Search results for "polyoxometalate"

showing 10 items of 86 documents

Magnetic excitations in an exchange-coupled tetramer cluster of cobalt (II): a study by inelastic neutron scattering

1992

Abstract The polyoxometalate K 10 [Co 4 (H 2 O) 2 (PW 9 O 34 ) 2 ].20H 2 O contains a ferromagnetically exchange-coupled tetramer of Co 11 encapsulated in between two diamagnetic molecules (PW 9 O 34 -9 . At 2.5K several inelastic peaks are observed in the energy range 1.5–7 meV, which are assigned to magnetic excitations in the cluster. A tentative interpretation of these data from an anisotropic exchange model yields a cobalt-cobalt interaction of 3meV (24cm -1 ) and an amount of anisotropy J xy / J z ≌0.6. These values are consistent with the magnetic susceptibility measurements.

Materials sciencechemistry.chemical_elementCondensed Matter PhysicsMagnetic susceptibilityInelastic neutron scatteringElectronic Optical and Magnetic MaterialschemistryTetramerPolyoxometalateCluster (physics)DiamagnetismElectrical and Electronic EngineeringAtomic physicsAnisotropyCobaltPhysica B: Condensed Matter
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Assembly of modular asymmetric organic-inorganic polyoxometalate hybrids into anisotropic nanostructures.

2010

Three organic-inorganic hybrid Mn-Anderson polyoxometalates (POMs), with both symmetrical and asymmetrical appended groups, have been synthesized, identified using electrospray mass spectrometry, and isolated using an approach that allows the three AA, BB, and AB compounds to be structurally characterized. Investigation of the self-assembly of the hybrids on hydrophilic surfaces reveals the formation of nanofibres with characteristics that reflect the nature of the substitution of the POM yielding a route to the programmed assembly of anisotropic hybrid nanostructures.

Models MolecularNanostructureElectrospray mass spectrometryChemistryGeneral ChemistryTungsten CompoundsBiochemistryCatalysisMass SpectrometryNanostructuresSelf-assembly Langmuir-Blodgett Scanning Force Microscopy Polyoxomethalates Hybrid Anysotropic NanostructuresColloid and Surface ChemistryChemical engineeringInorganic ChemicalsPolyoxometalateOrganic inorganicOrganic chemistryAnisotropyOrganic ChemicalsAnisotropySettore CHIM/02 - Chimica FisicaHybridJournal of the American Chemical Society
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Two Novel Polyoxometalate-Encapsulated Metal–Organic Nanotube Frameworks as Stable and Highly Efficient Electrocatalysts for Hydrogen Evolution React…

2018

Two novel polyoxometalate (POM)-encapsulated metal–organic nanotube (MONT) framework crystalline materials with unprecedented copper-mixed ligands, HUST-200 and HUST-201, have been successfully synthesized by an effective synthesis strategy. The encapsulation not only provides a shield to increase the chemical stability, but also does not affect its catalytic activity, and, therefore, the crystalline materials are very active for HER (H+ can diffuse easily through the pores of the MONTs). Remarkably, HUST-200 displays a low overpotential of 131 mV (catalytic current density is equal to 10 mA·cm–2). This work thus offers a new way for devising HER electrocatalysts with low cost using POM-enc…

NanotubeMaterials scienceCrystalline materials02 engineering and technologyOverpotential010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysisMetalChemical engineeringvisual_artPolyoxometalatevisual_art.visual_art_mediumGeneral Materials ScienceHydrogen evolutionChemical stability0210 nano-technologyACS Applied Materials & Interfaces
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Recent advances in polyoxometalate-containing molecular conductors

2005

The recent advances in crystalline conducting molecular materials based on polyoxometalates (POMs) and organic donors of the tetrathiafulvalene (TTF) family or perylene are discussed. We emphasise the wide diversity of POM structural types and the variety of packing architectures for the organic molecules that can be induced by these inorganic anions. Besides structural effects, we show that these hybrids can have interesting electric and/or magnetic properties. Thus, in the last years the common belief that this type of radical salts containing such big and highly charged anions could only exhibit poor conducting properties has been refuted by the production of new materials exhibiting hig…

New materialsNanotechnologyOrganic moleculesInorganic ChemistryMetalchemistry.chemical_compoundchemistryvisual_artPolyoxometalateMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryMolecular materialsElectrical conductorTetrathiafulvalenePeryleneCoordination Chemistry Reviews
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Poly(polyoxotungstate)s with 20 Nickel Centers: From Nanoclusters to One-Dimensional Chains

2009

NickelCrystallographychemistryPolyoxometalateCluster (physics)chemistry.chemical_elementGeneral MedicineGeneral ChemistryPhotochemistryCatalysisNanoclustersAngewandte Chemie International Edition
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Polyoxometalate salts of cationic nitronyl nitroxide free radicals

2008

The cationic nitronyl nitroxide free radical of the N-methylpyridinium type p-MepyNN + has been combined with [Mo 8 0 26 ] 4- and Keggin [SiW 12 0 40 ] 4- polyanions to afford salts ( p-MepyNN) 4 [Mo 8 0 26 ] DMSO (DMSO = dimethylsulfoxide) (1) and (p-MepyNN)4[SiW 12 0 40 ] 6DMF (DMF = dimethylformamide) (2). Herein, their structural and magnetic properties are described.

Nitroxide mediated radical polymerizationChemistryMagnetismRadicalCationic polymerizationGeneral ChemistryCondensed Matter PhysicsPhotochemistrychemistry.chemical_compoundMetallatePolyoxometalatePolymer chemistryDimethylformamideGeneral Materials ScienceGroup 2 organometallic chemistrySolid State Sciences
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Restricting Magnetic Interaction Pathways in Polyoxometalate Salts of Cationic Nitronyl Nitroxide Free Radicals

2004

Abstract : Salts 1 and 2 that combine the [W 6 O 19 ] 2- Lindqvist anion with the cationic nitronyl nitroxide (NN) free radicals p -MepyNN + and n Bu 3 NCH 2 NN + , respectively, have been synthesized and their structural and magnetic properties have been studied. Keywords: Nitroxide radicals, polyoxometalates, magnetism. Introduction Ferromagnetism based on purely organic materials has raised a lot of interest during the last decade [1]. Most of the studies have been performed with nitronyl nitroxide (NN) radicals due to their persistence, stability and ease of functionalization [2]. Bulk ferromagnetism in these compounds arises from ferromagnetic interactions between open-shell molecules …

Nitroxide mediated radical polymerizationFree RadicalsMagnetismPharmaceutical ScienceCrystallography X-RayPhotochemistryCrystal engineeringArticleNitroxide radicalsAnalytical Chemistrylcsh:QD241-441Magneticslcsh:Organic chemistryCationsDrug DiscoveryAntiferromagnetismMoleculepolyoxometalatesPhysical and Theoretical Chemistrymagnetism.ChemistryOrganic ChemistryIntermolecular forceTemperatureTungsten CompoundsCrystallographyFerromagnetismChemistry (miscellaneous)PolyoxometalateMolecular MedicineNitrogen OxidesDimerizationMolecules
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Gd-based single-ion magnets with tunable magnetic anisotropy: Molecular design of spin qubits

2012

et al.

PhysicsMagnetic anisotropyPhysics and Astronomy (all)Condensed matter physicsPulsed EPRPolyoxometalateIsotropyGeneral Physics and AstronomyFigure of meritMoleculeQuantum tunnellingIon
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Magnetic excitations in polyoxometalate tetrameric clusters

1997

Abstract The metal-oxide clusters with formula [M4(D2O)2(PW9O34)2]10− which contain a tetrameric magnetic cluster M4O16 provide an ideal series for the study of magnetic exchange interactions in polymetallic molecular clusters. To get a more direct information on the splitting of the spin states caused by the exchange interactions we have performed inelastic neutron scattering measurements on the Co, Mn and Ni clusters. Magnetic excitations have been observed in the range 0.5–6 meV. A tentative interpretation of these data from a Heisenberg exchange Hamiltonian and a single ion zero-field splitting is presented for Ni cluster.

PhysicsSpin statesSingle ionCondensed Matter PhysicsInelastic neutron scatteringElectronic Optical and Magnetic MaterialsMagnetic anisotropysymbols.namesakeFerromagnetismPolyoxometalateCluster (physics)symbolsElectrical and Electronic EngineeringAtomic physicsHamiltonian (quantum mechanics)Physica B: Condensed Matter
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Single-Crystal-to-Single-Crystal Anion Exchange in a Gadolinium MOF: Incorporation of POMs and [AuCl4]−

2016

The encapsulation of functional molecules inside porous coordination polymers (also known as metal-organic frameworks, MOFs) has become of great interest in recent years at the field of multifunctional materials. In this article, we present a study of the effects of size and charge in the anion exchange process of a Gd based MOF, involving molecular species like polyoxometalates (POMs), and [AuCl4]−. This post-synthetic modification has been characterized by IR, EDAX, and single crystal diffraction, which have provided unequivocal evidence of the location of the anion molecules in the framework.

Polymers and PlasticsGadoliniumInorganic chemistryPorous Coordination Polymerschemistry.chemical_element010402 general chemistry01 natural sciencesArticleSingle Crystal DiffractionIonlcsh:QD241-441lcsh:Organic chemistryFunctional importanceanion exchangeMoleculepolyoxometalatesMaterialsIon exchange010405 organic chemistryGeneral ChemistryMOFs; anion exchange; polyoxometalatesMOFs0104 chemical sciencesCrystallographychemistryCristallsCompostos de coordinacióSingle crystalPolymers
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