Organic–inorganic hybrid poly(silsesquioxane) monoliths with controlled macro- and mesopores

Abstract

Siloxane-based organic–inorganic hybrid monoliths with well-defined macropores and/or mesopores have been synthesized by a sol–gel process, accompanied by polymerization-induced phase separation. Using aklyltrialkoxysilanes and alkylene-bridged alkoxysilanes, two different categories of organosiloxane networks have been characterized in view of macroporosity (based on phase separation) and mesoporosity (supramolecularly templated by surfactants). While the alkyl-terminated poly(siloxane) networks exhibit substantial surface hydrophobicity accompanied by mechanical flexibility, the alkylene-bridged networks behave much more similarly to those prepared from tetraalkoxysilanes with regard to surface hydrophilicity, mechanical rigidness and mesopore-forming ability. The supramolecular templating of mesopores embedded in the gel skeletons (which comprise well-defined macroporous networks) has proven to give a wide variety of hierarchically-designed macro–mesoporous hybrid materials.