Search results for "Antiferromagnet"
showing 10 items of 506 documents
Magneto-structural study on a series of rhenium(IV) complexes containing biimH2, pyim and bipy ligands
2008
Abstract Three rhenium(IV) mononuclear compounds of formulae [ReCl4(biimH2)] · 2DMF (1), [ReCl4(pyim)] · DMF (2) and [ReCl4(bipy)] (3) (biimH2 = 2,2′-biimidazole, pyim = 2-(2′-pyridyl)imidazole, bipy = 2,2′-bipyridine and DMF = N,N-dimethylformamide) have been prepared and characterized. The crystal structure of 2 was determined by single crystal X-ray diffraction. Compound 2 crystallizes in the monoclinic system with P21/c as space group. The rhenium atom is six-coordinated by four Cl atoms and two nitrogen atoms from a bidentate pyim ligand [average values of Re–Cl and Re–N bonds lengths being 2.330(2) and 2.117(4) A, respectively]. The magnetic properties were investigated from susceptib…
Trinuclear N,N-Bridged Copper(II) Complexes Involving a Cu3OH Core: [Cu3(μ3-OH)L3A(H2O)2]A·(H2O)x {L = 3-Acetylamino-1,2,4-triazolate; A = CF3SO3, N…
2000
The reaction of Haat [Haat = (3-acetylamino-1,2,4-triazole)] with aquated Cu(CF3SO3)2, Cu(NO3)2, and Cu(ClO4)2, respectively, in water results in the trinuclear complexes [Cu3(OH)(aat)3(CF3SO3)(H2O)2](CF3SO3) (1), [Cu3(OH)(aat)3(NO3)(H2O)2](NO3).(H2O)2 (2), and [Cu3(OH)(aat)3(ClO4)(H2O)2](ClO4) (3). The synthesis, X-ray structure, and magnetic and spectroscopic properties of the three title complexes are described. The cation of the three complexes is trinuclear with a Cu3OH skeleton which has the N-N diazine grouping of a triazole ring as bridge between each pair of copper atoms. The Cu3OH units have an average Cu-O distance of 1.991(6) (1), 2.000(6) (2), and 2.007(6) (3) A, an average Cu-…
FeMoO4 Revisited: Crosslike 90° Noncollinear Antiferromagnetic Structure Caused by Dzyaloshinskii–Moriya Interaction
2021
The ground state of Fe2+ (S = 2) in α- and β-FeMoO4 is investigated by experiments including X-ray diffraction, Raman scattering, and 57Fe–Mossbauer spectroscopy below 300 K and evaluated by theore...
A step further in the comprehension of the magnetic coupling in gadolinium(III)-based carboxylate complexes
2013
Three new gadolinium(III) complexes of formula [Gd4(bta) 3(H2O)16]n·12nH2O (1), [Gd4(bta)3(H2O)12] n·18nH2O (2) and [Gd2(H 2bta)(bta)(H2O)2]n·4nH 2O (3) (H4bta = 1,2,4,5-benzenetetracarboxylic acid) have been synthesized and their structures determined by X-ray diffraction. 1 and 3 are three-dimensional compounds whereas 2 exhibits a two-dimensional structure. The ability of the bta4- to adopt different coordination modes accounts for these high dimensionalities although it precludes a rational structural design. The structures of 1-3 have in common the double oxo-carboxylate bridge between gadolinium(III) ions (μ-O: κ2O,O′) either as a discrete units (1 and 2) or as a chain (3) and one (3)…
Antiferromagnetic Interactions in Copper(II) µ-Oxalato Dinuclear Complexes: The Role of the Counterion
2018
We report the preparation, crystal structure determination, magnetic properties and DFT calculations of five oxalato-bridged dicopper(II) complexes of formula [Cu-2(bpy)(2-)(H2O)(2)(C2O4)](CF3SO3)(2) (1), [Cu-2(bpy)(2)(C2O4)](PF6)(2) (2), [Cu-2(bpy)(2)(C2O4)](ClO4)(2) (3), [Cu-2(bpy)(2)Cl-2(C2O4)]center dot H2O (4) and [Cu-2(bpy)(2)(NO2)(2)(C2O4)] (5) (bpy = 2,2'-bipyridine and C2O42-= oxalate). Compounds 1, 2, 4 and 5 crystallize in the monoclinic system and 3 crystallizes in the triclinic system. The oxalate ligands in 1-5 adopt the bis-bidentate coordination mode and the two bpy molecules act as terminal ligands. The coordination of the counterions and the surroundings of the copper(II) …
The magnetic resonance of Gd3+ in Gd2Se3 near the phase transition and up to 300 K
1985
Temperature dependences of the width of the Gd2Sc3 ESR lines are investigated. The observed width is satisfactory explained by a dipole mechanism narrowed by exchange interaction. Changes of the Gd2Se3 ESR line at T = 6 K are due to antiferromagnetic ordering in the sample. Es wird die Temperaturabhangigkeit der ESR-Linienbreite von Gd2Se3 untersucht. Die beobachtete Breite wird durch einen Dipolmechanismus mit Verschmelzung durch Austauschwechselwirkung beschrieben. Anderungen der Gd2Se3-ESR-Linie bei T = 6 K werden infolge antiferromagnetischer Ordnung in der Probe hervorgerufen.
Electric Field Control of Spin-Dependent Dissipative Electron Transfer Dynamics in Mixed-Valence Molecules
2015
We demonstrate that the borderline class II/III magnetic MV dimers, which can be referred to as single molecule multiferroics, provide a unique possibility to achieve electric field control of the electron transfer (ET) dynamics. As an example, we consider a MV dimer d2-d1 in which an extra electron is delocalized over two spin-cores (s0 = 1/2), and the ET is spin-dependent due to the double exchange mechanism. It is assumed that the “extra” electron is coupled to the only intramolecular vibration, and a weak coupling to the dissipative subsystem (thermal bath) is taken into account. The vibronic energy levels and the wave functions of the isolated dimer (quantum part of the system) are num…
Magnetic and structural approach for understanding the electrochemical behavior of LiNi0.33Co0.33Mn0.33O2 positive electrode material
2013
Abstract A systematic study has been performed to investigate the structural and magnetic changes in LiNi 0.33 Mn 0.33 Co 0.33 O 2 , a member of the LiNi y Mn y Co 1–2 y O 2 series, upon chemical lithium deintercalation. Structural characterization of the chemically delithiated Li x Ni 0.33 Mn 0.33 Co 0.33 O 2 samples indicates that the initial rhombohedral symmetry (α-NaFeO 2 type structure) is maintained in the whole 0.3 ≤ x ≤ 1.0 composition range. Less than 1% variation in the hexagonal unit cell volume was evidenced showing a good structural stability of this sample. SEM pictures of the delithiated phases confirm this stability. Indeed, the particle size average undergoes a small dec…
Synthesis, structural analysis, and magnetic properties of ethylmalonate-manganese(II) complexes
2011
12 páginas, 10 figuras, 6 tablas.-- et al.
Slow relaxation of the magnetization in Oximato-bridged heterobimetallic Copper(II)-Manganese(III) chains
2011
The use of the oximato-containing copper(II) complexes, [Cu(Hdeg)2] (H2deg = diethylglyoxime), [Cu(Hmeg)2] (H2meg = methylethylglyoxime) and [Cu(Hdmg)2] (H2dmg = dimethylglyoxime), as ligands toward manganese(II) acetate in methanol afforded the heterobimetallic compounds of formula [MnCu(deg)2(CH3COO)(H2O)2] (1), [MnCu(meg)2(CH3COO)(H2O)2] (2) and [MnCu(dmg)2(CH3COO)(H2O)2] (3) where the starting manganese(II) ion was oxidized to manganese(III) by air. In the lack of single crystals suitable for X-ray diffraction analysis, X-ray absorption techniques (EXAFS and XANES) at 40 K were used for the structural characterization of 1-3. The analysis of the X-ray absorption data reveals that 1-3 ar…