JOURNAL ARTICLE

K2[FeII 3(P2O7)2(H2O)2]

Juan YangXin ZhangBiao LiuWei SunYa‐Xi Huang

Year: 2012 Journal:   Acta Crystallographica Section E Structure Reports Online Vol: 68 (6)Pages: i47-i48   Publisher: International Union of Crystallography

Abstract

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.

Keywords:
Physics

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Topics

Magnetism in coordination complexes
Physical Sciences →  Materials Science →  Electronic, Optical and Magnetic Materials
Metal-Organic Frameworks: Synthesis and Applications
Physical Sciences →  Chemistry →  Inorganic Chemistry
Chemical Synthesis and Characterization
Physical Sciences →  Environmental Science →  Industrial and Manufacturing Engineering

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