Search results for "Curie's law"
showing 8 items of 8 documents
Synthesis, crystal structure and magnetic properties of [Cu(bpym)(mal)(H2O)]·6H2O and [Cu2(bpym)(mal)2(H2O)2]·4H2O (bpym=2,2′-bipyrimidine, H2mal=mal…
2001
Abstract Two new mixed-ligand complexes of formula [Cu(bpym)(mal)(H2O)]·6H2O (1) and [Cu2(bpym)(mal)2(H2O)2]·4H2O (2) (bpym=2,2′-bipyrimidine and H2mal=malonic acid) have been synthesised and characterised by X-ray diffraction methods. The crystal structure of 1 consists of mononuclear [Cu(bpym)(mal)(H2O)] units in which the copper atom shows a slightly distorted square-pyramidal environment with two bpym-nitrogen and two malonate-oxygen atoms forming the equatorial plane and a water molecule in the axial position. The structure of 2 is built by centrosymmetric bpym-bridged dinuclear [Cu2(bpym)(mal)2(H2O)2] units, in which the geometry of each Cu(II) ion is similar to that found in 1. Malon…
Geometric, electronic, and magnetic structure ofCo2FeSi: Curie temperature and magnetic moment measurements and calculations
2005
In this work a simple concept was used for a systematic search for materials with high spin polarization. It is based on two semiempirical models. First, the Slater-Pauling rule was used for estimation of the magnetic moment. This model is well supported by electronic structure calculations. The second model was found particularly for ${\mathrm{Co}}_{2}$ based Heusler compounds when comparing their magnetic properties. It turned out that these compounds exhibit seemingly a linear dependence of the Curie temperature as function of the magnetic moment. Stimulated by these models, ${\mathrm{Co}}_{2}\mathrm{FeSi}$ was revisited. The compound was investigated in detail concerning its geometrical…
Magnetic and electronic properties of double perovskites and estimation of their Curie temperatures byab initiocalculations
2008
First principles electronic structure calculations have been carried out on ordered double perovskites Sr_2B'B"O_6 (for B' = Cr or Fe and B" 4d and 5d transition metal elements) with increasing number of valence electrons at the B-sites, and on Ba_2MnReO_6 as well as Ba_2FeMoO_6. The Curie temperatures are estimated ab initio from the electronic structures obtained with the local spin-density functional approximation, full-potential generalized gradient approximation and/or the LDA+U method (U - Hubbard parameter). Frozen spin-spirals are used to model the excited states needed to evaluate the spherical approximation for the Curie temperatures. In cases, where the induced moments on the oxy…
Synthesis Crystal Structure and Magnetic Properties of the Trinuclear Nickel(II) Complex Bis[(μ-thiocyanato-N)bis(μ-pyridazine-N1,N2)bis(thiocyanato-…
2000
Unusual single N-bridging thiocyanato and double pyridazine (pdz) bridges occur in the linear trinuclear nickel(II) complex of formula [Ni3(pdz)6(NCS)6]. The compound exhibits a quasi Curie law behavior, the antiferromagnetic coupling through the double 1,2-diazine links being nearly compensated by the ferromagnetic exchange through the single N-bridging thiocyanato.
All-cis-1,2,3,4,5,6-cyclohexanehexacarboxylate two-dimensional gadolinium(III) complexes: Synthesis, X-ray crystal structure and magnetic properties
2010
Abstract The first gadolinium(III) complexes with the trideprotonated form of the 1,2,3,4,5,6-cyclohexanehexacarboxylic acid (H3clhex3−) of formulae [Gd(H3clhex)(H2O)4]n·3nH2O (1) and [Gd(H3clhex)(H2O)4]n·6nH2O (2) have been prepared through the gel technique and their structures determined by single crystal X-ray diffraction. The structure of 1 is made up of 63 honey-comb layers which are generated by [Gd(H2O)4]3+ cations and H3clhex3− anions acting as three-fold nodes and three-fold connectors, respectively. The structure of 2 consists of a [44,62] two-dimensional network extended in the ac plane where the H3clhex−3 groups act as four-fold connectors and the [Gd(H2O)4]3+ units as four-fol…
A new eight-coordinate complex of manganese(II): synthesis, crystal structure, spectroscopy and magnetic properties of [Mn(Hoxam)2(H2O)4] (H2oxam=oxa…
2001
Abstract The crystal structure of an eight-coordinate manganese(II) compound containing oxamato and water molecules as ligands [Mn(Hoxam)2(H2O)4], were H2oxam=oxamic acid, has been determined by X-ray diffraction on single-crystals. The coordinated oxygen atoms are located at the vertices (corners) of a distorted bicapped trigonal antiprism. Hydrogen bonding is responsible for an extended 3D-network. The magnetic susceptibility data of the compound have been investigated. χMT follows the Curie law, at very low temperatures χMT decreases smoothly due to weak intermolecular interactions and/or due to a small zero field splitting of the sextuplet spin state of the Mn(II).
[Criii(L)(CN)4]−: a new building block in designing cyanide-bridged 4,2-ribbon-like chains {[Criii(L)(CN)4]2Mn(H2O)2}·nH2O [L = 2-aminomethylpyridine…
2005
The preparation, X-ray crystallography and magnetic study of compounds PPh4[Cr(ampy)(CN)4]·H2O (1), PPh4[Cr(phen)(CN)4]·H2O·CH3OH (2), {[Cr(ampy)(CN)4]2Mn(H2O)2}·6H2O (3) and {[Cr(phen)(CN)4]2Mn(H2O)2}·4H2O (4), with PPh4+ = tetraphenylphosphonium cation, ampy = 2-aminomethylpyridine and phen = 1,10-phenanthroline, are reported here. 1 and 2 are mononuclear complexes whereas 3 and 4 are 4,2-ribbon-like bimetallic chains. The magnetic properties of 1–4 were investigated in the temperature range 1.9–300 K. A quasi Curie law behaviour for a magnetically isolated spin quartet is observed for 1 and 2. Compounds 3 and 4 are ferrimagnetic CrIII2MnII chains, which exhibit a metamagnetic behaviour, …
Radical cation salts based on BEDT-TTF and the paramagnetic anion [Cr(NCS)6]3−
1999
Abstract A new radical cation salt formulated as (ET)5.5[Cr(NCS)6] (ET = BEDT-TTF = bis(ethylene)dithiotetrathiafulvalene) has been synthesised and characterised by X-ray diffraction and magnetic measurements. The structure shows the presence of alternating layers of the ET units and mixed layers of anions and an isolated ET molecule. The magnetic susceptibility data in the temperature range 2–300 K show a Curie law with C = 1.771 cm3.K.mol−1 and Nα = 1.20.10−5 cm3.mol−1, in agreement with the presence of isolated Cr(III) without any contribution from the organic part.