Abstract
AbstractThe reinvestigation of the pseudo‐binary systems MBr–BiBr3 (M = Rb, Cs) revealed two new phases with composition MBi2Br7. Both compounds are hygroscopic and show brilliant yellow color. The crystal structures were solved from X‐ray single crystal diffraction data. The isostructural compounds adopt a new structure type in the triclinic space group P$\bar{1}$. The lattice parameters are a = 755.68(3) pm, b = 952.56(3) pm, c = 1044.00(4) pm, α = 76.400(2)°, β = 84.590(2)°, γ = 76.652(2)° for RbBi2Br7 and a = 758.71(5) pm, b = 958.23(7) pm, c = 1060.24(7) pm, α = 76.194(3)°, β = 83.844(4)°, γ = 76.338(3)° for CsBi2Br7. The crystal structures consist of M+ cations in anticuboctahedral coordination by bromide ions and bromidobismuthate(III) layers 2∞[Bi2Br7]–. The 2D layers comprise pairs of BiBr6 octahedra sharing a common edge. The Bi2Br10 double octahedra are further connected by common vertices. The bismuth(III) atoms increase their mutual distance in the double octahedra by off‐centering so that the BiBr6 octahedra are distorted. The CsBi2Br7 type can be interpreted as a common hexagonal close sphere packing of M and Br atoms, in which 1/4 of the octahedral voids are filled by Bi atoms. The structure type was systematically analyzed and compared with alternative types of common packings. The existence of a compound with the suggested composition CsBiBr4 could not be verified experimentally.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Zeitschrift für anorganische und allgemeine Chemie
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.