Mg1 + x Ir1 − x (x = 0, 0.037 and 0.054), a binary intermetallic compound with a new orthorhombic structure type determined from powder and single-crystal X-ray diffraction

2004 ◽  
Vol 60 (3) ◽  
pp. 272-281 ◽  
Author(s):  
Radovan Černý ◽  
Guillaume Renaudin ◽  
Vincent Favre-Nicolin ◽  
Viktor Hlukhyy ◽  
Rainer Pöttgen

The new binary compound Mg1 + x Ir1 − x (x = 0–0.054) was prepared by melting the elements in the Mg:Ir ratio 2:3 in a sealed tantalum tube under an argon atmosphere in an induction furnace (single crystals) or by annealing cold-pressed pellets of the starting composition Mg:Ir 1:1 in an autoclave under an argon atmosphere (powder sample). The structure was independently solved from high-resolution synchrotron powder and single-crystal X-ray data: Pearson symbol oC304, space group Cmca, lattice parameters from synchrotron powder data a = 18.46948 (6), b = 16.17450 (5), c = 16.82131 (5) Å. Mg1 + x Ir1 − x is a topologically close-packed phase, containing 13 Ir and 12 Mg atoms in the asymmetric unit, and has a narrow homogeneity range. Nearly all the atoms have Frank–Kasper-related coordination polyhedra, with the exception of two Ir atoms, and this compound contains the shortest Ir—Ir distances ever observed. The solution of a rather complex crystal structure from powder diffraction, which was fully confirmed by the single-crystal method, shows the power of powder diffraction in combination with the high-resolution data and the global optimization method.

2013 ◽  
Vol 69 (2) ◽  
pp. i11-i12 ◽  
Author(s):  
Yongho Kee ◽  
Hoseop Yun

The structure of Li3V2(PO4)3has been reinvestigated from single-crystal X-ray data. Although the results of the previous studies (all based on powder diffraction data) are comparable with our redetermination, all atoms were refined with anisotropic displacement parameters in the current study, and the resulting bond lengths are more accurate than those determined from powder diffraction data. The title compound adopts the Li3Fe2(PO4)3structure type. The structure is composed of VO6octahedra and PO4tetrahedra by sharing O atoms to form the three-dimensional anionic framework∞3[V2(PO4)3]3−. The positions of the Li+ions in the empty channels can vary depending on the synthetic conditions. Bond-valence-sum calculations showed structures that are similar to the results of the present study seem to be more stable compared with others. The classical charge balance of the title compound can be represented as [Li+]3[V3+]2[P5+]3[O2−]12.


1991 ◽  
Vol 24 (5) ◽  
pp. 888-892 ◽  
Author(s):  
V. A. Trunov ◽  
A. L. Malyshev ◽  
D. Yu. Chernyshov ◽  
A. I. Kurbakov ◽  
M. M. Korsukova ◽  
...  

1999 ◽  
Vol 32 (6) ◽  
pp. 1084-1089 ◽  
Author(s):  
R. B. Von Dreele

By combining high-resolution X-ray powder diffraction data and stereochemical restraints, Rietveld refinement of protein crystal structures has been shown to be feasible. A refinement of the 1261-atom protein metmyoglobin was achieved by combining 5338 stereochemical restraints with a 4648-step (dmin= 3.3 Å) powder diffraction pattern to give the residualsRwp= 2.32%,Rp= 1.66%,R(F2) = 3.10%. The resulting tertiary structure of the protein is essentially identical to that obtained from previous single-crystal studies.


2015 ◽  
Vol 71 (12) ◽  
pp. 1548-1550
Author(s):  
Andrea V. Hoffmann ◽  
Viktor Hlukhyy ◽  
Thomas F. Fässler

The crystal structure of the binary compound tetracalcium triarsenide, Ca4As3, was investigated by single-crystal X-ray diffraction. Ca4As3crystallizes in the Ba4P3structure type and is thus a homologue of isotypic Sr4As3. The unit cell contains 32 Ca2+cations, 16 As3−isolated anions and four centrosymmetric [As2]4–dumbbells. The As atoms in each of the dumbbells are connected by a single bond, thus this calcium arsenide is a Zintl phase.


2007 ◽  
Vol 63 (3) ◽  
pp. 505-509 ◽  
Author(s):  
B. Dittrich ◽  
P. Munshi ◽  
M. A. Spackman

The structure of L-ornithine hydrochloride, C5H13N2O_2^+Cl−, has been redetermined at 100 K by single-crystal X-ray diffraction within a project that aims to generate accurate bond-distance restraints for the invariom refinement of proteins. The high-resolution data were subject to an invariom and a multipole refinement, and the resulting electron densities on a grid were compared. Improvements in the conventional R factor obtained by multipole modelling were smaller than in other structures containing solely the elements CHNO owing to Cl core scattering. Cruickshank's diffraction-component precision index and Stevens & Coppens suitability factor are discussed.


2017 ◽  
Vol 73 (7) ◽  
pp. 1037-1040
Author(s):  
Konstantin E. German ◽  
Mikhail S. Grigoriev ◽  
Bogdan L. Garashchenko ◽  
Alexander V. Kopytin ◽  
Ekaterina A. Tyupina

The redetermination of the title compound, sodium pertechnate, from single-crystal CCD data recorded both at 296 and 100 K confirms previous studies based on X-ray powder diffraction film data [Schwochau (1962).Z. Naturforsch. Teil A,17, 630; Keller & Kanellakopulos (1963).Radiochim. Acta,1, 107–108] and neutron powder diffraction data using the Rietveld method [Weaveret al.(2017).Inorg. Chem.12, 677–681], but reveals a considerable improvement in precision. The standard uncertainties of the room-temperature structure determination are about seven times lower than those of the neutron diffraction structure determination and about 13 times lower at 100 K, due to the decrease in the amplitude of librations. The crystal expansion could be approximated linearly with a thermal volumic expansion coefficient of 1.19 (12) × 10−4K−1. NaTcO4adopts the scheelite (CaWO4) structure type in space group typeI41/awith Na and Tc atoms (both with site symmetry -4) replacing Ca and W atoms, respectively.


RSC Advances ◽  
2014 ◽  
Vol 4 (96) ◽  
pp. 53602-53607 ◽  
Author(s):  
Hai-Feng Li ◽  
Andrew Wildes ◽  
Binyang Hou ◽  
Cong Zhang ◽  
Berthold Schmitz ◽  
...  

The magnetization, crystal structure, and thermal expansion of a nearly stoichiometric Sr1.04(3)Er2.09(6)O4.00(1)single crystal have been studied by PPMS measurements and in-house and high-resolution synchrotron X-ray powder diffraction.


2007 ◽  
Vol 62 (7) ◽  
pp. 896-900 ◽  
Author(s):  
Volodymyr Babizhetskyy ◽  
Arndt Simon ◽  
Kurt Hiebl

Abstract The structure of CeB4 has been determined by single crystal X-ray diffraction. The compound crystallizes in the ThB4 structure type (space group P4/mbm, a = 7.2034(8), c = 4.1006(5) Å; 270 reflections with Fo ≥ 4σ (Fo), R1 = 0.023, wR2 = 0.052). The results of the magnetic and electrical resistivity measurements indicate a strong f-d hybridization of the 4 f electrons of the cerium atom


Sign in / Sign up

Export Citation Format

Share Document