Search results for "Exchange interaction"

showing 10 items of 80 documents

Ferromagnetic kinetic exchange interaction in magnetic insulators

2020

The superexchange theory predicts dominant antiferromagnetic kinetic interaction when the orbitals accommodating magnetic electrons are covalently bonded through diamagnetic bridging atoms/groups. Here we show that explicit consideration of magnetic and (leading) bridging orbitals, together with the electron transfer between the former, reveals a strong ferromagnetic kinetic exchange contribution. First principle calculations show that it is comparable in strength with antiferromagnetic superexchange in a number of magnetic materials with diamagnetic metal bridges. In particular, it is responsible for a very large ferromagnetic coupling ($-10$ meV) between the iron ions in a Fe$^{3+}$-Co$^{…

Work (thermodynamics)magneettiset ominaisuudetMaterials scienceelectronic-structurePhysics MultidisciplinaryFOS: Physical sciencesmagnetic couplingelektronitmagneettikentätKinetic energyteoriatORBITAL PHYSICSCondensed Matter - Strongly Correlated ElectronsCondensed Matter::Materials ScienceANTIFERROMAGNETISMHUBBARD-MODELPhysics - Chemical PhysicsSUPEREXCHANGE INTERACTIONSdensity functional theoryChemical Physics (physics.chem-ph)Condensed Matter - Materials SciencecomplexesScience & TechnologyStrongly Correlated Electrons (cond-mat.str-el)Condensed matter physicsCRYSTALmagnetic insulatorsPhysicsSUPERCONDUCTIVITYExchange interactionMaterials Science (cond-mat.mtrl-sci)transitionORDERhubbard-modelsuperexchange interactionsWannier function methodsELECTRONIC-STRUCTUREFerromagnetismPhysical SciencesCondensed Matter::Strongly Correlated ElectronsCOMPLEXESTRANSITION
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Molecular squares of Ni(II) and Cu(II): ferromagnetic exchange interaction mediated by syn-anti carboxylate-bridging.

2009

The synthesis of four discrete tetranuclear complexes {[Ni(II)(L(2))][ClO(4)]}(4).MeCN (1), {[Cu(II)(L(1))(O(3)SCF(3))]}(4).H(2)O (), {[Cu(II)(L(3))(OClO(3))]}(4).MeCN () and {[Cu(II)(L(4))][ClO(4)]}(4).3MeCN.4H(2)O (4), supported by a closely similar group of carboxylate-appended (2-pyridyl)alkylamine ligands [L(1)(-): 3-[N-methyl-{2-(pyridin-2-yl)ethyl}amino]propionate; L(2)(-): 3-[(2-(pyridin-2-yl)ethyl){2-(pyridin-2-yl)methyl}amino]propionate; L(3)(-): 3-[N-isopropyl-{2-(pyridin-2-yl)methyl}amino]propionate and L(4)(2-): 3-[N-{2-(pyridin-2-yl)methyl}amino]-bis(propionate)] is described. Structural characterization reveals that each Ni(II) centre in 1 has square-pyramidal Ni(II)N(3)O(2) …

chemistry.chemical_classificationStereochemistryLigandExchange interactionIonInorganic Chemistrychemistry.chemical_compoundCrystallographyOxygen atomchemistryFerromagnetismPropionateMoleculeCarboxylateDalton transactions (Cambridge, England : 2003)
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Exploring the exchange interaction in a mixed valence {CoII4CoIII2} hexanuclear cluster with novel topology

2012

Abstract Reaction between [Co2(μ-OH2)(μ-Piv)2(Piv)2(HPiv)4] and a (salicylidene)ethanolamine ligand under ambient reaction conditions, affords hexanuclear complexes [CoIII2CoII4(Piv)8(HPiv)2(L)2(OH)2] (1–2). Both products have been characterized crystallographically and found to be mixed-valent, containing divalent and trivalent Co centers. Down to 30 K, the variable-temperature magnetic susceptibility data are dominated by the single-ion properties of high spin Co(II) centers with distorted-octahedral coordination geometries. Below this temperature, the effect of intramolecular ferromagnetic exchange interactions becomes apparent. Magnetic data has been analyzed in terms of ground isolated…

chemistry.chemical_classificationValence (chemistry)ChemistryExchange interactionCrystal structureMagnetic susceptibilityDivalentInorganic ChemistryMagnetizationCrystallographyFerromagnetismIntramolecular forceMaterials ChemistryPhysical and Theoretical ChemistryPolyhedron
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Hexanuclear copper(ii) cage with {Cu3O⋯H⋯OCu3} core supported by a dicompartmental oxime ligand with m-xylyl spacer: synthesis, molecular structure a…

2010

A new dicompartmental dioxime ligand (H(2)L) with m-xylyl spacer between the donor sites has been synthesised by Schiff-base condensation of α,α'-diamino-m-xylene and diacetyl monooxime. The ligand reacts with copper(ii) salts giving rise to hexanuclear tricationic copper(II) cage complexes [Cu(II)(6)(μ(3)-O···H···O-μ(3))L(3)(H(2)O)(6)]X(3) (X = BF(4), 1a; X = ClO(4), 1b). The complexes have been characterised by different analytical and spectroscopic techniques and confirmed the hexanuclear structure even in solution. Single crystal X-ray diffraction studies of both the complexes revealed a very similar core structure with three dicompartmental ligands supporting two triangular Cu(3)O core…

crystal structureHydrogen bondLigandExchange interactionHexanuclear copper complexchemistry.chemical_elementCrystallography X-RayLigandsOximeHexanuclear copper complex; oxime; crystal structureoximeCopperInorganic ChemistryMagneticschemistry.chemical_compoundCrystallographychemistryUnpaired electronOximesOrganometallic CompoundsMoleculeSingle crystalCopperDalton Transactions
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Three-dimensional bimetallic octacyanidometalates $[M^{IV}{(\mu-CN)_{4}Mn^{II}(H_{2}O)_2}_2 \cdot 4H_{2}O]_{n}$ (M=Nb,Mo,W) : synthesis, single-cryst…

2008

Abstract We report the synthesis, the single-crystal X-ray crystallographic structures and the magnetic properties of three new isostructural cyanido-bridged networks: [M IV {(μ-CN) 4 Mn II (H 2 O) 2 } 2 ·4H 2 O] n [M IV  = Nb IV ( 1 ), Mo IV ( 2 ), W IV ( 3 )]. For compound 1 , the magnetic properties reveal a ferrimagnetic phase below 50 K. In contrast, compounds 2 and 3 show a paramagnetic behaviour with no magnetic ordering down to 2 K. The only electronic difference between the two kinds of compounds is the presence of two paired electrons on Mo IV ( 2 ) and W IV ( 3 ) (d 2 electronic configuration, S  = 0) with no possible exchange interactions with Mn II ions (d 5 electronic configur…

magnetic exchange interactionMagnetismGeneral Chemical Engineering010402 general chemistry01 natural sciencesMagnetizationParamagnetismcrystal structuresunpaired electronsstructure cristallineAntiferromagnetismIsostructural010405 organic chemistryChemistrymolecule-based magnetsGeneral Chemistrypont cyanure3. Good health0104 chemical sciencesCrystallographycyanido bridgeUnpaired electronoctacyanométallatesoctacyanidometalatesCurie temperatureinteraction d'échange magnétiqueelectronscélibatairesaimants à précurseurs moléculairesMolecule-based magnets
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Theoretical and computational studies of magnetic anisotropy and exchange coupling in molecular systems

2018

The field of molecular magnetism studies the magnetic properties of molecular systems as opposed to conventional metal-based magnets. The high chemical modifiability of the constituting molecules makes such materials highly versatile, and the small size of the building blocks leads to the rise of various quantum mechanical phenomena, such as tunneling and entanglement. These phenomena can then be further utilized in the construction of nanoscale quantum devices. This dissertation describes computational and theoretical studies in the field of molecular magnetism using state-of-the-art quantum chemical methods based on ab initio multireference approaches and broken symmetry density functional t…

organic magnetsmagnetic anisotropymagneettiset ominaisuudetCASPT2tiheysfunktionaaliteoriamolecular magnetismexchange interactionmolekyylitkompleksiyhdisteetorganometalliyhdisteetCASSCFDFTspin-orbit couplingquantum chemistrybroken symmetry DFTkvanttikemiaendohedral metallo-fullereneslanthanidessingle-molecule magnetsmagnetismiNEVPT2orgaaniset yhdisteet
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Chirality selective spin interactions mediated by the moving superconducting condensate

2018

We show that superconducting correlations in the presence of nonzero condensate velocity can mediate the peculiar interaction between localized spins that breaks the global inversion symmetry of magnetic moments. The proposed interaction mechanism is capable of removing fundamental degeneracies between topologically distinct magnetic textures. For the generic system of three magnetic impurities in the current-carrying superconductor, we find the energy term proportional to spin chirality. In realistic superconductor/ferromagnetic/superconductor setups we reveal significant energy differences between various magnetic textures with opposite chiralities. We calculate Josephson energies of junc…

suprajohtavuushelicoidal magnetic textureskyrmionsCondensed Matter::Superconductivityimpurities in superconductorsmagnetic textureexchange interactionJosephson effectmagnetismiRKKY interactionspin texturemagnetic vorticessuprajohteet
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Chirality selective spin interactions mediated by the moving superconducting condensate

2018

We show that superconducting correlations in the presence of nonzero condensate velocity can mediate the peculiar interaction between localized spins that breaks the global inversion symmetry of magnetic moments. The proposed interaction mechanism is capable of removing fundamental degeneracies between topologically distinct magnetic textures. For the generic system of three magnetic impurities in the current-carrying superconductor, we find the energy term proportional to spin chirality. In realistic superconductor/ferromagnetic/superconductor setups we reveal significant energy differences between various magnetic textures with opposite chiralities. We calculate Josephson energies of junc…

suprajohtavuusskyrmionsmagnetic textureexchange interaction02 engineering and technology01 natural sciencessuprajohteetCondensed Matter::Superconductivityimpurities in superconductors0103 physical sciencesmagnetismi010306 general physicsSpin (physics)RKKY interactionPhysicsSuperconductivityMagnetic momentSpintronicsCondensed matter physicsSpinsta114SkyrmionJosephson effect021001 nanoscience & nanotechnologyChirality (electromagnetism)Ferromagnetismhelicoidal magnetic texture0210 nano-technologymagnetic vorticesPhysical Review B
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Beyond the spin model: exchange coupling in molecular magnets with unquenched orbital angular momenta.

2011

In this critical review we review the problem of exchange interactions in polynuclear metal complexes involving orbitally degenerate metal ions. The key feature of these systems is that, in general, they carry an unquenched orbital angular momentum that manifests itself in all their magnetic properties. Thus, interest in degenerate systems involves fundamental problems related to basic models in magnetism. In particular, the conventional Heisenberg-Dirac-Van Vleck model becomes inapplicable even as an approximation. In the first part we attempt to answer two key questions, namely which theoretical tools are to be used in the case of degeneracy, and how these tools can be employed. We demons…

symbols.namesakeMagnetic anisotropyAngular momentumExchange biasZeeman effectCondensed matter physicsMagnetismChemistryExchange interactionDegenerate energy levelssymbolsGeneral ChemistryHamiltonian (quantum mechanics)Chemical Society reviews
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ChemInform Abstract: Magnetic Exchange Between Metal Ions with Unquenched Orbital Angular Momenta: Basic Concepts and Relevance to Molecular Magnetism

2010

This review article is a first attempt to give a systematic and comprehensive description (in the framework of the unified theoretical approach) of the exchange interactions in polynuclear systems based on orbitally degenerate metal ions in the context of their relevance to the modern molecular magnetism. Interest in these systems is related to the fundamental problems of magnetism and at the same time steered by a number of impressive potential applications of molecular magnets, like high-density memory storage units, nanoscale qubits, spintronics and photoswitchable devices. In the presence of orbital degeneracy, the conventional spin Hamiltonian (Heisenberg–Dirac–van Vleck model) becomes…

symbols.namesakeTheoretical physicsSpintronicsMagnetismChemistryQubitExchange interactionDegenerate energy levelssymbolsContext (language use)General MedicineHamiltonian (quantum mechanics)Degeneracy (mathematics)ChemInform
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