![[HTML version]](/e/graphics/htmlborder.gif)
![[PDF version]](/e/graphics/pdfborder.gif)
![[CIF]](/e/graphics/cifborder.gif)
![[3d view]](/e/graphics/3dviewborder.gif)
![[Structure Factors]](/e/graphics/structurefactorsborder.gif)
![[Supplementary Material]](/e/graphics/supplementarymaterialsborder.gif)
![[CIF check Report]](/e/graphics/checkcifborder.gif)
![[Issue contents]](/e/graphics/issuecontentsborder.gif)
![[Open access]](/e/graphics/free.gif)
Acta Cryst. (2009). E65, i78 [ doi:10.1107/S1600536809041622 ]
Abstract: The title compound, K2Sm(MoO4)(PO4), has been prepared under atmospheric conditions using a high temperature solution growth (HTSG) method. The structure of K2Sm(MoO4)(PO4) is isotypic with other A2M(MoO4)(PO4) compounds, where A = Na or K, and M = trivalent rare earth cation. It can be described as being built up from two-dimensional anionic layers with composition [Sm(MoO4)(PO4)]2- that are stacked along the c axis and are interconnected by K+ cations which are in an eightfold coordination by O atoms. The SmO8, MoO4 and PO4 polyhedra exhibit 2 symmetry.
Online 17 October 2009
Copyright © International Union of Crystallography
IUCr Webmaster