Search results for "METAL"

showing 10 items of 7908 documents

On the Road to MM′X Polymers: Redox Properties of Heterometallic Ni···Pt Paddlewheel Complexes

2014

On the quest of heterometallic mixed-valence MM'X chains, we have prepared two stable discrete bimetallic compounds: the reduced (PPN)[ClNi(μ-OSCPh)4Pt] (PPN = bis(triphenylphosphine)iminium; OSCPh = benzothiocarboxylato) and the oxidized [(H2O)Ni(μ-OSCPh)4PtCl] species. The role of the aqua and chlorido axial ligands is crucial to facilitate oxidation of the {Ni(μ-OSCPh)4Pt} core. Experimental and theoretical analyses indicate that a NiPt-Cl/Cl-NiPt isomerization process occurs in the oxidized species. The electronic structure of the reduced system shows two unpaired electrons, one located in a d(x(2)-y(2)) orbital of the Ni(II) ion and a second in the antibonding d(z(2)-dz(2)) combination…

010405 organic chemistryChemistryIminium010402 general chemistryPhotochemistryAntibonding molecular orbital01 natural sciencesRedox0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundUnpaired electron[CHIM]Chemical SciencesMolecular orbitalPhysical and Theoretical ChemistryTriphenylphosphineBimetallic stripIsomerizationComputingMilieux_MISCELLANEOUS
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Hybrid Molecular Materials Based upon Magnetic Polyoxometalates and Organic π-Electron Donors:  Syntheses, Structures, and Properties of Bis(ethylene…

1998

International audience; The syntheses, crystal structures, and physical properties of the series of radical salts made with bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF or ET) and monosubstituted α-Keggin polyoxoanions of formula [XZ(H2O)M11O39]5- (XZM11 = Si(IV)Fe(III)Mo11, Si(IV)Cr(III)W11, P(V)Con(II)W11, P(V)Ni(II)W11, P(V)Cu(II)W11 P(V)Zn(II)W11, P(V)Mn(II)W11, and P(V)Mn(II)Mo11) containing a magnetic metal ion Z on a peripheral octahedral site of the Keggin union are reported. They all crystallize in two related series called α2 and α3. The general structure consists of alternating layers of the organic donor and the Keggin polyoxometalates. While the stoichiometry and α-packing a…

010405 organic chemistryChemistryInorganic chemistryGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesIonMetalCrystallographychemistry.chemical_compoundColloid and Surface ChemistryOctahedronPolymerizationvisual_artPhase (matter)visual_art.visual_art_medium[CHIM]Chemical SciencesStoichiometryTetrathiafulvaleneJournal of the American Chemical Society
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A decacobalt(ii) cluster with triple-sandwich structure obtained by partial reductive hydrolysis of a pentacobalt(ii/iii) Weakley-type polyoxometalat…

2016

Partial reductive hydrolysis of a penta-CoII/III cluster [CoII4(H2O)2(CoIIIW9O34)(PW9O34)]12− (1) leads to the formation of [Co2{Co3(H2O)(Co(OH)2W7O26)(PW9O34)}2]22− (2). This polyoxometalate is made up of two capping [PW9O34]9− units and two bridging [W7O26]10− units that assemble to encapsulate a novel deca-CoII cluster core comprising octahedral and tetrahedral CoII ions.

010405 organic chemistryChemistryInorganic chemistryMetals and AlloysGeneral ChemistryType (model theory)010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHydrolysisCrystallographyOctahedronPolyoxometalateMaterials ChemistryCeramics and CompositesCluster (physics)Chemical communications (Cambridge, England)
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Electrochemical instability of highly fluorinated tetraphenyl borates and syntheses of their respective biphenyls

2018

Highly fluorinated tetraphenyl borate anions are of importance as weakly coordinating anions in metalorganic reactions. However, at high positive potentials their electrochemical stability in organic solvents is not sufficient. This was investigated by a comprehensive cyclic voltammetry study and can be used synthetically to generate highly fluorinated biphenyls.

010405 organic chemistryChemistryInorganic chemistryMetals and Alloyschemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesInstabilityCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMaterials ChemistryCeramics and CompositesCyclic voltammetryBoronChemical Communications
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Electrochemical, Spectroelectrochemical, and Structural Studies of Mono- and Diphosphorylated Zinc Porphyrins and Their Self-Assemblies

2019

International audience; Three series of porphyrins containing a Zn(II) central metal ion and zero, one or two phosphoryl groups at the meso-positions of the macrocycle were characterized as to their electrochemical, spectroscopic and structural properties in non-aqueous media. The investigated compounds are represented as 5,15-bis(4'-R-phenyl)porphyrinatozinc, 10-(diethoxyphosphoryl)-5,15-bis(4'-R-phenyl)porphyrinatozinc and 5,15-bis(diethoxyphosphoryl)-10,20-bis(4'-R-phenyl)porphyrinatozinc, where R = OMe, Me, H or CN. Linear-free energy relationships are observed between the measured redox potentials at room temperature and the electronic nature of the substituents at the 5 and 15 meso-ph…

010405 organic chemistryChemistryInorganic chemistrychemistry.chemical_elementZinc010402 general chemistryElectrochemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetal[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryvisual_artvisual_art.visual_art_medium[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry
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Localization of alkali metal ions in sodium-promoted palladium catalysts as studied by low energy ion scattering and transmission electron microscopy

1996

Three series of palladium-based catalysts have been studied by Low Energy Ion Scattering (LEIS) and Transmission Electron Microscopy (TEM). The first series is comprised of Na-Pd/SiO{sub 2} catalysts, obtained by addition of palladium to a silica support and by further addition of sodium ions with a Na/Pd atomic ratio (R) equal to 0,6.4 and 25.6. The second series consists of palladium catalysts supported on natural pumice, in which, due to a different loading of supported palladium, R{prime}, the (Na+K)/Pd atomic ratio, is equal to 17.0 and 39.4. The third series is represented by two palladium-based catalysts supported on {open_quotes}model pumices,{close_quotes} synthetic silico-aluminat…

010405 organic chemistryChemistryInorganic chemistrychemistry.chemical_element[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryAlkali metal01 natural sciencesCatalysis0104 chemical sciencesCatalysisIonMetalTransition metalLow-energy ion scatteringvisual_artvisual_art.visual_art_mediumAtomic ratioPhysical and Theoretical ChemistryPalladium
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The nature of interactions of benzene with CF3I and CF3CH2I

2019

In situ grown crystals of CF3I and CF3CH2I are dominated by I⋯I and F⋯F interactions. Their co-crystals with benzene, (CF3I)2·C6H6 and CF3CH2I·C6H6, contain two completely different sets of intermolecular interactions. (CF3I)2·C6H6 shows a unique halogen-bond type: above-the-bond C–I⋯πC6H6 interactions. CF3CH2I·C6H6 shows above-the-centre C–H⋯πC6H6 interactions. These interactions are electrostatically dominated type II halogen bonds between single halogenoalkane molecules and weaker dispersion dominated interactions between the co-crystal components. The observed preferences for benzene for the two binding partners match with calculated molecular electrostatic potentials.

010405 organic chemistryChemistryIntermolecular forceMetals and AlloysGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundChemical physicsHalogenMaterials ChemistryCeramics and CompositesMoleculeDispersion (chemistry)BenzeneChemical Communications
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Theoretical search for very short metal-actinide bonds: NUIr and isoelectronic systems.

2004

, respectively. These analogues provide anexample ofthe isolobal principle, now without any outsideligands onthePt atom,asituation describedasits “autogenicisolobality”. These systems have multiple C Pt bonds. Theisolobal principle of Hoffmann refers to the similar chemicalbehaviorofansphybridandametalatomwithligands,-ML

010405 organic chemistryChemistryIsolobal principleGeneral ChemistryGeneral MedicineActinide010402 general chemistryIridiumMultiple bonds01 natural sciencesCatalysisComputer chemistry0104 chemical sciencesMetalCrystallographyDensity functional calculationsvisual_artAtomddc:540visual_art.visual_art_mediumPhysical chemistryUraniumMultiple bondingAngewandte Chemie (International ed. in English)
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Synthesis of copper(II) and gold(III) bis(NHC)-pincer complexes

2016

Abstract CuII and AuIII chlorido complexes bearing the bis(NHC) carbazolide pincer ligand (bimca) were synthesized by transmetallation from the respective lithium complex [Li(bimca)] (NHC=N-heterocyclic carbene). In the case of copper, two different molecular structures were obtained depending on the copper source. With Cu(II) chloride the paramagnetic mononuclear [Cu(bimca)Cl] complex is formed and has been characterized by EPR spectroscopy and X-ray structure analysis, while copper(I) chloride leads under oxidation to a dinuclear structure in which two cationic [CuII(bimca)] moieties are bridged by one chlorido ligand. The positive charge is compensated by the [CuCl2]− counter ion, as pro…

010405 organic chemistryChemistryLigandCationic polymerizationchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCopperMedicinal chemistry0104 chemical sciencesPincer movementlaw.inventionchemistry.chemical_compoundTransmetalationlawElectron paramagnetic resonancePincer ligandCarbeneZeitschrift für Naturforschung B
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Soluble Heterometallic Coordination Polymers Based on a Bis-terpyridine-Functionalized Dioxocyclam Ligand

2010

Soluble homo- and heterometallic coordination polymers containing transition metal cations (Cu(2+), Fe(2+), Co(2+), and Ni(2+) ions) were prepared in a two-step procedure using a polytopic bis(terpyridine)dioxocyclam ligand 1H(2) (dioxocyclam = 1,4,8,11-tetraazacyclotetradecane-5,7-dione). These supramolecular systems incorporate two different metal complexes, the metal cations being located both between two terpyridine units and in the macrocyclic framework. The characterization of these soluble architectures was investigated by cyclic voltammetry, mass spectrometry, viscosimetry, and UV-vis absorption and electron paramagnetic resonance (EPR) spectroscopies. Our results clearly indicate t…

010405 organic chemistryChemistryLigandMetal ions in aqueous solutionSupramolecular chemistry010402 general chemistryPhotochemistry01 natural sciences[ CHIM ] Chemical Sciences0104 chemical scienceslaw.inventionInorganic ChemistryMetalchemistry.chemical_compoundTransition metallawvisual_artPolymer chemistryvisual_art.visual_art_medium[CHIM]Chemical SciencesPhysical and Theoretical ChemistryTerpyridineCyclic voltammetryElectron paramagnetic resonanceComputingMilieux_MISCELLANEOUS
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