Search results for "metal coordination"

showing 4 items of 4 documents

The Pyridyl Functional Groups Guide the Formation of Pd Nanoparticles Inside A Porous Poly(4-Vinyl-Pyridine)

2015

The reactivity of palladium acetate inside a poly(4-vinylpyridine-co-divinylbenzene) polymer is strongly influenced by the establishment of interaction between the Pd precursor and the pyridyl functional group in the polymer. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and simultaneous X-ray absorption near edge structure (XANES) and small angle X-ray scattering (SAXS) techniques have been applied to monitor the reactivity of palladium acetate in the presence of H-2 and CO as a function of temperature. H-2 reduces palladium acetate to Pd nanoparticles and acetic acid. The pyridyl groups in the polymer play a vital role both in stabilizing the formed acetic acid, thu…

INFRARED-SPECTRADiffuse reflectance infrared fourier transformpolymersmall angle X-ray scatteringInfrared spectroscopychemistry.chemical_elementPALLADIUM(II) ACETATEIR spectroscopy; nanoparticles; palladium; polymers; small angle X-ray scattering; X-ray absorption spectroscopyPhotochemistryCatalysisCatalysisInorganic ChemistryAcetic acidchemistry.chemical_compoundRUTHENIUM NANOPARTICLESPARTICLE FORMATIONENVIRONMENTALLY BENIGNReactivity (chemistry)Physical and Theoretical ChemistryCARBON-MONOXIDEpolymerschemistry.chemical_classificationPOLYMERIC SUPPORTSnanoparticleIN-SITUOrganic ChemistryIR spectroscopy; nanoparticles; palladium; polymers; small angle X-ray scattering; X-ray absorption spectroscopy; Inorganic Chemistry; Organic Chemistry; Physical and Theoretical Chemistry; CatalysisX-ray absorption spectroscopyPolymerpalladiumchemistryIR spectroscopynanoparticlesPalladium(II) acetateTRANSITION-METAL COORDINATIONRESOLVED SAXS ANALYSISPalladium
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Phosphorus-Chalcogen Ring Expansion and Metal Coordination

2017

The reactivity of 4-membered (RPCh)2 rings (Ch = S, Se) that contain phosphorus in the +3 oxidation state is reported. These compounds undergo ring expansion to (RPCh)3 with the addition of a Lewis base. The 6-membered rings were found to be more stable than the 4-membered precursors, and the mechanism of their formation was investigated experimentally and by density functional theory calculations. The computational work identified two plausible mechanisms involving a phosphinidene chalcogenide intermediate, either as a free species or stabilized by a suitable base. Both the 4- and 6-membered rings were found to react with coinage metals, giving the same products: (RPCh)3 rings bound to the…

metal coordination010405 organic chemistryChemistryInorganic chemistryCoinage metals010402 general chemistryRing (chemistry)01 natural sciences0104 chemical sciencesInorganic ChemistryMetalCrystallographyChalcogenring expansionOxidation statePhosphinidenevisual_artvisual_art.visual_art_mediumReactivity (chemistry)Lewis acids and basesPhysical and Theoretical Chemistryphosphorus-chalcogenta116
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CH vs. HC—Promiscuous Metal Sponges in Antimicrobial Peptides and Metallophores

2023

Histidine and cysteine residues, with their imidazole and thiol moieties that deprotonate at approximately physiological pH values, are primary binding sites for Zn(II), Ni(II) and Fe(II) ions and are thus ubiquitous both in peptidic metallophores and in antimicrobial peptides that may use nutritional immunity as a way to limit pathogenicity during infection. We focus on metal complex solution equilibria of model sequences encompassing Cys–His and His–Cys motifs, showing that the position of histidine and cysteine residues in the sequence has a crucial impact on its coordination properties. CH and HC motifs occur as many as 411 times in the antimicrobial peptide database, while …

metal coordinationOrganic ChemistryPharmaceutical ScienceAnalytical Chemistrybioinorganic chemistryantimicrobial peptidesthermodynamicspotentiometryChemistry (miscellaneous)Drug DiscoveryMolecular Medicinebioinorganic chemistry; antimicrobial peptides; metallophores; thermodynamics; potentiometry; metal coordinationmetallophoresPhysical and Theoretical ChemistryMolecules
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Zn2+ and Cu2+ complexes of a fluorescent scorpiand-type oxadiazole azamacrocyclic ligand: crystal structures, solution studies and optical properties

2020

A ligand comprised of a macrocyclic pyridinophane core having a pendant arm containing a secondary amine group linked through a methylene spacer to a pyridyl–oxadiazole–phenyl (PyPD) fluorescent system has been prepared (L). The crystal structures of [ZnL](ClO4)2 and [CuL](ClO4)2 show that M2+ is coordinated to all the nitrogen atoms of the macrocyclic core, the secondary amine of the pendant arm and the nitrogen atom of the pyridine group of the fluorescent moiety, the latter bond being clearly weaker than the one with the pyridine of the macrocycle. Solution studies showed the formation of a highly stable Cu2+ complex with 1 : 1 stoichiometry, whereas with Zn2+ least stable complexes were…

metal coordinationspectroscopic behaviourLigandzincOxadiazoleCrystal structureFluorescenceInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryPyridineMoietyAzacyclophanes oxadiazole scorpiand metal coordination zinc spectroscopic behaviourAmine gas treatingMethyleneAzacyclophanesoxadiazolescorpiandDalton Transactions
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