The magnetic properties of rhenium halides. II. Rhenium trichloride

1965 ◽  
Vol 18 (4) ◽  
pp. 441 ◽  
Author(s):  
D Brown ◽  
R Colton
Keyword(s):  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Low Temperature ◽  
Powder Diffraction ◽  
Infrared Spectra ◽  
X Ray ◽  
Temperature Modification ◽  
Rhenium Halides

Magnetic susceptibility measurements have been made on anhydrous rhenium trichloride and the dihydrate, ReCl3,2H2O. Infrared spectra and X-ray powder diffraction studies are reported for anhydrous rhenium trichloride and the possible existence of a low temperature modification of the trichloride is discussed.

MAGNETIC AND STRUCTURAL PROPERTIES OF SOME ABa2Cu3O7−δ SUPERCONDUCTORS

1987 ◽  
Vol 01 (03n04) ◽  
pp. 989-992 ◽  
Author(s):  
M.T. Causa ◽  
S.M. Dutrús ◽  
C. Fainstein ◽  
G. Nieva ◽  
H.R. Salva ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Electrical Resistivity ◽  
Magnetic Susceptibility ◽  
Specific Heat ◽  
Powder Diffraction ◽  
Magnetic Moments ◽  
Superconducting Properties ◽  
X Ray ◽  
Structural Modifications

We report here normal and superconducting properties of ABa 2 Cu 3 O 7−δ (with A=Y, Gd, Dy, and Er) and of Fe doped YBa2Cu3O7−δ . Results from X-ray powder diffraction, electrical resistivity, magnetic susceptibility, ESR, and specific heat measurements are presented, leading to a characterization of the magnetic properties of these materials. The effect of structural modifications of the lattice on the superconducting properties and the relative insensitivity of Tc to the presence of magnetic moments is discussed.

Superconductivity and Normal-State Properties of (Y1-x-yZrxCay)Ba2Cu3O7-δ Compounds

1998 ◽  
Vol 12 (28) ◽  
pp. 1175-1183 ◽  
Author(s):  
I. Gr. Deac ◽  
A. V. Pop ◽  
V. Pop ◽  
R. Tetean ◽  
D. Kovacs ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Powder Diffraction ◽  
Normal State ◽  
Lattice Parameters ◽  
Temperature Dependent ◽  
Dopant Content ◽  
X Ray ◽  
Electrical And Magnetic Properties ◽  
Normal State Properties

The electrical and magnetic properties of ( Y 1-x-y Zr x Ca y) Ba 2 Cu 3 O 7-δ ceramics are investigated by using resistivity, ac and dc susceptibility measurements. X-ray powder diffraction has been used to find the lattice parameters of the samples. The samples are orthorhombic, except the sample with x=0.15 and y=0.2 which is tetragonal. All the samples are superconducting. There is no significant change in Tc for the Zr-doped ( Y 1-x Zr x) Ba 2 Cu 3 O 7-δ samples, while for the ( Y 0.85-y Zr 0.15 Ca y) Ba 2 Cu 3 O 7-δ compounds the Tc decrease with the dopant content and they show temperature dependent dc magnetic susceptibility, in the normal state.

Synthesis and Characterization of Magnetic Rubidium Superoxide, RbO2

2019 ◽  
Vol 966 ◽  
pp. 237-242
Author(s):  
Fahmi Astuti ◽  
Mizuki Miyajima ◽  
Takahito Fukuda ◽  
Masashi Kodani ◽  
Takehito Nakano ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Spin Relaxation ◽  
Powder Diffraction ◽  
Solution Method ◽  
Muon Spin ◽  
Muon Spin Relaxation ◽  
Synthesis And Characterization ◽  
X Ray

Polycrystalline rubidium superoxide (RbO2) has been synthesized by using solution method followed by the reaction process under the cooling condition of-40 °C. X-ray Powder Diffraction (XRD) spectra showed that RbO2 was successfully synthesized by this method. The magnetic susceptibility and pulsed muon spin relaxation (μSR) measurements were carried out in order to study the magnetic properties of RbO2.

Structure and Magnetic Properties of (Cr,Ni)4-xCoxSi

2019 ◽  
Vol 289 ◽  
pp. 108-113
Author(s):  
Romana Iryna Martyniak ◽  
Nataliya Muts ◽  
Olga Sichevych ◽  
Horst Borrmann ◽  
Matej Bobnar ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Cell Parameter ◽  
Powder Diffraction Data ◽  
X Ray ◽  
Pearson Symbol ◽  
Paramagnetic Behaviour

The crystal structure of the (Cr,Ni)4Si phase with and without Co was refined from X-ray powder diffraction data. The compound crystallises with an Au4Al-type structure (Pearson symbol cP20, space group P213): unit-cell parameter a = 0.611959(6) nm for the composition (Cr0.312Ni0.688)4Si, a = 0.612094(6) nm for (Cr0.375Ni0.625)4Si, and a = 0.612316(6) nm for (Cr0.337Co0.063Ni0.600)4Si. The magnetic susceptibility was measured in external fields up to 7 T at temperatures between 1.8 and 400 K. The three investigated samples exhibited paramagnetic behaviour described by the modified Curie-Weiss law: χ0 = 146∙10-6 emu g-at.-1, μeff = 0.21 μB/atom, θP = -13 K for (Cr0.312Ni0.688)4Si; χ0 = 158∙10-6 emu g-at.-1, μeff = 0.20 μB/atom, θP = -15 K for (Cr0.375Ni0.625)4Si; χ0 = 169∙10-6 emu g-at.-1, μeff = 0.18 μB/atom, θP = -52 K for (Cr0.337Co0.063Ni0.600)4Si.

X-ray Structure Refinement and Vibrational Spectroscopy of Ca8Gd2 (PO4)6 O2

2013 ◽  
Vol 12 (10) ◽  
pp. 719-726
Author(s):  
R. Ayadi ◽  
Mohamed Boujelbene ◽  
T. Mhiri
Keyword(s):  
Solid State ◽  
General Formula ◽  
Vibrational Spectroscopy ◽  
Powder Diffraction ◽  
Infrared Spectra ◽  
Solid State Reaction ◽  
Structure Refinement ◽  
Unit Cell ◽  
Cell Group ◽  
X Ray

The present paper is interested in the study of compounds from the apatite family with the general formula Ca10 (PO4)6A2. It particularly brings to light the exploitation of the distinctive stereochemistries of two Ca positions in apatite. In fact, Gd-Bearing oxyapatiteCa8 Gd2 (PO4)6O2 has been synthesized by solid state reaction and characterized by X-ray powder diffraction. The site occupancies of substituents is0.3333 in Gd and 0.3333 for Ca in the Ca(1) position and 0. 5 for Gd in the Ca (2) position.  Besides, the observed frequencies in the Raman and infrared spectra were explained and discussed on the basis of unit-cell group analyses.

Cobalt(II) Mercury Tetrathiocyanate Complexes with Lewis Bases

1973 ◽  
Vol 51 (3) ◽  
pp. 438-447 ◽  
Author(s):  
R. Makhija ◽  
L. Pazdernik ◽  
R. Rivest
Keyword(s):  
Magnetic Susceptibility ◽  
Powder Diffraction ◽  
Elemental Analysis ◽  
Far Infrared ◽  
Crystalline Solid ◽  
Ultraviolet Spectroscopy ◽  
X Ray ◽  
Lewis Bases ◽  
Polydentate Ligands

A new series of octahedral cobalt(II) complexes are formed when CoX2(X = Cl, Br, I, SCN) reacts with Hg(SCN)2 in the presence of Lewis bases. These complexes of stoichiometry CoHg(SCN)4•2L (L = THF, dioxane, pyridine, aniline) are pink to violet solids which slowly decompose to the blue crystalline solid, CoHg(SCN)4, the stable magnetic susceptibility standard. On further reaction of CoHg(SCN)4•2THF with mono-, bi-, and polydentate ligands in dry ethanol, complexes of the following types are obtained: CoHg(SCN)4•2L (L = PΦ3), CoHg(SCN)4•2LL (LL = trien), CoHg(SCN)4•3LL (LL = en, bipy), and CoHg(SCN)4•4LL (LL = phen). The stoichiometry of these were determined by elemental analysis. Possible structures of these are discussed with the help of mid and far infrared, visible, and ultraviolet spectroscopy, magnetic susceptibility, and X-ray powder diffraction. Some new i.r. bands like Co—P, Co—N, and Hg—S are assigned in the low region.

Crystal structure of potassium tetraperoxomolybdate (VI) K2[Mo(O2)4]

2005 ◽  
Vol 20 (3) ◽  
pp. 203-206 ◽  
Author(s):  
M. Grzywa ◽  
M. Różycka ◽  
W. Łasocha
Keyword(s):  
Crystal Structure ◽  
Low Temperature ◽  
Diffraction Pattern ◽  
Powder Diffraction ◽  
Rietveld Method ◽  
Structure Refinement ◽  
Crystal Structure Refinement ◽  
Unit Cell Parameters ◽  
X Ray ◽  
Cell Parameters

Potassium tetraperoxomolybdate (VI) K2[Mo(O2)4] was prepared, and its X-ray powder diffraction pattern was recorded at low temperature (258 K). The unit cell parameters were refined to a=10.7891(2) Å, α=64.925(3)°, space group R−3c (167), Z=6. The compound is isostructural with potassium tetraperoxotungstate (VI) K2[W(O2)4] (Stomberg, 1988). The sample of K2[Mo(O2)4] was characterized by analytical investigations, and the results of crystal structure refinement by Rietveld method are presented; final RP and RWP are 9.79% and 12.37%, respectively.

Synthesis, Structure and Magnetism of ErCoIn5

2004 ◽  
Vol 848 ◽  
Author(s):  
Evan Lyle Thomas ◽  
Erin E. Erickson ◽  
Monica Moldovan ◽  
David P. Young ◽  
Julia Y. Chan
Keyword(s):  
Magnetic Properties ◽  
Electrical Resistivity ◽  
Magnetic Susceptibility ◽  
Single Crystal ◽  
Experimental Results ◽  
Flux Growth ◽  
X Ray Diffraction ◽  
Metallic Behavior ◽  
X Ray ◽  
Growth Method

AbstractA new member of the LnMIn5 family, ErCoIn5, has been synthesized by a flux-growth method. The structure of ErCoIn5 was determined by single crystal X-ray diffraction. It crystallizes in the tetragonal space group P4/mmm, Z = 1, with lattice parameters a = 4.5400(4) and c = 7.3970(7) Å, and V = 152.46(2) Å3. Electrical resistivity data show metallic behavior. Magnetic susceptibility measurements show this compound to be antiferromagnetic with TN = 5.1 K. We compare these experimental results with those of LaCoIn5 in an effort to better understand the effect of the structural trends observed on the transport and magnetic properties.

Synthesis, Structure, and Characterization of La1−xBax (0 ≤ x ≤ 1)

1992 ◽  
Vol 271 ◽  
Author(s):  
Joseph E. Sunstrom ◽  
Susan M. Kauzlarich
Keyword(s):  
Magnetic Susceptibility ◽  
Powder Diffraction ◽  
Single Phase ◽  
Gravimetric Analysis ◽  
Thermal Gravimetric ◽  
Temperature Dependent ◽  
X Ray ◽  
Early Transition Metal ◽  
Arc Melting

ABSTRACTThe compounds La1−xBaxTiO3 (0 ≤ × ≤ 1) have been prepared by arc melting stoichiometric amounts of LaTiO3 and BaTiO3. Single phase samples can be made for the entire stoichiometry range. The polycrystalline samples have been characterized by thermal gravimetric analysis, X-ray powder diffraction, and temperature dependent magnetic susceptibility. This series of compounds has been studied as a possible candidate for an early transition metal superconductor.

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