Potassium beryllium selenate dihydrate, K2Be(SeO 4)2 2H2O: Preparation, structure and infrared spectroscopy

Author(s)
Mitko Georgiev, Donka Stoilova, Manfred Wildner, V Karadjova
Abstract

The solubility in the three-component system K2SeO 4-BeSeO4-H2O at 25°C is studied by the method of isothermal decrease of supersaturation. A new compound, K 2Be(SeO4)2ž2H2O, is formed in a wide concentration range (from solutions containing 39.40 mass% beryllium selenate and 8.50 mass% potassium selenate up to solutions containing 7.02 mass% beryllium selenate and 51.14 mass% potassium selenate). K 2Be(SeO4)2ž2H2O crystallizes in the monoclinic space group P21/c (a.503(2), b.846(1), c=7.491(1) A°, ß•.77(1)°, V15.5 A°3, Z=4, R1=0.026 for 4220 Fo>4s(Fo) and 153 variables). The crystal structure is composed of [Be(SeO4)2(H 2O)2]2- groups, formed by a BeO4 tetrahedron sharing two corners with SeO4 tetrahedra. These units are linked via potassium cations and comparatively strong hydrogen bonds to double layers and further to a three-dimensional framework structure. K 2Be(SeO4)2ž2H2O is isotypic with the corresponding sulfate compound, K2Be(SO4) 2ž2H2O. The strengths of the hydrogen bonds in the title compound as deduced from the infrared wavenumbers of the uncoupled OD stretches of matrix-isolated HDO molecules (isotopically dilute sample) are discussed in terms of the Ow?O hydrogen bond distances, the different hydrogen bond acceptor capabilities of the selenate oxygen atoms and the strong Be-OH2 interactions (synergetic effect). The intramolecular O-H bond lengths are derived from the ?OD vs. rOH correlation curve. Œ 2005 Elsevier B.V. All rights reserved.

Organisation(s)
Department of Mineralogy and Crystallography
External organisation(s)
Technical University of Sofia, Bulgarian Academy of Sciences (BAS)
Journal
Journal of Molecular Structure
Volume
752
Pages
158-165
No. of pages
8
ISSN
0022-2860
Publication date
2005
Peer reviewed
Yes
Austrian Fields of Science 2012
105113 Crystallography, 1030 Physics, Astronomy
Portal url
https://ucrisportal.univie.ac.at/en/publications/b9fec24b-5b91-4877-a308-bd760e24569d