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14 citations found for Shvanskaya, L.

Search for Shvanskaya, L. in the World Directory of Crystallographers

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A new modification of CsMnPO4 (β-phase) is discussed in a superspace approach. Structural relations with topologically and chemically similar compounds are shown.

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Acta Cryst. (2023). A79, C786
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Two novel com­pounds, namely, K2Mn3(H2O)2[P2O7]2 and KMn(H2O)2[Al2(PO4)3], are members of the A2M3(H2O)2[P2O7]2 and AM2+(H2O)2[M3+2(PO4)3] morphotropic series with atoms of alkali (A) and first-row transition (M) metals. A study of the magnetic susceptibility of KMn(H2O)2[Al2(PO4)3] revealed its paramagnetic behaviour.

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Acta Cryst. (2018). A74, e331
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The crystal structures of three novel caesium borophosphates with chain-type anionic fragments are reported. Relationships between new and known phases are discussed in terms of the effect of the initial crystallization medium on the structure.

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The novel compound Cs2CuAl4O8 was synthesized from a phosphate flux and its structure was determined from single-crystal X-ray diffraction data; topological relations with zeolite-like phases are discussed. The quantum ground state of this compound is gapped spin liquid.

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Acta Cryst A. (2013). A69, s448
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New compounds, KCuAl[PO4]2 (I) and K(Al,Zn)2[(P,Si)O4]2 (II), obtained hydrothermally, were studied by single-crystal X-ray diffraction. Based on its structure, (I) is a potentially electrochemically active material and/or possible low-temperature antiferromagnet. The phase (II) was established to be a product of epitaxial intergrowth of phosphate KAlZn[PO4]2 and silicate KAlSi[SiO4]2 components with close crystal structures, thus providing a single diffraction pattern.

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The crystal structure of RbMn4(PO4)3, which was synthesized hydro­thermally, has been refined in the space group Pnnm (D2h12). At low temperatures, the compound orders into a canted anti­ferromagnetic state with finite spontaneous magnetization.

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In the crystal structure of KMn2V3O10, tetramers of MnO6 octahedra sharing edges and trimers of VO4 tetrahedra sharing vertices are linked in a three-dimensional framework with channels occupied by K3+ ions. The novel representative in the rare family of trivanadates orders antiferromagnetically at TN = 8.2 K.


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