Search results for "Magnetic Susceptibility"
showing 10 items of 516 documents
Synthesis, characterisation, crystal structures, and magnetic properties of one-dimensional oxalato-bridged metal(II) complexes with 3-hydroxypyridin…
2001
One-dimensional oxalato-bridged metal(II) compounds of formula [M(-ox)(L)2]n [L = 3-hydroxypyridine (pyOH) or isoquinoline (isq)] have been synthesised and characterised by FT-IR spectroscopy, TG-DTA techniques, variable-temperature magnetic measurements and X-ray diffraction methods. The complexes [M(-ox)(pyOH)2]n [M= Co (1), Ni (2)] are isomorphous and crystallise in the orthorhombic space group Pnab. The compounds [M(-ox)(isq)2]n [M= Co (3), Ni (4), Cu (5)] are also isomorphous and belong to the monoclinic space group C2/c. Crystal structures consist of zig-zag chains in which cis-[M(L)2] 2 + units are sequentially bridged by bis-bidentate oxalato ligands with intrachain M···M distances …
Unique direct synthesis of cyanide-bridged Fe2Cu2 molecular squares by destruction of sodium nitroprusside
2009
Abstract The one-pot reaction of copper powder, sodium nitroprusside, ammonium thiocyanate and 2,2′-bipyridine (bpy) in acetonitrile solution at ambient conditions of air and water yields the novel heterometallic [Fe2Cu2(bpy)6(μ-CN)4(NCS)2]2[Fe(CN)5(NO)](NCS)2·5H2O complex 1, which has been structurally and magnetically characterized. The most prominent feature of this complex is the unique tetranuclear Fe 2 II Cu 2 II squares comprised [Cu(bpy)NCS]+ and [Fe(bpy)2]2+ corners with CN edges. The Cu⋯Cu and Fe⋯Fe separations are ∼6.72 and ∼7.73 A, respectively. The variable-temperature magnetic susceptibility study revealed that a very weak antiferromagnetic coupling is active between Cu(II) ce…
Synthesis, crystal structure and magnetic properties of [Cr2Cu2(bpy)4(ox)5]·2H2O. An oxalato-bridged heterometallic tetramer
2003
A new heterometallic tetramer of formula [Cr2Cu 2(bpy)4(ox)5]·2H2O (1) (bpy=2,2′-bipyridine; ox=oxalate dianion) has been prepared and characterised by single-crystal X-ray diffraction, magnetic susceptibility measurements and ESR spectroscopy. The tetranuclear unit in 1 can be viewed as the combination of two terminal [Cr(bpy)2(ox)]- units with a central oxalato-bridged copper(II) dimer. The chromium ions are in a distorted octahedral environment with metal-ligand distances ranging from 1.944(4) to 2.064(5) A. The copper(II) centres lie in an axially distorted octahedron. The axial positions are occupied by one oxygen atom belonging to the central bridging oxalate anion [O(9)-Cu(1): 2.245(…
Magnetic Excitations in Polyoxometalate Clusters Observed by Inelastic Neutron Scattering: Evidence for Anisotropic Ferromagnetic Exchange Interacti…
1999
The ground-state properties of the tetranuclear Co2+ cluster [Co4(H2O)2(PW9O34)2]10- were investigated by combining specific heat, magnetic susceptibility, and magnetization measurements with a detailed inelastic neutron scattering (INS) study on a fully deuterated sample of K10[Co4(H2O)2(PW9O34)2]·22H2O. As a result of the single ion anisotropy of the octahedral Co2+, the appropriate exchange Hamiltonian of the Co4 spin cluster is anisotropic. INS turns out to be essential for the determination of energy splittings in the ground state resulting from the coupling. Besides the energy pattern, INS provides information about the wave functions of the split ground-state components of the spin c…
Magnetic Excitations in Polyoxometalate Clusters Observed by Inelastic Neutron Scattering: Evidence for Ferromagnetic Exchange Interactions and Spin…
1999
The ground-state properties of the tetranuclear Ni2+ cluster [Ni4(H2O)2(PW9O34)2]10- were investigated by combining magnetic susceptibility and magnetization measurements with a detailed inelastic neutron scattering (INS) study on a fully deuterated sample of K6Na4[Ni4(H2O)2(PW9O34)2]·24H2O. The temperature dependence of the magnetic susceptibility indicates a ferromagnetic coupling of the four constituent Ni2+ ions (s = 1), and a low-temperature magnetization study provides the magnitude of the S = 4 ground-multiplet splitting due to the single-ion anisotropy of the Ni2+ ions. Besides a more direct and precise determination of the anisotropic S = 4 ground-multiplet splitting, INS enabled t…
Structure, magnetizability, and nuclear magnetic shielding tensors of bis-heteropentalenes. IV. Dihydrophospholophosphole isomers
2005
The geometry of the heteropentalenes formed by two phosphole units has been determined at the DFT level. The magnetic susceptibility and the nuclear magnetic shielding at the nuclei of these systems have also been calculated using gauge-including atomic orbitals and a large Gaussian basis set to achieve near Hartree-Fock estimates. A comparative study of the various isomers, of their flattened analogs, and of the parent phosphole molecule, shows that the [3,4-c] isomer is the most aromatic system in the set considered, assuming diatropicity and degree of planarity as indicators, even if it is the less stable in terms of total molecular energy. Plots of magnetic field-induced current densiti…
Building-block process for the synthesis of new chromium(iii) malonate complexes
2010
We describe the crystal structures of two bimetallic compounds with the malonate and an exo-polydentate N-donor ligand {[Cu(tren)]4[Cr2(mal)4(OH)2]}(ClO4)4·8H2O (3) and [Ni(Htren)2][Cr2(mal)4(OH)2]·8H2O (4) which are prepared from the dinuclear K4[Cr2(mal)4(OH)2]·6H2O precursor (2) [tren = tris(2-aminoethyl)amine and H2mal = malonic acid]. Their crystal packing and supramolecular structures are analyzed in the context of the influence of the dichromium(III) [Cr2(mal)4(OH)2]4− unit, which acts as a building-block. Different supramolecular motifs built up from hydrogen bonds are discussed, and their self-assembly to yield a 3D arrangement is described. The magnetic properties of the compounds…
A dihydrogen arsenate-mediated supramolecular network: crystal structure and magnetic properties of {[(bipy)Cu(μ-H2AsO4)(H2AsO4)]2}n
2002
Treatment of an aqueous suspension of Cu(OH)2 and 2,2′-bipyridine (bipy) with either Na2HAsO4·7H2O (1∶1∶2) or As2O5 (1∶1∶1) yields single crystals of {[(bipy)Cu(μ-H2AsO4)(H2AsO4)]2}n, 1, on standing. The solid-state structure of 1 consists of a three dimensional supramolecular network, supported by a combination of coordination covalent, hydrogen bonding and face-to-face π–π interactions. Variable temperature magnetic susceptibility measurements reveal very weak antiferromagnetic coupling between Cu(II) centres across the dihydrogen arsenate bridges (J = −0.58 cm−1).
Layered Molecule-Based Magnets Formed by Decamethylmetallocenium Cations and Two-Dimensional Bimetallic Complexes [MIIRuIII(ox)3]−(MII=;Mn, Fe, Co, C…
2001
Abstract A new series of hybrid organometallic-inorganic layered magnets with formula [Z III Cp * 2 ] [M II Ru III (ox) 3 ] ( Z III =Co and Fe; M II =Mn, Fe, Co, Cu, and Zn; ox=oxalate: Cp * =pentamethylcyclopentadienyl) has been prepared. All of these compounds are isostructural to the previously reported [ Z III Cp * 2 ] [ M II M III (ox) 3 ] ( M III =Cr, Fe) series and crystallize in the monoclinic space group C 2/ m , as found by powder X-ray diffraction analysis. They are novel examples of magnetic materials formed by bimetallic oxalate-based extended layers separated by layers of organometallic cations. The magnetic properties of all these compounds have been investigated (ac and dc m…
Magnetic polyoxometalates: anisotropic exchange interactions in the moiety of [(NaOH2)Co3(H2O)(P2W15O56)2]17-.
2005
The magnetic exchange interactions in a C0(3)(11) moiety encapsulated in Na(17) [(NaOH(2))Co(3)(H(2)O)(P(2)W(15)O(56))(2)] (NaCo(3)) were studied by a combination of magnetic measurements (magnetic susceptibility and low-temperature magnetization), with a detailed Inelastic Neutron Scattering (INS) investigation. The novel structure of the salt was determined by X-ray crystallography. The ferromagnetic Co(3)O(14) triangular cluster core consists of three octahedrally oxo-coordinated Co(II) ions sharing edges. According to the single-ion anisotropy and spin-orbit coupling usually assumed for octahedral Co(II) ions, the appropiate exchange Hamiltonian to describe the ground-state properties o…