SYNTHESIS OPTIMIZATION AND STRUCTURE-ANALYSIS OF THE ZINCOSILICATE MOLECULAR-SIEVE VPI-9

Citation
Lb. Mccusker et al., SYNTHESIS OPTIMIZATION AND STRUCTURE-ANALYSIS OF THE ZINCOSILICATE MOLECULAR-SIEVE VPI-9, Microporous materials, 6(5-6), 1996, pp. 295-309
Citations number
18
Categorie Soggetti
Chemistry Physical","Material Science","Chemistry Applied
Journal title
ISSN journal
09276513
Volume
6
Issue
5-6
Year of publication
1996
Pages
295 - 309
Database
ISI
SICI code
0927-6513(1996)6:5-6<295:SOASOT>2.0.ZU;2-N
Abstract
The synthesis of the zincosilicate molecular sieve VPI-9 has been opti mized to produce a pure and highly crystalline material reproducibly. Its complex framework topology (structure type code VM) has been deter mined in the space group P4(2)/ncm (a=9.8946, c=36.8715 Angstrom) from high resolution synchrotron powder diffraction data collected on an N H4+-exchanged sample. Attempts to solve the structure by conventional methods or by exploiting anomalous scattering effects were unsuccessfu l. However, the application of a new approach to structure solution fr om powder data (FOCUS), which incorporates some of the principles used intuitively in model building into an automated structure determinati on procedure, generated the correct framework. With 7 T-sites, this fr amework topology is the most complex yet solved from powder diffractio n data without manual intervention. The topology can be described in t erms of two types of layers joined via isolated tetrahedra. One layer is a simple 4.8(2) net, and the other contains chains of pairs of [5(3 )3] polyhedra. There is a 2-dimensional 8-ring channel system between the [5(3)3] polyhedra layers. Rietveld refinement of the structure of VPI-9 in the as-synthesized form (Rb44K4[Si96Zn24O240]. 48H(2)O) requi red a doubling of the c-axis (a = 9.8837, c = 73.6505 Angstrom; V = 71 95 Angstrom(3)), and a reduction of the symmetry to P4(1)2(1)2. In add ition to the 15 T-atoms and 30 oxygens in the framework, 9 Rb, 2 K and 3 H2O positions could be located within the 8-ring channels. Refineme nt of the 170 structural parameters using synchrotron data converged w ith R(wp) = 0.147 (R(exp) = 0.099) and R(F) = 0.069. The Zn atoms in t he framework are completely ordered in layers. Each Zn is surrounded b y four Si, and each Si by three Si and one Zn. The peaks in the Si-29 MAS NMR spectrum can be interpreted very convincingly in terms of the average Si-O-T angles found in the refinement. While the structure of VPI-9 has several features in common with those of the related zincosi licate molecular sieves VPI-7 and RUB-17, such as the framework densit y, 4.8(2) layers, 3-rings, and a subunit containing Zn, there are also some interesting differences, which might be related to the lower Zn concentration in VPI-9.