Received 19 July 2013
aLaboratoire de Chimie du Solide Appliquée, Faculté des Sciences, Université Mohammed V-Agdal, Avenue Ibn Battouta, BP 1014, Rabat, Morocco, and bLaboratoire des Matériaux Céramiques et Procédés Associés EA 2443, Université de Valenciennes et du Hainaut - Cambrésis Le Mont Houy, 59313 Valenciennes, France
Correspondence e-mail: firstname.lastname@example.org
The title compound, strontium trimanganese tris(orthophosphate), was synthesized under hydrothermal conditions. Its structure is isotypic to that of the lead analogue PbMnII2MnIII(PO4)3. Two O atoms are in general positions, whereas all others atoms are in special positions. The Sr and one P atom exhibit mm2 symmetry, the MnII atom 2/m symmetry, the MnIII atom and the other P atom .2. symmetry and two O atoms are located on mirror planes. The three-dimensional network of the crystal structure is made up of two types of chains running parallel to . One chain is linear and is composed of alternating MnIIIO6 octahedra and PO4 tetrahedra sharing vertices; the other chain has a zigzag arrangement and is built up from two edge-sharing MnIIO6 octahedra connected to PO4 tetrahedra by edges and vertices. The two types of chains are linked through PO4 tetrahedra, leading to the formation of channels parallel to  and  in which the SrII ions are located. They are surrounded by eight O atoms in the form of a slightly distorted bicapped trigonal prism.
For the isotypic lead analogue, see: Alhakmi et al. (2013). For compounds with related structures, see: Adam et al. (2009); Assani et al. (2011a,b,c); Moore & Ito (1979). For applications of related compounds, see: Trad et al. (2010). For the by-product phase, see: Moore & Araki (1973). For bond-valence analysis, see: Brown & Altermatt (1985).
Data collection: APEX2 (Bruker, 2009); cell refinement: SAINT (Bruker, 2009); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 2012) and DIAMOND (Brandenburg, 2006); software used to prepare material for publication: publCIF (Westrip, 2010).
Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: WM2761 ).
The authors thank the Unit of Support for Technical and Scientific Research (UATRS, CNRST) for the X-ray measurements.
Adam, L., Guesdon, A. & Raveau, B. (2009). J. Solid State Chem. 182, 2338-2343.
Alhakmi, G., Assani, A., Saadi, M. & El Ammari, L. (2013). Acta Cryst. E69, i40.
Assani, A., El Ammari, L., Zriouil, M. & Saadi, M. (2011a). Acta Cryst. E67, i41.
Assani, A., El Ammari, L., Zriouil, M. & Saadi, M. (2011b). Acta Cryst. E67, i40.
Assani, A., Saadi, M., Zriouil, M. & El Ammari, L. (2011c). Acta Cryst. E67, i5.
Brandenburg, K. (2006). DIAMOND. Crystal Impact GbR, Bonn, Germany.
Brown, I. D. & Altermatt, D. (1985). Acta Cryst. B41, 244-247.
Bruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.
Farrugia, L. J. (2012). J. Appl. Cryst. 45, 849-854.
Moore, P. B. & Araki, T. (1973). Am. Mineral. 58, 302-307.
Moore, P. B. & Ito, J. (1979). Mineral. Mag. 43, 227-35.
Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.
Trad, K., Carlier, D., Croguennec, L., Wattiaux, A., Ben Amara, M. & Delmas, C. (2010). Chem. Mater. 22, 5554-5562.
Westrip, S. P. (2010). J. Appl. Cryst. 43, 920-925.