Modulated structure of Lu4AlCu2B9O23 from low-temperature single-crystal X-ray data.

Acta Crystallogr B Struct Sci Cryst Eng Mater

Institute of Crystallography RAS, Leninskii prospect 59, 119333 Moscow, Russian Federation.

Published: August 2013

A second-order phase transition with both displacive and disorder mechanisms was discovered in Lu4AlCu2B9O23 using single-crystal X-ray diffraction techniques by cooling down the sample to 110 K. Low-temperature structure modulations are mainly associated with Cu atoms surrounded by O atoms. The fivefold asymmetric environment leads to a special copper position splitting into a pair of general ones so that four O atoms coordinate each of them. Each copper site is 50% occupied at room temperature, but at lower temperature statistical disorder gives occupation and displacive modulations with a wavevector of q = 0.132c*. Tetragonal P\bar 42(1)m symmetry of the non-modulated phase transforms into an orthorhombic (3+1)-dimensional symmetry, P21212(00γ)00s, whereas the \bar 4 axis becomes the twinning axis.

Download full-text PDF

Source
http://dx.doi.org/10.1107/S2052519213014231DOI Listing

Publication Analysis

Top Keywords

single-crystal x-ray
8
modulated structure
4
structure lu4alcu2b9o23
4
lu4alcu2b9o23 low-temperature
4
low-temperature single-crystal
4
x-ray data
4
data second-order
4
second-order phase
4
phase transition
4
transition displacive
4

Similar Publications

Helical Quintulene: Synthesis, Chirality, and Supramolecular Assembly.

Angew Chem Int Ed Engl

January 2025

Xiamen University, Department of Chemistry, Siminnan Road 422, 361005, Xiamen, CHINA.

Quintulene is a quintuply symmetrical cycloarene with a positively curved molecular geometry. First described by Staab and Sauer in 1984, its successful synthesis was not achieved until 2020. Due to the challenges posed by its positive curvature, structural extensions of quintulene have been studied rarely.

View Article and Find Full Text PDF

A novel ternary boride, NiPtB ( = 0.5), was obtained by argon-arc melting of the elements followed by annealing at 750 °C. It exhibits a new structure type with the space group ( = 2.

View Article and Find Full Text PDF

In a systematic study, six pseudopolymorphic coordination polymers containing the ditopic 1,3-di(pyridin-4-yl)urea ligand (4bpu) constructed with d metal cations, possessing the formula {[M(4bpu)I]S} [(M = Zn, Cd and Hg), (S = MeOH or EtOH)], namely Zn-MeOH, Zn-EtOH, Cd-MeOH, Cd-EtOH, Hg- and Hg-EtOH were obtained. The title compounds were characterized by single-crystal X-ray diffraction analysis (SC-XRD), elemental analysis (CHN), FT-IR spectroscopy, thermogravimetric analysis (TGA), and powder X-ray diffraction (PXRD). The diffraction studies show that these compounds are isostructural 1D zig-zag chain coordination polymers which is also confirmed using XPac 2.

View Article and Find Full Text PDF

A volatile heteroleptic open ruthenocene has been synthesised and characterised by NMR and single crystal X-ray diffraction. Using this compound as a precursor and oxygen as a co-reactant, a highly conductive Ru film has been deposited on Si with native oxide at 220 °C. Under the same deposition conditions, the film thickness obtained with the new compound has almost doubled compared to its homoleptic analogue.

View Article and Find Full Text PDF

The structural stability of the energetic material 2,2',4,4',6,6'-hexanitrostilbene (-HNS) under high pressure is critical for optimizing its detonation performance and low sensitivity. However, its structural response to external pressure has not been sufficiently investigated. In this study, high-pressure single-crystal X-ray diffraction data of -HNS demonstrate that the sample exhibits pronounced anisotropic strain, demonstrating an unusual negative linear compressibility (NLC) along the axis, with a coefficient of -4.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!