Tetrahedral framework structures: polymorphic phase transition with reorientation of hexagonal helical channels in the Zintl compound Na2ZnSn5 and its relation to Na5Zn(2+x)Sn(10-x).

Two modifications of the new Zintl compound Na2ZnSn5 were synthesized by direct reactions of the elements. hP-Na2ZnSn5, which is metastable under standard conditions, is obtained by fast cooling of a melt of stoichiometric composition. Slow cooling of such a melt or tempering of hP-Na2ZnSn5 (e.g., at 300 °C) leads to the thermodynamically stable tI-Na2ZnSn5. Both phases show an open framework structure of four-bonded Zn and Sn atoms exhibiting hexagonal helical channels in which the Na atoms are situated with disorder. Whereas the Zn-Sn network of hP-Na2ZnSn5 is analogous to known Tr-Sn networks (Tr = Ga, In), tI-Na2ZnSn5 features a closely related novel framework with a different channel structure. In the structure model for hP-Na2ZnSn5 there is only one, Zn/Sn mixed occupied, site for the framework atoms, whereas Zn and Sn are fully ordered on three sites in the case of tI-Na2ZnSn5. The phase transition from hP-Na2ZnSn5 to tI-Na2ZnSn5 was studied using high-temperature powder and single-crystal X-ray diffraction methods. Na2ZnSn5 is stable up to about 350 °C and does not melt congruently but decomposes to form Na5Zn(2+x)Sn(10-x). DFT band structure calculations (TB-LMTO-ASA) were performed with ordered model structures which were deduced from a conceivable pathway for the interconversion of the two polymorphic structures of Na2ZnSn5. A band gap at the Fermi level, as expected for a Zintl phase, is found for the ordered structure of tI-Na2ZnSn5. On the basis of an analysis of the relationship between the network structures of the Sn-rich Na-Zn-Sn phases, a general perspective for novel open framework structures with exclusively four-bonded atoms is given.