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K(2)[Fe(II) (3)(P(2)O(7))(2)(H(2)O)(2)]
The title compound, dipotassium diaquabis(diphosphato)triferrate(II), K(2)[Fe(II) (3)(P(2)O(7))(2)(H(2)O)(2)], was synthesized under solvothermal conditions. The crystal structure is isotypic with its Co analogue. In the structure, there are two crystallographically distinct Fe positions; one lies...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379056/ https://www.ncbi.nlm.nih.gov/pubmed/22719277 http://dx.doi.org/10.1107/S1600536812021484 |
Sumario: | The title compound, dipotassium diaquabis(diphosphato)triferrate(II), K(2)[Fe(II) (3)(P(2)O(7))(2)(H(2)O)(2)], was synthesized under solvothermal conditions. The crystal structure is isotypic with its Co analogue. In the structure, there are two crystallographically distinct Fe positions; one lies on an inversion center, the other on a general position. The first Fe(2+) cation adopts a regular octahedral coordination with six O atoms, whereas the other is coordinated by five O atoms and a water molecule. The [FeO(6)] octahedron shares its trans-edges with an adjacent [FeO(5)(H(2)O)] octahedron; in turn, the [FeO(5)(H(2)O)] octahedron shares skew-edges with a neighbouring [FeO(6)] octahedron and an [FeO(5)(H(2)O)] octahedron, resulting in a zigzag octahedral chain running along [001]. The zigzag chains are linked to each other by the P(2)O(7) diphosphate groups, leading to a corrugated iron diphosphate layer, [Fe(3)(P(2)O(7))(2)(H(2)O)(2)](2−), parallel to (100). The interlayer space is occupied by K(+) cations, which adopt an eight-coordination to seven O atoms and one water molecule from a neighbouring iron diphosphate layer. Thus, the K(+) ions not only compensate the negative charge of the layer but also link the layers into a network structure. |
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