The hexaazidosilicate(IV) ion: Synthesis, properties, and molecular structure

The reaction of SiCl4 with an excess of (PPN)N3 (PPN+ = [(Ph3P)2N]+) affords selectively (PPN)2[Si(N3)6] (1). Simultaneous thermal analysis (TG-DTA) shows that the hexaazidosilicate salt is remarkably stable, melting at Tonex = 214 °C. Melting of 1 is followed by two distinct exothermic decomposition processes at Ton = 256 and 321 °C, the first one involving elimination of N2 and the second one degradation of the PPN cations and evolution of Si(N3)4, N2, and some HN3. The crystal structure of 1 consists of discrete PPN+ cations and S2 symmetric [Si(N3)6]2- anions, which have a very rare, octahedral SiN6 framework and the highest nitrogen content (90%) among the hexaazidometallates reported so far. The IR, Raman, 29Si, and 14N NMR spectra of 1 in CH3CN suggest in combination with the calculated spectra the presence of intact [Si(N3)6]2--anions of S6 symmetry in solution. Geometry optimizations with various methods and basis sets show an S6 symmetric structure to be the most stable [Si(N3)6]2- isomer, the calculated bonding parameters comparing well with the experimental values. Copyright © 2002 American Chemical Society.