scholarly journals Structural determination of the low-temperature phases of globular organic molecules by powder X-ray diffraction

1996 ◽  
Vol 52 (a1) ◽  
pp. C548-C548
Author(s):  
A. J. Mora ◽  
A. N. Fitch
Hyomen Kagaku ◽  
2016 ◽  
Vol 37 (9) ◽  
pp. 429-434 ◽  
Author(s):  
Ryohei TSURUTA ◽  
Yuta MIZUNO ◽  
Takuya HOSOKAI ◽  
Tomoyuki KOGANEZAWA ◽  
Hisao ISHII ◽  
...  

2021 ◽  
Author(s):  
Zhehao Huang ◽  
Tom Willhammar ◽  
Xiaodong Zou

Three-dimensional electron diffraction is a powerful tool for accurate structure determination of zeolite, MOF, and COF crystals that are too small for X-ray diffraction. By revealing the structural details, the properties of the materials can be understood, and new materials and applications can be designed.


2021 ◽  
Vol 45 (2) ◽  
pp. 167-173
Author(s):  
Lalmi Khier ◽  
Lakel Abdelghani ◽  
Djamel Maouche

In this work, we have studied the Kaolin M1 and M2 by the X-ray diffraction method, and we have focused on mullite phase which is the main phase present in common in both products. An update of the program of the method of Stokes was carried out, it was necessary to the microstructural analysis. The completed version is less sensitive to the choice by excess of the number of coefficients of Fourier with regard to the effect of truncation and the office plurality of the errors. The determination of the symmetry of the cell of the principal phase (mullite) in the studied fritted Kaolins was carried out. In Kaolin M1, the size of crystallites of the dominant phase varies between 80 to 170 Å. In Kaolin M2, the size of the crystalline grains of mullite varies between 100 to 400 Å. The size of crystallites was confirmed by the joint method of Williamson-Hall. A distribution of sizes of crystallites was carried out. It shows a dominance of the size of approximately 140 Å for the principal phase of Kaolin M1 and a dominance of the size of approximately 230 Å for the same principal phase of Kaolin M2. By the study of the profiles of line by DRX, it appears very clearly that the principal phase of the various sintered Kaolins, mullite, is free from internal microstrains. It is the case of the mixtures fritted not only at low temperature (1100℃) during 1 hour but also the case of the mixtures of the type ‘chamotte’ cooks with 1350℃ during very long times.


1989 ◽  
Vol 32 (2) ◽  
pp. 171-177 ◽  
Author(s):  
M.P. Da Silva ◽  
A.A. Bernussi ◽  
G.M. Gualberto

1989 ◽  
Vol 42 (7) ◽  
pp. 1155 ◽  
Author(s):  
J Baldas ◽  
SF Colmanet

The crystal structure of [AsPh4] [TcOCl4] (1) has been determined by X-ray diffraction. Crystals are tetragonal, space group P4/n, a 12.664(1), c 7.822(1) � , Z = 2. Refinement based on 912 data measured with Cu Ka radiation converged with R 0.059. The structure consists of discrete [AsPh4]+ cations and [TcOCl4]- anions with the technetium atom in a square-pyramidal environment. In contrast to an earlier structural determination of the [TcOCl]-anion in [N(PPh3)2] [TcOCl4], the [TcOCl4]-anion in (1) possesses ideal symmetry. The Tc =O bond length is 1.593(8) � with Tc -CI 2.309(2) �.


1969 ◽  
Vol 47 (6) ◽  
pp. 1093-1094 ◽  
Author(s):  
M. Mathew ◽  
Gus J. Palenik

The crystal structure of 1,2-bis(diphenylphosphineoxido)ethane copper(II) chloride has been determined by X-ray diffraction techniques. The compound is the first structural determination of a CuCl2–phosphineoxide adduct and exhibits some very large distortions from the ideal tetrahedral symmetry. The Cl—Cu—O angle is 140.2° and the Cu—Cl distance of 2.195 Å is shorter than in other CuCl2 complexes.


2002 ◽  
Vol 41 (20) ◽  
pp. 5300-5312 ◽  
Author(s):  
L. Valencia ◽  
J. Martinez ◽  
A. Macías ◽  
R. Bastida ◽  
R. A. Carvalho ◽  
...  

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