Search results for "Paramagnetism"

showing 10 items of 354 documents

n-cluster models in a transverse magnetic field

2017

In this paper we analize a family of one dimensional fully analytically solvable models, named the n-cluster models in a transverse magnetic field, in which a many-body cluster interaction competes with a uniform transverse magnetic field. These models, independently by the cluster size n + 2, exibit a quantum phase transition, that separates a paramagnetic phase from a cluster one, that corresponds to a nematic ordered phase or a symmetry-protected topological ordered phase for even or odd n respectively. Due to the symmetries of the spin correlation functions, we prove that these models have no genuine n+2-partite entanglement. On the contrary, a non vanishing concurrence arises between s…

Statistics and ProbabilityQuantum phase transitionPhysicsQuantum PhysicsStatistical Mechanics (cond-mat.stat-mech)SpinsFOS: Physical sciencesStatistical and Nonlinear PhysicsQuantum entanglementCondensed Matter Physics01 natural sciences010305 fluids & plasmasMagnetic fieldParamagnetismQuantum mechanics0103 physical sciencesCluster (physics)quantum complex systemsStatistics Probability and UncertaintyQuantum informationQuantum Physics (quant-ph)010306 general physicsCondensed Matter - Statistical MechanicsSpin-½
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Identification of clusters of companies in stock indices via Potts super-paramagnetic transitions

2000

The clustering of companies within a specific stock market index is studied by means of super-paramagnetic transitions of an appropriate q-state Potts model where the spins correspond to companies and the interactions are functions of the correlation coefficients determined from the time dependence of the companies' individual stock prices. The method is a generalization of the clustering algorithm by Domany et. al. to the case of anti-ferromagnetic interactions corresponding to anti-correlations. For the Dow Jones Industrial Average where no anti-correlations were observed in the investigated time period, the previous results obtained by different tools were well reproduced. For the Standa…

Statistics and ProbabilityStatistical Mechanics (cond-mat.stat-mech)SpinsFOS: Physical sciencesCondensed Matter PhysicsStock market indexParamagnetismCluster (physics)Statistical physicsCluster analysisStock (geology)Condensed Matter - Statistical MechanicsPotts modelMathematics
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Effect of Cyanato, Azido, Carboxylato, and Carbonato Ligands on the Formation of Cobalt(II) Polyoxometalates: Characterization, Magnetic, and Electro…

2007

Five Co(II) silicotungstate complexes are reported. The centrosymmetric heptanuclear compound K(20)[{(B-beta-SiW(9)O(33)(OH))(beta-SiW(8)O(29)(OH)(2))Co(3)(H(2)O)}(2)Co(H(2)O)(2)]47 H(2)O (1) consists of two {(B-beta-SiW(9)O(33)(OH))(beta-SiW(8)O(29)(OH)(2))Co(3)(H(2)O)} units connected by a {CoO(4)(H(2)O)(2)} group. In the chiral species K(7)[Co(1.5)(H(2)O)(7))][(gamma-SiW(10)O(36))(beta-SiW(8)O(30)(OH))Co(4)(OH)(H(2)O)(7)]36 H(2)O (2), a {gamma-SiW(10)O(36)} and a {beta-SiW(8)O(30)(OH)} unit enclose a mononuclear {CoO(4)(H(2)O)(2)} group and a {Co(3)O(7)(OH)(H(2)O)(5)} fragment. The two trinuclear Co(II) clusters present in 1 enclose a mu(4)-O atom, while in 2 a mu(3)-OH bridging group co…

Stereochemistry010405 organic chemistryOrganic ChemistryCenter (category theory)chemistry.chemical_elementGeneral ChemistryGeneral Medicine[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysis0104 chemical sciencesRedox ActivityParamagnetismCrystallographychemistryElectronic effectCompound K[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]CobaltComputingMilieux_MISCELLANEOUS
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The Series of Molecular Conductors and Superconductors ET4[AFe(C2O4)3]·PhX (ET = bis(ethylenedithio)tetrathiafulvalene; (C2O4)2– = oxalate; A+ = H3O+…

2011

An extensive series of radical salts formed by the organic donor bis(ethylenedithio)tetrathiafulvalene (ET), the paramagnetic tris(oxalato)ferrate(III) anion [Fe(C(2)O(4))(3)](3-), and halobenzene guest molecules has been synthesized and characterized. The change of the halogen atom in this series has allowed the study of the effect of the size and charge polarization on the crystal structures and physical properties while keeping the geometry of the guest molecule. The general formula of the salts is ET(4)[A(I)Fe(C(2)O(4))(3)]·G with A/G = H(3)O(+)/PhF (1); H(3)O(+)/PhCl (2); H(3)O(+)/PhBr (3), and K(+)/PhI (4), (crystal data at room temperature: (1) monoclinic, space group C2/c with a = 1…

StereochemistryChemistryCrystal structureZero field splittingTriclinic crystal systemInorganic ChemistryCrystalCrystallographyParamagnetismchemistry.chemical_compoundHalobenzenePhysical and Theoretical ChemistryTetrathiafulvaleneMonoclinic crystal systemInorganic Chemistry
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Synthesis, X‐ray Studies and Magnetic Properties of Dinuclear Ni II and Cu II Complexes Bridged by the Azo‐2,2′‐bipyridine Ligand

2003

Two new paramagnetic transition metal complexes that contain the bridging ligand azo-2,2-bipyridine (abpy) have been prepared and characterized by X-ray crystallography and magnetic susceptibility measurements. The compound [Ni2(µ-abpy)(CH3CN)2(NO3)4]·2CH3CN (1·2CH3CN) crystallizes in the triclinic space group P1 ¯ with a = 8.290(5) A u , b = 8.343(5) A u , c = 11.180(5) A u , α = 105.36(3)°, β = 94.39(3)°, γ = 107.56(3)°, V = 700.5(7) A u 3 and Z = 1. The related salt [Cu2(µ

StereochemistryChemistryLigandchemistry.chemical_elementBridging ligandTriclinic crystal systemMagnetic susceptibility22'-BipyridineInorganic ChemistryCrystallographyParamagnetismNickelchemistry.chemical_compoundTransition metalEuropean Journal of Inorganic 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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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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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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Nanoporosity, Inclusion Chemistry, and Spin Crossover in Orthogonally Interlocked Two-Dimensional Metal-Organic Frameworks

2015

[Fe(tvp)(2)(NCS)(2)] (1) (tvp=trans-(4,4-vinylenedipyridine)) consists of two independent perpendicular stacks of mutually interpenetrated two-dimensional grids. This uncommon supramolecular conformation defines square-sectional nanochannels (diagonal approximate to 2.2nm) in which inclusion molecules are located. The guest-loaded framework 1@guest displays complete thermal spin-crossover (SCO) behavior with the characteristic temperature T-1/2 dependent on the guest molecule, whereas the guest-free species 1 is paramagnetic whatever the temperature. For the benzene-guest derivatives, the characteristic SCO temperature T-1/2 decreases as the Hammet sigma(p) parameter increases. In general, …

StereochemistryIronOrganic ChemistrySupramolecular chemistryInclusion compoundsInterpenetrationGeneral ChemistryMetal-organic frameworksSpin crossoverCatalysischemistry.chemical_compoundParamagnetismCrystallographyBenzonitrilechemistrySpin crossoverFISICA APLICADAPerpendicularMoleculeMetal-organic frameworkAcetonitrileChemistry - A European Journal
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A novel polynitrile ligand with different coordination modes: Synthesis, structure and magnetic properties of the series [M(tcnoprOH)2(H2O)2] (M=Mn, …

2008

International audience; A novel polynitrile ligand (tcnoprOH− = [(NC)2CC(OCH2CH2CH2OH)C(CN)2]−) with up to five potentially coordinating groups has been synthesized in a one-pot reaction from a cyclic acetal and malononitrile. The combination of this novel ligand with different transition metal ions has led to the synthesis of two different structural types with the same formula but with different coordination modes in the ligand. Mn(II) and Cu(II) lead to a μ2-N,O-coordinating mode in the series of compounds formulated as [M(N,O-tcnoprOH)2(H2O)2] (M = MnII (1) and CuII (2)), whereas Co(II) and, most probably Ni(II), lead to a μ2-N,N′-coordinating mode in [Co(N,N′-tcnoprOH)2(H2O)2] (3). Bot…

StereochemistryMetal ions in aqueous solutionZero field splitting[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesAnalytical ChemistryInorganic ChemistryPolynitrile ligandschemistry.chemical_compoundParamagnetismGroup (periodic table)Magnetic properties[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistrySpectroscopyMalononitrile010405 organic chemistryLigandOrganic ChemistryAcetalMagnetic chains3. Good health0104 chemical sciencesCrystallographychemistryChain complexesDerivative (chemistry)
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