic acetal and malononitrile. The combination of this novel ligand with different transition metal ions has led to the synthesis of two different structural types with the same formula but with different coordination modes in the ligand. Mn(II) and Cu(II) lead to a μ2-N,O-coordinating mode in the series of compounds formulated as [M(N,O-tcnoprOH)2(H2O)2] (M = MnII (1) and CuII (2)), whereas Co(II) and, most probably Ni(II), lead to a μ2-N,N′-coordinating mode in [Co(N,N′-tcnoprOH)2(H2O)2] (3). Bot…

StereochemistryMetal ions in aqueous solutionZero field splitting[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesAnalytical ChemistryInorganic ChemistryPolynitrile ligandschemistry.chemical_compoundParamagnetismGroup (periodic table)Magnetic properties[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistrySpectroscopyMalononitrile010405 organic chemistryLigandOrganic ChemistryAcetalMagnetic chains3. Good health0104 chemical sciencesCrystallographychemistryChain complexesDerivative (chemistry)
researchProduct

Binuclear Cu2+ complex mediated discrimination between L-glutamate and L-aspartate in water.

2005

L-Glutamate and L-aspartate selectivity is achieved by the action of two Cu2+ metal ions rightly disposed in a cyclophanetype macrocyclic framework; electrochemical sensing of glutamate has been achieved by adsorption of the copper complexes on graphite electrodes. Verdejo Viu, Begoña, Begona.Verdejo@uv.es ; Domenech Carbo, Antonio, Antonio.Domenech@uv.es ; Jimenez Garcia, Hermas Rafael, Hermas.Jimenez@uv.es ; Soriano Soto, Concepción, Concepcion.Soriano@uv.es ; Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es

StereochemistryUNESCO::QUÍMICAMetal ions in aqueous solutionL-Aspartatechemistry.chemical_elementGlutamic AcidElectrochemistry:QUÍMICA [UNESCO]Medicinal chemistryCatalysisAdsorptionMaterials ChemistryElectrochemistryOrganometallic CompoundsAspartic AcidUNESCO::QUÍMICA::Química inorgánicaElectrochemicalMetals and AlloysGlutamate receptorWaterBinuclear Cu2General ChemistryCyclophanetype macrocyclic framework:QUÍMICA::Química inorgánica [UNESCO]CopperSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryL glutamateL-aspartateBinuclear Cu2 ; L-glutamate ; L-aspartate ; Water ; Cyclophanetype macrocyclic framework ; ElectrochemicalCeramics and CompositesL-glutamateSelectivityCopperChemical communications (Cambridge, England)
researchProduct

Binding abilities of dehydropeptides towards Cu(II) and Ni(II) ions. Impact of Z–E isomerization on metal ion binding

2002

The study on the binding ability of dehydro-tri- and tetrapeptides has shown that the alpha,beta-double bond has a critical effect on the peptide coordination to metal ions. It may affect the binding of the vicinal amide nitrogens by the electronic effect and stabilize the complex due to steric effects. The (Z) isomer is the most effective in stabilizing of the complexes formed. The presence of large side chain in the dehydroamino acid residue may also be critical for the coordination mode in the metallopeptide systems.

Steric effectsNickel(II) complexesE–Z isomersMetal ion bindingChemistryMetal ions in aqueous solutionPhotochemistryBiochemistryisomerizationInorganic ChemistryMetalCrystallographychemistry.chemical_compounddehydropeptidesAmidevisual_artSide chainvisual_art.visual_art_mediumElectronic effectCopper(II) complexesIsomerizationVicinalJournal of Inorganic Biochemistry : an interdisciplinary journal
researchProduct

Metal-functionalized covalent organic frameworks as precursors of supercapacitive porous N-doped graphene

2017

Covalent Organic Frameworks (COFs) based on polyimine with several metal ions (FeIII, CoII and NiII) adsorbed into their cavities have shown the ability to generate N-doped porous graphene from their pyrolysis under controlled conditions. These highly corrugated and porous graphene sheets exhibit high values of specific capacitance, which make them useful as electrode materials for supercapacitors.

SupercapacitorMaterials scienceRenewable Energy Sustainability and the EnvironmentMetal ions in aqueous solutionInorganic chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCapacitance0104 chemical sciencesMetalAdsorptionChemical engineeringCovalent bondvisual_artvisual_art.visual_art_mediumGeneral Materials Sciencecovalent organic frameworks0210 nano-technologyPorosityPyrolysis
researchProduct

Electrochemical identification of metal ions in archaeological ceramic glazes by stripping voltammetry at graphite/polyester composite electrodes

2002

The electrochemical response of metal ions in different samples of coloured ceramic tin-lead glazes attached to graphite/polyester composite electrodes is described. In addition to the ubiquous signals for lead, reductive dissolution processes are followed by anodic stripping peaks for Co, Cu, Sb, Mn, Sn and Fe, enabling the direct identification of such elements in microsamples proceeding from archaeological glazed tiles from Valencia (Spain) workshops (16th-18th century). Additional anodic and cathodic peaks corresponding to redox processes involving metal species in solution generated during stripping processes are also used. Peak potentials, Tafel plots and shape parameters are used for…

Tafel equationAnodic stripping voltammetryStripping (chemistry)ChemistryMetal ions in aqueous solutionvisual_artvisual_art.visual_art_mediumGraphiteCeramicVoltammetryDissolutionArchaeologyAnalytical ChemistryTalanta
researchProduct

Sensing of Transition Metals by Top-Down Carbon Dots

2021

Carbon quantum dots (CQDs) are a new class of carbon-rich materials with a range of unique optical and structural properties. They can be defined as carbon nanoparticles, with sizes in the range of 1–10 nm, displaying absorption and emission activities in the UV-VIS range. Depending on the structure, CQDs display a wide variability of properties, which provides the possibility of finely tuning them for several applications. The great advantages of CQDs are certainly the ease of synthesis, non-toxicity, and the strong interactions with the surrounding environment. Based on this, CQDs are especially promising as selective chemosensors. The present study reports on carbon quantum dots synthesi…

TechnologyMaterials scienceAbsorption spectroscopyQH301-705.5Metal ions in aqueous solutionQC1-999chemistry.chemical_elementPhotochemistryIonTransition metalcarbon dotsGeneral Materials ScienceBiology (General)Absorption (electromagnetic radiation)InstrumentationQD1-999sensingFluid Flow and Transfer ProcessesProcess Chemistry and TechnologyTPhysicsGeneral EngineeringEngineering (General). Civil engineering (General)FluorescenceComputer Science ApplicationsChemistrychemistrySurface modificationfluorescenceTA1-2040CarbonApplied Sciences
researchProduct

New coordination polymers based on a novel polynitrile ligand: Synthesis, structure and magnetic properties of the series [M(tcnoetOH)2(4,4′-bpy)(H2O…

2008

International audience; A novel polynitrile anionic ligand, tcnoetOH−(=[(NC)2CC(OCH2CH2OH)C(CN)2]−), has been synthesized by a one-pot reaction from a cyclic acetal and malononitrile. This ligand has been successfully used to prepare, with 4,4′-bpy as co-ligand, a novel series of coordination polymers formulated as [M(tcnoetOH)2(4,4′-bpy)(H2O)2] with M(II) = Fe (1), Co (2) and Ni (3). These isostructural compounds present a linear chain structure consisting of octahedrally coordinated metal ions bridged by trans 4,4′-bpy ligands. The coordination sphere of the metal ions is completed with two terminal tcnoetOH− ligand and two water molecules. The magnetic properties indicate that the three …

Transition metal complexesCoordination sphere010405 organic chemistryChemistryLigandMetal ions in aqueous solutionInorganic chemistryZero field splitting010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryParamagnetismCrystallographychemistry.chemical_compoundPolynitrileMagnetic propertiesMaterials ChemistryMolecule[CHIM]Chemical SciencesPhysical and Theoretical ChemistryIsostructuralChain complexesMalononitrile
researchProduct

Improvement of photo-stability of LLDPE-based nanocomposites

2006

LLDPE-based nanocomposites undergo faster photo-oxidation than the unfilled matrix and the extent of their physical properties deterioration, namely elongation at break and tensile strength, is dependent on the organo-nanoclay loading. The observed acceleration is not due to faster photo-oxidation but rather due to a reduction of the oxidation induction time. The presence in the organoclays of trace amounts of metal ions may be promoting catalytic photodegradation. While UV absorbers provide useful protection, use of a metal deactivator has been found to greatly enhance the photo-stability of the LLDPE-based nanocomposites. Combinations of a metal deactivator and UV absorber yield synergist…

Yield (engineering)NanocompositeMaterials sciencePolymers and PlasticsMetal ions in aqueous solutionCondensed Matter PhysicsLinear low-density polyethyleneMetalMetal deactivatorMechanics of Materialsvisual_artUltimate tensile strengthMaterials Chemistryvisual_art.visual_art_mediumComposite materialPhotodegradation
researchProduct