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Hydrocarbon-Bridged Polysiloxane and Polysilsesquioxane Network Materials.§

Published online by Cambridge University Press:  21 February 2011

Gregory M. Jamison
Affiliation:
Properties of Organic Materials Department, Sandia National Laboratories, Albuquerque, New Mexico 87185-0367
Douglas A. Loy
Affiliation:
Properties of Organic Materials Department, Sandia National Laboratories, Albuquerque, New Mexico 87185-0367
Roger A. Assinkt
Affiliation:
Properties of Organic Materials Department, Sandia National Laboratories, Albuquerque, New Mexico 87185-0367
Kenneth J. Shea
Affiliation:
Department of Chemistry, University of California Irvine, Irvine, California 92717
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Abstract

Hexylene-and phenylene-bridged polymethylsiloxane xerogels X-2 and X-4, respectively, were prepared by the sol-gel hydrolysis and condensation of 1, 6-bis(diethoxymethyl-silyl)hexane 1 and 1, 4-bis(diethoxymethysilyl)benzene 2 under acidic and basic conditions. These polymerizations afforded network polymers in the form of wet gels within several hours. The gels were processed to afford xerogels whose characteristics (determined by solid state 13C and 29Si CP MAS NMR spectroscopy and nitrogen sorption porosimetry) were compared and contrasted with those of their analogous polysilsesquioxanes. 29Si CP MAS NMR indicates a high, degree of hydrolysis and polycondensation; porosimetry measurements reveal that the materials have significant surface areas, save for the acid-catalyzed hexylene gels X-2.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

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Footnotes

§

This research was supported by the United States Department of Energy under contract No.DE-AC04-94AL85000.

§

This research was supported by the United States Department of Energy under contract No. DE-AC04-94AL85000.

References

REFERENCES

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