Search results for "Metal Ion"

showing 10 items of 297 documents

Synthesis, Crystal Structures, and Magnetic Properties of a New Family of Heterometallic Cyanide-Bridged FeIII2MII2 (M = Mn, Ni, and Co) Square Compl…

2011

New heterobimetallic tetranuclear complexes of formula [Fe(III){B(pz)(4)}(CN)(2)(μ-CN)Mn(II)(bpy)(2)](2)(ClO(4))(2)·CH(3)CN (1), [Fe(III){HB(pz)(3)}(CN)(2)(μ-CN)Ni(II)(dmphen)(2)](2)(ClO(4))(2)·2CH(3)OH (2a), [Fe(III){B(pz)(4)}(CN)(2)(μ-CN)Ni(II)(dmphen)(2)](2)(ClO(4))(2)·2CH(3)OH (2b), [Fe(III){HB(pz)(3)}(CN)(2)(μ-CN)Co(II)(dmphen)(2)](2)(ClO(4))(2)·2CH(3)OH (3a), and [Fe(III){B(pz)(4)}(CN)(2)(μ-CN)Co(II)(dmphen)(2)](2)(ClO(4))(2)·2CH(3)OH (3b), [HB(pz)(3)(-) = hydrotris(1-pyrazolyl)borate, B(Pz)(4)(-) = tetrakis(1-pyrazolyl)borate, dmphen = 2,9-dimethyl-1,10-phenanthroline, bpy = 2,2'-bipyridine] have been synthesized and structurally and magnetically characterized. Complexes 1-3b have be…

DenticitySpin statesChemistryStereochemistryLigandMetal ions in aqueous solutionCrystal structureInorganic ChemistryBipyridinechemistry.chemical_compoundCrystallographyPerchlorateAntiferromagnetismPhysical and Theoretical ChemistryInorganic Chemistry
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Structural properties and applications of multidentate [O,N,O,X'] aminobisphenolate metal complexies

2012

Abstract Aminobisphenols with side-arm donors are versatile tetradentate ligands that effectively coordinate to the metal ions in a tripodal fashion. Most of the metal ions form electrically neutral isolable complexes with aminobisphenolates with different side chains. However, some anionic complexes and zwitterions are also described. The coordination geometry of the metal centre can be controlled by the ligand design. Especially, the ortho -substituents of the phenolate moieties as well as the nature of side-arm donor influence the structure and reactivity of the complexes formed. Depending on the metal ion and the ligand environment, the complexes formed can be monomeric or dimeric ones.…

DenticityStereochemistryChemistryLigandMetal ions in aqueous solutionNon-innocent ligandInorganic ChemistryMetalCrystallographyvisual_artMaterials Chemistryvisual_art.visual_art_mediumReactivity (chemistry)Physical and Theoretical ChemistryMetal aquo complexta116Coordination geometryCoordination Chemistry Reviews
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Bis‐μ‐pyrazolate‐Bridged Dinickel(II) and Dicopper(II) Complexes: An Example of Stereoelectronic Preference of Metal Ions and Stabilization of Mixed‐…

2007

New dimeric nickel(II) and copper(II) complexes [(L)Ni(μ-L′)]2[ClO4]21 and [(L)Cu(μ-L′)]2[ClO4]22, [2-[3-(2′-pyridyl)pyrazol-1-ylmethyl]pyridine (L) and 3-(2-pyridyl)pyrazole (HL′)] have been synthesized, structurally characterized, and their absorption, magnetic, EPR and redox properties investigated. The crystal structure of 1·MeCN reveals a planar {Ni2(μ-L′)2}2+ core [Ni···Ni separation: 4.0765(10) A] in which each distorted octahedral NiII ions is terminally coordinated by a tridentate ligand L and bridged by two HL′ units, in their deprotonated form. The structural analysis of 2·2MeCN reveals two five-coordinate CuII ions, each terminally coordinated by adopting only a bidentate coordi…

DenticityStereochemistryChemistryMetal ions in aqueous solutionCrystal structurePyrazolelaw.inventionInorganic ChemistryCrystallographychemistry.chemical_compoundDeprotonationOctahedronlawPyridineElectron paramagnetic resonanceEuropean Journal of Inorganic Chemistry
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New family of thiocyanate-bridged Re(IV)-SCN-M(II) (M = Ni, Co, Fe, and Mn) heterobimetallic compounds: synthesis, crystal structure, and magnetic pr…

2012

The heterobimetallic complexes of formula [(Me(2)phen)(2)M(μ-NCS)Re(NCS)(5)]·CH(3)CN [Me(2)phen = 2,9-dimethyl-1,10-phenanthroline and M = Ni (1), Co (2), Fe (3), and Mn (4)] have been prepared, and their crystal structures have been determined by X-ray diffraction on single crystals. Compounds 1-4 crystallize in the monoclinic C2/c space group, and their structure consists of neutral [(Me(2)phen)(2)M(μ-NCS)Re(NCS)(5)] heterodinuclear units with a Re-SCN-M bridge. Each Re(IV) ion in this series is six-coordinated with one sulfur and five nitrogen atoms from six thiocyanate groups building a somewhat distorted octahedral environment, whereas the M(II) metal ions are five-coordinated with fou…

DenticityThiocyanateMetal ions in aqueous solutionInorganic chemistryCrystal structureInorganic ChemistryTrigonal bipyramidal molecular geometryCrystallographychemistry.chemical_compoundOctahedronchemistryMoleculePhysical and Theoretical ChemistryMonoclinic crystal systemInorganic chemistry
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Construction of Coordination Polymers from Semirigid Ditopic 2,2′-Biimidazole Derivatives: Synthesis, Crystal Structures, and Characterization

2017

Eight coordination polymers (CPs), {[Ag(L1)]ClO4}n (1), {[Ag(L2)1.5]ClO4·C2H3N}n (2a), {[Ag(L2)]ClO4}n (2b), [Zn(L1)Cl2]n (3), {[Zn(L2)Cl2]·CHCl3}n (4), {[Cu(L1)2Cl]Cl·H2O}n (5), [Cu2(L2)(μ-Cl)2]n (6), and [Cu4(L2)(μ-Cl)4]n (7) were synthesized via self-assembly of corresponding metal ions and biimidazole based ditopic ligands, 1,1′-bis(pyridin-3-ylmethyl)-2,2′-biimidazole L1 and 1,1′-bis(pyridin-4-ylmethyl)-2,2′-biimidazole L2. These ligands possess conformational flexibility and two pairs of coordination sites: pyridine nitrogen (NPy) atoms and imidazole nitrogen (NIm) atoms. Depending on the metal center in CPs, the biimidazole compounds act as tetra- (1, 7), tri- (2a), or bidentate (2a,…

Denticitykemia010405 organic chemistryStereochemistryMetal ions in aqueous solutionCenter (category theory)General ChemistryCrystal structureNuclear magnetic resonance spectroscopy010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencescoordination polymersCrystallographychemistry.chemical_compoundchemistryPyridineImidazoleGeneral Materials Sciencepolymeeritta116Single crystalpolymersCrystal Growth & Design
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Determination of Phenol by Preconcentration‐Direct Chemiluminescence in a FIA Assembly

2005

Abstract The determination of phenol in water samples is proposed with the aid of a flow‐injection system. The analytical procedure is based on the direct chemiluminometric emission by oxidation of the analyte with potassium permanganate in acidic medium. The flow assembly is provided with a solid‐phase reactor filled with a resin type XAD‐4 for analyte preconcentration. A large study of potential interferences, namely, amino acids reaching water through degradation of organic matter; metals and inorganic metal ions typically present in water interfering with the CL emission of the parent compound, was performed. The calibration graph was linear over the phenol concentration range 1.0–20.0 …

Detection limitAnalyteChemistryCalibration curveMetal ions in aqueous solutionBiochemistry (medical)Clinical BiochemistryInorganic chemistryBiochemistryAnalytical Chemistrylaw.inventionStandard curvePotassium permanganatechemistry.chemical_compoundlawElectrochemistryPhenolSpectroscopyChemiluminescenceAnalytical Letters
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Influence of water sample storage protocols in chemiluminescence detection of trace elements.

2002

This paper shows the influence of different sample storage protocols, on the chemiluminescence signal of some metal ions. The storage protocols studied were: acid addition (HCl or HNO(3)) and no reagent addition to filtered and refrigerated (T=4 degrees C) samples. Light emission was produced for the chemiluminescence reaction between luminol and hydrogen peroxide in buffer carbonate conditions (pH 10.8) catalysed by Cr(III), Co(II) and Cu(II). Batch and/or flow modes in different conditions were tested. Fe(II), Fe(III), Ni(II) and Mn(II) did not give chemiluminescence in the studied conditions. A parallel study of sensitivity and selectivity was performed. Then the presence or absence of t…

Detection limitMetal ions in aqueous solutionAnalytical chemistryAnalytical ChemistryLuminollaw.inventionchemistry.chemical_compoundchemistrylawReagentLight emissionHydrogen peroxideMasking agentChemiluminescenceTalanta
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Metal ions modify DNA-protecting and mutagen-scavenging capacities of the AV-153 1,4-dihydropyridine.

2019

Abstract 1,4-Dihydropyridines (1,4-DHP) possess important biochemical and pharmacological properties, including antioxidant and antimutagenic activities. AV-153-Na, an antimutagenic and DNA-repair enhancing compound was shown to interact with DNA by intercalation. Here we studied DNA binding of several AV-153 salts to evaluate the impact of AV-153 modifications on its DNA binding capacity, the ability to scavenge the peroxynitrite, to protect HeLa and B-cells cells against DNA damage. Affinity of the AV-153 salts to DNA measured by a fluorescence assay was dependent on the metal ion forming a salt in position 4 of the 1,4-DHP, and it decreased as follows: Mg > Na > Ca > Li > Rb > K. AV-153-…

DihydropyridinesAntioxidantDNA RepairDNA damageHealth Toxicology and Mutagenesismedicine.medical_treatmentMetal ions in aqueous solutionIntercalation (chemistry)[SDV.CAN]Life Sciences [q-bio]/CancerMutagen02 engineering and technologymedicine.disease_causeNiacinAntioxidantsHeLa03 medical and health scienceschemistry.chemical_compoundPeroxynitrous AcidGeneticsmedicineHumansDrug InteractionsDNA Breaks Single-StrandedComputingMilieux_MISCELLANEOUS030304 developmental biology0303 health sciencesB-Lymphocytesbiology021001 nanoscience & nanotechnologybiology.organism_classificationIntercalating AgentsRecombinant ProteinsOxidative StresschemistryMetalsBiophysicstat Gene Products Human Immunodeficiency VirusComet AssaySingle-Cell Analysis0210 nano-technologyDNAPeroxynitriteDNA DamageHeLa CellsMutation research. Genetic toxicology and environmental mutagenesis
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Simultaneous Removal and Recovery of Metal Ions and Dyes from Wastewater through Montmorillonite Clay Mineral

2019

The main objective of this work was to evaluate the potential of Montmorillonite nanoclay (Mt), readily and inexpensively available, for the simultaneous adsorption (and removal) of two classes of pollutants: metal ions and dyes. The attention was focused on two &ldquo

DyeGeneral Chemical EngineeringMetal ions in aqueous solutionGroundwater remediation02 engineering and technologyAdsorption; Dyes; Metal ions; Montmorillonite; Wastewaters010501 environmental sciences01 natural sciencesdyesmetal ionArticlechemistry.chemical_compoundsymbols.namesakeAdsorptionGeneral Materials ScienceCrystal violetMetal ionwastewater0105 earth and related environmental sciencesSettore CHIM/02 - Chimica FisicaMontmorilloniteSettore GEO/06 - MineralogiaAqueous solutionLangmuir adsorption modelmetal ions021001 nanoscience & nanotechnologyWastewatersMontmorilloniteWastewaterChemical engineeringchemistryadsorptionsymbolsAdsorption0210 nano-technologywastewatersNanomaterials
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Trace element fractionation through halite crystallisation: Geochemical mechanisms and environmental implications

2019

Halite is an important mineral for industry, agriculture and food production. It crystallises after water evaporation, while the progressive growth of dissolved metal ions in brines is occurring. Then, halite exploitation may provide the delivery of metal ions in the environment and the mechanism of this trace element accumulation should be studied. In this work we investigate the distribution of lanthanides and Y (hereafter named Rare Earth Elements, REE), Zr and Hf between crystallising halite and brines in the Dead Sea as geochemical tools for recognising the mechanism of metal ion removal from brines and accumulation in halite. Halite forms cubic crystals where octahedral planes sometim…

Environmental Engineering010504 meteorology & atmospheric sciencesEvaporiteChemistryMetal ions in aqueous solutionInorganic chemistryDead Sea Zr-Hf decoupling Ab-initio calculation REE Environmental pollution De-icing saltTrace elementEnvironmental pollution010501 environmental sciencesengineering.material01 natural sciencesPollutionMetalCrystalvisual_artengineeringvisual_art.visual_art_mediumEnvironmental ChemistryHaliteWaste Management and DisposalDissolution0105 earth and related environmental sciencesScience of The Total Environment
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