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EN
This paper presents the results of investigation of magnetic properties in Cu/Ni multilayer systems. Based on the investigation of Ni/Cu and Cu/Ni systems with different thickness of magnetic and non-magnetic layers it was proved that the presence of ferromagnetic (F-F) and antiferromagnetic (A-F) exchange couplings depends on the quality of layers in artificial superlattice and on the state and type of free surface, superlattice structure and its roughness.
EN
The strategy of "complex as ligand" allowed us to synthesize two new _-oxamido- bridged copper(II)-chromium(III) heterotetranuclear complexes formulated as [Cu3(oxae)3Cr](ClO4)3 (1) and [Cu3(oxpn)3Cr](ClO4)3 (2), where oxae and oxpn represent N,N_-bis(2-aminoethyl)oxamido and N,N_-bis(3-aminopropyl)oxamido dianions, respectively. Based on elemental analyses, molar conductivity and magnetic moment (room-temperature) measurements, IR, ESR and electronic spectral studies, these complexes are proposed to have oxamido-bridged structures consisting of three copper(II) ions and a chromium(III) ion, in which the chromium(III) ion has an octahedral environment and the three copper(II) ions have a square-planar environment. The two heterotetranuclear complexes were further characterized by variable-temperature magnetic susceptibility (3~300 K) measurements and the magnetic data have been used to deduce the indicated heterotetranuclear structure. The results derived from least-squares fit of the experimental data have confirmed the ferromagnetic interaction between the adjacent copper(II) and chromium(III) ions through the oxamido-bridge within each molecule. On the basis of the spin Hamiltonian operator, H=-2J(S Cu1 . S Cr+S Cu2 . S Cr + S Cu3 . S cr) , the magnetic analyses were carried out for the two copper(II)-chromium(III) heterotetranuclear complexes and the spin-coupling constants (J) were evaluated as +13.98 cm-1 for (1) and +12.65 cm-1 for (2). The results indicate that the bridging oxamido should be able to transmit ferromagnetic interaction in the strict orthogonality [Cu3 IICrIII] system. The influence of the symmetry of the magnetic orbitals on the nature of the magnetic interaction between the paramagnetic centers is preliminarily discussed.
EN
Ten new copper(II)-lanthanide(III) heterobinuclear complexes bridged by N,N'-bis[3- (dimethylamino)propyl]oxamido dianions (dmoxpn) and end-capped with 2,2'-bipyridine (bpy), namely, Cu(dmoxpn)Ln(bpy)2(NO3)3 (Ln = La, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb), have been synthesized and characterized by elemental analyses, molar conductivity measurements, and spectroscopic (IR, UV, ESR) studies. The Cu(dmoxpn)Gd(bpy)2(NO3)3 complex was further characterized by variable-temperature magnetic susceptibility (4.2~300 K) measurements and the magnetic data have been also used to deduce the indicated heterobinuclear structure. The results derived from least-squares fit of the experimental data have confirmed that the adjacent copper(II) and gadolinium(III) ions through the oxamido-bridge in the complex are ferromagnetically coupled with the exchange integral J(Cu-Gd) = +8.59 cm-1. A plausible mechanism for the ferromagnetic coupling between gadolinium(III) and copper(II) is discussed in terms of spin-polarization.
EN
Novel copper(II), cobalt(II) and manganese(II) binuclear complexes have been synthesized, namely [Cu2(3-NO2-phth)(phen)4](ClO4)2 and [M2(3-NO2-phth)(phen)4(H2O)2](ClO4)2, whereM=Co orMn, phen = 1,10-phenanthroline and 3-NO2-phth denotes 3-nitro-phthalate dianion. Magnetic susceptibility measurements between 4.2-300 K (or 77-300 K) demonstrate a ferromagnetic interaction between two copper(II) ions in the Cu-Cu complex, and a weak antiferromagnetic interaction between the metal ions in Co-Co and Mn-Mn complexes. Based on spin Hamiltonian operator, _H = -2J _ S1_ _ S2 (S1=S2 = 1/2, S1=S2 = 3/2 or S1 = S2 = 5/2), J is found to be equal to +5.26 cm-1, -1.72 cm-1 and -0.62 cm-1 for the Cu-Cu, Co-Co and Mn-Mn complexes, respectively
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