Search results for "antiferromagnetism"

showing 10 items of 471 documents

Synthesis, crystal structure and magnetic properties of [Cu2(bpym)(N3)4] (bpym=2,2′-bipyrimidine)

1993

Abstract The compound of formula [Cu 2 (bpym)(N 3 ) 4 ] (bpym=2,2′-bipyrimidine) has been synthesized and its crystal structure determined by X-ray diffraction methods. It crystallizes in the monoclinic space group P 2 1 / n with cell constants: a =10.071(2), b =6.376(1), c =11.617(2) A and β=95.93(1)°; V =742.0(2) A 3 , D (calc., Z =2)=2.029 g cm −3 , M r =453.4, F (000)=448, λ (Mo Kα)=0.71073 A, μ (Mo Kα)=29.1 cm −1 and T =298 K. A total of 2027 reflections was collected over the range 3⩽2θ⩽55°; of these, 1723 were unique and 1427 were considered as observed ( I >3σ( I )) and used in the structural analysis. The final R and R w residuals were 0.0275 and 0.0328, respectively. The structure…

StereochemistryChemistryCrystal structureMagnetic susceptibilityInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronX-ray crystallographyMaterials ChemistryAntiferromagnetismMoleculeAzidePhysical and Theoretical ChemistryMonoclinic crystal systemInorganica Chimica Acta
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Iron(III), chromium(III) and cobalt(II) complexes with squarate: Synthesis, crystal structure and magnetic properties

2011

The preparation and variable temperature-magnetic investigation of three squarate-containing complexes of formula [Fe 2 (OH) 2 (C 4 O 4 ) 2 (H 2 O) 4 ]·2H 2 O ( 1 ) [Cr 2 (OH) 2 (C 4 O 4 ) 2 (H 2 O) 4 ]·2H 2 O ( 2 ) and [Co(C 4 O 4 )(H 2 O) 4 ] n ( 3 ) [H 2 C 4 O 4  = 3.4-dihydroxycyclobutene-1,2-dione (squaric acid)] together with the crystal structures of 1 and 3 are reported. Complex 1 contains discrete centrosymmetric [Fe 2 (OH) 2 (C 4 O 4 ) 2 (H 2 O) 4 ] diiron(II) units where the iron pairs are joined by a di-μ-hydroxo bridge and two squarate ligands acting as bridging groups through adjacent oxygen atoms. Two coordinated water molecules in cis position complete the octahedral environ…

StereochemistryChemistrychemistry.chemical_elementCrystal structureSquaric acidInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronIntramolecular forceMaterials ChemistryAntiferromagnetismMoleculePhysical and Theoretical ChemistryIsostructuralCobaltInorganica Chimica Acta
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A Comparative Structural and Magnetic Study of Three Compounds Based on the Cluster Unit M4Cl8(THF)6 (M=Mn, Fe, Co)

2001

Treatment of anhydrous M Cl 2 phases with THF under refluxing conditions leads to excision of the clusters M 4 Cl 8 (THF) 6 ( M =Fe (1), Co (3)) and dimensional reduction to the chain of clusters, {Mn 4 Cl 8 (THF) 6 (Mn(THF) 2 Cl 2 } ∞ , (2). All three compounds were isolated in high yields as crystalline materials and subjected to comprehensive magnetic studies. X-ray structures of the three compounds were performed to verify the nature of the compounds, but only the Mn derivative is discussed in detail due to the fact that the structures of the Fe and Co clusters were reported earlier. The molecular structures of M 4 Cl 8 (THF) 6 ( M =Fe, Co) consist of a rhombic arrrangement of metal ion…

StereochemistryCrystal structureCondensed Matter PhysicsMagnetic susceptibilityElectronic Optical and Magnetic MaterialsInorganic ChemistryMetalCrystallographyMagnetizationchemistry.chemical_compoundchemistryOctahedronvisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumMoleculeAntiferromagnetismPhysical and Theoretical ChemistryTetrahydrofuranJournal of Solid State Chemistry
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Synthesis, crystal structure and magnetic properties of two alternating double μ1,1 and μ1,3 azido bridged Cu(ii) and Ni(ii) chains

2014

Two new alternating μ1,1- and μ1,3-azido bridged chains, [Cu(N3)2(mtn)]n (1) and [Ni(N3)2(mtn)]n (2) where mtn = N-methyl-1,3-propanediamine, have been synthesized and characterized by single crystal X-ray diffraction. In both complexes, each metal atom is coordinated to six nitrogen atoms from four azide anions and one N-methyl-1,3-propanediamine molecule in a distorted octahedral geometry. In 1, the basal-apical double μ1,1-azido bridged Cu(ii)-dimers are connected through two asymmetric μ1,3-N3 bridges to form a 1D chain in which one of the azide acts as a μ1,1,3 bridge while the other one is terminal. The structure of 2 is very similar but one of the azide ions acts as μ1,1 and the othe…

StereochemistryCrystal structureInorganic ChemistryMetalchemistry.chemical_compoundCrystallographyParamagnetismchemistryvisual_artOctahedral molecular geometryvisual_art.visual_art_mediumAntiferromagnetismMoleculeAzideSingle crystalDalton Trans.
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Oxo-Vanadium(IV) Dihydrogen Phosphate: Preparation, Magnetic Study, and Heterogeneous Catalytic Epoxidation

2008

A layered oxo-vanadium(IV) dihydrogen phosphate, {VO(H2PO 4)2} n has been synthesized hydrothermally and characterized by several physicochemical methods. Single-crystal X-ray analysis (crystal system, tetragonal; space group, P4/ ncc; unit cell dimensions, a = b = 8.9632(4), c = 7.9768(32) A) of {VO(H2PO4) 2} n reveals that the compound has an extended two-dimensional structure. The VO2+ moieties are connected through bridging H 2PO4 (-) ions, and this type of connection propagates parallel to the crystallographic ab plane which gives rise to a layered structure. The layers are staked parallel to the crystallographic c axis with a separation between the layers of ca. 4.0 A. Magnetic suscep…

StereochemistryCrystal systemVanadiumchemistry.chemical_elementSurfaces and InterfacesAtmospheric temperature rangeCondensed Matter PhysicsMagnetic susceptibilityCatalysisTetragonal crystal systemchemistry.chemical_compoundCrystallographychemistryElectrochemistryAntiferromagnetismGeneral Materials ScienceAcetonitrileSpectroscopyLangmuir
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Magnetic properties of vanadium(IV)-based extended systems: [(VO)3(μ-PO4)2(2,2′-bpy)(μ-OH2)]*1/3H2O and (VO)2H4P2O9

2013

International audience; The magnetic properties of [(VO)3(μ-PO4)2(2,2′-bpy)(μ-OH2)]1/3H2O (1) and (VO)2H4P2O9 (2), a tubular and a layered vanadium(IV) phosphates containing triply oxido bridged VIV dimers, are analyzed considering the Bleaney-Bowers S = 1/2 dimer model. In compound 1 the presence of an additional VIV connected with the VIV dimers through μ1,2-PO43− bridges is described with a Curie-Weiss type correction. This model reproduces the magnetic properties of compound 1 with g = 1.956, Jdim = −102.1 cm−1, θ = −0.4 cm−1 and Nα = 278 × 10−6 emu mol−1. In compound 2, the presence of a small percentage of paramagnetic impurity has to be considered to account for the divergence of χm …

StereochemistryDimermolecular magnetismVanadiumchemistry.chemical_elementVPO02 engineering and technology010402 general chemistry01 natural sciencesDFTInorganic ChemistryParamagnetismchemistry.chemical_compoundImpurityhybrid materialsMaterials ChemistryAntiferromagnetismPhysical and Theoretical Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographyMonomerchemistrySuperexchangevanadium0210 nano-technologyHybrid material
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S-shaped decanuclear heterometallic [Ni8Ln2] complexes [Ln(iii) = Gd, Tb, Dy and Ho]: theoretical modeling of the magnetic properties of the gadolini…

2014

The reaction of 8-quinolinol-2-carboaldoxime (LH2) with Ni(II) and Ln(III) salts afforded the heterometallic decanuclear compounds [Ni8Dy2(μ3-OH)2(L)8(LH)2(H2O)6](ClO4)2·16H2O (1), [Ni8Gd2(μ3-OH)2(L)8(LH)2(H2O)4(MeOH)2](NO3)2·12H2O (2), [Ni8Ho2(μ3-OH)2(L)8(LH)2(H2O)4(MeOH)2](ClO4)2·2MeOH·12H2O (3) and [Ni8Tb2 (μ3-OH)2(L)8(LH)2(MeOH)4(OMe)2]·2CH2Cl2·8H2O (4). While compounds 1-3 are dicationic, compound 4 is neutral. These compounds possess an S-shaped architecture and comprise a long chain of metal ions bound to each other. In all the complexes, the eight Ni(II) and two Ln(III) ions of the multimetallic ensemble are hold together by two μ3-OH, eight dianionic (L(2-)) and two monoanionic oxi…

StereochemistryGadoliniumMetal ions in aqueous solutionchemistry.chemical_elementOximeIonInorganic Chemistrychemistry.chemical_compoundMolecular wireCrystallographychemistryFerromagnetismAntiferromagnetismDerivative (chemistry)Dalton Trans.
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Intramolecular ferro- and antiferromagnetic interactions in oxo-carboxylate bridged digadolinium(iii) complexes

2010

Two new digadolinium(III) complexes with monocarboxylate ligands, [Gd2(pac)6(H2O)4] (1) and [Gd2(tpac)6(H2O)4] (2) (Hpac = pentanoic acid and Htpac = 3-thiopheneacetic acid), have been prepared and their structures determined by X-ray diffraction on single crystals. Their structures consist of neutral and isolated digadolinium(III) units, containing six monocarboxylate ligands and four coordinated water molecules, the bridging skeleton being built by a muO(1):kappa2O(1)O(2) framework. This structural pattern has already been observed in the parent acetate-containing compound [Gd2(ac)6(H2O)4] x 4 H2O (3) whose structure and magnetic properties were reported elsewhere (L. Cañadillas-Delgado, …

StereochemistryGadoliniumchemistry.chemical_elementAtmospheric temperature rangeMagnetic susceptibilitySquare antiprismInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryIntramolecular forceAntiferromagnetismMoleculeCarboxylateDalton Transactions
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Dinuclear and two- and three-dimensional gadolinium(III) complexes with mono- and dicarboxylate ligands: synthesis, structure and magnetic properties

2009

Three new gadolinium(III) complexes with carboxylate ligands of formula [Gd2(ac)6(H2O)4]·2H2O (1), [Gd2(ac)2(fum)2(H2O)4]n (2) and [Gd2(ox)(fum)2(H2O)4]n·4nH2O (3) (ac = acetate, fum = fumarate and ox = oxalate) have been prepared and their structures determined by X-ray diffraction on single crystals. The structure of 1 is made up of discrete centrosymmetric di-µ-oxo(carboxylate acetate)digadolinium(III) units with an intramolecular Gd⋯Gd separation of 4.1589(3) A. Each gadolinium atom in 1 is nine-coordinated with two water molecules and seven carboxylate-oxygen atoms from four acetate ligands building a monocapped square antiprism environment. Compound 2 exhibits a sheet-like structure, …

StereochemistryGadoliniumchemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsMagnetic susceptibilityOxalateSquare antiprismchemistry.chemical_compoundCrystallographychemistryIntramolecular forceAntiferromagnetismMoleculeGeneral Materials ScienceCarboxylateCrystEngComm
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Charge transfer salts containing a paramagnetic cyano-complex and iodine substituted organic donor involving –I(donor)···N(anion)-interactions

2005

Abstract The preparation, crystal structures, EHT band calculation and optical properties of two new charge transfer salts, namely (DIET)2[Fe(bpca)(CN)3] (1) and (DIEDO)2[Fe(bpca)(CN)3] (2), where bpca = bis(2-pyridylcarbonyl)amide anion, DIET = diiodoethylenedithotetrathiavalene and DIEDO = diiodoethylenedioxotetrathiavalene are reported. The magnetic properties of 2 and those of the low-spin iron(III) precursor of formula (PPh4)[Fe(bpca)(CN)3]·H2O (3) were also investigated in the temperature range 1.9–205 K. Crystal data; (1): monoclinic P21, a = 8.8238(2)A, b = 13.2891(3) A, c = 18.5042(5) A, β = 91.115(1)°, Z = 2, R = 0.0710 for 7021 independent reflections with I > 2 σ(I) and (2): Mon…

StereochemistryGeneral Chemical EngineeringInfrared spectroscopyGeneral ChemistryCrystal structureAtmospheric temperature rangeParamagnetismchemistry.chemical_compoundCrystallographychemistryAmideMoleculeAntiferromagnetismMonoclinic crystal systemComptes Rendus Chimie
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