Single crystals of yttrium penta-phosphate(V), YP(5)O(14), were obtained by solid-state reaction. The ortho-rhom-bic title compound belongs to the family of ultraphosphates and is the second polymorph of this composition. It is isotypic with its Ho and Er analogues. The structure contains two bridging Q(2)-type PO(4) tetra-hedra and one branching Q(3)-type PO(4) tetra-hedron, leading to infinite ultraphosphate ribbons running along the a axis. The coordination polyhedron around the Y(3+) cation may be described as distorted bicapped trigonal-prismatic. The YO(8) polyhedra are isolated from each other. They are linked by corner-sharing to the O atoms of six Q(2)-type and of two Q(3)-type PO(4) tetra-hedra into a three-dimensional framework.
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http://dx.doi.org/10.1107/S1600536809007193 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
February 2024
TU Wien, Institute for Chemical Technologies and Analytics, Division of Structural Chemistry, Getreidemarkt 9/E164-05-01, 1060 Vienna, Austria.
Single crystals of two basic cadmium phosphates, dicadmium orthophosphate hydroxide, Cd(PO)OH, and penta-cadmium bis-(orthophosphate) tetra-kis-(hydroxide), Cd(PO)(OH), were obtained under hydro-thermal conditions. Cd(PO)OH adopts the triplite [(Mn,Fe)(PO)F] structure type. Its asymmetric unit comprises two Cd, one P and five O sites, all situated at the general Wyckoff position 8 of space group 2/; two of the O atoms are positionally disordered over two sites, and the H atom could not be localized.
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December 2023
Laboratoire de Chimie Appliquée des Matériaux, Centre des Sciences des Matériaux, Faculty of Science, Mohammed V University in Rabat, Avenue Ibn Batouta, BP 1014, Rabat, Morocco.
Single crystals of tricadmium orthophosphate, Cd(PO), have been synthesized successfully by the hydro-thermal route, while its powder form was obtained by a solid-solid process. The corresponding crystal structure was determined using X-ray diffraction data in the monoclinic space group 2/. The crystal structure consists of CdO or CdO dimers linked together by PO tetra-hedra through sharing vertices or edges.
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January 2023
Laboratoire de Chimie Appliquée des Matériaux, Centre des Sciences des Matériaux, Faculty of Science, Mohammed V University in Rabat, Avenue Ibn Batouta, BP 1014, Rabat, Morocco.
The orthophosphate BaNiFe(PO) has been synthesized by a solid-state reaction route and characterized by single-crystal X-ray diffraction and energy-dispersive X-ray spectroscopy. The crystal structure comprises (100) sheets made up of [NiO] dimers that are linked to two PO tetra-hedra common edges and vertices and of linear infinite [010] chains of corner-sharing [FeO] octa-hedra and [PO] tetra-hedra. The linkage of the sheets and chains into a framework is accomplished through common vertices of PO tetra-hedra and [FeO] octa-hedra.
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July 2022
Laboratoire de Chimie Appliquée des Matériaux, Centre des Sciences des Matériaux, Faculty of Science, Mohammed V University in Rabat, Avenue Ibn Batouta, BP 1014, Rabat, Morocco.
Single crystals of β-KCoFe(PO), potassium cobalt(II) iron(III) bis-(ortho-phosphate), were grown from the melt under atmospheric conditions. This phosphate crystallizes isotypically with KZnFe(PO) in space group 2/, adopting a zeolite- type of structure. The structure of the present phosphate is distinguished by an occupational disorder of the two transition-metal sites with ratios Fe:Co of 0.
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December 2021
Shenzhen Key Laboratory of Solid State Batteries, Academy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Shenzhen 518055, People's Republic of China.
Single crystals of the langbeinite-type phosphates KNaTiFe(PO) and KNaTiFe(PO) were grown by crystallization from high-temperature self-fluxes in the system NaO-KO-PO-TiO-FeO using fixed molar ratios of (Na+K):P = 1.0, Ti:P = 0.20 and Na:K = 1.
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