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The structure of sodium calcium magnesium iron phosphate, (Na0,38,Ca0,31)MgFe2P3O12, consists of an [MgFe2(PO4)3]- framework, built up by chains of edge-sharing (FeO6-FeO6-MgO6) octahedra running along the [\overline 101] direction. The chains are linked together via the common corners of phosphate tetrahedra to form sheets parallel to the ab plane. Adjacent sheets are also connected through PO4 tetrahedra, thus giving rise to an open framework with two different kinds of channels where the Na+ and Ca2+ cations are located.

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Tripotassium triiron(III) tetraarsenate, K3Fe3(AsO4)4, has been synthesized at high temperature by solid-state reaction. The structure is built up from corner- and edge-sharing between FeO6 octahedra and AsO4 tetrahedra. The structure can be described as infinite anionic layers parallel to the (010) plane. Alkali metal cations are located in the interlayer space. The relationship between the title compound and K3Fe3(PO4)4·H2O structures is discussed. The title compound is isostructural with K3Cr3(AsO4)4.

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The crystal structure of the new iron(III) arsenate, viz. tricaesium diiron(III) tris(arsenate), Cs3Fe2(AsO4)3, is built up from corner-sharing AsO4 tetrahedra and FeO5 trigonal bipyramids forming a three-dimensional open framework, which contains two channels running along the c axis where the Cs+ cations are located. This compound is a rare example of an oxide possessing Fe exclusively in trigonal-bipyramidal coordination.

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The structure of the title compound, sodium lithium decavanadate eicosahydrate, Na5.22Li0.78[V10O28]·20H2O, is characterised by [V10O28]6- polyanions which are linked by hydrogen bonds and Na+ ions. The centrosymmetric [V10O28]6- polyanion consists of ten distorted VO6 edge-sharing octahedra.
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