Search results for "Chela"

showing 10 items of 415 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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Effects of preorganization in the chelation of UO22+ by hydroxamate ligands: cyclic PIPO– vs linear NMA–

2018

International audience; Many siderophores incorporate as bidentate chelating subunits linear and more seldomly cyclic hydroxamate groups. In this work, a comparative study of the uranyl binding properties in aqueous solution of two monohydroxamic acids, the prototypical linear N-methylacetohydroxamic acid (NMAH) and the cyclic analog 1-hydroxypiperidine-2-one (PIPOH), has been carried out. The complex [UO2(PIPO)(2)(H2O)] crystallized from slightly acidic water solutions (pH < 5), and its molecular structure was determined by X-ray diffraction. The uranyl speciation in the presence of both ligands has been thoroughly investigated in a 0.1 M KNO3 medium at 298.2 K by the combined use of four …

DenticitySpeciation010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesCatalysisMetalchemistry.chemical_compounduranylMaterials Chemistry[CHIM.CRIS]Chemical Sciences/CristallographyMoleculeChelation[CHIM.COOR]Chemical Sciences/Coordination chemistry[PHYS]Physics [physics]Aqueous solutionLigandChemistryN-methylacetohydroxamic acidGeneral ChemistryUranyl0104 chemical sciencesCrystallographyStability constants of complexesvisual_artSolution thermodynamicscyclic hydroxamic acidvisual_art.visual_art_medium[CHIM.RADIO]Chemical Sciences/Radiochemistry
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Synthesis and structural investigations on R2Sn(IV)-D-aldonic acid complexes (R = methyl; butyl). Their effect on a new toxicity test organism,Liza s…

2008

Eight R2Sn(IV)-D-aldonate complexes [(R = Me, Bu; D-aldonate = D-galactonate2− (Galn), D-Gluconate2− (Glun), D-Gulonate2− (Guln), D-Ribonate2− (Ribn)], five of which are new derivatives, have been synthesized and structurally characterized both in solid and solution state by IR, 119Sn Mossbauer and 1H, 13C, 119Sn NMR spectroscopies, showing that ligands act as dianonic chelating agents. In solution phase, NMR data suggest that the bidentate chelation is attained by the O1 carboxylate and the vicinal O2 alkoxide atoms, which can be dynamically extended to a third binding site (O4) competing with O2. In Me2Sn(IV)-D-gluconate complex the occurrence of a self-association process leading to a di…

DenticityStereochemistryGeneral Chemistryorganotin(IV)NMRMossbauerInorganic Chemistrychemistry.chemical_compoundchemistrycarbohydrateSettore CHIM/03 - Chimica Generale E InorganicaAlkoxideAldonic acidToxicityhistopathologyTributyltinChelationCarboxylateBinding siteApplied Organometallic Chemistry
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Part 2. Synthesis, characterization and X-ray structure of a new enantiomerically pure bis-equatorial dirhodium(II) compound

2001

Abstract The UV irradiation of an acetone solution of Rh2(O2CCF3)4 and the chiral phosphane (1S, 2S, 5R)-(2-hydroxy-5-isopropenyl-2-methyl-cyclohexyl)diphenylphosphane, (+)PPh2(CHR*OH) leads to the formation of two diastereoisomeric bis-equatorial compounds of formula Rh2(μ-O2CCF3)2(η1-O2CCF3)2(η2-(+)PPh2(CHR*OH))2 P(+)2 and M(+)2 in a 1.5:1 ratio, respectively. Both compounds have been separated by standard column chromatography. The characterization of the enantiomer M(+)2 has been accomplished by X-ray crystallography. The molecular structure consists of an Rh2 4+ unit bridged by two trifluoroacetate ligands. The coordination of each metal center is fulfilled by one phosphine acting …

DenticityStereochemistryLigandMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundColumn chromatographychemistryMaterials ChemistryMoleculeChelationPhysical and Theoretical ChemistryEnantiomerPhosphineInorganica Chimica Acta
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Mono- and Bidentate Phosphine Ligands in the Palladium-Catalyzed Methyl Acrylate Dimerization

2003

The influence of several phosphine ligands on the activity, selectivity and stability of the catalytic system Pd(acac)2, ligand, [HOEt2][BF4] was studied in the dimerization of methyl acrylate (MA). It was found that the catalyst's activity increased with increasing the basicity of the monodentate ligands used, whereas bulky phosphines lowered the linearity of the dimers and the reaction rates. With chelating P N-, P P-, and P As-ligands the Pd-catalyst could be efficiently stabilized during the reaction. The use of 1-dibutylphosphino-2-dimethylaminoethane as ammonium tetrafluoroborate salt allowed the highest overall activity.

DenticityTetrafluoroborateLigandchemistry.chemical_elementGeneral ChemistryMedicinal chemistryCatalysischemistry.chemical_compoundchemistryOrganic chemistryChelationMethyl acrylatePhosphinePalladiumAdvanced Synthesis &amp; Catalysis
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Direct arylation of heterocycles: the performances of ferrocene-based polyphosphane ligands in palladium-catalyzed C-H bond activation

2010

International audience; The palladium-catalyzed direct arylation of alkylated- furan, thiophene, and thiazole and benzoxazole heterocycles with electronically and sterically deactivated bromoarenes was selectively and efficiently promoted by ferrocenyl polyphosphanes. In this C[BOND]H bond activation reaction of heteroaromatics, the performances of polydentate di-, tri-, and tetraphosphane ligands were compared, showing that the triphosphane 1,1′,2-tris(diphenylphosphino)-4-tert-butylferrocene 3 was the most effective for the coupling. The introduction of more electron-donating (iPr) or electron-withdrawing (furyl) groups on the phosphorus atoms did not improve the ligand performances. The …

Denticitychemistry.chemical_elementCH activation010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisThiopheneOrganic chemistryChelation[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryThiazoleheterocycles010405 organic chemistryLigandOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[CHIM.CATA]Chemical Sciences/CatalysisBenzoxazolepalladiumhomogeneous catalysis0104 chemical sciencesTriphosphanechemistryligands effectsPalladium
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Optical recognition and removal of Hg(II) using a new self-chemosensor based on a modified amino-functionalized Al-MOF

2017

Abstract We developed a simple self-chemical optical sensor for the monitoring and removal of ultra-trace levels of Hg(II) from aqueous media. The development of this sensor was based on the covalent attachment of amino-functionalized aluminum-based MOF particles with ninhydrin. The new sensor is densely coated with a chelating ligand to permit an ultra-fast, selective, pH-dependent visualization for removal of Hg(II) with detection limit (LOD∼0.494 μg L−1). Monitoring was accomplished via both a colorimetric signal visible to the naked eye as well as UV–vis absorption spectroscopy. Digital image-based colorimetric analysis has also used as a semi-quantitative analysis for determination the…

Detection limitAbsorption spectroscopyMetals and AlloysAnalytical chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryCovalent bondNinhydrinMaterials ChemistryChelationNaked eyeElectrical and Electronic Engineering0210 nano-technologyColorimetric analysisInstrumentationSilver oxideNuclear chemistrySensors and Actuators B: Chemical
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Gas-chromatographic elemental analysis via di(trifluorethyl)dithiocarbamato-chelates

1986

The capillary-gas-chromatographic conditions for the determination of trace metals after extraction from aqueous solution are optimized by coupling of capillaries and improvement of injection technique. Different detectors (FID and ECD) are tested. pH range and buffer systems for extraction of metal chelates are discussed.

Detection limitAqueous solutionChromatographyChemistryClinical BiochemistryExtraction (chemistry)General MedicineAnalytical ChemistryMetalElemental analysisvisual_artvisual_art.visual_art_mediumPh rangeGeneral Materials ScienceChelationTrace metalFresenius' Zeitschrift für analytische Chemie
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Hybrid Chelator-Based PSMA Radiopharmaceuticals: Translational Approach

2021

(1) Background: Prostate-specific membrane antigen (PSMA) has been extensively studied in the last decade. It became a promising biological target in the diagnosis and therapy of PSMA-expressing cancer diseases. Although there are several radiolabeled PSMA inhibitors available, the search for new compounds with improved pharmacokinetic properties and simplified synthesis is still ongoing. In this study, we developed PSMA ligands with two different hybrid chelators and a modified linker. Both compounds have displayed a promising pharmacokinetic profile. (2) Methods: DATA5m.SA.KuE and AAZTA5.SA.KuE were synthesized. DATA5m.SA.KuE was labeled with gallium-68 and radiochemical yields of various…

Diagnostic ImagingGlutamate Carboxypeptidase IIBiodistributionmedia_common.quotation_subjectPharmaceutical ScienceOrganic chemistryChemistry Techniques Syntheticurologic and male genital diseasesArticleAnalytical ChemistryTranslational Research BiomedicalMicechemistry.chemical_compoundhybrid chelatorNude mouseQD241-441In vivoNeoplasmsDrug DiscoveryLNCaPAnimalsHumansChelationradionuclide diagnosis and therapyPhysical and Theoretical ChemistryInternalizationChelating Agentsmedia_commonMolecular StructurebiologyChemistryRadiochemistrybiology.organism_classificationDisease Models AnimalKineticsChemistry (miscellaneous)Isotope LabelingAntigens SurfaceHeterograftsMolecular MedicineRadiopharmaceuticalsAmmonium acetateEx vivoprostate specific membrane antigen PSMAProtein BindingMolecules
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Ligand-Based Charge-Transfer Luminescence in Ionic Cyclometalated Iridium(III) Complexes Bearing a Pyrene-Functionalized Bipyridine Ligand: A Joint T…

2012

Two new heteroleptic iridium(III) complexes [Ir(ppy)(2)(pyr(2)bpy)][PF(6)] ([1a][PF(6)]) and [Ir(dfppy)(2)(pyr(2)bpy)][PF(6)] ([2a][PF(6)]), where Hppy = 2-phenylpyridine, Hdfppy = 2-(3,5-difluorophenyl)pyridine, and pyr(2)bpy = 5,5'-bis(pyren-1-yl)-2,2'-bipyridine, have been synthesized and fully characterized. The single-crystal structures of pyr(2)bpy and the complexes 4{[1a][PF(6)]}·2CH(2)Cl(2)·9H(2)O and [2a][PF(6)]·0.25CH(2)Cl(2)·H(2)O have been determined. The effect of the pyrene substituents on the electronic properties is investigated through a comprehensive photophysical and theoretical study on the two complexes in comparison to reference complexes without substituents on the an…

ELECTROLUMINESCENT DEVICESAbsorption spectroscopyEMITTING ELECTROCHEMICAL-CELLSchemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesInorganic ChemistryBipyridinechemistry.chemical_compoundPyridineCRYSTAL-STRUCTURESIridiumPhysical and Theoretical ChemistryCHELATED RUTHENIUM(II) COMPLEXEXACT-EXCHANGEChemistryLigand021001 nanoscience & nanotechnologyTRANSITION-METAL-COMPLEXES0104 chemical sciences3. Good healthCrystallographyPHOTOPHYSICAL PROPERTIESQUANTUM YIELDSIntramolecular forcePyreneEXCITED-STATE PROPERTIESSENSITIZED SOLAR-CELLS0210 nano-technologyLuminescenceInorg. Chem.
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