Structures of six industrial benzimidazolone pigments from laboratory powder diffraction data

2009 ◽  
Vol 65 (2) ◽  
pp. 200-211 ◽  
Author(s):  
Jacco van de Streek ◽  
Jürgen Brüning ◽  
Svetlana N. Ivashevskaya ◽  
Martin Ermrich ◽  
Erich F. Paulus ◽  
...  
Keyword(s):  
Crystal Structures ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Real Space ◽  
Powder Diffraction Data ◽  
Intermolecular Hydrogen Bonds ◽  
Rietveld Refinements ◽  
Hydrogen Bonding Pattern ◽  
Β Phase ◽  
Α Phase

The crystal structures of six industrially produced benzimidazolone pigments [Pigment Orange 36 (β phase), Pigment Orange 62, Pigment Yellow 151, Pigment Yellow 154 (α phase), Pigment Yellow 181 (β phase) and Pigment Yellow 194] were determined from laboratory X-ray powder diffraction data by means of real-space methods using the programs DASH and MRIA, respectively. Subsequent Rietveld refinements were carried out with TOPAS. The crystal phases correspond to those produced industrially. Additionally, the crystal structures of the non-commercial compound `BIRZIL' (a chloro derivative of Pigment Yellow 194) and of a dimethylsulfoxide solvate of Pigment Yellow 154 were determined by single-crystal structure analyses. All eight crystal structures are different; the six industrial pigments even exhibit five different hydrogen-bond topologies. Apparently, the good application properties of the benzimidazolone pigments are not the result of one specific hydrogen-bonding pattern, but are the result of a combination of efficient molecular packing and strong intermolecular hydrogen bonds.

Industrial azomethine nickel complex pigments. Four crystal structures from X-ray powder diffraction data

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Jürgen Brüning ◽  
Svetlana N. Ivashevskaya ◽  
Jacco van de Streek ◽  
Edith Alig ◽  
Martin U. Schmidt
Keyword(s):  
Crystal Structures ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Rietveld Method ◽  
Laboratory Data ◽  
Real Space ◽  
Planar Geometry ◽  
Powder Diffraction Data ◽  
Β Phase ◽  
Α Phase

Abstract The crystal structures of the azomethine nickel complexes Pigment Orange 68 (P.O.68, C29H18N4O3Ni), Pigment Red 257 (P.R.257, C16H4Cl8N6O2Ni), and Solvent Brown 53 (S.Br.53, C18H10N4O2Ni) were determined from powder diffraction data. The compounds are industrially used for the colouration of plastics and coatings. P.O.68 exists in two polymorphic forms, the commercial one is the α-phase. The crystal structures were solved from laboratory data using real-space methods and refined by the Rietveld method. For the Rietveld refinement of α-P.O.68, synchrotron data were employed. In all structures, the Ni2+ ion is coordinated by two N atoms and two O atoms in a square-planar geometry. Both phases of P.O.68 crystallise in P21/c, Z = 4. In both structures, the molecules form dimers via an inversion centre, with Ni-to-Ni distances of 3.606 Å (α-phase) and 3.286 Å (β-phase). The dimers are stacked into columns. Neighbouring columns are connected by hydrogen bonds: one classical N–H⋅⋅⋅O bond, and one N–H⋅⋅⋅π bond to the naphthalene moiety of a molecule in the neighbouring stack. P.R.257 crystallises in P21/c, Z = 2, with molecules on inversion centres. The molecules show a typical van der Waals packing without close Ni-Ni contacts. S.Br.53 exhibits Pbcn symmetry with Z = 8. The molecules form columns with Ni-to-Ni distances of 3.508 Å.

Structures of three dehydration products of bischofite from in situ synchrotron powder diffraction data (MgCl2·nH2O; n = 1, 2, 4)

2007 ◽  
Vol 63 (2) ◽  
pp. 235-242 ◽  
Author(s):  
Kunihisa Sugimoto ◽  
Robert E. Dinnebier ◽  
Jonathan C. Hanson
Keyword(s):  
Crystal Structures ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Similarity Criteria ◽  
Powder Diffraction Data ◽  
Rietveld Refinements ◽  
Synchrotron Powder Diffraction ◽  
Magnesia Concrete ◽  
First Time

High-quality in situ synchrotron powder diffraction data have been used to investigate the decomposition products of bischofite in the temperature range 298 ≤ T ≤ 873 K. At least eight phases could be identified: MgCl2·nH2O (n = 1, 2, 4 and 6), MgOHCl·nH2O (0 ≤ n ≤ 1.0), MgCl2 and MgO. The crystal structures of three magnesium chloride hydrates MgCl2·nH2O (n = 1, 2, 4) were determined ab initio, replacing published Rietveld refinements from low-quality powder diffraction data based on similarity criteria. MgCl2·4H2O was found to be disordered and has been correctly determined for the first time. The crystal structures of bischofite and MgCl2·4H2O consist of discrete Mg(H2O)6 and MgCl2(H2O)4 octahedra, respectively. The crystal structure of MgCl2·2H2O is formed by single chains of edge-sharing MgCl2(H2O)4 octahedra, while in the case of MgCl2·H2O double chains of edge-sharing MgCl(H2O)5 octahedra are found. The phases in the system MgCl2–H2O are intermediates in the technologically important process of MgO and subsequently Mg production. The same phases were recently found to be of key importance in the understanding of cracks in certain magnesia concrete floors.

The crystal structures of solvent-free alkali-metal squarates from powder diffraction data

2005 ◽  
Vol 220 (11) ◽  
Author(s):  
Robert E. Dinnebier ◽  
Hanne Nuss ◽  
Martin Jansen
Keyword(s):  
High Resolution ◽  
Alkali Metal ◽  
Crystal Structures ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Room Temperature ◽  
Solvent Free ◽  
Crystallographic Data ◽  
Powder Diffraction Data ◽  
X Ray

AbstractThe crystal structures of solvent-free lithium, sodium, rubidium, and cesium squarates have been determined from high resolution synchrotron and X-ray laboratory powder patterns. Crystallographic data at room temperature of Li

Challenging structure determination from powder diffraction data: two pharmaceutical salts and one cocrystal with Z′ = 2

2019 ◽  
Vol 234 (4) ◽  
pp. 257-268 ◽  
Author(s):  
Carina Schlesinger ◽  
Michael Bolte ◽  
Martin U. Schmidt
Keyword(s):  
Single Crystal ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Structure Determination ◽  
Real Space ◽  
Powder Diffraction Data ◽  
The Real ◽  
Pharmaceutical Salts ◽  
Structure Solution ◽  
Space Method

Abstract Structure solution of molecular crystals from powder diffraction data by real-space methods becomes challenging when the total number of degrees of freedom (DoF) for molecular position, orientation and intramolecular torsions exceeds a value of 20. Here we describe the structure determination from powder diffraction data of three pharmaceutical salts or cocrystals, each with four molecules per asymmetric unit on general position: Lamivudine camphorsulfonate (1, P 21, Z=4, Z′=2; 31 DoF), Theophylline benzamide (2, P 41, Z=8, Z′=2; 23 DoF) and Aminoglutethimide camphorsulfonate hemihydrate [3, P 21, Z=4, Z′=2; 31 DoF (if the H2O molecule is ignored)]. In the salts 1 and 3 the cations and anions have two intramolecular DoF each. The molecules in the cocrystal 2 are rigid. The structures of 1 and 2 could be solved without major problems by DASH using simulated annealing. For compound 3, indexing, space group determination and Pawley fit proceeded without problems, but the structure could not be solved by the real-space method, despite extensive trials. By chance, a single crystal of 3 was obtained and the structure was determined by single-crystal X-ray diffraction. A post-analysis revealed that the failure of the real-space method could neither be explained by common sources of error such as incorrect indexing, wrong space group, phase impurities, preferred orientation, spottiness or wrong assumptions on the molecular geometry or other user errors, nor by the real-space method itself. Finally, is turned out that the structure solution failed because of problems in the extraction of the integrated reflection intensities in the Pawley fit. With suitable extracted reflection intensities the structure of 3 could be determined in a routine way.

The BaAl4 Structure and its Derivatives from the R-Zn-Ga Systems

2012 ◽  
Vol 194 ◽  
pp. 5-9 ◽  
Author(s):  
Yuriy Verbovytskyy ◽  
Antonio Pereira Gonçalves
Keyword(s):  
Crystal Structures ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Powder Diffraction Data ◽  
Space Group ◽  
X Ray ◽  
First Time

Seven new ternary RZn1+xGa3-x (R = Ce, Pr, Nd, Sm, Ho and Er) and R5Zn2Ga17 (R = Ce) phases are synthesized for the first time. Their crystal structures are solved on basis of X-ray powder diffraction data. The above mentioned compounds belong to the BaAl4 (space group I4/mmm) and Rb5Hg19 (space group I4/m) structure types. Details of the structure of the Ce5Zn2Ga17 compound and relationship with RZn2-xGa2+x (BaAl4 type) and R3Zn8-xGa3+x (La3Al11 type) are briefly discussed.

NanoPDF64: software package for theoretical calculation and quantitative real-space analysis of powder diffraction data of nanocrystals

2017 ◽  
Vol 50 (6) ◽  
pp. 1821-1829 ◽  
Author(s):  
Kazimierz Skrobas ◽  
Svitlana Stelmakh ◽  
Stanislaw Gierlotka ◽  
Bogdan F. Palosz
Keyword(s):  
Powder Diffraction ◽  
Diffraction Data ◽  
Analytical Formula ◽  
Real Space ◽  
Distribution Functions ◽  
Powder Diffraction Data ◽  
Space Analysis ◽  
Atomic Vibrations ◽  
Hexagonal Close Packed Structure ◽  
Diffraction Patterns

NanoPDF64is a tool designed for structural analysis of nanocrystals based on examination of powder diffraction data with application of real-space analysis. The program allows for fast building of models of nanocrystals consisting of up to several hundred thousand atoms with either cubic or hexagonal close packed structure. The nanocrystal structure may be modified by introducing stacking faults, density modulation waves (i.e.the core–shell model) and thermal atomic vibrations. The program calculates diffraction patterns and, by Fourier transform, the reduced pair distribution functionsG(r) for the models. ExperimentalG(r)s may be quantitatively analyzed by least-squares fitting with an analytical formula.

Sign in / Sign up

Export Citation Format

Share Document