Search results for "Magnetism"

showing 10 items of 1934 documents

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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Unexpected magnetic topology in the heterobimetallic [ReIVBr4(μ-ox)CuII(bpy)2] compound

2011

Abstract A novel oxalato-bridged rhenium(IV)-copper(II) compound, namely [ReIVBr4(μ-ox)CuII(bpy)2] (1), has been obtained by reacting (PPh4)2[ReBr4(ox)] with Cu(CF3SO3)2 and 2,2′-bpy in CH3CN, and its crystal structure determined by single-crystal X-ray diffraction. Intermolecular Br⋯Br interactions and nonbonding Cu⋯Br type contacts between the heterobimetallic dinuclear units lead to a two-dimensional supramolecular structure. Compound 1 behaves magnetically as a [ReIVCuII]2 tetranuclear species with weak antiferromagnetic interactions through the oxalato bridge and intermolecular Br⋯Br contacts.

Inorganic ChemistryCrystallographychemistryStereochemistryIntermolecular forceMaterials ChemistrySupramolecular chemistryAntiferromagnetismchemistry.chemical_elementCrystal structurePhysical and Theoretical ChemistryRheniumTopology (chemistry)Inorganica Chimica Acta
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An Azide-Bridged Copper(II) Ferromagnetic Chain Compound Exhibiting Metamagnetic Behavior

1997

The one-dimensional chain complex [Cu(2)(mgr;(2)-1,1-N(3))(2)(mgr;(2)-1,3-NO(3))(2)(mgr;(2)-1,3-Me(3)NCH(2)CO(2))(2)](n)() (1) contains three different bridge groups,mgr;(2)-1,1-azide (end-on),mgr;(2)-nitrate, andmgr;(2)-syn,syn-carboxylate, arranged so that the azide and carboxylate groups bridge equatorially and dictate the intrachain magnetic behavior between the copper magnetic orbitals. Variable-temperature magnetic susceptibility studies at low field, and magnetization studies at variable field, reveal dominant intrachain ferromagnetism (J = 26 cm(-)(1)) but also much weaker interchain ferromagnetism (THETAV; = 2.3 K) and antiferromagnetism (J(eff) = -0.18 cm(-)(1)). The structure has…

Inorganic ChemistryCrystallographychemistry.chemical_compoundChain (algebraic topology)FerromagnetismChemistrychemistry.chemical_elementAzidePhysical and Theoretical ChemistryBridge (interpersonal)CopperInorganic Chemistry
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Spin canting in an unprecedented three-dimensional pyrophosphate- and 2,2'-bipyrimidine-bridged cobalt(II) framework.

2008

The three-dimensional cobalt(ii) compound of formula {[Co(2)(P(2)O(7))(bpym)(2)].12H(2)O}(n), where the pyrophosphate and 2,2'-bipyrimidine act as bridging ligands, is a new example of a spin-canted antiferromagnet with T(c) = 19 K.

Inorganic ChemistryCrystallographychemistry.chemical_compoundChemistryInorganic chemistryAntiferromagnetismchemistry.chemical_elementCobaltPyrophosphateSpin cantingDalton transactions (Cambridge, England : 2003)
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