Abstract
Bisfunctional dichlorosilanes were reacted with tetrasilanol of double-decker shaped octaphenylsilsesquioxane (DDSQ) to form fully condensed DDSQ compounds. The crystallographic and thermal characteristics of these compounds were examined. For compounds capped with dichlorosilanes bearing linear aliphatic moieties, as the number of carbon increases from methyl to n-butyl (from 1 to 4) the melting temperature, Tm, dropped from 546 K to 416 K. While for compounds capped with cycloaliphatic, as the moiety changes from cyclopentyl to cyclohexyl, the value of Tm increases from 533 K to 555 K. Surprising, the highest Tm observed was that when capping was done using diisopropyl dichlorosilane. A Tm of around 565 K was observed, which was even higher as compare to diphenyl dichlorosilane capped DDSQ, which had Tm of about 526 K. Phase behavior of binary and ternary mixtures of these condensed DDSQ was also investigated. To our surprise, mixtures of these compounds form eutectic. The eutectic points were calculated based on ideal binary and ternary eutectic from the thermal properties of pure components. Depending on the crystallography, experimental observations of eutectic match well with calculated values.
Phase Behavior of Selected Condensed Double-Decker Shaped Silsesquioxane Compounds
