Search results for "FERROMAGNETIC"

showing 10 items of 81 documents

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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Redox switching of the antiferromagnetic coupling in permethylated dicopper(ii) paracyclophanes

2012

A unique magnetic electroswitching behavior has been observed in an oxamato-based permethylated dicopper(II) paracyclophane; upon reversible one-electron oxidation of the double tetramethyl-substituted p-phenylenediamidate bridging skeleton, the spin alignment of the two Cu(II) ions (S(Cu) = ½) changes from antiparallel (OFF) to parallel (ON) in the resulting dicopper(II) π-radical cation species.

ChemistryMetals and AlloysGeneral ChemistryPhotochemistryRedoxCatalysisAntiferromagnetic couplingSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographyMaterials ChemistryCeramics and CompositesAntiparallel (electronics)Chemical Communications
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Relatively strong intramolecular antiferromagnetic coupling in a neutral Cr(III)2Nb(V)2 heterobimetallic molecular square.

2015

A relatively large antiferromagnetic interaction between the two chromium(III) ions from the molecular square [{Cr(dmso)4}2{Nb(μ-O)2(C2O4)2}2] () (J = -12.0 cm(-1)) is mediated by the diamagnetic oxo-Nb(V)-oxo pathway, its nature and magnitude being substantiated by DFT type theoretical calculations.

ChemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryType (model theory)CatalysisAntiferromagnetic couplingSquare (algebra)Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographyChromiumComputational chemistryIntramolecular forceMaterials ChemistryCeramics and CompositesDiamagnetismAntiferromagnetismChemical communications (Cambridge, England)
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Formation of a novel ferromagnetic end-to-end cyanate bridged homochiral helical copper(ii) Schiff base complex via spontaneous symmetry breaking

2014

A homochiral helical coordination polymer of copper(II) has been synthesized using achiral precursors via spontaneous symmetry breaking and has been confirmed by single crystal X-ray diffraction and solid-state CD spectroscopy. The variable temperature magnetic measurements indicate the presence of weak ferromagnetic exchange interactions mediated by end-to-end cyanate bridges (J = +0.12 cm(-1)).

Circular dichroismSchiff baseStereochemistryChemistryCoordination polymerSpontaneous symmetry breakingchemistry.chemical_elementcircular dichroism spectroscopyCyanateferromagnetismsingle crystalsCopperX-ray diffractionInorganic ChemistryCrystallographychemistry.chemical_compoundfunctional groupsFerromagnetismcopperferromagnetic materialsta116Single crystalDalton Transactions
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New Heusler Compounds and Their Properties

2013

Spintronics is a multidisciplinary field and a new research area. New materials must be found for satisfying the different types of requirement. The search for stable half-metallic ferromagnets and ferromagnetic semiconductors with Curie temperatures higher than room temperature is still a challenge for solid state scientists. A general understanding of how structures are related to properties is a necessary prerequisite for material design. Computational simulations are an important tool for a rational design of new materials. The new developments in this new field are reported from the point of view of material scientists.

Condensed Matter::Materials ScienceMaterials scienceSpintronicsField (physics)Spin polarizationFerromagnetismCurieFerromagnetic semiconductorNew materialsNanotechnologyMaterial Design
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One-dimensional oxalato-bridged copper(II) complex possessing two structurally different metallic centres

2001

Abstract The crystal structure of the oxalato-bridged copper(II) compound [Cu2(μ-ox)2(ampy)3]n 1 (ox=oxalate dianion, ampy=2-amino-3-methylpyridine) consists of infinite corrugated one-dimensional chains in which two types of copper(II) centres, five- and six-coordinated, are bridged sequentially by asymmetric bis-bidentate oxalato ligands. Magnetic susceptibility measurements show the occurrence of a significant intrachain antiferromagnetic coupling (J=−22.9 cm −1 ) .

Copper complexChemistryInorganic chemistrychemistry.chemical_elementCrystal structureCopperMagnetic susceptibilityOxalateAntiferromagnetic couplingInorganic ChemistryMetalCrystallographychemistry.chemical_compoundvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryInorganic Chemistry Communications
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Stoichiometry of LiNiO2 Studied by Mössbauer Spectroscopy

2002

From the 61Ni and 57Fe Mossbauer spectroscopy data follows the cationic site assignment in Li1−x Ni1+x O2. Our data explain the ferromagnetic properties of this material because of the appearance of Ni2+ (S = 1) among Ni3+ (S = 1/2) in Ni3+O2 hexagonal planes. We have no evidence for the ferromagnetic interaction between the NiO2 layers through the excess Ni2+ ions substituting the Li+ ions. The presence of Ni2+ found in the Ni3+O2 planes explains the absence of the Jahn-Teller distortions probably because of the electronic transfer between the Ni3+ and Ni2+ ions.

CrystallographyFerromagnetismMössbauer effectFerromagnetic material propertiesChemistryJahn–Teller effectMössbauer spectroscopyStoichiometryCharged particleIon
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Coexistence of spin-crossover and antiferromagnetic coupling phenomena in the novel dinuclear Fe(II) complex [Fe(dpa)(NCS)2]2bpym

2003

Abstract The iron(II) spin crossover dinuclear compound [Fe(dpa)(NCS) 2 ] 2 bpym where dpa = 2,2 ′ -dipyridylamine and bpym = 2,2 ′ -bipyrimidine has been synthesized and characterized. Variable-temperature magnetic susceptibility and 57 Fe Mossbauer spectroscopy data provide evidence for a rather complete and continuous S=2 ( HS )↔S=0 (LS) spin-crossover behavior taking place in the temperature range 400–50 K (T 1/2 =245 K ) without the presence of a plateau at 50% of conversion. The absence of such plateau, which is characteristic of all dinuclear compounds so far studied, is interpreted in terms of synergetic effect between intramolecular and intermolecular interactions.

CrystallographyNuclear magnetic resonanceChemistrySpin crossoverIntramolecular forceMössbauer spectroscopyIntermolecular forceGeneral Physics and AstronomyPhysical and Theoretical ChemistryAtmospheric temperature rangePlateau (mathematics)Magnetic susceptibilityAntiferromagnetic couplingChemical Physics Letters
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Interplay of Antiferromagnetic Coupling and Spin Crossover in Dinuclear Iron(II) Complexes

2003

This article reports on the study of the interplay between magnetic coupling and spin transition in 2,2′-bipyrimidine (bpym)-bridged iron(II) dinuclear compounds. Coexistence of both phenomena has been observed in [Fe(bpym)(NCS)2]2bpym, [Fe(bpym)(NCSe)2]2bpym and [Fe(bt)(NCS)2]2bpym (bpym = 2,2′-bipyrimidine, bt = 2,2′-bithiazoline) by the action of external physical factors namely pressure or electromagnetic radiation. Competition between magnetic exchange and spin crossover has been studied in [Fe(bpym)(NCS)2]2bpym at 6.3 kbar. LIESST experiments carried out in [Fe(bpym)(NCSe)2]2bpym and [Fe(bt)(NCS)2]2bpym at 4.2 K have shown that is possible to achieve dinuclear molecules with different…

CrystallographySpin statesCondensed matter physicsChemistrySpin crossoverSpin transitionMoleculeInductive couplingLIESSTAntiferromagnetic couplingMagnetic exchange
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Cyanide-bridged Fe(III)–Co(II) bis double zigzag chains with a slow relaxation of the magnetisation

2003

Reaction of [FeIII(bipy)(CN)4]¯ with fully solvated MII cations [M = Co (1) and Mn (2)] produces the isostructural bis double zigzag chains [[FeIII(bipy)(CN)4]2MII(H2O)]·MeCN·1/2H2O; 1 exhibits intrachain ferromagnetic and interchain antiferromagnetic couplings, slow magnetic relaxation and hysteresis effects. Luminita Marilena, Toma, Luminita.Toma@uv.es ; Lescouezec, Alain Francois Rodri, Alain.Lescouezec@uv.es ; Lloret Pastor, Francisco, Francisco.Lloret@uv.es ; Julve Olcina, Miguel, Miguel.Julve@uv.es

Cyanide-bridged Fe(III)–Co(II)CyanideUNESCO::QUÍMICA:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundMagnetizationMaterials ChemistryAntiferromagnetismIsostructuralHysteresis effectsCondensed matter physicsUNESCO::QUÍMICA::Química inorgánicaRelaxation (NMR)Metals and AlloysGeneral ChemistryCyanide-bridged Fe(III)–Co(II) ; Slow relaxation ; Ferromagnetic ; Antiferromagnetic ; Hysteresis effectsAntiferromagnetic:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyHysteresischemistryZigzagFerromagnetismFerromagneticCeramics and CompositesSlow relaxation
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