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Single crystals of the lanthanide-containing iridate, disamarium sodium iridium hexaoxide, Sm2NaIrO6, were prepared via high-temperature flux growth and structurally characterized by single-crystal X-ray diffraction. The compound crystallizes in the monoclinic space group P21/n and is a double perovskite, consisting of a 1:1 ordered rock-salt-type lattice of corner-shared NaO6 and IrO6 distorted octahedra. Samarium occupies the eightfold coordination site generated by the connectivity of the octahedra.

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The asymmetric unit of the title compound, [Co(C2H8N2)3][Bi2I9], crystallizes in the ortho­rhom­bic space group Cmc21. The asymmetric unit contains half of a [Co(en)3]3+ cation (en is ethyl­enediamine) and half of a [Bi2I9]3- anion. Both species are located on mirror planes, requiring the [Co(en)3]3+ cation to be present as a statistically disordered mixture of both enantiomeric forms. Crystals were grown solvothermally from an ethanol-water solvent mixture using rac-[Co(en)3]I3 and bis­muth triiodide as starting materials. The compound is a rare example of a mixed-metal halobismuthate material.

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The asymmetric unit of the title compound, [Co(C12H8N2)3](I3)2, contains one [Co(1,10-phenanthroline)3]2+ cation, half each of two centrosymmetric triiodide anions, and one complete triiodide anion. The title compound was synthesized solvothermally from Co(NO3)2, 1,10-phenanthroline, and SnI2, where the SnI2 reagent serves only as a source of I atoms.

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In the one-dimensional title polymer, [Cu(C8H4F3O2S)2(C12H10N4)]n or [Cu(L)2(tta)2] [tta is α-thenoyl­trifluoro­acetonato and L is 1,4-bis­(4-pyrid­yl)-2,3-diaza-1,3-butadiene], Cu2+ lies on a center of inversion. It is axially coordinated by two pyridyl N atoms from two different L ligands and equatorially coordinated by four O atoms from two chelating tta ligands. The ligand L propagates the one-dimensional chain structure by serving as a bridging ligand between two Cu octa­hedra via Cu—N coordinate bonds.
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