POLY(UREIDOSILAZANES) - PRECERAMIC POLYMERIC PRECURSORS FOR SILICON CARBONITRIDE AND SILICON-NITRIDE - SYNTHESIS, CHARACTERIZATION, AND PYROLYTIC CONVERSION TO SI3N4 SIC CERAMICS/

Citation
D. Seyferth et al., POLY(UREIDOSILAZANES) - PRECERAMIC POLYMERIC PRECURSORS FOR SILICON CARBONITRIDE AND SILICON-NITRIDE - SYNTHESIS, CHARACTERIZATION, AND PYROLYTIC CONVERSION TO SI3N4 SIC CERAMICS/, Chemistry of materials, 7(11), 1995, pp. 2058-2066
Citations number
37
Categorie Soggetti
Chemistry Physical","Material Science
Journal title
ISSN journal
08974756
Volume
7
Issue
11
Year of publication
1995
Pages
2058 - 2066
Database
ISI
SICI code
0897-4756(1995)7:11<2058:P-PPPF>2.0.ZU;2-W
Abstract
The mixture of cyclo-[CH3Si(H)NH](n) oligomers obtained in the ammonol ysis of CH3SiHCl2 has been converted to material of higher molecular w eight by the reaction with urea (between 4:1 and 12:1 CH3Si(H)NH unit/ urea ratio) in pyridine at 85 degrees C. The resulting poly(ureidosila zanes) (PUSZ) were obtained as white solids, gums or oils, depending o n the CH3-Si(H)NH/urea ratio used. Their pyrolysis in a flow of argon to 1000 degrees C gave black silicon carbonitride in high yield. In a flow of ammonia, their pyrolysis to 1000 degrees C resulted in grayish -white silicon nitride ceramics with a carbon content of less than 2%. DRIFTS, TGA-MS, TGA-FTIR, cross-polarization, and single-pulse magic angle spinning solid state NMR as well as solution-state NMR spectrosc opy were employed in the characterization of the PUSZs and in the inve stigation of their pyrolytic conversion to ceramic materials. Selectiv e isotopic labeling using C-13- and N-15-labeled urea was particularly useful in NMR studies aimed at determining the constitution of the po ly(ureidosilanes).