Search results for "Ferro"

showing 10 items of 2451 documents

Magnetic Excitations in Polyoxometalate Clusters Observed by Inelastic Neutron Scattering:  Evidence for Ferromagnetic Exchange Interactions and Spin…

1999

The ground-state properties of the tetranuclear Ni2+ cluster [Ni4(H2O)2(PW9O34)2]10- were investigated by combining magnetic susceptibility and magnetization measurements with a detailed inelastic neutron scattering (INS) study on a fully deuterated sample of K6Na4[Ni4(H2O)2(PW9O34)2]·24H2O. The temperature dependence of the magnetic susceptibility indicates a ferromagnetic coupling of the four constituent Ni2+ ions (s = 1), and a low-temperature magnetization study provides the magnitude of the S = 4 ground-multiplet splitting due to the single-ion anisotropy of the Ni2+ ions. Besides a more direct and precise determination of the anisotropic S = 4 ground-multiplet splitting, INS enabled t…

ChemistryGeneral ChemistryBiochemistryMolecular physicsMagnetic susceptibilityCatalysisInelastic neutron scatteringCrystallographyMagnetizationColloid and Surface ChemistryDeuteriumFerromagnetismExcited stateCondensed Matter::Strongly Correlated ElectronsSpin (physics)AnisotropyJournal of the American Chemical Society
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Climate Over the Ages; Is the Environment Stable?

2010

As described in Chaps. 3 and 4, the advent of oxygenic photosynthesis triggered worldwide environmental changes. A world that had been reductive passed over into a state in which free dioxygen was available in the oceans and the atmosphere. We have already described the likely catastrophic effects on an anaerobic biota, but the changes were much broader than that. Dioxygen in the seas led to major changes in seawater chemistry. Iron, which had previously been soluble as ferrous salts, was precipitated in the ferric form. Copper, which had been insoluble in the anaerobic ocean as cuprous sulphide (Cu+-state), now became moderately soluble in the cupric form (Cu++-state).

ChemistryGreat Oxygenation EventEnvironmental chemistryFerrous saltsmedicineCambrian explosionFerricchemistry.chemical_elementSeawaterBiotaPhotosynthesisCoppermedicine.drug
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A dihydrogen arsenate-mediated supramolecular network: crystal structure and magnetic properties of {[(bipy)Cu(μ-H2AsO4)(H2AsO4)]2}n

2002

Treatment of an aqueous suspension of Cu(OH)2 and 2,2′-bipyridine (bipy) with either Na2HAsO4·7H2O (1∶1∶2) or As2O5 (1∶1∶1) yields single crystals of {[(bipy)Cu(μ-H2AsO4)(H2AsO4)]2}n, 1, on standing. The solid-state structure of 1 consists of a three dimensional supramolecular network, supported by a combination of coordination covalent, hydrogen bonding and face-to-face π–π interactions. Variable temperature magnetic susceptibility measurements reveal very weak antiferromagnetic coupling between Cu(II) centres across the dihydrogen arsenate bridges (J = −0.58 cm−1).

ChemistryHydrogen bondSupramolecular chemistryArsenateGeneral ChemistryCrystal structureCondensed Matter PhysicsMagnetic susceptibilityAqueous suspensionAntiferromagnetic couplingCrystallographychemistry.chemical_compoundCovalent bondGeneral Materials ScienceCrystEngComm
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New Features in the dynamics of a ferroin-catalyzed Belousov-Zhabotinsky reaction induced by a zwitterionic surfactant

2008

Abstract Interactions between reaction–diffusion systems and aggregated host environments are a subject of widespread interest. In this work, the behavior of the Belousov–Zhabotinsky reaction was investigated in a micellar environment formed by the zwitterionic surfactant N-tetradecyl-N,N-dimethylamine oxide (C14DMAO). The appearance of an induction period with a threshold-like dependence upon the surfactant concentration, was detected at [C14DMAO] = 5.0 × 10−3 mol dm−3. These new features were explained in terms of the segregation ability typical of the amphiphilic self-assembling systems. Numerical simulations were also performed to confirm the proposed mechanism.

ChemistryInduction periodInorganic chemistryOxideGeneral Physics and AstronomyPhotochemistryCatalysischemistry.chemical_compoundBelousov–Zhabotinsky reactionPulmonary surfactantAmphiphileFerroinPhysical and Theoretical ChemistryBelousov–Zhabotinsky reaction zwitterionic surfactantSettore CHIM/02 - Chimica Fisica
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Magnetic polyoxometalates: anisotropic exchange interactions in the moiety of [(NaOH2)Co3(H2O)(P2W15O56)2]17-.

2005

The magnetic exchange interactions in a C0(3)(11) moiety encapsulated in Na(17) [(NaOH(2))Co(3)(H(2)O)(P(2)W(15)O(56))(2)] (NaCo(3)) were studied by a combination of magnetic measurements (magnetic susceptibility and low-temperature magnetization), with a detailed Inelastic Neutron Scattering (INS) investigation. The novel structure of the salt was determined by X-ray crystallography. The ferromagnetic Co(3)O(14) triangular cluster core consists of three octahedrally oxo-coordinated Co(II) ions sharing edges. According to the single-ion anisotropy and spin-orbit coupling usually assumed for octahedral Co(II) ions, the appropiate exchange Hamiltonian to describe the ground-state properties o…

ChemistryInorganic chemistryMagnetic susceptibilityInelastic neutron scatteringInorganic ChemistryCrystallographyMagnetizationFerromagnetismOctahedronMolecular symmetryMoietyCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryAnisotropyInorganic chemistry
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Molecule-Based Magnets Formed by Bimetallic Three-Dimensional Oxalate Networks and Chiral Tris(bipyridyl) Complex Cations. The Series [ZII(bpy)3][ClO…

2000

The synthesis, structure, and physical properties of the series of molecular magnets formulated as [ZII(bpy)3][ClO4][MIICrIII(ox)3] (ZII = Ru, Fe, Co, and Ni; MII = Mn, Fe, Co, Ni, Cu, and Zn; ox = oxalate dianion) are presented. All the compounds are isostructural to the [Ru(bpy)3][ClO4][MnCr(ox)3] member whose structure (cubic space group P4(1)32 with a = 15.506(2) A, Z = 4) consists of a three-dimensional bimetallic network formed by alternating MII and CrIII ions connected by oxalate anions. The identical chirality (lambda in the solved crystal) of all the metallic centers determines the 3D chiral structure adopted by these compounds. The anionic 3D sublattice leaves some holes where th…

ChemistryInorganic chemistryOxalateInorganic ChemistryCrystalMetalchemistry.chemical_compoundCrystallographyFerromagnetismvisual_artvisual_art.visual_art_mediumPhysical and Theoretical ChemistryIsostructuralChirality (chemistry)Bimetallic stripMolecule-based magnetsInorganic Chemistry
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Synthesis, Crystal Structure and Magneto‐Structural Correlation of an Unusual Thiocyanato‐Bridged Nickel( II ) Compound, [Ni(μ‐NCS)(dpt)(NCS)] 2 [Ni(…

2003

Reaction of Ni(ClO4)2·6H2O with bis(3-aminopropyl)amine (dpt) and ammonium thiocyanate produces the novel thiocyanato-bridged nickel(II) compound [Ni(μ-NCS)(dpt)(NCS)]2[Ni(μ-NCS)(dpt)(NCS)]4, which has been structurally characterised. The structure determination reveals that there are two different molecules in the crystal lattice; one is dinuclear and other is tetranuclear. Low-temperature magnetic measurements show that there are ferro- as well as antiferromagnetic interactions. The ferromagnetic interaction arises from the dinuclear part and the doubly bridged part of the tetranuclear unit; the antiferromagnetic interaction occurs between singly bridged nickel centres in the tetranuclear…

ChemistryInorganic chemistrychemistry.chemical_elementCrystal structureInorganic ChemistryCrystallographyNickelchemistry.chemical_compoundFerromagnetismStructural correlationAntiferromagnetismMoleculeAmine gas treatingAmmonium thiocyanateEuropean Journal of Inorganic Chemistry
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Trans-dicyanobis(acetylacetonato)ruthenate(III) as a precursor to build novel cyanide-bridged RuIII–MII bimetallic compounds [M=Co and Ni]

2006

Abstract The use of the mononuclear complex trans-[Ru(acac)2(CN)2]− as a ligand towards the preformed species [Ni2L(H2O)2Cl2], [Co(dmphen)](NO3)2, [Ni(dmphen)](NO3)2 and [Co(H2O)6](NO3)2 afforded the novel cyanide-bridged bimetallic compounds of formula [{Ru(acac)2(CN)2}{Ni2(L)(H2O)2}]{Ru(acac)2(CN)2}·2H2O (1), [{Ru(acac)2(CN)2}{Co(dmphen)(NO3)}]·H2O (2) and [{Ru(acac)2(CN)2}{Ni(dmphen)(NO3)}]·H2O (3) and [{Ru(acac)2(CN)2}2Co] (4) [Hacac = acetylacetone, dmphen = 2,9-dimethylphenanthroline and H2L = 11,23-dimethyl-3,7,15,19-tetrazatricyclo[19.3.1.19,13]hexacosa-2,7,9,11,13(26),14,19,21(25),22,24-decaene-25,26-diol]. Their syntheses, X-ray crystal structures and magnetic properties are repor…

ChemistryInorganic chemistrychemistry.chemical_elementCrystal structureRutheniumInorganic ChemistryCrystallographyNickelOctahedronMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryIsostructuralCobaltBimetallic stripCoordination Chemistry Reviews
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A New Heptanuclear Cobalt(II) Cluster Encapsulated in a Novel Heteropolyoxometalate Topology:  Synthesis, Structure, and Magnetic Properties of [Co7(…

2004

The synthesis and the structural and magnetic characterization of a novel heptanuclear cobalt cluster encapsulated in a heteropolyoxotungstate is reported. This complex shows how it is possible to control the nuclearity of the Co clusters formed in a tungstate solution by slightly changing the synthetic conditions, and the relevance of pH in this regard. This heptanuclear complex [Co7(H2O)2(OH)2P2W25O94]16- (Co7) crystallizes in the triclinic space group P1 (a = 12.3403(6) A, b = 22.5966(11) A, c = 23.2645(12) A, α = 68.7830(11)°, β = 83.7981(12)°, γ = 78.5423(13)°, V = 5922.4(5) A3, Z = 2) and is formed by six CoO6 octahedra from two Co3 trimers sustained by Keggin trivacant fragments held…

ChemistryInorganic chemistrychemistry.chemical_elementTriclinic crystal systemInorganic ChemistryCrystallographychemistry.chemical_compoundTungstateOctahedronGroup (periodic table)TetrahedronCluster (physics)AntiferromagnetismPhysical and Theoretical ChemistryCobaltInorganic Chemistry
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An Iron-Based Molecular Redox Switch as a Model for Iron Release from Enterobactin via the Salicylate Binding Mode

2001

The iron release mechanism from protonated ferric enterobactin [Fe(III)(enterobactinH(3))] via the salicylate binding mode was probed. For this purpose, a tripodal dodecadentate ligand incorporating three salicylamide (OO) and three bipyridine (NN) binding sites was synthesized as well as iron complexes thereof. It was shown that a ferric ion coordinates selectively to the hard salicylamides and a ferrous ion binds to the softer bipyridines. Upon reduction or oxidation, the iron translocates reversibly and intramolecularly from one site to the other, thus displaying switchlike properties. Both states were characterized by cyclic voltammetry and visible and Mössbauer spectroscopy. The Mössba…

ChemistryLigandInorganic chemistryProtonationRedoxFerrousInorganic ChemistryBipyridinechemistry.chemical_compoundEnterobactinPolymer chemistrymedicineFerricPhysical and Theoretical ChemistryCyclic voltammetrymedicine.drugInorganic Chemistry
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