Search results for "antiferromagnetism"

showing 10 items of 471 documents

Hybrid Organic/Inorganic Molecular Materials Formed by Tetrathiafulvalene Radicals and Magnetic Trimeric Clusters of Dimetallic Oxalate‐Bridged Compl…

2003

The first examples of trimeric, dimetallic, pure oxalate-bridged complexes [ox = (C2O4)2−] have been synthesized and characterized structurally and magnetically for the two new series of crystalline molecular assemblies formulated as (TTF)4{MII(H2O)2[MIII(ox)3]2}·nH2O [for MIII = Cr; MII = Mn (1), Fe (2), Co (3), Ni (4), Cu (5) and Zn (6); for MIII = Fe; MII = Mn (7), Fe (8), Co (9), Ni (10) and Zn (11)]. Both series (Cr2M and Fe2M) are isostructural. The crystal structure of (TTF)4{Mn(H2O)2[Cr(ox)3]2}⋅14H2O (1) [monoclinic, space group C2/c (no. 15), a = 13.240(5) A, b = 19.450(5) A, c = 27.690(5) A, β = 97.63(5)°, V = 7068(3) A3 and Z = 4] shows alternating layers of the organic radical T…

chemistry.chemical_classificationCrystal structureOxalateCoordination complexInorganic ChemistryMagnetizationchemistry.chemical_compoundCrystallographyNuclear magnetic resonancechemistryAntiferromagnetismIsostructuralTetrathiafulvaleneMonoclinic crystal systemEuropean Journal of Inorganic Chemistry
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New dinuclear copper complexes incorporating bis(imidazolyl) based ligands and bidentate–monodentate oxalate bridges. Crystal structure and magnetic …

2016

Abstract This paper reports the synthesis, X-ray crystal structure and magnetic characterization of two novel copper(II) dinuclear compounds including bis(imidazolyl) ligands and oxalate anions, [Cu2(BIM)2(C2O4)2]·4H2O (1) (BIM = bis(2-imidazolyl)methane) and [Cu2(BIK)2(C2O4)2] (2) (BIK = bis(2-imidazolyl)ketone). The oxalate anion acts as bidentate–monodentate in both cases, although it exhibits different coordination bridging modes: whereas in compound 1 a μ1,1,2-oxalato is observed, a μ1,2,3-oxalato is found in compound 2. In both cases, the 3D framework is held together by a combination of H-bonding and aromatic-aromatic interactions provided by the convenient structural features of BIM…

chemistry.chemical_classificationDenticityKetone010405 organic chemistryStereochemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesCopperMagnetic susceptibilityOxalate0104 chemical scienceslaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrylawMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryElectron paramagnetic resonancePolyhedron
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1‑Phenyl-3-(pyrid-2-yl)benzo[e][1,2,4]triazinyl: The First "Blatter Radical" for Coordination Chemistry

2014

A neutral air- and moisture-stable N,N′-chelating radical ligand, 1-phenyl-3-(pyrid-2-yl)benzo[e][1,2,4]triazinyl (1) was synthesized and characterized by electron paramagnetic resonance spectroscopy, X-ray crystallography, and magnetic measurements. Subsequent reaction of 1 with Cu(hfac)2·2H2O (hfac = hexafluoroacetylacetonate) under ambient conditions afforded the coordination complex Cu(1)(hfac)2 in which the radical binds to the metal in a bidentate fashion. Magnetic susceptibility data collected from 1.8 to 300 K indicate a strong ferromagnetic metal-radical interaction in the complex and weak antiferromagnetic radical···radical interactions between the Cu(1)(hfac)2 units. Detailed com…

chemistry.chemical_classificationDenticityStereochemistryLigandpysyvät radikaalitRadicalmetal complexes[CHIM.INOR]Chemical Sciences/Inorganic chemistryMedicinal chemistryMagnetic susceptibilityCoordination complexInorganic ChemistryMetalParamagnetismCoordination Chemistrystable radicalschemistryBlatter radikaalivisual_artvisual_art.visual_art_mediumAntiferromagnetismBlatter radicalPhysical and Theoretical Chemistryta116metallikompleksit
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Neutron-scattering studies on CeM2Ge2(M=Ag, Au, and Ru)

1992

The results of elastic, quasielastic, and inelastic neutron-scattering studies on polycrystalline CeM 2 Ge 2 (M=Ag, Au, and Ru) are presented. All compounds reveal long-range magnetic order at low temperatures. Ferromagnetic (M=Ru), antiferromagnetic (M=Au), and incommensurate (M=Ag) structures were detected. Using time-of-flight (TOF) techniques, the crystalline electric-field splittings were determined. With high-resolution TOF experiments the temperature and wave-vector dependence of the magnetic relaxation rate was studied

chemistry.chemical_classificationElastic scatteringMaterials scienceCondensed matter physicsMagnetic structureNuclear TheoryAnalytical chemistryNeutron scatteringInelastic scatteringchemistryFerromagnetismAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsCrystalliteNuclear ExperimentInorganic compoundPhysical Review B
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Syntheses, structures and magnetic properties of cyano-bridged one-dimensional Ln3+–Fe3+ (Ln = La, Dy, Ho and Yb) coordination polymers

2019

Four new heterometallic one-dimensional coordination polymers with formulae trans-[La(o-phen)3(H2O)(μ-CN)2Fe(CN)4]·7H2O (1) and trans-[Ln(H2O)2(phen)2(μ-CN)2Fe(CN)4]·nH2O [Ln/n = Dy/8 (2), Ho/7 (3) and Yb/7 (4), (o-phen = 1,10-phenanthroline)] have been synthesized by reacting Ln(NO3)3·xH2O with K3[Fe(CN)6] and 1,10-phenanthroline. The structures of 1–4 have been established by single crystal X-ray diffraction. Polymer 1 presents a chain structure with three o-phen ligands coordinated to La3+ and [Fe(CN)6]3− complexes connecting them through two trans CN− ligands to form a linear chain. Compounds 2–4 are solvates and contain Ln3+ ions coordinated to two o-phen ligands and also bridged by [F…

chemistry.chemical_classificationHydrogen bond02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMagnetic susceptibilityCatalysis0104 chemical sciencesIonCrystallographychemistryMaterials ChemistryCluster (physics)MoleculeAntiferromagnetism0210 nano-technologySingle crystalNew Journal of Chemistry
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Oxalate‐Based 3D Chiral Magnets: The Series [Z II (bpy) 3 ][ClO 4 ][M II Fe III (ox) 3 ] (Z II = Fe, Ru; M II = Mn, Fe; bpy = 2,2'‐Bipyridine; ox = O…

2005

The synthesis, structure, and physical properties of the oxalate-based molecular magnets with the formula [ZII(bpy)3][ClO4][MIIFeIII(ox)3] (ZII = Fe, Ru; MII = Mn, Fe; bpy = 2,2'-bipyridine; ox = oxalate dianion) are presented here. All compounds are isostructural and crystallize in the chiral cubic space group P4132, and contain three-dimensional dimetallic networks formed by alternating MII and MIII ions that are connected by oxalate anions. These compounds exhibit strong antiferromagnetic interactions that give rise to magnetic ordering as ferrimagnets or weak ferromagnets, with critical temperatures of up to 20 K, which is twice as high as those found for the isostructural magnets based…

chemistry.chemical_classificationInorganic chemistry22'-BipyridineOxalateCoordination complexInorganic ChemistryBipyridinechemistry.chemical_compoundCrystallographychemistryFerromagnetismMössbauer spectroscopyAntiferromagnetismIsostructuralEuropean Journal of Inorganic Chemistry
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New hexanuclear FeIII clusters with the gem-diol hydrated form of di(2-pyridyl)ketone and carboxylato ligands: Crystal structures and magnetic proper…

2019

Abstract The hexanuclear compounds [Fe6O2Cl2{(py)2CO2}2(pyOH)2(pyCOO)2(ButCOO)6] (1) and [Fe6O2{(py)2CO2}2(pyCOO)4(ButCOO)6] (2) were obtained by condensation of the trinuclear μ3-oxo-centered iron(III) pivalate [Fe3O(ButCOO)6(H2O)3]+ in the presence of di(2-pyridyl)ketone [(py)2CO] in MeCN at ambient temperature. Both complexes contain an analogous core which can be described as two {Fe3O}7+ units joined by gem-diolato (py)2CO22− bridges. Variable-temperature magnetic susceptibility measurements in polycrystalline samples of 1 and 2 reveal strong antiferromagnetic couplings between the iron(III) ions leading to S = 0 ground states.

chemistry.chemical_classificationKetone010405 organic chemistryDiolCondensationCrystal structure010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesIonInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryMaterials ChemistryAntiferromagnetismCrystallitePhysical and Theoretical ChemistryPolyhedron
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Structural and magnetic properties of polynuclear oximate copper complexes with different topologies

2017

Abstract Two new copper(II) complexes containing the methyl(2-pyridyl)ketone oxime ligand (mpkoH) [Cu3(OH)(ClO4)2(mpko)3]·CH3OH (1) and [Cu(ClO4)(mpko)(mpkoH)]n (2) have been prepared from Cu(ClO4)2 and mpkoH in different metal-to-ligand molar ratios. In addition, the compound [Cu{(mpko)2BF2}(H2O)](BF4) (3) [(mpko)2BF2 is the fluoroboration product of the oxime] has been obtained when replacing Cu(ClO4)2 by Cu(BF4)2. Compound 1 is an isolated triangle with a {Cu3(µ3-OH)}5+ core, whereas 2 is a chain of CuII ions linked by anionic mpko− bridges. 1 exhibits strong antiferromagnetic competing interactions, as well as antisymmetric exchange. On the other hand, very weak ferromagnetic interactio…

chemistry.chemical_classificationKetoneAntisymmetric exchange010405 organic chemistryLigandInorganic chemistrychemistry.chemical_element010402 general chemistryOxime01 natural sciencesCopper0104 chemical scienceslaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryFerromagnetismlawMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryElectron paramagnetic resonancePolyhedron
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Discrete unusual mixed-bridged trinuclear CoIII2CoII and pentanuclear NiII coordination complexes supported by a phenolate-based ligand: theoretical …

2021

Two new complexes [CoIII2CoII(μ-OL)2(μ-OOCCH3)2(μ-N3)2(N3)2]·Et2O (1·Et2O) and [NiII5(μ-OL)4(μ-OOCCH3)2(OOCCH3)2(μ-N3)2]·CH3CN (2) (HOL = 2-((2-(pyridin-2-yl)ethylamino)methyl)phenol) have been synthesized and characterized by elemental analysis, IR, and UV/Vis spectroscopy. Structural analysis revealed that 1 is a discrete trinuclear and 2 is a discrete pentanuclear coordination complex. In complex 1, terminal metal (CoIII) is in a distorted octahedral MN4O2 environment where coordination is satisfied by two nitrogen atoms and one oxygen atom of the ligand, and an oxygen atom from the acetate group and two nitrogen atoms from azide (one each from the bridging and terminal ones). The centra…

chemistry.chemical_classificationLigandGeneral ChemistryCrystal structureMagnetic susceptibilityCatalysisCoordination complexchemistry.chemical_compoundCrystallographychemistryOctahedronPyridineMaterials ChemistryAntiferromagnetismAzideNew Journal of Chemistry
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Chiral Molecular Magnets: Synthesis, Structure, and Magnetic Behavior of the Series [M(L-tart)] (M = MnII, FeII, CoII, NiII;L-tart = (2R,3R)-(+)-tart…

2006

A new series of layered magnets with the formula [M(L-tartrate)] (M = Mn(II), Co(II), Fe(II), Ni(II); L-tartrate = (2R,3R)-(+)-tartrate) has been prepared. All of these compounds are isostructural and crystallize in the chiral orthorhombic space group I222, as found by X-ray structure analysis. Their structure consists of a three-dimensional polymeric network in which each metal shows distorted octahedral coordination bound to four L-tartrate ligands, two of which chelate through an alcohol and a carboxylate group and the other two bind terminally through a monodentate carboxylate group. The chirality of the ligand imposes a Delta conformation on all metal centers. Magnetically, the paramag…

chemistry.chemical_classificationLigandStereochemistryOrganic ChemistryGeneral ChemistryCatalysisCoordination complexCondensed Matter::Materials Sciencechemistry.chemical_compoundParamagnetismCrystallographychemistryFerromagnetismAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsCarboxylateIsostructuralSpontaneous magnetizationChemistry - A European Journal
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