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A New Catalytic Method for Producing Preceramic Polysilazanes

Published online by Cambridge University Press:  28 February 2011

Yigal D. Blum
Affiliation:
Contribution from the Organometallic Chemistry and the Ceramics Programs and the Polymer Sciences Department, SRI International, Menlo Park, CA 94025
Richard M. Laine
Affiliation:
Contribution from the Organometallic Chemistry and the Ceramics Programs and the Polymer Sciences Department, SRI International, Menlo Park, CA 94025
Kenneth B. Schwartz
Affiliation:
Contribution from the Organometallic Chemistry and the Ceramics Programs and the Polymer Sciences Department, SRI International, Menlo Park, CA 94025
David J. Rowcliffe
Affiliation:
Contribution from the Organometallic Chemistry and the Ceramics Programs and the Polymer Sciences Department, SRI International, Menlo Park, CA 94025
Robert C. Bening
Affiliation:
Contribution from the Organometallic Chemistry and the Ceramics Programs and the Polymer Sciences Department, SRI International, Menlo Park, CA 94025
David B. Cotts
Affiliation:
Contribution from the Organometallic Chemistry and the Ceramics Programs and the Polymer Sciences Department, SRI International, Menlo Park, CA 94025
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Abstract

A transition metal (e.g., Ru3 (CO)12, Pt/C) catalyzed process for Si-N bond formation is discussed that provides a new route to mono-, oligo-, and polysilazanes. The catalysts function by activating Si-H bonds in the pres-ence of ammonia. Polymeric silazanes can also be produced from oligomers in the presence of ammonia at low temperatures. This method allows us to control or modify the composition of the polysilazane during or after the polymeriza-tion. A variety of polysilazanes were prepared and converted to Si3 N4 with ceramic yields ranging from 55%-85%. By varying the monomers and reaction conditions, we can control the nitrogen and carbon content in the preceramic polymers, which enables us to obtain ceramic products that are primarily Si3N4and simultaneously minimizes the coproduction of SiC and C.

Type
Articles
Copyright
Copyright © Materials Research Society 1986

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References

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