Sodium aluminogermanate hydroxosodalite hydrate Na6+x[Al6Ge6O24](OH)x · nH2O (x ≈ 1.6, n ≈ 3.0)

Synthesis, phase transitions and dynamical disorder of the hydrogen dihydroxide anion, H3O2, in the Cubic high‐temperature form

verfasst von
Michael Wiebcke, Peter Sieger, Jürgen Felsche, Günter Engelhardt, Peter Behrens, Jürg Schefer
Abstract

Crystalline sodium aluminogermanate hydroxosodalite hydrate Na6+x[Al6Ge6O24](OH)x · nH2O with x ≈ 1.6 and n ≈ 3.0 has been synthesized by reacting Al2O3, GeO2 and NaOH solution under hydrothermal conditions, and characterized by means of simultaneous thermal analysis, differential scanning calorimetry, X‐ray and neutron diffraction as well as 1H and 23Na MAS NMR and IR spectroscopy. The material undergoes a reversible structural phase transition at Tc = 166 K (heating mode), which is actually a complex two‐step transformation as detected in DSC measurements. Structure refinements of the cubic high‐temperature form (cell constant a = 9.034(2) Å, room temperature) with single‐crystal X‐ray and powder neutron diffraction data have not yielded overall satisfactory results, probably due to the solid‐solution character of the hydrosodalite. The refinements nevertheless demonstrate that (i) the sodalite host framework is a strictly alternating array of corner‐linked AlO4 and GeO4 tetrahedra, and (ii) most polyhedral [4668] cavities are occupied by four sodium cations and one orientationally disordered hydrogen dihydroxide anion, H3O2, which possesses a strong central hydrogen bond. Variable‐temperature 1H MAS NMR spectra unambiguously confirm the presence of H3O2 ions and, in addition, reveal a dynamical intraionic exchange between the central and terminal protons and a rotational diffusion of those anions to occur in the high‐temperature form. The nature of the guest complexes filling the remaining cages could not be unambiguously determined. Results are compared with those obtained in recent studies on the related sodium aluminosilicate hydrosodalite system of the general formula Na6+x[Al6Si6O24] (OH)x · nH2O.

Externe Organisation(en)
Universität Konstanz
Universität Stuttgart
Paul Scherrer Institut (PSI)
Typ
Artikel
Journal
ZAAC ‐ Journal of Inorganic and General Chemistry
Band
619
Seiten
1321-1329
Anzahl der Seiten
9
ISSN
0044-2313
Publikationsdatum
07.1993
Publikationsstatus
Veröffentlicht
Peer-reviewed
Ja
ASJC Scopus Sachgebiete
Anorganische Chemie
Elektronische Version(en)
https://doi.org/10.1002/zaac.19936190728 (Zugang: Geschlossen)