Search results for "Exchange Interactions"

showing 10 items of 14 documents

High‐nuclearity mixed‐valence magnetic clusters : A general solution of the double exchange problem

1996

We report here a general solution of the double‐exchange problem in the high‐nuclearity mixed valence systems containing arbitrary number P of the electrons delocalized over the network of N (P<N) localized spins. The developed approach is based on the successive (chainlike) spin‐coupling scheme and takes full advantage from the quantum angular momentum theory. In the framework of this approach the closed‐form analytical expressions are deduced for the matrix elements of the double exchange interaction, two‐electron transfer, and three‐center interaction that can be referred to as the potential exchange transfer. For the arbitrary nuclearity mixed‐valence systems the matrix elements of all …

Angular momentumValence (chemistry)SpinsChemistryExchange interactionExchange InteractionsGeneral Physics and AstronomyElectron TransferQuantum numberLocalized StatesUNESCO::FÍSICA::Química físicaDelocalized electronMolecular ClustersQuantum mechanicsMixed−Valence CompoundsPhysical and Theoretical ChemistryMatrix ElementsSpin−Lattice Relaxation:FÍSICA::Química física [UNESCO]Exchange Interactions ; Molecular Clusters ; Matrix Elements ; Electron Transfer ; Localized States ; Spin−Lattice Relaxation ; Mixed−Valence CompoundsQuantumBasis set
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Ferrimagnetic Heisenberg chain; influence of a random exchange interaction

1985

We report on the magnetic behavior of ‘‘rigid’’ ferrimagnetic chains isolated in bimetallic complexes of the EDTA and ‘‘flexible’’ ones obtained in the amorphous variety. As shown by LAXS, the only noteworthy difference in the amorphous state is the random distribution of bond angles between nearest neighbors within chains. The ‘‘rigid’’ bimetallic chains in CoNi(EDTA)6H2O are described in terms of Heisenberg model with an exchange coupling J=−7.5 K. The behavior of the amorphous variety somewhat differs, following the law X=AT−0.8 typical of REHAC. A classical spin chain model involving a J distribution and alternating g factors allows to explain successfully the temperature dependence of …

Chemical BondsMagnetic PropertiesExchange InteractionsEdtaGeneral Physics and AstronomyNickel CompoundsMagnetic SusceptibilityFerrimagnetic MaterialsFerrimagnetism:FÍSICA [UNESCO]HydratesExchange Interactions ; Ferrimagnetic Materials ; Chains ; Heisenberg Model ; Amorphous State ; Chemical Bonds ; Magnetic Susceptibility ; Cobalt Compounds ; Nickel Compounds ; Hydrates ; Edta ; Ferrimagnetism ; Magnetic PropertiesBimetallic stripCondensed matter physicsChemistryHeisenberg modelExchange interactionUNESCO::FÍSICAAmorphous StateChainsMagnetic susceptibilityAmorphous solidMolecular geometryChemical bondFerrimagnetismHeisenberg ModelCobalt Compounds
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Magnetic exchange interaction in a pair of orbitally degenerate ions: Magnetic anisotropy of [Ti2Cl9]−3

2001

The theory of the kinetic exchange in a pair of orbitally degenerate ions developed by the authors [J. Phys. Chem. A 102, 200 (1998)] is applied to the case of face-shared bioctahedral dimer (overall D3h-symmetry). The effective kinetic exchange Hamiltonian is found for a 2T2–2T2 system taking into account all relevant transfer pathways and charge-transfer crystal field states. The influence of different transfer integrals involved in the kinetic exchange on the energy pattern and magnetic properties of the system is examined. The role of other related interactions (trigonal crystal field, spin–orbit coupling) is also discussed in detail. Using the pseudoangular momentum representation and …

Condensed matter physicsChemistryDegenerate energy levelsGeneral Physics and AstronomyTrigonal crystal systemKinetic energyNegative ionsExchange interactions (electron)Magnetic exchangeIonUNESCO::FÍSICA::Química físicaMagnetic anisotropysymbols.namesakeTitanium compounds ; Magnetic anisotropy ; Negative ions ; Exchange interactions (electron)Quantum mechanicssymbolsTitanium compoundsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Hamiltonian (quantum mechanics)Magnetic anisotropy
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Syntheses, Structures, Magnetic Properties, and Density Functional Theory Magneto-Structural Correlations of Bis(μ-phenoxo) and Bis(μ-phenoxo)-μ-acet…

2013

The bis(mu-phenoxo) (FeNiIII)-Ni-II compound [Fe-III(N-3)(2)LNiII(H2O)(CH3CN)](ClO4) (1) and the bis(mu-phenoxo)-mu-acetate/bis(mu-phenoxo)-bis(mu-acetate) (FeNiII)-Ni-III compound {[Fe-III(OAc)LNiII(H2O)(mu-OAc)](0.6)center dot[(FeLNiII)-L-III(mu-OAc)(2)](0.4)}(ClO4)center dot 1.1H(2)O (2) have been synthesized from the Robson type tetraiminodiphenol macrocyclic ligand H2L, which is the [2 + 2] condensation product of 4-methyl-2,6-diformylphenol and 2,2'-dimethy1-1,3-diaminopropane. Single-crystal X-ray structures of both compounds have been determined. The cationic part of the dinuclear compound 2 is a cocrystal of the two species [Fe-III(OAc)LNiII(H2O)(mu-OAc)](+) (2A) and [(FeLNiII)-L-I…

Coordination ClustersCopper(Ii) ComplexesSingle-Molecule MagnetTransition-Metal-ComplexesChemistryStereochemistryTheoretical ExplorationExchange InteractionsCationic polymerizationCocrystalAnisotropy BarrierInorganic ChemistryCrystallographyFerromagnetismAntiferromagnetismLanthanide ComplexesDensity functional theoryMacrocyclic ligandPhysical and Theoretical ChemistrySpin Ground-StateGaussian-Basis SetsInorganic Chemistry
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A field induced ferromagnetic-like transition below 2.8 K in Li2CuO2: An experimental and theoretical study

1998

The low temperature magnetic properties of the Li2CuO2 compound have been investigated by means of superconducting quantum interference device magnetometry. We find in addition to an antiferromagnetic phase below 9.5 K a ferromagnetic-like steep rise of the magnetization around 2.8 K. The observed low temperature behavior is discussed by considering second and fourth order magnetocrystalline effective anisotropy coefficients, in addition to the exchange couplings reported in the literature. Work at the Institut de Ciencia dels Materials was supported by the Spanish Comisión Interministerial de Ciencia y Technología Grant No. CICYT MAT 96-1037.

Field (physics)MagnetometerExchange InteractionsGeneral Physics and AstronomyExchange Interactions (Electron)Magnetizationlaw.inventionMagnetizationMagnetisationAntiferromagnetism:FÍSICA [UNESCO]lawPhase (matter)Magnetic propertiesFerromagnetic MaterialsCopper OxidesLi2CuO2AntiferromagnetismAntiferromagnetic MaterialsLithium OxidesAnisotropyCondensed matter physicsTemperature Range 0000-0013 KChemistryTemperature DependenceUNESCO::FÍSICALithium Compounds ; Ferromagnetic-Antiferromagnetic Transitions ; Ferromagnetic Materials ; Antiferromagnetic Materials ; Magnetisation ; Magnetic Anisotropy ; Exchange Interactions (Electron) ; Lithium Oxides ; Copper Oxides ; Magnetization ; Exchange Interactions ; Antiferromagnetism ; Ferromagnetism ; Temperature Dependence ; Temperature Range 0000-0013 KMagnetic AnisotropyMagnetic anisotropyFerromagnetismLithium CompoundsFerromagnetismFerromagnetic-Antiferromagnetic TransitionsJournal of Applied Physics
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Magnetic field-controlled 0−π transitions and their experimental signatures in superconductor-ferromagnet-superconductor junctions

2019

Superconductor-ferromagnet-superconductor Josephson junctions are known to exist in the $0$ and $\pi$ states with the transitions between them controlled by the temperature and ferromagnetic interlayer thickness. We demonstrate that these transitions can be controlled also by the external magnetic field directed perpendicular to the layers. By varying the ratio of diffusion coefficients in superconducting and ferromagnetic layers, these field-controlled transitions can be made detectable for arbitrary large value of the exchange energy in the ferromagnet. We also show that the $0$-$\pi$ transitions in the perpendicular field can be observed as the specific features of the flux-flow conducti…

Josephson effectMaterials sciencePhysics and Astronomy (miscellaneous)Field (physics)superconducting devices02 engineering and technologyConductivitymagnetic fieldssuperconductorsmagneettikentät01 natural sciencessuprajohteetCondensed Matter::Materials ScienceCondensed Matter::Superconductivity0103 physical sciencesferromagnetic materialsPerpendicular010302 applied physicsSuperconductivityCondensed matter physicsCondensed Matter - SuperconductivityExchange interaction021001 nanoscience & nanotechnologyCondensed Matter::Mesoscopic Systems and Quantum Hall Effect3. Good healthMagnetic fieldexchange interactionsFerromagnetismCondensed Matter::Strongly Correlated Electrons0210 nano-technology
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1D antiferromagnetism in spin‐alternating bimetallic chains

1990

The magnetic and thermal properties of the ordered bimetallic chain CoNi(EDTA)⋅6H2O in the very low‐temperature range are reported. The magnetic behavior does not exhibit the characteristic features of 1D ferrimagnets, but a continuous decrease of χmT towards zero at absolute zero. This 1D antiferromagnetic behavior results from an accidental compensation between the moments located at the two sublattices. This behavior, as well as the specific‐heat results, are modeled on the basis of an Ising‐exchange model that considers both alternating spins and Landé factors, and a zero‐field splitting on the Ni site. Eugenio.Coronado@uv.es ; Fernando.Sapina@uv.es

Magnetic PropertiesEdtaExchange InteractionsGeneral Physics and AstronomyNickel CompoundsCobalt Compounds ; Nickel Compounds ; Edta ; Hydrates ; Magnetic Properties ; One−Dimensional Systems ; Ultralow Temperature ; Antiferromagnetism ; Magnetic Moments ; Exchange Interactions ; Ising Model ; Anisotropy ; Specific HeatMagnetic MomentsAntiferromagnetism:FÍSICA [UNESCO]AntiferromagnetismHydratesAnisotropyBimetallic stripAbsolute zeroSpin-½Condensed matter physicsMagnetic momentSpinsChemistryUNESCO::FÍSICAOne−Dimensional SystemsUltralow TemperatureSpecific HeatIsing ModelAnisotropyCondensed Matter::Strongly Correlated ElectronsIsing modelCobalt Compounds
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The ferrimagnetic compounds CoM[M’(EDTA)]2⋅4H2O(M,M’=Co,Ni): Magnetic characterization of CoCo[Ni(EDTA)2]⋅4H2O

1990

Under the terms of the Creative Commons Attribution (CC BY) license to their work.

Magnetic PropertiesExchange InteractionsEdtaNickel CompoundsGeneral Physics and AstronomyBimetalsFerrimagnetic MaterialsCondensed Matter::Materials ScienceNuclear magnetic resonance:FÍSICA [UNESCO]FerrimagnetismNickel compoundsCocoHydratesSpin (physics)Bimetallic stripChemistryUNESCO::FÍSICABimetals ; Magnetic Properties ; Exchange Interactions ; Cobalt Compounds ; Nickel Compounds ; Ferrimagnetic Materials ; Ising Model ; Edta ; HydratesCharacterization (materials science)CrystallographyIsing ModelOctahedronCondensed Matter::Strongly Correlated ElectronsIsing modelCobalt CompoundsJournal of Applied Physics
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Magnetic exchange interactions in the heteropoly complexes [M4(H2O)2(PW9O34)2]10− [M=Co(II) and Cu(II)]

1990

The magnetic properties of the heteropolyanions [M4(H2O)2(PW9O34)2]10− [M=Co(II) and Cu(II)] down to 4 K are reported. Their individual heteropoly molecules contain a rhomblike arrangement formed by four coplanar MO6 octahedra sharing edges. The magnetic properties support an intramolecular ferromagnetic exchange in the Co(II) tetramer, and antiferromagnetic exchange in the Cu(II) tetramer. These behaviors are discussed assuming anisotropic exchange in the Co(II) compound, and Heisenberg exchange in the Cu(II) compound. Carlos.Gomez@uv.es

Magnetic PropertiesExchange InteractionsGeneral Physics and AstronomyCopper ComplexesAntiferromagnetismTetramerVery Low TemperatureAntiferromagnetismMoleculeAnisotropy:FÍSICA::Química física [UNESCO]Cobalt Complexes ; Copper Complexes ; Heteropolyanions ; Magnetic Properties ; Exchange Interactions ; Ferromagnetism ; Antiferromagnetism ; Anisotropy ; Heisenberg Model ; Ultralow Temperature ; Very Low TemperatureCondensed matter physicsChemistryHeisenberg modelUltralow TemperatureUNESCO::FÍSICA::Química físicaCrystallographyOctahedronFerromagnetismIntramolecular forceFerromagnetismHeisenberg ModelAnisotropyCobalt ComplexesHeteropolyanions
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Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, andMagnetic Properties

2015

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, MnII, FeII, CoII, or NiII, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)2] and [Fe(1)(hfac)2] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the meta…

Magnetic susceptibility measurementsAntiferromagnetic couplingIron compoundsLigands01 natural sciencesNickelheterosyklitMetal ionsta116Cobalt compoundsChelationChemistryMetal–radical interactionsMagnetismSingle crystal x-ray diffractionRadicals[CHIM.MATE]Chemical Sciences/Material chemistrymetal-radical interactionsradicalsexchange interactionsChemistrykoordinaatiokemiaUnpaired electronPositive ionsMetalsSynthesis (chemical)visual_artradikaalitvisual_art.visual_art_mediumElectronic structureCoordinating propertiesmagneettiset ominaisuudetX ray diffractionRadicalInorganic chemistryRadical interactionsElectronic structureHeterocycles010402 general chemistryCatalysisMagnetic susceptibilityMetalElectronic structure calculationsMetal complexesMagnetic properties[CHIM.COOR]Chemical Sciences/Coordination chemistrymetalli-radikaali -vuorovaikutuksetManganeseheterocycles010405 organic chemistryLigandCrystal structureOrganic ChemistryGeneral ChemistryMagnetic susceptibility0104 chemical sciencesCrystallographyOctahedronFerromagnetismExchange interactionscoordination chemistrySingle crystalsmagnetic propertiesCoordination reactions
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