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The asymmetric unit of the compound (NH4)7(HPO4)2(PO4) consists of two hydrogen phosphate anions, one phosphate anion and seven ammonium cations, all of them located in general positions. The two [PO3(OH)]2− anions are linked to the PO43− anion via an O—H...O hydrogen bond to form a three-anion unit, which is surrounded by the ammonium cations. The anions and cations are further connected via N—H...O hydrogen bonding.

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The title compound, {[Er(C4H4O4)(H2O)3]Cl·2H2O}n, crystallizes with an infinite polymeric structure, in which erbium(III) ions on twofold rotation axes are bridged by centrosymmetric succinate dianions. The carboxyl­ate groups of the dicarboxyl­ate coordinate in a tridentate-bridging manner to the otherwise water-coordinated ErIII ion. The structure is completed by Cl anions and uncoordinated water molecules.

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Black single crystals of tetra­samarium(II) oxide hexa­iodide, Sm4OI6, were obtained from a reaction of SmI3, SmOI, NaI, and Na in a sealed tantalum container. Sm4OI6 crystallizes in space group P63mc and, like many M4OX6 type oxide halides of divalent metals, adopts the anti-K6HgS4/Na6ZnO4 type of structure, with K6HgS4 ≃ I6OSm4. A tetra­hedron of samarium(II) that incorporates an oxide ion is surrounded by 18 iodide ions which are connected further into a three-dimensional non-centrosymmetric structure. The O atom and one of the Sm atoms occupy sites with 3m symmetry, whereas the second Sm atom and both I atoms are located at sites with m symmetry.

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Yellow crystals of the title compound, poly[[aqua­lithium(I)]-μ3-iodo­fumarato], [Li(HOOC—CH=CI—COO)(H2O)]n, crystallized unexpectedly from an aqueous solution containing acetyl­ene­dicarboxylic acid and LiI. The lithium cation is coordinated tetra­hedrally by four O atoms of three iodo­fumarate anions and one water mol­ecule. These tetra­hedra are connected such that a layered coordination polymer is formed.
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