Search results for "magnetism."

showing 10 items of 1879 documents

Diphenoxo-Bridged NiIILnIII Dinuclear Complexes as Platforms for Heterotrimetallic (LnIIINiII)2RuIII Systems with a High-Magnetic-Moment Ground State…

2012

The first examples of pentanuclear heterotrimetallic [(LnNi)(2)Ru] [Ln(3+) = Gd (1) and Dy (2)] complexes were prepared and magnetostructurally characterized. They exhibit ferromagnetic interactions, leading to a high-magnetic-moment ground state.

Inorganic ChemistryCrystallographyMagnetic momentFerromagnetismChemistryStereochemistryStructure (category theory)Physical and Theoretical ChemistryGround stateta116Inorganic Chemistry
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Slow relaxation of the magnetization in a 4,2-wavelike Fe(III)2Co(II) heterobimetallic chain.

2012

The reaction of the low-spin iron(III) complex [Fe(dmbpy)(CN)(4)](-) (1) with fully solvated cobalt(II) ions affords the cyanide-bridged heterobimetallic chain {[Fe(III)(dmbpy)(CN)(4)](2)Co(II)(H(2)O)(2)}(n) · 4nH(2)O (2), which exhibits intrachain ferromagnetic coupling and double slow relaxation of the magnetization.

Inorganic ChemistryCrystallographyMagnetizationCondensed matter physicschemistryFerromagnetismChain (algebraic topology)Relaxation (NMR)chemistry.chemical_elementPhysical and Theoretical ChemistryCobaltIonInorganic chemistry
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[Fe(III)(dmbpy)(CN)4]-: a new building block for designing single-chain magnets.

2012

We herein present the synthesis and magneto-structural study of a new family of heterobimetallic chains of general formula {[Fe(III)(dmbpy)(CN)(4)](2)M(II)(H(2)O)(2)}(n)·pnH(2)O [dmbpy = 4,4'-dimethyl-2,2'-bipyridine; M = Mn (2), Cu (3), Ni (4) and Co (5) with p = 4 (2), 3 (3), 9 (4) and 3.5 (5)] which were prepared by using the mononuclear PPh(4)[Fe(III)(dmbpy)(CN)(4)]·3H(2)O (1) building block (PPh(4)(+) = tetraphenylphosphonium) as a ligand toward fully solvated M(II) ions. The structure of 1 consists of discrete [Fe(III)(dmbpy)(CN)(4)](-) anions, tetraphenylphosphonium cations and noncoordinated water molecules. Complexes 2-5 are isostructural compounds whose structure consists of neutr…

Inorganic ChemistryCrystallographyMagnetizationFerromagnetismFerrimagnetismLigandChemistryStereochemistryRelaxation (NMR)MoleculeIsostructuralIonDalton transactions (Cambridge, England : 2003)
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Synthesis, crystal structures and magnetic properties of cyanide- and phenolate-bridged [MIIINiII]2tetranuclear complexes (M = Fe and Cr)

2005

The binuclear complex NiII2L(H2O)2(ClO4)2 (1) and the neutral tetranuclear bimetallic compounds [{MIII(phen)(CN)4}2{NiII2L(H2O)2}]·2CH3CN with M = Fe (2) and Cr (3) [H2L = 11,23-dimethyl-3,7,15,19-tetraazatricyclo[19.3.1.19,13]hexacosa-2,7,9,11,13(26),14,19,21(25),22,24-decaene-25,26-diol] have been synthesized and the structures of 2 and 3 determined by single crystal X-ray diffraction. 2 and 3 are isostructural compounds whose structure is made up of centrosymmetric binuclear cations [Ni2(L)(H2O)2]2+ and two peripheral [M(phen)(CN)4]− anions [M = Fe (2) and Cr (3)] acting as monodentate ligands towards the nickel atoms through one of their four cyanide nitrogen atoms. The environment of t…

Inorganic ChemistryCrystallographyNickelDenticityChemistryIntramolecular forceInorganic chemistryAntiferromagnetismMoleculechemistry.chemical_elementDensity functional theoryCrystal structureIsostructuralDalton Trans.
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Structural, magnetic and related attributes of some oximate-bridged tetranuclear nickel(ii) rhombs and a dinuclear congenerElectronic supplementary i…

2003

New oximate-bridged tetranuclear nickel(II) complexes of compositions {Ni(Dien)}2(μ3-OH)2{Ni2(Moda)4}(ClO4)2·Solv (Solv = H2O, 1a; Solv = 2CH3NO2, 1b; Solv = 2H2O·2C4H8O2, 1c), {Ni(Sdien)}2(μ3-OH)2{Ni2(Moda)4}(ClO4)2·H2O (2), {Ni(Odien)}2(μ3-OH)2{Ni2(Moda)4}(ClO4)2·0.6H2O (3), {Ni(Dien)}2(μ3-OH)2{Ni2(Inaf)4}(ClO4)2·CH3NO2 (4) and {Ni(Odien)}2(μ3-OH)2{Ni2(Inaf)4}(ClO4)2·2NaClO4·2H2O (5) and the dinuclear complex (Ni{Odien})2(Moda)2(ClO4)2 (6) have been prepared (Dien = 1,5-diamino-3-azapentane, Odien = 1,5-diamino-3-oxapentane, Sdien = 1,5-diamino-3-thiapentane, ModaH = butane-2,3-dione monooxime, InafH = phenylglyoxaldoxime). X-ray examination revealed similar structures for 1a, 1b, 1c, 2 a…

Inorganic ChemistryCrystallographyNickelFerromagnetismchemistryMagnetochemistryStereochemistryAntiferromagnetismchemistry.chemical_elementSpectroscopyCoupling (probability)Antiferromagnetic couplingDalton Transactions
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Spin crossover and photomagnetism in dinuclear iron(II) compounds

2007

Abstract In this paper, we review recent work reported in the field of molecular spin crossover phenomena in dinuclear compounds. Following a comprehensive overview on the synthesis and properties of new iron(II) dinuclear compounds presenting the spin crossover phenomenon, we focus this review on recent efforts made in studying and understanding the photo-physical properties of the {[Fe(L)(NCX)2]2bpym} (L = bt or bpym, X = S or Se) family of compounds. Finally, literature on the different theoretical approaches treating the static and dynamic properties of dinuclear complexes presenting two-step thermal spin transition is briefly summarized.

Inorganic ChemistryCrystallographyNuclear magnetic resonanceChemistrySpin crossoverMaterials ChemistrySpin transitionPhysical and Theoretical ChemistryPhotomagnetismLIESSTCoordination Chemistry Reviews
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Towards Molecular Conductors with a Spin‐Crossover Phenomenon:Crystal Structures, Magnetic Properties and Mössbauer Spectra of[Fe(salten)Mepepy][M(dm…

2005

Three new iron(III) compounds of formula [Fe(salten)Mepepy][M(dmit)2]·CH3CN (M = Ni, Pd, Pt; H2salten = 4-azaheptamethylene-1,7-bis(salicylideneiminate); Mepepy = 1-(pyridin-4-yl)-2-(N-methylpyrrol-2-yl) ethane; dmit2– = 1,3-dithiole-2-thione-4,5-dithiolato) have been synthesised and the crystal structure of each compound has been solved at different temperatures. The structures consist of alternating layers of [M(dmit)2]– units and [Fe(salten)Mepepy] cations. In the Ni compound photo-isomerisation of the Mepepy ligand can be observed in dichloromethane solution. The temperature dependence of the magnetic susceptibility of the compounds reveals a gradual S = 5/2 blabla S = 1/2 spin crossove…

Inorganic ChemistryCrystallographyNuclear magnetic resonanceOxidation stateChemistrySpin crossoverMössbauer spectroscopyX-ray crystallographyAntiferromagnetismCrystal structureMagnetic susceptibilityHyperfine structureEuropean Journal of Inorganic Chemistry
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Eight‐Coordinate Endohedral Rhenium, Osmium and Iridium Atoms in Rare‐Earth Halide Cluster Complexes

2010

Endohedral (interstitial) atoms are essential for almost all of the rare-earth halide cluster complexes. Most of these contain octahedral clusters, some are isolated, but the majority exhibits condensation by common edges to structures of higher dimensionality. Higher coordination numbers of the endohedral atoms are rare. Four examples of extended cluster complexes with eight-coordinate endohedral atoms of sixth-period elements (Re, Os, Ir) are presented. In the quasi-isostructural, non-isotypic halides (ReGd 4 )Br 4 and {OsSc 4 }-Cl 4 , square antiprisms of gadolinium and scandium atoms, respectively, are connected by two common faces to chains, surrounded and loosely connected by halogeni…

Inorganic ChemistryCrystallographyParamagnetismChemical bondChemistryCoordination numberInorganic chemistryEndohedral fullereneCluster (physics)chemistry.chemical_elementOsmiumCrystal structureScandiumEuropean Journal of Inorganic Chemistry
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Synthesis and structure of a paramagnetic Mo3S4 incomplete cuboidal cluster with seven cluster skeletal electrons

2012

The electron precise incomplete cuboidal complex [Mo(3)S(4)(dppe)(3)Br(3)]Br (1a) with 6 cluster skeletal electrons (CSE) and its halogen-mixed analogue [Mo(3)S(4)(dppe)(3)(Br,Cl)(3)](Br,Cl) (1b) can be smoothly reduced to the paramagnetic [Mo(3)S(4)(dppe)(3)X(3)] clusters (2a, X = Br; 2b, X = Cl/Br) with 7 CSE by treatment with liquid Ga.

Inorganic ChemistryCrystallographyParamagnetismComputational chemistryChemistryCluster (physics)Electron
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Structure and Magnetic Properties of the Ferromagnetic Cu3Cl126- Trimer in [(NH3C2H4)3NH]2Cu3Cl14

2004

The crystal structure consists of a strongly hydrogen bonded network of tris(N-ethylammonium)ammonium cations, Cu3Cl12(6)- trimeric species, and Cl- anions. The Cu3Cl12(6)- trimers are formed by two distorted tetrahedral CuCl4(2)- anions linked to a central square planar CuCl4(2)- anion via semicoordinate Cu-Cl...Cu mu1 bridges. The central copper ion shows only small deviations from ideal D4h symmetry, while the terminal copper ions show a mild distortion from D2d symmetry with an average trans Cl-Cu-Cl angle of 136.0 degrees. The semicoordinate linkages provide a ferromagnetic exchange pathway between the copper ions with J/k = 6.91(3) K. Short Cl...Cl contacts (3.67-3.90 angstoms) lead t…

Inorganic ChemistryCrystallographyPlanarFerromagnetismChemistryTetrahedronchemistry.chemical_elementTrimerCrystal structurePhysical and Theoretical ChemistryCopperSymmetry (physics)IonInorganic Chemistry
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