ChemInform Abstract: Crystal Structure and Magnetic Ordering in ErFe6Ge6 Studied by X-Ray, Neutron Diffraction and Magnetic Measurements.

ChemInform ◽  
2010 ◽  
Vol 28 (48) ◽  
pp. no-no
Author(s):  
O. OLEKSYN ◽  
P. SCHOBINGER-PAPAMANTELLOS ◽  
J. RODRIGUEZ-CARVAJAL ◽  
E. BRUECK ◽  
K. H. J. BUSCHOW
Keyword(s):  
Crystal Structure ◽  
Neutron Diffraction ◽  
Magnetic Measurements ◽  
Magnetic Ordering ◽  
X Ray

Crystal structure and magnetic ordering in ErFe6Ge6 studied by X-ray, neutron diffraction and magnetic measurements

1997 ◽  
Vol 257 (1-2) ◽  
pp. 36-45 ◽  
Author(s):  
O. Oleksyn ◽  
P. Schobinger-Papamantellos ◽  
J. Rodríguez-Carvajal ◽  
E. Brück ◽  
K.H.J. Buschow
Keyword(s):  
Crystal Structure ◽  
Neutron Diffraction ◽  
Magnetic Measurements ◽  
Magnetic Ordering ◽  
X Ray

Structural and Magnetic Properties of La0.7Sr0.3Mn1-xNixO3 (x=0.05, 0.1, 0.2, 0.3, 0.4)

2011 ◽  
Vol 1327 ◽  
Author(s):  
Thomas F. Creel ◽  
Jinbo B. Yang ◽  
Mehmet Kahveci ◽  
Jagat Lamsal ◽  
Satish K. Malik ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Neutron Diffraction ◽  
Diffraction Data ◽  
Magnetic Measurements ◽  
Magnetic Ordering ◽  
Neutron Diffraction Data ◽  
Space Group ◽  
X Ray ◽  
Antiferromagnetic Ordering ◽  
Structural And Magnetic Properties

ABSTRACTWe have studied the structural and magnetic properties of La0.7Sr0.3Mn1-xNixO3 (x=0.05, 0.10, 0.20, 0.30, and 0.40) perovskites using x-ray and neutron diffraction and magnetic measurements. To our knowledge, there exists no neutron diffraction data available for this group of perovskite compositions. Neutron (λ = 1.479Å) and x-ray (λ = 1.5481Å; Cu Kα) powder diffraction indicate that for x ≥ 0.1 all samples are two-phase with a rhombohedral perovskite structure (space group R-3c) and a small amount of NiO (space group Fm3m). Neutron diffraction data for the perovskite phase at 12K and 300K show ferromagnetic ordering for x ≤ 0.2 and antiferromagnetic ordering for x = 0.4. However, for x = 0.3, neutron diffraction data at 12K show coexisting ferromagnetic and antiferromagnetic ordering while at 300K no magnetic ordering is found. Magnetic measurements indicate that the Curie temperature decreases with increasing Ni content. The NiO phase for all samples was found to have antiferromagnetic ordering at 12K and 300K. The magnetic measurements are consistent with the neutron diffraction data and together indicate long-range magnetic ordering for samples at low temperature and transitions from ferromagnetic to paramagnetic to antiferromagnetic ordering for samples at room temperature.

X-ray and neutron diffraction study of the defect crystal structure of the as-grown nonstoichiometric phase Y0.715Ca0.285F2.715

2013 ◽  
Vol 58 (4) ◽  
pp. 575-585 ◽  
Author(s):  
N. B. Bolotina ◽  
A. I. Kalyukanov ◽  
T. S. Chernaya ◽  
I. A. Verin ◽  
I. I. Buchinskaya ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Neutron Diffraction ◽  
Diffraction Study ◽  
Neutron Diffraction Study ◽  
Nonstoichiometric Phase ◽  
X Ray ◽  
Defect Crystal

scholarly journals Pressure-cooking of explosives—the crystal structure of ε-RDX as determined by X-ray and neutron diffraction

2010 ◽  
Vol 46 (31) ◽  
pp. 5662 ◽  
Author(s):  
David I. A. Millar ◽  
Iain D. H. Oswald ◽  
Christopher Barry ◽  
Duncan J. Francis ◽  
William G. Marshall ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Neutron Diffraction ◽  
Pressure Cooking ◽  
X Ray

scholarly journals Synthesis, Crystal Structure and Magnetic Properties of Bixbyite-type Vanadium Oxide Nitrides

2009 ◽  
Vol 64 (3) ◽  
pp. 281-286 ◽  
Author(s):  
Suliman Nakhal ◽  
Wilfried Hermes ◽  
Thorsten Ressler ◽  
Rainer Pöttgen ◽  
Martin Lerch
Keyword(s):  
Crystal Structure ◽  
Vanadium Oxide ◽  
Magnetic Ordering ◽  
Vanadium Oxides ◽  
Detectable Amount ◽  
X Ray Diffraction ◽  
X Ray ◽  
Vanadium Sulfide ◽  
Structure Result ◽  
X Ray Absorption

Ammonolysis of vanadium sulfide leads to the formation of bixbyite-type vanadium oxide nitrides. Small amounts of nitrogen incorporated in the structure result in the stabilization of the bixbyite type not known for vanadium oxides. The crystal structure was investigated using X-ray diffraction and X-ray absorption spectroscopy. At temperatures above 550 °C the powders decompose to corundumtype V2O3 containing no detectable amount of nitrogen. Below 39 K magnetic ordering is observed.

Cyano-Bridged Bimetallic Complexes of Copper(II) with Nitroprusside. Crystal Structure of [Cu(H2NCH2CH(NH2)CH3)2Fe(CN)5NO] . H2O

2000 ◽  
Vol 53 (3) ◽  
pp. 225 ◽  
Author(s):  
Zdenek Smékal ◽  
Zdenek Trávnícek ◽  
Jaromír Marek ◽  
Milan Nádvornik
Keyword(s):  
Crystal Structure ◽  
Structural Analysis ◽  
Magnetic Measurements ◽  
X Ray ◽  
Cyanide Group ◽  
Cyanide Ligand ◽  
Binuclear Structure ◽  
Tetragonal Pyramidal ◽  
Cyanide Ligands ◽  
Diamine Ligands

Five new complexes of compositions [Cu(1,2-pn)2Fe(CN)5NO]·H2O (1,2-pn = propane-1,2-diamine) and [Cu(L)Fe(CN)5NO]·xH2O (L = tmen (N,N,N′,N′-tetramethylethane-1,2-diamine), x = 0.5; L = trimeen (N,N,N′-trimethylethane-1,2-diamine), x = 1; L = dien (N-(2-aminoethyl)ethane-1,2-diamine), x = 0; L = medpt (N-(3-aminopropyl)-N-methylpropane-1,3-diamine), x = 2) have been isolated from the reaction mixture of Cu(ClO4)2·6H2O (or CuCl2·2H2O), the amine and Na2 [Fe(CN)5NO]·2H2O in water. The complexes have been characterized by infrared and ultraviolet–visible spectroscopies, and magnetic measurements. Single-crystal X-ray structural analysis revealed that the [Cu(1,2-pn)2Fe(CN)5NO]·H2O complex assumes a cyanide-bridged binuclear structure in which iron(II) is six-coordinated by five cyanide ligands and one nitrosyl group (the nitrosyl group lies cis to the bridging cyanide group), while copper(II) is five-coordinated by two propane-1,2-diamine ligands and a bridging cyanide ligand in a distorted tetragonal pyramidal arrangement.

ChemInform Abstract: THE CRYSTAL STRUCTURE OF CUBIC INDIUM TRIHYDROXIDE BY X-RAY AND NEUTRON DIFFRACTION METHODS

1979 ◽  
Vol 10 (24) ◽  
Author(s):  
D. F. MULLICA ◽  
G. W. BEALL ◽  
W. O. MILLIGAN ◽  
J. D. KORP ◽  
I. BERNAL
Keyword(s):  
Crystal Structure ◽  
Neutron Diffraction ◽  
X Ray

Magnetic and Structural Properties of Ferrimagnetic Bioceramics

2005 ◽  
Vol 473-474 ◽  
pp. 117-122 ◽  
Author(s):  
A.C. Kis ◽  
Th. Leventouri ◽  
J.R. Thompson
Keyword(s):  
Crystal Structure ◽  
Heat Treatment ◽  
Magnetic Properties ◽  
Calcium Phosphate ◽  
Powder Diffraction ◽  
Magnetic Measurements ◽  
Treatment Temperature ◽  
Monoclinic Crystal ◽  
X Ray ◽  
Phase Development

Structure and magnetic properties of ferrimagnetic bioceramics in the system {0.45(CaO, P2O5) ySiO2 xFe2O3 0.03Na2O}, x=0.05, 0.10, 0.15, 0.20, were studied by x-ray powder diffraction and magnetic measurements. Magnetite and calcium phosphate, crystallizing in the hexagonal and monoclinic crystal systems, are the major phases in the compounds. Phase development, crystal structure, and magnetic properties of the composites are determined by the specific starting composition of oxides and the heat-treatment temperature.

Sign in / Sign up

Export Citation Format

Share Document