The tris( tert- butoxy)siloxy complexes M[OSi(O t Bu) 3 ] 4 ( 1, M = Zr and 2, M = Hf) are efficient single-source precursors to homogeneous zirconia-silica and hafnia-silica materials. The ceramic conversions occur pyrolytically at low temperatures, give the theoretical yield for MO 2 ·4SiO 2 compositions, and occur without the incorporation of carbon. Compounds 1 and 2 are isomorphous, and crystallize as a mixture of two isomers. One isomer contains a 4-coordinate metal center, while the other is 5-coordinate and features a chelating η 2 -OSi(O t Bu) 3 ligand. The solid-state transformation of 1 to ZrO 2 ·4SiO 2 produces an open, fibrous material that is somewhat ordered with pores which are ∼20 nm in diameter. The solution-phase thermolysis of 1 produces a xerogel composed of small primary particles (≤∼5 nm). This xerogel possesses a high surface area (700 m 2 g - 1 for samples heated to 200 °C). Solutions of the precursors have been used to cast crack-free thin films of MO 2 ·4SiO 2 . The MO 2 ·4SiO 2 materials are amorphous as initially formed, and subsequent crystallizations of tetragonal ZrO 2, monoclinic ZrO 2, and cristobalite occur at relatively high temperatures. The enhanced stabilization of the amorphous and tetragonal phases of zirconia, relative to those derived from many sol-gel systems, implies that these single-source precursors initially produce homogeneous materials and that subsequent crystallizations are to a large degree diffusion-controlled. Homogeneity in the initially formed ZrO 2 ·4SiO 2 material is also suggested by solid-state 29 Si NMR spectra. The molecular route to oxide materials described here represents an alternative to the sol-gel method and may offer certain advantages.
No takes yet. Share an insight, caveat, or question.
Terry et al. (1997) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: