





Acta Cryst. (1999). B55, 246-254 [doi:10.1107/S0108768198013044]
Abstract: Ammonioguanidinium hexafluorosilicate, CH8N
·SiF
, and bis(aminoguanidinium) hexafluorosilicate dihydrate, 2CH7N
·SiF
·2H2O, are new materials formed as by-products in course of preparing ferroelectric CH8N4ZrF6 in the presence of glassware. Their structures were determined for comparison with the corresponding hexafluorozirconates. All atoms including the eight H atoms in the CH8N
cation and the seven H atoms in the CH7N
cation have been located and refined with wR(F2) = 0.0653, R = 0.0255, S = 1.146 and wR(F2) = 0.0745, R = 0.0301, S = 1.065, respectively. The N2C-N-N backbone of the 2+ cation is close to planarity, while that of the 1+ cation does not differ significantly from planarity. The SiF
octahedron is nearly ideally regular in both materials, with
F interactions in CH8N4SiF6 results in a relatively dense variant of the NaCl structure. In addition to similar forces, the dihydrate is also characterized by the role of the water molecule with its strong NH
O interactions; its packing efficiency is, however, appreciably less than that of the anhydrous hexafluorosilicate with an
8% increase in void space. Cleaved crystals of the dihydrate are frequently twinned across the (001) composition plane, with a twofold rotation about the b axis as the twin operation.
Online 1 April 1999
![]() ![]() Structure factor file (CIF format) (61.2 kbytes) | |
![]() ![]() Structure factor file (CIF format) (65.1 kbytes) | |
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