Search results for "Metal ions in aqueous solution"

showing 10 items of 256 documents

DNA-binding of nickel(II), copper(II) and zinc(II) complexes: structure-affinity relationships

2013

Abstract Nickel(II), copper(II) and zinc(II) complexes with the same ligands normally display analogous coordination geometry and binding mode toward DNA. However, although qualitatively alike in structure and properties, different DNA-binding ability has often been observed. This review surveys the most recent examples of binding of the three metal ions complexed with monodentate and chelating bidentate to tetradentate ligands to DNA. An attempt has also been made to rationalize the observed trend in the values of the intrinsic DNA-binding constant, Kb, in terms of structural and chemical features.

DenticityMetal ions in aqueous solutionInorganic chemistryBinding constantchemistry.chemical_elementZincDNABinding constantCopperSettore CHIM/08 - Chimica FarmaceuticaInorganic ChemistryNickelCrystallographyZincchemistryNickelSettore CHIM/03 - Chimica Generale E InorganicaMaterials ChemistryChelationPhysical and Theoretical ChemistryCopperCoordination geometry
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Characterization of complexes formed between [Me2Sn(IV)]2+ and carboxymethylcelluloses.

2006

Complexes formed between carboxymethylcellulose (CMC) and the [Me(2)Sn(IV)]2+ cation have been prepared in the solid state and characterized by FTIR and Mossbauer spectroscopy. The complexes contained CMC with varying molar weight and degree of carboxylation, and the complexes were isolated both from acidic and from neutral solutions at varying metal-to-ligand ratios. The characteristic vibration bands of the ligands were identified from their pH-dependent FTIR spectra. In the organotin(IV) complexes obtained at pH approximately 2, the -COO- moieties were found to be coordinated in a monodentate manner, and the band characteristic of the protonated (unbound) -COO- group(s) was also identifi…

DenticityMetal ions in aqueous solutionInorganic chemistryInfrared spectroscopyBiochemistryAnalytical ChemistrySpectroscopy MossbauerDeprotonationSpectroscopy Fourier Transform InfraredOrganotin CompoundsCarboxymethylcelluloseValence (chemistry)Sn(IV)Molecular StructureLigandChemistryOrganic ChemistryStructureTin CompoundsGeneral MedicineQuadrupole splittingInfrared spectraTrigonal bipyramidal molecular geometryCrystallographyCarboxymethylcellulose SodiumMössbauer spectraCarbohydrate research
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Co-existence of ferro- and antiferromagnetic interactions in a hexanuclear mixed-valence CoIII2MnII2MnIV2 cluster sustained by a multidentate Schiff …

2019

The successful utilization of the “direct synthesis” approach yielded the unprecedented hexanuclear complex of formula [Co2MnII2MnIV2(L1)4Cl2(μ3-O)2(dmf)4]·2dmf (1) (H3L is the Schiff base derived from the condensation of salicylaldehyde and 3-aminopropane-1,2-diol). Single crystal X-ray analysis revealed that 1 crystallizes in the monoclinic system P21/c and it contains a rare mixed-valence {CoIII2MnII2MnIV2(μ2-O)8(μ3-O)2} core where all metal ions are linked through the phenolato and alkoxo groups of the L3− ligand. Besides the charge balance resulting from the X-ray structure, the oxidation state of the metal ions has been confirmed by XPS spectroscopy. Cryomagnetic studies indicate the …

DenticitySchiff baseValence (chemistry)Materials scienceSpin states010405 organic chemistryMetal ions in aqueous solution010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOxidation state[CHIM]Chemical SciencesAntiferromagnetism[CHIM.COOR]Chemical Sciences/Coordination chemistryComputingMilieux_MISCELLANEOUSMonoclinic crystal systemDalton Transactions
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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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