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Unusual cis and trans architecture of dihydrofunctional double-decker shaped silsesquioxane and synthesis of its ethyl bridged π-conjugated arene derivatives
| Content Provider | Semantic Scholar |
|---|---|
| Author | Walczak, Marcin Januszewski, Rafał Majchrzak, Mariusz Kubicki, Marek Dudziec, Beata Marciniec, Bogdan |
| Copyright Year | 2017 |
| Abstract | 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. |
| Starting Page | 3290 |
| Ending Page | 3296 |
| Page Count | 7 |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/C7NJ00255F |
| Volume Number | 41 |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/c7/nj/c7nj00255f/c7nj00255f1.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/C7NJ00255F |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |