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Redetermination of the low-temperature polymorph of Li(2)MnSiO(4) from single-crystal X-ray data.


ABSTRACT: Crystals of dilithium manganese(II) silicate were grown under high-temperature hydro-thermal conditions in the system LiOH-MnO(2)-SiO(2). The title compound crystallizes in the ?(II)-Li(3)PO(4) structure type. The coordination polyhedra of all cations are slightly distorted tetra-hedra (m symmetry for MnO(4) and SiO(4)), which are linked by corner-sharing to each other. The vertices of the tetra-hedra point to the same direction perpendicular to the distorted hexa-gonal close-packed (hcp) array of O atoms within which half of the tetra-hedral voids are occupied by cations. In comparison with the previous refinement from powder X-ray data [Dominko et al. (2006 ?). Electrochem. Commun.8, 217-222], the present reinvestigation from single-crystal X-ray data allows a more precise determination of the distribution of the Li(+) and Mn(2+) cations, giving a perfectly site-ordered structure model for both Li(+) and Mn(2+).

SUBMITTER: Sato M 

PROVIDER: S-EPMC3435565 | biostudies-literature | 2012 Sep

REPOSITORIES: biostudies-literature

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Redetermination of the low-temperature polymorph of Li(2)MnSiO(4) from single-crystal X-ray data.

Sato Mineo M   Ishigaki Tadashi T   Uematsu Kazuyoshi K   Toda Kenji K   Okawa Hirokazu H  

Acta crystallographica. Section E, Structure reports online 20120815 Pt 9


Crystals of dilithium manganese(II) silicate were grown under high-temperature hydro-thermal conditions in the system LiOH-MnO(2)-SiO(2). The title compound crystallizes in the β(II)-Li(3)PO(4) structure type. The coordination polyhedra of all cations are slightly distorted tetra-hedra (m symmetry for MnO(4) and SiO(4)), which are linked by corner-sharing to each other. The vertices of the tetra-hedra point to the same direction perpendicular to the distorted hexa-gonal close-packed (hcp) array  ...[more]

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