Larrea Edurne S, Mesa José Luis, Legarra Estibaliz, Aguayo Andrés Tomás, Arriortua Maria Isabel
Dpto. Mineralogía y Petrología, Universidad del País Vasco, UPV/EHU, Sarrina s/n, 48940 Leioa, Spain.
Dpto. Química Inorgánica, Universidad del País Vasco, UPV/EHU, Sarrina s/n, 48940 Leioa, Spain.
Acta Crystallogr E Crystallogr Commun. 2016 Jan 1;72(Pt 1):63-5. doi: 10.1107/S2056989015024007.
Single crystals of the title compound, potassium hexa-phosphito-penta-ferrate(II,III) hemihydrate, K0.75[Fe(II) 3.75Fe(III) 1.25(HPO3)6]·0.5H2O, were grown under mild hydro-thermal conditions. The crystal structure is isotypic with Li1.43[Fe(II) 4.43Fe(III) 0.57(HPO3)6]·1.5H2O and (NH4)2[Fe(II) 5(HPO3)6] and exhibits a Fe(II) 3.75Fe(III) 1.25(HPO3)6 open framework with disordered K(+) (occupancy 3/4) as counter-cations. The anionic framework is based on (001) sheets of two [FeO6] octa-hedra (one with point group symmetry 3.. and one with point group symmetry .2.) linked along [001] through HPO3 oxoanions. Each sheet is constructed from 12-membered rings of edge-sharing [FeO6] octa-hedra, giving rise to channels with a radius of ca 3.1 Å where the K(+) cations and likewise disordered water mol-ecules (occupancy 1/4) are located. O⋯O contacts between the water mol-ecule and framework O atoms of 2.864 (5) Å indicate hydrogen-bonding inter-actions of medium strength. The infrared spectrum of the compound shows vibrational bands typical for phosphite and water groups. The Mössbauer spectrum is in accordance with the presence of Fe(II) and Fe(III) ions.
标题化合物六亚磷酸根五铁(II,III)酸钾半水合物K₀.₇₅[Fe(II)₃.₇₅Fe(III)₁.₂₅(HPO₃)₆]·0.5H₂O的单晶在温和水热条件下生长。其晶体结构与Li₁.₄₃[Fe(II)₄.₄₃Fe(III)₀.₅₇(HPO₃)₆]·1.5H₂O和(NH₄)₂[Fe(II)₅(HPO₃)₆]同型,呈现出一个Fe(II)₃.₇₅Fe(III)₁.₂₅(HPO₃)₆开放骨架,其中无序的K⁺(占有率3/4)作为抗衡阳离子。阴离子骨架基于由两个[FeO₆]八面体(一个具有点群对称性3..,一个具有点群对称性.2.)组成的(001)片层,它们通过HPO₃含氧阴离子沿[001]方向相连。每片层由共边[FeO₆]八面体的12元环构成,形成半径约为3.1 Å的通道,K⁺阳离子以及同样无序的水分子(占有率1/4)位于其中。水分子与骨架O原子之间的O⋯O接触距离为2.864(5) Å,表明存在中等强度的氢键相互作用。该化合物的红外光谱显示出亚磷酸根和水基团典型的振动带。穆斯堡尔谱与Fe(II)和Fe(III)离子的存在相符。