Search results for "Magnetic Susceptibility"

showing 10 items of 516 documents

Spin crossover in iron(II) tris(2-(2′-pyridyl)benzimidazole) complex monitored by variable temperature methods: synchrotron powder diffraction, DSC, …

2003

Abstract The thermal expansion of the spin crossover system [Fe(pybzim) 3 ](ClO 4 ) 2  · H 2 O (pybzim=2-(2 ′ -pyridyl)benzimidazole) has been determined from powder X-ray data between 50 and 250 K; the wavelength of the synchrotron source was 1.21888(1) A. The unit cell parameters of the triclinic crystal system were a =12.091 A, b =12.225 A, c =14.083 A, α =77.70°, β =80.35°, γ =74.35°, and V =1944.9 A 3 at 250 K. In addition to the linear thermal expansion of the unit cell volume, an extra expansion due to the low-spin (LS) to high-spin (HS) transition is observed. The V ( T ) function shows a sudden increase comparable with the step in the effective magnetic moment at the transition reg…

CrystallographyExtended X-ray absorption fine structureMagnetic momentChemistrySpin crossoverAnalytical chemistryGeneral Physics and AstronomyInfrared spectroscopyPhysical and Theoretical ChemistryTriclinic crystal systemMole fractionMagnetic susceptibilityPowder diffractionChemical Physics
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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…

CrystallographyFerromagnetismChemistryInorganic chemistryTetrahedronchemistry.chemical_elementTrimerGeneral MedicineCrystal structureMagnetic susceptibilityCopperSymmetry (physics)IonChemInform
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Coexistence of spin-crossover and antiferromagnetic coupling phenomena in the novel dinuclear Fe(II) complex [Fe(dpa)(NCS)2]2bpym

2003

Abstract The iron(II) spin crossover dinuclear compound [Fe(dpa)(NCS) 2 ] 2 bpym where dpa = 2,2 ′ -dipyridylamine and bpym = 2,2 ′ -bipyrimidine has been synthesized and characterized. Variable-temperature magnetic susceptibility and 57 Fe Mossbauer spectroscopy data provide evidence for a rather complete and continuous S=2 ( HS )↔S=0 (LS) spin-crossover behavior taking place in the temperature range 400–50 K (T 1/2 =245 K ) without the presence of a plateau at 50% of conversion. The absence of such plateau, which is characteristic of all dinuclear compounds so far studied, is interpreted in terms of synergetic effect between intramolecular and intermolecular interactions.

CrystallographyNuclear magnetic resonanceChemistrySpin crossoverIntramolecular forceMössbauer spectroscopyIntermolecular forceGeneral Physics and AstronomyPhysical and Theoretical ChemistryAtmospheric temperature rangePlateau (mathematics)Magnetic susceptibilityAntiferromagnetic couplingChemical Physics Letters
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Pressure-Induced Spin State Conversion in Antiferromagnetically Coupled Fe(II) Dinuclear Complexes

2001

The effect of pressure on the thermal dependence of the magnetic susceptibility has been investigated in the 2,2‘-bipyrimidine (bpm)-bridged iron(II) complexes of formula {[Fe(L)(NCX)2]2bpm} (X = S...

CrystallographyNuclear magnetic resonanceMaterials scienceSpin statesThermalMaterials ChemistryPhysical and Theoretical ChemistryMagnetic susceptibilitySurfaces Coatings and FilmsThe Journal of Physical Chemistry B
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Polymorphism and Pressure Driven Thermal Spin Crossover Phenomenon in [Fe(abpt)2(NCX)2] (X=S, and Se): Synthesis,Structure and Magnetic Properties

2002

The monomeric compounds [Fe(abpt 2(NCX)2(X = S (1), Se (2) and abpt = 4-amino- 3,5-bis(pyridin-2-yl)-1,2,4-triazole) have been synthesized and characterized. They crystallize in the monoclinic P21/n space group with a = 11.637(2) A, b = 9.8021(14) A, c = 12.9838(12) A, β = 101.126(14)°, and Z=2 for 1, and a= 11.601(2) A, b = 9.6666(14) A, c = 12.883(2) A, β = 101.449(10)°, and Z = 2 for 2. The unit cell contains a pair mononuclear [Fe(abpt)2(NCX)21 units related by a center of symmetry. Each iron atom, located at a molecular inversion center, is in a distorted octahedral environment. Four of the six nitrogen atoms coordinated to the Fe(II) ion belong to the pyridine-N(1) and triazole-N(2) r…

CrystallographyNuclear magnetic resonanceOctahedronChemistrySpin crossoverAtomSpin transitionAtmospheric temperature rangeMagnetic susceptibilityMonoclinic crystal systemIon
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ChemInform Abstract: Ferric Phosphite: Dimers of Face-Sharing Fe(III)O6 Octahedra. Crystal Structure Redetermination, Moessbauer Spectra, Magnetic Su…

2010

CrystallographyOctahedronChemistrymedicineFerricGeneral MedicineCrystal structureMagnetic susceptibilityHeat capacitySpectral linemedicine.drugChemInform
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A 'Butterfly'-shaped Water Tetramer in a Cu4 Complex Supported by a Hydrazone Ligand: Synthesis, Crystal Structure, Magnetic Properties, and Quantum …

2009

A potentially tetradentate NOOO donor hydrazone ligand, LH2 (condensation product of benzhydrazide with O-vanillin) generates a tetranuclear CuII complex [Cu4(L)4]·4H2O (1), whose void spaces are occupied by water tetramers presenting a ‘butterfly’ conformation with the highest dihedral angle reported to date, as revealed by its X-ray crystal structure. 1 has also been characterized using various spectroscopic techniques, including IR, UV-vis, and elemental analysis. Variable temperature magnetic susceptibility measurements reveal the presence of moderate antiferromagnetic intra-tetramer coupling between the four CuII centres connected through simple oxo groups of the hydrazone ligand with…

CrystallographyTetramerChemistryAb initio quantum chemistry methodsSupramolecular chemistryPhysical chemistryDensity functional theoryGeneral ChemistryCrystal structureDihedral angleMagnetic susceptibilityQuantum chemistryAustralian Journal of Chemistry
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Magnetization and61Ni Mössbauer effect study of the ternary arsenide CrNiAs

2008

The results of x-ray diffraction, dc magnetization, and 61Ni M?ssbauer spectroscopy studies of the ternary arsenide CrNiAs are reported. This compound crystallizes in the orthorhombic Fe2P-type structure (space group ) with the lattice parameters a = 6.1128(2)?? and c = 3.6585(1)??. CrNiAs is a mean-field ferromagnet with Curie temperature TC = 171.9(1)?K and the critical exponents ? = 0.514(18), ? = 1.010(16), and ? = 2.922(10). The temperature dependence of the magnetic susceptibility above TC follows the modified Curie?Weiss law with a paramagnetic Curie temperature of 176.0(3)?K and effective magnetic moment per transition metal atom of 2.42(1)??B. The magnetic moment per formula unit a…

Curie–Weiss lawCondensed matter physicsMagnetic momentChemistryCondensed Matter PhysicsMagnetic susceptibilitysymbols.namesakeMagnetizationFerromagnetismsymbolsCurie temperatureGeneral Materials ScienceHyperfine structureDebye modelJournal of Physics: Condensed Matter
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Itinerant Electron Metamagnetism in η-Carbide-Type Compound Co3Mo3C

2010

We report the magnetic properties of the cobalt molybdenum η-carbide-type compounds Co 3 Mo 3 C and Co 3 Mo 3 N. The magnetic susceptibility χ of Co 3 Mo 3 C shows a Curie–Weiss temperature dependence at high temperatures and a broad maximum at around 100 K, whereas that of Co 3 Mo 3 N shows a nearly temperature-independent enhanced Pauli paramagnetic behavior. The absence of a magnetic long-range order was confirmed by the nuclear magnetic resonance technique in both the compounds. As expected from the broad maximum of χ, we observed an itinerant electron metamagnetic transition at around 37 T in Co 3 Mo 3 C.

Curie–Weiss lawMaterials scienceCondensed matter physicsGeneral Physics and Astronomychemistry.chemical_elementMagnetic susceptibilityCarbideCrystallographyParamagnetismchemistryMolybdenumCurie temperatureCobaltMetamagnetismJournal of the Physical Society of Japan
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Synthesis, crystal structure and magnetic properties of a new cyanide-bridged mixed-valence copper(I)/copper(II) clathrate

2013

A unique cyanide-bridge mixed-valence CuI/CuII clathrate of formula [CuI2(CN)3][{CuII(tren)}2(μ-CN)](CF3SO3)2 [tren = tris(2-aminoethyl)amine] containing cyanide-bridged [{CuII(tren)}2(μ-CN)]3 + binuclear cations stacked between anionic honeycomb layered copper(I) cyanide networks, was synthesized and structurally characterized by single crystal X-ray diffraction. Variable-temperature magnetic susceptibility studies showed that the cyanide bridge mediates a strong antiferromagnetic interaction between the copper(II) centers (J = − 160 cm− 1, the spin Hamiltonian being defined as H = − JSA⋅SB).

Cyanide bridgeMixed-valence copper(III) complexesValence (chemistry)Binuclear complexCyanideInorganic chemistrychemistry.chemical_elementCrystal structureMagnetic susceptibilityCopperInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryCrystal structuresMagnetic propertiesMaterials ChemistryAntiferromagnetismAmine gas treatingPhysical and Theoretical ChemistrySingle crystalInorganic Chemistry Communications
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