Silyl- and disilanyl-1,3-butadiyne polymers from hexachloro-1,3-butadiene
Abstract
Organosilane polymers having recurring silylene-1,3-butadiyne and/or disilylene-1,3-butadiyne units are prepared in a one-pot synthesis from hexachlorobutadiene. Depending on the organic substituents (R and R[prime]), these polymers have useful film-forming properties, and are converted to the ceramic, silicon carbide upon heating a very uniform high char yields. They can also be pulled into fibers. The polymers are thermally crosslinked above 100 C.
- Inventors:
- Issue Date:
- OSTI Identifier:
- 7021190
- Patent Number(s):
- 4965332
- Application Number:
- PPN: US 7-352825
- Assignee:
- Iowa State Univ. Research Foundation, Inc., Ames, IA (United States)
- DOE Contract Number:
- W-7405-ENG-82
- Resource Type:
- Patent
- Resource Relation:
- Patent File Date: 16 May 1989
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 36 MATERIALS SCIENCE; 37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; ORGANIC POLYMERS; SYNTHESIS; SILICON CARBIDES; PRECURSOR; CROSS-LINKING; EXTRUSION; ORGANIC CHLORINE COMPOUNDS; ORGANIC SILICON COMPOUNDS; CARBIDES; CARBON COMPOUNDS; CHEMICAL REACTIONS; FABRICATION; MATERIALS WORKING; ORGANIC COMPOUNDS; ORGANIC HALOGEN COMPOUNDS; POLYMERIZATION; POLYMERS; SILICON COMPOUNDS; 360201* - Ceramics, Cermets, & Refractories- Preparation & Fabrication; 400201 - Chemical & Physicochemical Properties
Citation Formats
Barton, T J, and Ijadi-Maghsoodi, S. Silyl- and disilanyl-1,3-butadiyne polymers from hexachloro-1,3-butadiene. United States: N. p., 1990.
Web.
Barton, T J, & Ijadi-Maghsoodi, S. Silyl- and disilanyl-1,3-butadiyne polymers from hexachloro-1,3-butadiene. United States.
Barton, T J, and Ijadi-Maghsoodi, S. Tue .
"Silyl- and disilanyl-1,3-butadiyne polymers from hexachloro-1,3-butadiene". United States.
@article{osti_7021190,
title = {Silyl- and disilanyl-1,3-butadiyne polymers from hexachloro-1,3-butadiene},
author = {Barton, T J and Ijadi-Maghsoodi, S},
abstractNote = {Organosilane polymers having recurring silylene-1,3-butadiyne and/or disilylene-1,3-butadiyne units are prepared in a one-pot synthesis from hexachlorobutadiene. Depending on the organic substituents (R and R[prime]), these polymers have useful film-forming properties, and are converted to the ceramic, silicon carbide upon heating a very uniform high char yields. They can also be pulled into fibers. The polymers are thermally crosslinked above 100 C.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {1990},
month = {10}
}
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