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Method for making polysilsesquioxanes and organohydridosilanes

Patent 6284908 Issued on September 4, 2001. Estimated Expiration Date: Icon_subject September 25, 2020. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Method of cleaving organosiloxanes
Patent #: 4417067
Issued on: 11/22/1983
Inventor: Kotzsch ,   et al.

Preparation of polymethylsilsesquioxane
Patent #: 4528390
Issued on: 07/09/1985
Inventor: Kimura

Method for decomposing polysiloxane
Patent #: 5504235
Issued on: 04/02/1996
Inventor: Hirose, et al.

Process for decomposing siloxane bond-containing compound
Patent #: 5892087
Issued on: 04/06/1999
Inventor: Yang, et al.

Synthesis of siloxane resins Patent #: 6043330
Issued on: 03/28/2000
Inventor: Hacker, et al.

Inventors

Assignee

Application

No. 669101 filed on 09/25/2000

US Classes:

556/467, Plural silicons in a reactant528/14, Material is a metal-containing material528/21Material is a nitrogen-containing compound

Examiners

Primary: Shaver, Paul F.

Attorney, Agent or Firm

International Class

C07F 012/08

Abstract

A method for disproportionation of an oligohydridosiloxane to produce a polysilsesquioxane compound and an organohydridosilane compound when contacted with a basic catalyst. The basic catalyst can be a tetraalkylammonium hydroxide, an alkali metal hydroxide, and an alkali earth hydroxide. These basic catalysts are generally dissolved in an organic solvent for delivery. The hydroxide catalysts are attractive because many readily decompose by heating above 150° C., thus being easily removed from the final materials. The oligohydridosiloxane is contacted with the basic catalyst under conditions effective to catalytically convert the oligohydridosiloxane into a polysilsesquioxane compound and an organohydridosilane compound. The reaction can occur in either an inert or oxidative atmosphere and can occur without heating, at room temperature. Both polysilsesquioxane foams and gels of the formula (RSiO1.5)n can be produced.

Other References

  • Laine, R., Rahn, J. Youngdahl, K., Babonneau, F., Hoppe, M., Zhang, Z., and Harrod, J., "Synthesis and high-temperature chemistry of methylsilsesquioxane polymers produced by titanium-catalyzed redistribution of methylhydridooligo-and -polysiloxanes," Chem. Mater., 1990, 2, 464-472
  • Xin, S., Aitken, C., Harrod, J., Mu, Y., and Samuel, E., "Redistribution reactions of alkoxy- and siloxysilanes, catalyzed by dimethyltitanocene," Can. J. Chem., 1990, 68, 471-476
  • Rahimian, K., Assink, R. and Loy, D., "Polymethylsilsesquioxanes through base-catalyzed redistribution of oligomethylhydridosiloxanes," Polymer Preprints, American Chemical Society, 2000, 41(1), 512-513
  • Rahimian, K., Assink, R., Lang, D., and Loy, D., "Polysilsesquioxanes through base-catalyzed redistribution of oligohydridosiloxanes," Polymer Preprints, American Chemical Society, 2000, 41 (2), 1277-127
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