Article ID Journal Published Year Pages File Type
1324253 Journal of Organometallic Chemistry 2010 5 Pages PDF
Abstract

Cage octasilsesquioxane with various substituents were obtained by the condensation reaction of various all-cis cyclic tetrasiloxanetetraol (R-T4-tetraol, R = phenyl, p-tolyl, i-butyl, naphthyl) with benzyltrimethylammonium hydroxide or tetrabutylammonium fluoride as a catalyst. Co-condensation of phenyl-T4-tetraol with phenyl-d5-T4-tetraol or with p-tolyl-T4-tetraol were found to proceed through reshuffling process evidenced by scrambling of the substituents. Pure octa(4-bromo-substituted phenyl)octasilsesquioxane was synthesized for the first time from tetra(4-bromo-substituted phenyl)tetrasiloxanetetraol sodium salt.

Graphical abstractCage octasilsesquioxanes were obtained from sodium salt of cyclic tetrasiloxanetetraols.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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