Crystal structure of a sodium, zinc and iron(III)-based non-stoichiometric phosphate with an alluaudite-like structure: Na1.67Zn1.67Fe1.33(PO4)3
The new title compound, disodium dizinc iron(III) tris-(phosphate), Na1.67Zn1.67Fe1.33(PO4)3, which belongs to the alluaudite family, has been synthesized by solid-state reactions. In this structure, all atoms are in general positions except for four, which are located on special positions of the C2...
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Published in | Acta crystallographica. Section E, Crystallographic communications Vol. 71; no. Pt 6; pp. 690 - 692 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
International Union of Crystallography
01.06.2015
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Abstract | The new title compound, disodium dizinc iron(III) tris-(phosphate), Na1.67Zn1.67Fe1.33(PO4)3, which belongs to the alluaudite family, has been synthesized by solid-state reactions. In this structure, all atoms are in general positions except for four, which are located on special positions of the C2/c space group. This structure is characterized by cation substitutional disorder at two sites, one situated on the special position 4e (2) and the other on the general position 8f. The 4e site is partially occupied by Na(+) [0.332 (3)], whereas the 8f site is entirely filled by a mixture of Fe and Zn. The full-occupancy sodium and zinc atoms are located at the Wyckoff positions on the inversion center 4a (-1) and on the twofold rotation axis 4e, respectively. Refinement of the occupancy ratios, bond-valence analysis and the electrical neutrality requirement of the structure lead to the given composition for the title compound. The three-dimensional framework of this structure consists of kinked chains of edge-sharing octa-hedra stacked parallel to [10-1]. The chains are formed by a succession of trimers based on [ZnO6] octa-hedra and the mixed-cation Fe(III)/Zn(II) [(Fe/Zn)O6] octa-hedra [Fe(III):Zn(III) ratio 0.668 (3)/0.332 (3)]. Continuous chains are held together by PO4 phosphate groups, forming polyhedral sheets perpendicular to [010]. The stacked sheets delimit two types of tunnels parallel to the c axis in which the sodium cations are located. Each Na(+) cation is coordinated by eight O atoms. The disorder of Na in the tunnel might presage ionic mobility for this material. |
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AbstractList | The new title compound, disodium dizinc iron(III) tris(phosphate), Na1.67Zn1.67Fe1.33(PO4)3, which belongs to the alluaudite family, has been synthesized by solid-state reactions. In this structure, all atoms are in general positions except for four, which are located on special positions of the C2/c space group. This structure is characterized by cation substitutional disorder at two sites, one situated on the special position 4e (2) and the other on the general position 8f. The 4e site is partially occupied by Na+ [0.332 (3)], whereas the 8f site is entirely filled by a mixture of Fe and Zn. The full-occupancy sodium and zinc atoms are located at the Wyckoff positions on the inversion center 4a (-1) and on the twofold rotation axis 4e, respectively. Refinement of the occupancy ratios, bond-valence analysis and the electrical neutrality requirement of the structure lead to the given composition for the title compound. The three-dimensional framework of this structure consists of kinked chains of edge-sharing octahedra stacked parallel to [10-1]. The chains are formed by a succession of trimers based on [ZnO6] octahedra and the mixed-cation FeIII/ZnII [(Fe/Zn)O6] octahedra [FeIII:ZnIII ratio 0.668 (3)/0.332 (3)]. Continuous chains are held together by PO4 phosphate groups, forming polyhedral sheets perpendicular to [010]. The stacked sheets delimit two types of tunnels parallel to the c axis in which the sodium cations are located. Each Na+ cation is coordinated by eight O atoms. The disorder of Na in the tunnel might presage ionic mobility for this material. The new title compound, disodium dizinc iron(III) tris-(phosphate), Na1.67Zn1.67Fe1.33(PO4)3, which belongs to the alluaudite family, has been synthesized by solid-state reactions. In this structure, all atoms are in general positions except for four, which are located on special positions of the C2/c space group. This structure is characterized by cation substitutional disorder at two sites, one situated on the special position 4e (2) and the other on the general position 8f. The 4e site is partially occupied by Na(+) [0.332 (3)], whereas the 8f site is entirely filled by a mixture of Fe and Zn. The full-occupancy sodium and zinc atoms are located at the Wyckoff positions on the inversion center 4a (-1) and on the twofold rotation axis 4e, respectively. Refinement of the occupancy ratios, bond-valence analysis and the electrical neutrality requirement of the structure lead to the given composition for the title compound. The three-dimensional framework of this structure consists of kinked chains of edge-sharing octa-hedra stacked parallel to [10-1]. The chains are formed by a succession of trimers based on [ZnO6] octa-hedra and the mixed-cation Fe(III)/Zn(II) [(Fe/Zn)O6] octa-hedra [Fe(III):Zn(III) ratio 0.668 (3)/0.332 (3)]. Continuous chains are held together by PO4 phosphate groups, forming polyhedral sheets perpendicular to [010]. The stacked sheets delimit two types of tunnels parallel to the c axis in which the sodium cations are located. Each Na(+) cation is coordinated by eight O atoms. The disorder of Na in the tunnel might presage ionic mobility for this material. The transition-metal orthophosphate Na 1.67 Zn 1.67 Fe 1.33 (PO 4 ) 3 cristallizes in an alluaudite-type structure. The chains characterizing the alluaudite structure are then built up from [ M 2 O10] ( M = Fe/Zn) units alternating with [ZnO 6 ] octahedra. This structure is characterized by a cationic disorder in one tunnel and in the general position. The new title compound, disodium dizinc iron(III) tris(phosphate), Na 1.67 Zn 1.67 Fe 1.33 (PO 4 ) 3 , which belongs to the alluaudite family, has been synthesized by solid-state reactions. In this structure, all atoms are in general positions except for four, which are located on special positions of the C 2/ c space group. This structure is characterized by cation substitutional disorder at two sites, one situated on the special position 4 e (2) and the other on the general position 8 f . The 4 e site is partially occupied by Na + [0.332 (3)], whereas the 8 f site is entirely filled by a mixture of Fe and Zn. The full-occupancy sodium and zinc atoms are located at the Wyckoff positions on the inversion center 4 a (-1) and on the twofold rotation axis 4 e , respectively. Refinement of the occupancy ratios, bond-valence analysis and the electrical neutrality requirement of the structure lead to the given composition for the title compound. The three-dimensional framework of this structure consists of kinked chains of edge-sharing octahedra stacked parallel to [10-1]. The chains are formed by a succession of trimers based on [ZnO 6 ] octahedra and the mixed-cation Fe III /Zn II [(Fe/Zn)O 6 ] octahedra [Fe III :Zn III ratio 0.668 (3)/0.332 (3)]. Continuous chains are held together by PO 4 phosphate groups, forming polyhedral sheets perpendicular to [010]. The stacked sheets delimit two types of tunnels parallel to the c axis in which the sodium cations are located. Each Na + cation is coordinated by eight O atoms. The disorder of Na in the tunnel might presage ionic mobility for this material. |
Author | El Ammari, Lahcen Saadi, Mohamed Assani, Abderrazzak Khmiyas, Jamal |
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Keywords | Na1.67Zn1.67Fe1.33(PO4)3 crystal structure alluaudite structure type transition-metal phosphates solid-state reaction synthesis |
Language | English |
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Snippet | The new title compound, disodium dizinc iron(III) tris-(phosphate), Na1.67Zn1.67Fe1.33(PO4)3, which belongs to the alluaudite family, has been synthesized by... The transition-metal orthophosphate Na 1.67 Zn 1.67 Fe 1.33 (PO 4 ) 3 cristallizes in an alluaudite-type structure. The chains characterizing the alluaudite... The new title compound, disodium dizinc iron(III) tris(phosphate), Na1.67Zn1.67Fe1.33(PO4)3, which belongs to the alluaudite family, has been synthesized by... |
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SubjectTerms | alluaudite structure type crystal structure Na1.67Zn1.67Fe1.33(PO4)3 Research Communications solid-state reaction synthesis transition-metal phosphates |
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Title | Crystal structure of a sodium, zinc and iron(III)-based non-stoichiometric phosphate with an alluaudite-like structure: Na1.67Zn1.67Fe1.33(PO4)3 |
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