K9Y3[Si12O32]F2
Single-crystals of the title compound, nonapotassium triyttrium dodecasilicate difluoride, were obtained from flux synthesis experiments in the system SiO2—Y2O3—KF. The crystal structure belongs to the group of single-layer silicates and is based on silicate sheets parallel to (110). A single layer...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
International Union of Crystallography
2014-02-01
|
Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536814001470 |
id |
doaj-634ef21d1eb44ebcbd215fb5a9c661e3 |
---|---|
record_format |
Article |
spelling |
doaj-634ef21d1eb44ebcbd215fb5a9c661e32020-11-25T01:39:57ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682014-02-01702i11i1110.1107/S1600536814001470wm2792K9Y3[Si12O32]F2Volker Kahlenberg0Tanja Manninger1University of Innsbruck, Institute of Mineralogy & Petrography, Innrain 52, A-6020 Innsbruck, AustriaUniversity of Innsbruck, Institute of Mineralogy & Petrography, Innrain 52, A-6020 Innsbruck, AustriaSingle-crystals of the title compound, nonapotassium triyttrium dodecasilicate difluoride, were obtained from flux synthesis experiments in the system SiO2—Y2O3—KF. The crystal structure belongs to the group of single-layer silicates and is based on silicate sheets parallel to (110). A single layer contains secondary (Q2) and tertiary (Q3) silicate tetrahedra in the ratio 1:2 and is build up from six-, eight- and twelve-membered rings. The linkage between neighboring layers is achieved by two crystallographically independent Y3+ cations, which are coordinated by six oxygen ligands in form of distorted octahedra. Charge compensation is accomplished by incorporation of additional F− anions and K+ cations in the structural channels, forming anion-centred [F2K7] groups. Apart from one K+ and one Y3+ cation (each with site symmetry -1), the 30 crystallographically independent atoms reside on general positions.http://scripts.iucr.org/cgi-bin/paper?S1600536814001470 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Volker Kahlenberg Tanja Manninger |
spellingShingle |
Volker Kahlenberg Tanja Manninger K9Y3[Si12O32]F2 Acta Crystallographica Section E |
author_facet |
Volker Kahlenberg Tanja Manninger |
author_sort |
Volker Kahlenberg |
title |
K9Y3[Si12O32]F2 |
title_short |
K9Y3[Si12O32]F2 |
title_full |
K9Y3[Si12O32]F2 |
title_fullStr |
K9Y3[Si12O32]F2 |
title_full_unstemmed |
K9Y3[Si12O32]F2 |
title_sort |
k9y3[si12o32]f2 |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2014-02-01 |
description |
Single-crystals of the title compound, nonapotassium triyttrium dodecasilicate difluoride, were obtained from flux synthesis experiments in the system SiO2—Y2O3—KF. The crystal structure belongs to the group of single-layer silicates and is based on silicate sheets parallel to (110). A single layer contains secondary (Q2) and tertiary (Q3) silicate tetrahedra in the ratio 1:2 and is build up from six-, eight- and twelve-membered rings. The linkage between neighboring layers is achieved by two crystallographically independent Y3+ cations, which are coordinated by six oxygen ligands in form of distorted octahedra. Charge compensation is accomplished by incorporation of additional F− anions and K+ cations in the structural channels, forming anion-centred [F2K7] groups. Apart from one K+ and one Y3+ cation (each with site symmetry -1), the 30 crystallographically independent atoms reside on general positions. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536814001470 |
work_keys_str_mv |
AT volkerkahlenberg k9y3si12o32f2 AT tanjamanninger k9y3si12o32f2 |
_version_ |
1725048118576152576 |