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Sesquicaesium hemisodium tetracyanidoplatinate(II) sesquihydrate
The title compound, Cs(1.5)Na(0.5)[Pt(CN)(4)]·1.5H(2)O, was isolated from solution as a salt. The tetracyanidoplatinate (TCP) anions are stacked in a linear quasi-one-dimensional arrangement along the b axis, with Pt⋯Pt interactions of 3.6321 (5) Å. The mixed alkali metal TCP contains three distin...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008050/ https://www.ncbi.nlm.nih.gov/pubmed/21588473 http://dx.doi.org/10.1107/S1600536810032551 |
Sumario: | The title compound, Cs(1.5)Na(0.5)[Pt(CN)(4)]·1.5H(2)O, was isolated from solution as a salt. The tetracyanidoplatinate (TCP) anions are stacked in a linear quasi-one-dimensional arrangement along the b axis, with Pt⋯Pt interactions of 3.6321 (5) Å. The mixed alkali metal TCP contains three distinct alkali metal positions in the structure that do not show any mixed occupancy: Cs1 (site symmetry 2), Cs2 (general position) and Na1 (site symmetry [Image: see text]). The Na(+) ion contains an octahedral coordination environment composed of two water molecules and four N-terminal cyanides, which serve to bridge TCP anions. The Cs(+) cations contain mono- and bicapped square-prismatic environments, where the square prisms are formed from cyanide N atoms with water molecules capping the faces. The 1.5 water molecules per formula unit are a result of two fully occupied sites, one on a general position and one on a twofold rotation axis. Weak hydrogen-bonding interactions are observed between one water molecule and terminal N-atom acceptors from TCP, while the second water molecule is not involved in hydrogen bonding. |
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