Search results for "Susceptibility"

showing 10 items of 912 documents

EPR and Magnetic Susceptibility Studies of Cobalt(II)- and Nickel(II)-Substituted Azurins from Pseudomonas aeruginosa. Electronic Structure of the Ac…

1996

The electronic properties of cobalt(II)- and nickel(II)-substituted azurins from Pseudomonas aeruginosa have been investigated. EPR data for the cobalt derivative and paramagnetic susceptibility data for the nickel derivative are reported. The EPR spectrum of Co(II)−azurin shows the typical pattern of a Kramers' doublet (±1/2) associated with an S = 3/2 ground state in a distorted axial symmetry environment. The temperature dependence of the EPR intensities shows that this Kramers' doublet is the excited doublet and, therefore, that the corresponding zero-field splitting parameter D is negative (∼−3.5 cm-1). The mean g value is equal to 2.3. Nickel(II) azurin exhibits an effective magnetic …

Magnetic momentAnalytical chemistrychemistry.chemical_elementMagnetic susceptibilitylaw.inventionInorganic ChemistryParamagnetismCrystallographyNickelchemistrylawExcited statePhysical and Theoretical ChemistryGround stateElectron paramagnetic resonanceCobaltInorganic Chemistry
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Synthesis and magnetic characterization of trans-dichloroplatinum blues with creatinine

1992

Abstract By reaction of trans -[Pt II Cl 4 ] 2− with the amidate ligand creatinine two new paramagnetic blue platinum complexes have been obtained, namely violet and green varieties. These complexes have been characterized from thermal analysis, EPR and magnetic susceptibility. The violet complex has been formulated as trans -[Pt(creat)(H 2 O)Cl] 4 Cl. This compound has shown to be very stable, showing an extensive hyperfine structure in the powder EPR spectra. This result is a clear evidence of a tetranuclear oligomeric structure with one delocalized unpaired spin in the unit. EPR spectra in frozen solutions indicate that this mixed-valence complex maintains its oligomeric structure upon d…

Magnetic momentChemistryLigandStereochemistrychemistry.chemical_elementMagnetic susceptibilitylaw.inventionInorganic ChemistryParamagnetismCrystallographyDelocalized electronlawMaterials ChemistryPhysical and Theoretical ChemistryPlatinumElectron paramagnetic resonanceHyperfine structureInorganica Chimica Acta
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Uncompensated magnetization in the layered molecular antiferromagnet {N(n-C5H11)4[MnIIFeIII(ox)3]}∞

2009

Abstract Studies on the magnetic properties of the molecular antiferromagnetic material {N( n -C 5 H 11 ) 4 [Mn II Fe III (ox) 3 ]} ∞ , carried out by various physical techniques (AC/DC magnetic susceptibility, magnetization, heat capacity measurements and Mossbauer spectroscopy) at low temperatures, have been presented. Different experimental observations complement each other and provide a clue for the observation of an uncompensated magnetization below the Neel temperature and short-range correlations persisting high above T N . It is understood that the honeycomb layered structure of the compound contains non-equivalent magnetic sub-lattices, (Mn II –ox–Fe III A –...) and (Mn II –ox–Fe …

Magnetic momentCondensed matter physicsChemistryExchange interactionMagnetic susceptibilityMagnetic fieldInorganic ChemistryMagnetizationSpin waveMaterials ChemistryAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryNéel temperaturePolyhedron
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Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, andMagnetic Properties

2015

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, MnII, FeII, CoII, or NiII, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)2] and [Fe(1)(hfac)2] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the meta…

Magnetic susceptibility measurementsAntiferromagnetic couplingIron compoundsLigands01 natural sciencesNickelheterosyklitMetal ionsta116Cobalt compoundsChelationChemistryMetal–radical interactionsMagnetismSingle crystal x-ray diffractionRadicals[CHIM.MATE]Chemical Sciences/Material chemistrymetal-radical interactionsradicalsexchange interactionsChemistrykoordinaatiokemiaUnpaired electronPositive ionsMetalsSynthesis (chemical)visual_artradikaalitvisual_art.visual_art_mediumElectronic structureCoordinating propertiesmagneettiset ominaisuudetX ray diffractionRadicalInorganic chemistryRadical interactionsElectronic structureHeterocycles010402 general chemistryCatalysisMagnetic susceptibilityMetalElectronic structure calculationsMetal complexesMagnetic properties[CHIM.COOR]Chemical Sciences/Coordination chemistrymetalli-radikaali -vuorovaikutuksetManganeseheterocycles010405 organic chemistryLigandCrystal structureOrganic ChemistryGeneral ChemistryMagnetic susceptibility0104 chemical sciencesCrystallographyOctahedronFerromagnetismExchange interactionscoordination chemistrySingle crystalsmagnetic propertiesCoordination reactions
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Accidentally on purpose: construction of a ferromagnetic, oxime-based [MnIII2] dimer

2011

The serendipitous self-assembly of the complex [Mn(III)(2)Zn(II)(2)(Ph-sao)(2)(Ph-saoH)(4)(hmp)(2)] (1),whose magnetic core consists solely of two symmetry equivalent Mn(iii) ions linked by two symmetry equivalent -N-O- moieties, provides a relatively simple model complex with which to study the magneto-structural relationship in oxime-bridged Mn(III) cluster compounds. Dc magnetic susceptibility measurements reveal ferromagnetic (J = +2.2 cm(-1)) exchange resulting in an S = 4 ground state. Magnetisation measurements performed at low temperatures and high fields reveal the presence of significant anisotropy, with ac measurements confirming slow relaxation of the magnetisation and Single-Mo…

MagnetismChemistryRelaxation (NMR)Magnetic susceptibilitylaw.inventionInorganic ChemistryCrystallographyMagnetizationFerromagnetismComputational chemistrylawAnisotropyGround stateElectron paramagnetic resonanceDalton Transactions
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Magnetism and EPR spectra of the two‐sublattice manganese chain Mn2(EDTA)⋅9H2O

1990

We report on the magnetic behavior and single‐crystal EPR spectra of the chain complex Mn2(EDTA)⋅9H2O characterized by two different alternating sites for the manganese ions. Magnetic susceptibility data are indicative of weak antiferromagnetic exchange interactions between the manganese ions, showing a maximum of about 3 K. This behavior can be accurately described on the basis of a Heisenberg chain model that assumes classical spins, giving J/k=−0.72 K and g=2.0. The EPR spectra are typically low dimensional, with an angular dependence of the linewidth of the type (3 cos2 θ−1)n (n=4/3 or 2). Nevertheless, such a behavior cannot be reproduced from a one‐dimensional model with dipolar broad…

MagnetismEdtaExchange InteractionsGeneral Physics and Astronomychemistry.chemical_elementManganeseMagnetic SusceptibilityElectron Spin ResonanceIonlaw.inventionlaw:FÍSICA [UNESCO]AntiferromagnetismHydratesElectron paramagnetic resonanceLine WidthsCondensed matter physicsSpinsUNESCO::FÍSICAManganese ComplexesMagnetic susceptibilityOne−Dimensional CalculationsDipoleElectron Spin Resonance ; Manganese Complexes ; Edta ; Exchange Interactions ; Magnetic Susceptibility ; Line Widths ; One−Dimensional Calculations ; HydrateschemistryCondensed Matter::Strongly Correlated Electrons
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Ferromagnetism in [Mn(Cp*) 2 ] + ‐Derived Complexes: the “Miraculous” Stacking in [Mn(Cp*) 2 ][Ni(dmit) 2 ]

2003

The synthesis and characterisation (X-ray structure and magnetism) of metal complexes (Ni, Au) with the [Mn(Cp*)2]+ cation and the dmit2− and dmid2− ligands are reported. [Mn(Cp*)2][Ni(dmit)2] (1) and [Mn(Cp*)2][Au(dmit)2] (2) exhibit the same structural arrangement, built on stacks of [Ni(dmit)2]− pairs separated by two [Mn(Cp*)2]+ cations, showing a ···D+D+A−A−D+D+A−A−··· motif. On the contrary, the dmid2− derivative [Mn(Cp*)2][Ni(dmid)2]·CH3CN (3) exhibits a totally different structure, built on mixed layers composed of one [Ni(dmid)2]− unit separated by two [Mn(Cp*)2]+ cations, showing a ···D+D+A−D+D+A−···motif. The layers are separated from each other by perpendicular [Ni(dmid)2]− unit…

MagnetismLigandchemistry.chemical_elementManganeseMagnetic susceptibilityInorganic ChemistryMetalCrystallographyNuclear magnetic resonanceFerromagnetismchemistryFerrimagnetismvisual_artvisual_art.visual_art_mediumAntiferromagnetismEuropean Journal of Inorganic Chemistry
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Small clusters with Heisenberg antiferromagnetic exchange

2000

We study small symmetrical clusters of magnetic ions with Heisenberg antiferromagnetic exchange interaction. We calculate the magnetization and the specific heat as functions of applied magnetic field at zero and non-zero temperature. Results are given for both classical and quantum systems. At zero temperature the classical systems undergo a series of transitions where the symmetry changes as a function of applied field. The quantum systems show similar features to Ising systems previously studied.

MagnetizationCondensed matter physicsField (physics)Heisenberg modelChemistryExchange interactionQuantum systemAntiferromagnetismGeneral Materials ScienceIsing modelCondensed Matter PhysicsMagnetic susceptibilityJournal of Physics: Condensed Matter
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Hexahalorhenate(iv) salts of protonated ciprofloxacin: antibiotic-based single-ion magnets

2021

Two novel Re(IV) compounds of formula [H2cip][Hcip][ReCl6]Cl·H2O (1) and [Hcip]2[ReBr6] (2) [(H2cip)2+/(Hcip)+ = ciprofloxacindiium cation / ciprofloxacinium cation] have been synthesized and studied structurally and magnetically. 1 crystallizes in the monoclinic system with space group P21/c, whereas 2 crystallizes in the orthorhombic system with space group Pbca. 1 and 2 are hexahalorhenate(IV) salts obtained with the protonated ciprofloxacin antibiotic. In their crystal lattice, the [ReX6]2− [X = Cl(1) and Br(2)] anions are well separated from each other through the protonated ciprofloxacindiium (1) and ciprofloxacinium (1 and 2) cations, which are arranged without generating intermolecu…

MagnetizationCrystallographyParamagnetismHydrogen bondChemistryGeneral Materials ScienceProtonationOrthorhombic crystal systemGeneral ChemistryCrystal structureCondensed Matter PhysicsMagnetic susceptibilityMonoclinic crystal systemCrystEngComm
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High nuclearity magnetic clusters: Magnetic properties of a nine cobalt cluster encapsulated in a polyoxometalate, [Co9(OH)3(H2O)6(HPO4)2(PW9O34)3]16⊕

1994

MagnetizationCrystallographychemistryMechanics of MaterialsStereochemistryMechanical EngineeringPolyoxometalateCluster (physics)chemistry.chemical_elementGeneral Materials ScienceCobaltMagnetic susceptibilityIonAdvanced Materials
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