Abstract
Single crystals of the solid solution series Ca4+x
Y3–x
Si7O15+x
N5–x
were obtained by a solid-state reaction method using a flux for x = 0, 0.5 and 1, resulting in Ca4Y3Si7O15N5 (tetracalcium triyttrium heptasilicon oxynitride), Ca4.5Y2.5Si7O15.5N4.5 and Ca5Y2Si7O16N4 (pentacalcium diyttrium heptasilicon oxynitride). Single-crystal X-ray analysis revealed that the three compounds are isotypic and belong to space-group type P63/m. Ca2+ and Y3+ cations are distributed over two crystallographic sites (site symmetry \overline{3}.. and 1) in a disordered manner. The corresponding (Ca,Y)-centred polyhedra are connected by edge-sharing, resulting in the formation of a layer structure extending parallel to (001). Three [Si(O,N)]4 tetrahedra (two with point group symmetry m.., one with 3.. and half-occupancy) are condensed into an isolated [Si7(O,N)19] unit, in which an [Si(O,N)]4 tetrahedron is located at the center of a 12-membered oxynitride ring with composition [Si6O15N3]. The present compounds are the first to have such an [Si7(O,N)19] unit in their structures.
Funder
Ministry of Education, Culture, Sports, Science and Technology
Nippon Sheet Glass Foundation for Materials Science and Engineering
Dynamic Alliance for Open Innovation Bridging Human, Environment and Materials
Publisher
International Union of Crystallography (IUCr)
Subject
Condensed Matter Physics,General Materials Science,General Chemistry
Cited by
2 articles.
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