Rafał Januszewski

Unusual cis and trans architecture of dihydrofunctional double-decker shaped silsesquioxane and synthesis of its ethyl bridged π-conjugated arene derivatives

Double-decker silsesquioxanes have gained a high reputation in many branches of chemistry and process development. In particular, catalytic processes that convert double-decker silsesquioxanes into important functional classes of fine chemicals are a central topic of contemporary organosilicon chemistry. Although the 9,19-di(hydro)octaphenyl double-decker silsesquioxane (DDSQ-2SiH) is known, we report its cis and trans structure and X-ray structure for the first time. The combination of DDSQ-2SiH in a known hydrosilylation reaction protocol with precise reaction time control (FT-IR in situ apparatus) allowed us to selectively assemble a series of previously unreported molecular double-decker silsesquioxanes with ethyl bridged π-conjugated arenes. These compounds were used as a molecular model to obtain their respective macromolecular hybrid analogues. The obtained compounds were characterized spectroscopically and their thermal parameters were also verified.

A library of multisubstituted cyclotriphosphazenes – molecular scaffolds for hybrid materials

An effective approach for the syntheses of new di- and hexafunctional cyclotriphosphazenes, based on olefin or silylacetylene hydrosilylation with 4-dimethylsilylphenoxy cyclotriphosphazene derivatives, is reported. All new compounds obtained with high yields and selectivities were isolated and characterized by 1H, 13C, 29Si, 31P NMR and FT-IR techniques.