Search results for "Metal Ion"

showing 10 items of 297 documents

Homo- and Heterobinuclear Cu2+ and Zn2+ Complexes of Ditopic Aza Scorpiand Ligands as Superoxide Dismutase Mimics

2017

Two polytopic aza-scorpiand-like ligands, 6-[7-(diaminoethyl)-3,7-diazaheptyl]-3,6,9-triaza-1-(2,6-pyridina)cyclodecaphane (L1) and 6-[6′-[3,6,9-triaza-1-(2,6-pyridina)cyclodecaphan-6-yl]-3-azahexyl]-3,6,9-triaza-1-(2,6-pyridina)cyclodecaphane (L2), have been synthesized. The acid–base behavior and Cu2+, Zn2+, and Cu2+/Zn2+ mixed coordination have been analyzed by potentiometry, cyclic voltammetry, and UV–vis spectroscopy. The resolution of the crystal structures of [Cu2L2Cl2](ClO4)2·1.67H2O (1), [Cu2HL2Br2](ClO4)3·1.5H2O (2), and [CuZnL2Cl2](ClO4)2·1.64H2O (3) shows, in agreement with the solution data, the formation of homobinuclear Cu2+/Cu2+ and heterobinuclear Cu2+/Zn2+ complexes. The m…

biology010405 organic chemistryChemistryLigandStereochemistryMetal ions in aqueous solutionCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistrySuperoxide dismutaseCrystallographybiology.proteinPhysical and Theoretical ChemistryCyclic voltammetrySpectroscopyStoichiometryInorganic Chemistry
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Low temperature optical spectroscopy of cobalt-substituted hemocyanin from Carcinus maenas

1993

In this work we report the optical absorption spectra of three cobalt-substituted derivatives of hemocyanin (He) from Carcinus maenas, in the temperature range 300–20 K. The derivatives studied are the mononuclear (Co2+)-He with a single cobalt ion in the “CuA” site, the binuclear (Co2+)2-He and the binuclear mixed metal (Co2+-Cu1+)-He. At low temperature three main bands are clearly resolved; the temperature dependence of their zeroth, first and second moments sheds light on the stereodynamic properties in the surroundings of the chromophore. Within the limits of the reported analysis, in the binuclear derivatives the motions coupled to the chromophore appear to be “essentially harmonic” i…

biologyLigandMetal ions in aqueous solutionBiophysicsAnalytical chemistryActive sitechemistry.chemical_elementGeneral MedicineChromophoreAtmospheric temperature rangeCrystallographychemistrybiology.proteinSpectroscopyRotational–vibrational couplingCobaltEuropean Biophysics Journal
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Study of [2-(2’-pyridyl)imidazole] complexes to confirm two main characteristic thermoanalytical behaviors of transition metal complexes based on imi…

2016

Abstract Imidazole derivative ligands are recognized as useful models for biomimetic complexes. Among the inorganic–organic hybrid complexes, those with derivatives of imidazole heterocyclic N-donor ligands are interesting for their framework. In previous studies of complexes with imidazole derivative ligands, our group reported two main thermally induced decomposition behaviors supporting two different systematic decomposition trends. In this work, one of these characteristic decomposition mechanisms was again found. The final goal of these serial studies is the possibility to provide, by the experimental evidences, a prediction model of thermal stability and decomposition typical behavior…

biomimetic complexes; EGA; imidazole derivative complexes; TG-MS; transition metal ion complexes; chemical engineering (all); chemistry (all)Evolved gas analysisInorganic chemistrytransition metal ion complexes02 engineering and technology010402 general chemistryMass spectrometry01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundEGATransition metalPolymer chemistryImidazoleMoleculeThermal stabilitySettore CHIM/01 - Chimica Analiticabiomimetic complexesimidazole derivative complexes transition metal ion complexes biomimetic complexes EGA TG-MS021001 nanoscience & nanotechnologyimidazole derivative complexesDecomposition0104 chemical scienceschemistry (all)Fuel Technologychemical engineering (all)chemistryTG-MSMethanol0210 nano-technology
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Syntheses, characterization and properties of Cu(II)-, Mo(VI)- and U(VI) complexes with diaminotetraphenolate ligands

2013

catalytic studiesmagneettiset ominaisuudetkupariepäorgaaninen kemiadiaminotetraphenolsmetal ion extractiondiaminotetrafenolitkiderakenteeturaniumcrystal structuresmolybdenumuraanicoppermagnetic propertiesmolybdeeni
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Pseudopeptidic ligands: exploring the self-assembly of isophthaloylbisglycine (H2IBG) and divalent metal ions.

2012

We present a systematic study of the complexation of the new pseudopeptidic ligand isophthaloylbisglycine (H(2)IBG) with divalent metal ions of varying ionic radius. This work represents the initial employment of H(2)IBG in the coordination chemistry of alkaline earth, 3d transition, Zn(II) and Cd(II) metal elements. Infrared, NMR, thermal, magnetic, adsorption and theoretical studies of these compounds are also discussed.

chemistry.chemical_classificationAlkaline earth metalIonic radiusMagnetic Resonance SpectroscopySpectrophotometry InfraredInfraredLigandChemistryInorganic chemistryGlycineMolecular ConformationLigandsCoordination complexInorganic ChemistryMetalAdsorptionX-Ray DiffractionCoordination ComplexesMetalsDivalent metal ionsvisual_artvisual_art.visual_art_mediumQD0146ta116OligopeptidesDalton transactions (Cambridge, England : 2003)
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Cysteamine and its homoleptic complexes with group 12 metal ions. Differences in the coordination chemistry of ZnII, CdII, and HgII with a small N,S-…

2005

2-Ammoniumethanethiolate, (-)SCH(2)CH(2)NH(3)(+), the first structurally characterized zwitterionic ammoniumthiolate, is the stable form of cysteamine (HL) in the solid state and in aqueous solution. Reactions of ZnCl(2), Cd(Oac)(2), and HgCl(2) with cysteamine and NaOH in a 1:2:2 ratio, respectively, lead to the homoleptic complexes ML(2). Their single-crystal X-ray structures demonstrate basic differences in the coordination chemistry of Zn(II), Cd(II), and Hg(II). While chelating N,S-coordination modes are found for all metal ions, Zn(II) forms a mononuclear complex with a distorted tetrahedral Zn(N(2)S(2)) coordination mode, whereas Hg(II) displays a dimer with Hg(N(2)S(2)) coordinated …

chemistry.chemical_classificationAqueous solutionLigandStereochemistryMetal ions in aqueous solutionSolid-stateCoordination complexInorganic Chemistrychemistry.chemical_compoundchemistryGroup (periodic table)Polymer chemistryCysteaminePhysical and Theoretical ChemistryHomolepticInorganic chemistry
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Palladium(II) sequestration by phytate in aqueous solution. Speciation analysis and ionic medium effects.

2010

Environmental context.In the last 20 years, the demand for palladium and other platinum-group elements has intensified, causing a significant increase in their concentration in the environment, with particular accumulation in urban areas. Knowledge about Pd2+ speciation in aqueous media is fundamental for the understanding of its biological and environmental activity in contaminated areas. Phytic acid appears to be a good sequestering agent towards Pd2+ under various conditions, indicating its potential use in the remediation of contaminated sites. Abstract. Palladium(II) speciation in the presence of phytate (Phy12–) was studied by H+ ion selective electrode (ISE) potentiometry at 25°C in…

chemistry.chemical_classificationAqueous solutionMetal ions in aqueous solutionInorganic chemistryFluorescence spectrometrychemistry.chemical_elementcomplexes stability constantsPhytateIon selective electrodeDivalentMetalchemistryComplexesGeochemistry and PetrologyChemistry (miscellaneous)Ionic strengthvisual_artvisual_art.visual_art_mediumEnvironmental ChemistrySettore CHIM/01 - Chimica AnaliticaStability constantsComplexes; Stability constants; Phytate; PalladiumPalladiumPalladium
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Expanding the NUIG MOF family: synthesis and characterization of new MOFs for selective CO2 adsorption, metal ion removal from aqueous systems, and d…

2021

Metal organic frameworks (MOFs) have attracted considerable attention in recent years due to their use in a wide range of environmental, industrial and biomedical applications. The employment of benzophenone-4,4'-dicarboxylic acid (bphdcH2) in MOF chemistry provided access to the 3D mixed metal MOFs [CoNa2(bphdc)2(DMF)2]n (NUIG2) and [ZnK2(bphdc)2(DMF)2]n (NUIG3), and the 2D homometallic MOF [Co2(OH)(bphdcH)2(DMF)2(H2O)2]n(OH)·DMF (1·DMF). 1·DMF is based on a dinuclear SBU and consists of interpenetrating networks with an sql topology. Dc magnetic susceptibility studies were carried out in 1·DMF and revealed the presence of weak antiferomagnetic exchange interactions between the metal centr…

chemistry.chemical_classificationAqueous solutionMetal ions in aqueous solutionMagnetic susceptibilityInorganic ChemistryMetalAdsorptionDicarboxylic acidchemistryvisual_artPolymer chemistryvisual_art.visual_art_mediumMoleculeMetal-organic frameworkDalton Transactions
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Synthesis, characterization, and complexation of tetraarylborates with aromatic cations and their use in chemical sensors.

2005

Five aromatic borate anions, namely tetrakis(4-phenoxyphenyl)borate (1), tetrakis(biphenyl)borate (2), tetrakis(2-naphthyl)borate (3), tetrakis(4-phenylphenol)borate (4), and tetrakis(4-phenoxy)borate (5), have been prepared and tested as ion-recognition sites in chemical sensors for certain aromatic cations and metal ions. To gain further insight into the complexation of the cations, some complexes have been prepared and structurally characterized. The complexation behavior of 1 and 2 towards N-methylpyridinium (6), 1-ethyl-4-(methoxycarbonyl)pyridinium (7), tropylium (8), imidazolium (9), and 1-methylimidazolium (10) cations has been studied, and the stability constants of the complexes o…

chemistry.chemical_classificationBiphenylModels MolecularTetraphenylborateMolecular StructureMetal ions in aqueous solutionOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureCrystallography X-RayMedicinal chemistryHydrocarbons AromaticCatalysisIon selective electrodechemistry.chemical_compoundchemistryCationsBoratesNon-covalent interactionsPyridiniumBoronElectrodesChemistry (Weinheim an der Bergstrasse, Germany)
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A Co2O2 metallacycle exclusively supported by l-valine

2008

Abstract [Co2(OH)2( l -valine)4]·2.5H2O has been prepared under hydrothermal conditions and constitutes the first example of a [Co2O2] core supported exclusively by aminoacids. This synthetic dimetallic model for redox active metalloenzymes is one of the few binary aminoacid compounds of biologically relevant metal ions that has been structurally characterized, showing the possibilities of this synthetic approach for preparation of models in bioinorganic chemistry.

chemistry.chemical_classificationChemistryStereochemistryMetal ions in aqueous solutionBioinorganic chemistryGeneral ChemistryMetallacycleCondensed Matter PhysicsAmino acidValineHydrothermal synthesisGeneral Materials ScienceChirality (chemistry)Group 2 organometallic chemistrySolid State Sciences
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