Search results for "Chela"

showing 10 items of 415 documents

Binding ability of N-Para-amino-phenylsulfonyl derivatives of amino acids. Potentiometric and spectroscopic studies of Cu(II) complexes

1995

Abstract N-Para-amino-phenylsulfonyl derivatives of amino acids are very effective ligands for Cu(II) ions. Potentiometric and spectroscopic results have shown that Cu(II) ions are able to deprotonate and bind to sulfonamide nitrogen below pH 5 to form stable mono- and bis-[N − , COO − ] chelates. The basicity of sulfonamide nitrogen is lower than peptide amide nitrogen and no distinct anchoring site is necessary to promote the amide nitrogen deprotonation.

chemistry.chemical_classificationPotentiometric titrationchemistry.chemical_elementPeptideBiochemistryNitrogenMedicinal chemistrySulfonamideAmino acidInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryAmideOrganic chemistryChelationJournal of Inorganic Biochemistry
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Synthesis of [5]Rotaxanes Containing Bi- and Tridentate Coordination Sites in the Axis

2010

A new example of a linear [5]rotaxane has been synthesized by using the traditional "gathering-and-threading" approach but based on an unusual axle incorporating a symmetrical bis(bidentate) chelating fragment built on a 4,7-phenanthroline core. The stoppering reaction is particularly noteworthy since, instead of using a trivial bulky stopper as precursor to the blocking group, two semistoppered copper-complexed [2]pseudorotaxanes (namely [2]semirotaxanes) are used, which leads to the desired [5]rotaxane in good yield. The efficiency of the method relies on the use of "click" chemistry, with its very mild conditions, and on the protection by a transition-metal (copper(I)) of the various coo…

chemistry.chemical_classificationRotaxaneDenticityLigandStereochemistryclick chemistry; copper; lithium; rotaxanes; zincOrganic Chemistrychemistry.chemical_elementGeneral ChemistryZincCatalysischemistry.chemical_compoundCrystallographychemistryClick chemistryChelationTerpyridineCounterionChemistry - A European Journal
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Cyclic Analogs of Desferrioxamine E Siderophore for 68Ga Nuclear Imaging: Coordination Chemistry and Biological Activity in Staphylococcus aureus

2021

As multidrug-resistant bacteria are an emerging problem and threat to humanity, novel strategies for treatment and diagnostics are actively sought. We aim to utilize siderophores, iron-specific strong chelating agents produced by microbes, as gallium ion carriers for diagnosis, applying that Fe(III) can be successfully replaced by Ga(III) without losing biological properties of the investigated complex, which allows molecular imaging by positron emission tomography (PET). Here, we report synthesis, full solution chemistry, thermodynamic characterization, and the preliminary biological evaluation of biomimetic derivatives (FOX) of desferrioxamine E (FOXE) siderophore, radiolabeled with 68Ga …

chemistry.chemical_classificationSiderophorePotentiometric titrationchemistry.chemical_elementBiological activityCombinatorial chemistryCoordination complexInorganic Chemistrychemistry.chemical_compoundchemistryStability constants of complexesAmideparasitic diseasesChelationPhysical and Theoretical ChemistryGalliumInorganic Chemistry
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Synthesis of ruthenium(II) compounds with ortho-oxypyridinate ligands (hp). Crystal structure characterization of [Ru(η6-p-CH3C6H4CH(CH3)2)Cl(hp)]

1988

Abstract The reaction of [Ru(η6-p-cymene)Cl2]2 (p-cymene = p-CH3C6H4CH(CH3)2) with Nahp in THF yields [Ru(η6]-p-cymene)Cl(hp)] (1). The crystal structure of (1) has been determined by X-ray methods. (1) crystallizes in the space group Pbca, with a = 16.629(2), b = 10.201(3), c = 17.752(2) A. The compound contains one coordinated arene group, one chlorine and one hp group in a chelating coordination mode. The reaction of (1) with Aghp yields [Ru(η6-p-cymene)(hp)2] (2). The 13C NMR spectrum at - 70°C is consistent with a structure Ru(η6-p-cymene)(η2-hp)(η1-hp). At room temperature a rapid interconvertion between the two hp ligands occurs according to the observed 1H and 13C NMR spectra.

chemistry.chemical_classificationStereochemistrychemistry.chemical_elementCrystal structureNuclear magnetic resonance spectroscopyCarbon-13 NMRRutheniumInorganic ChemistryCrystallographychemistryX-ray crystallographyMaterials ChemistryMoleculeChelationPhysical and Theoretical ChemistryInorganic compoundPolyhedron
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Interaction of Dimethyltin(IV)2+ Cation with Gly-Gly, Gly-His, and Some Related Ligands. A New Case of a Metal Ion Able To Promote Peptide Nitrogen D…

1999

Equilibrium (pH-metric) and spectroscopic (1H,13C, and 119Sn NMR and 119Sn Mossbauer) studies were performed to characterize the interaction of the dimethyltin(IV) cation with glycine, glycyl-glycine (Gly-Gly), imidazole-4-acetic acid, histamine, histidine, glycyl-histamine, glycyl-histidine (Gly-His), and β-alanyl-histidine (carnosine). For histamine and glycyl-histamine (having only nitrogen donor atoms) no complex formation was detected. The hydrolyzed species of the dimethyltin(IV) cation are always dominant over the complexes formed with the other ligands, except with Gly-Gly and Gly-His. For these two ligands, {COO-,N-,NH2} coordinated complexes are dominant in the neutral pH range wi…

chemistry.chemical_classificationanimal structuresAqueous solutionintegumentary systemInorganic chemistryPeptideMedicinal chemistryInorganic ChemistryMetalchemistry.chemical_compoundTrigonal bipyramidal molecular geometryDeprotonationchemistryvisual_artembryonic structuresvisual_art.visual_art_mediumChelationCarboxylatePhysical and Theoretical ChemistryHistidineInorganic Chemistry
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Kinetics of alkaline phosphatase from pig kidney. Influence of complexing agents on stability and activity

1976

Metal ion-complexing agents, like KCN, EDTA etc., inactivate alkaline phosphatase of pig kidney. This inactivation is reversible at low concentrations of the complexing agents and irreversible at high concentrations. The reversible inhibition is probably due to removal of Zn2+ ions from the active site, where they are necessary for catalytic action, whereas the irreversible inhibition results from the removal of Zn2+ ions necessary for preservation of the structure. The inactivation is pseudo-first order. It depends on the concentration, size and charge of the complexing agents. β-Glycerophosphate and Mg2+ ions protect the enzyme from inactivation by complexing agents. Quantitative examinat…

chemistry.chemical_classificationbiologyDimerInorganic chemistryAllosteric regulationKineticsSubstrate (chemistry)Active siteCell BiologyCombinatorial chemistryBiochemistrychemistry.chemical_compoundEnzymechemistrybiology.proteinAlkaline phosphataseChelationMolecular BiologyBiochemical Journal
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Studies towards the development of lipophilic bifunctional N3S3 chelators for 68Ga

2010

Abstract The present study is concerned with a concept of charge-neutral, lipophilic, macrocyclic bifunctional chelators, suitable for the introduction of a gallium-68 label into small molecules. The synthesis of a novel bifunctional N3S3-type chelator, derived from 1,4,7-triazacyclononane, initial 68Ga-radiolabelling and the determination of stability and calculated lipophilicity of the compound are described. The 68Ga-labelled chelate was obtained in a maximum radiochemical yield of 93±5% after a reaction time of 2 min. It remained intact over 3 h in a DTPA-challenge and a transferrin challenge experiment, indicating sufficient stability for PET studies.

chemistry.chemical_classificationchemistry.chemical_compoundChemistryTransferrinYield (chemistry)LipophilicityOrganic chemistryChelationPhysical and Theoretical ChemistryBifunctionalCombinatorial chemistrySmall moleculeRadiochimica Acta
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Crystal structure of 2-methyl-1H-imidazol-3-ium aquatrichlorido(oxalato-κ2O,O′)stannate(IV)

2015

N—H⋯O, N—H⋯Cl and O—H⋯O hydrogen bonds between cations and anions in the complex salt (C4H7N2)+[Sn(H2O)Cl3(C2O4)]− are responsible for the formation of a three-dimensional network structure.

chemistry.chemical_classificationcrystal structureStannateLigandHydrogen bondorganotin(IV) complexInorganic chemistrychemistry.chemical_elementSalt (chemistry)General ChemistryCrystal structureCondensed Matter PhysicsMedicinal chemistryOxalateResearch Communicationslcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999hydrogen bondsGeneral Materials ScienceChelationTinActa Crystallographica Section E: Crystallographic Communications
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The Influence of the Amide Linkage in the FeIII-Binding Properties of Catechol-Modified Rosamine Derivatives

2015

The two new fluorescent ligands RosCat1 and RosCat2 contain catechol receptors connected to rosamine platforms through an amide linkage and were synthesized by using microwave-assisted coupling reactions of carboxyl- or amine-substituted rosamines with the corresponding catechol units and subsequent deprotection. RosCat1 possesses a reverse amide, whereas RosCat2 has the usual oriented amide bond (HNCO vs. CONH, respectively). The ligands were characterized by means of NMR spectroscopy, mass-spectrometry, and DFT calculations and X-ray crystallography studies for RosCat1. The influence of the amide linkage on the photophysical properties of the fluorescent ligands was assessed in different …

chemistry.chemical_classificationligand designCatecholChemistryStereochemistryOrganic ChemistryChemistry (all)Quantum yieldGeneral ChemistryNuclear magnetic resonance spectroscopyamideCatalysisCoupling reactionCoordination complexCrystallographychemistry.chemical_compoundironSettore CHIM/03 - Chimica Generale E InorganicaAmidePeptide bondChelationcoordination modemass spectrometry
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Fluorescent Type II Materials from Naphthylmethyl Polyamine Precursors

2004

Speciation studies in aqueous solution on the interaction of Cu2+ and Zn2+ with a series of polyaminic ligands N-naphthalen-1-ylmethyl-N′-{2-[(naphthalen-1-ylmethyl)-amino]-ethyl}-ethane-1,2-diamine (Ll), N-naphthalen-1-ylmethyl-N′-(2-{2-[(naphthalen-1-ylmethyl)-amino]-ethylamino}-ethyl)-ethane-1,2-diamine (L2) and N-naphthalen-1-ylmethyl-N′-[2-(2-{2-[(naphthalen-1-ylmethyl)-amino]-ethylamino}-ethylamino)-ethyl]-ethane-1,2-diamine (L3) containing two naphthylmethyl groups at their termini and N 1-(2-{2-[(naphthalen-1-ylmethyl)-amino]-ethylamino}-ethyl)-ethane-1,2-diamine (L4) containing just one naphthylmethyl group have been carried out at 298.1 K in 0.15 mol dm−3 NaCl. In the case of the …

chemistry.chemical_compoundAqueous solutionchemistryMetal ions in aqueous solutionInorganic chemistryChelationGeneral ChemistryPolyamineMedicinal chemistryFluorescenceSupramolecular Chemistry
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