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Preparation and characterization of aryl-substituted polysilsesquioxanes
Polymerizations of aryltrialkoxysilanes generally afford soluble oligomeric or polymeric aryl-substituted silsesquioxanes. This is in spite of being based on trifunctional precursors capable of forming highly crosslinked and insoluble network polymers. In this study, soluble phenyl, benzyl, and phenethyl-substituted silsesquioxane oligomers and polymers were prepared by hydrolyzing their respective triethoxysilyl precursor with water or aqueous acid. Additional samples of the polymers were prepared by heating the materials at 100 C or 200 C under vacuum in order to drive the condensation chemistry. One sample of polybenzylsilsesquioxane was heated at 200 C with catalytic NaOH. The resulting materials were characterized using solution {sup 1}H, {sup 13}C, and {sup 29}Si NMR spectroscopy, gel permeation chromatography, and differential scanning calorimetry. Of particular interest was the effect of the aryl substituent, and processing conditions on the molecular weight and glass transition temperatures of the polysilsesquioxanes.