An efficient multi-gram access in a two-step synthesis to soluble, nine-atomic, silylated silicon clusters.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39715754.
- Also identified by DOI 10.1038/s41467-024-55211-z and PMC identifier 11666712.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Silicon is by far the most important semiconducting material. However, solution-based synthetic approaches for unsaturated silicon-rich molecules require less efficient multi-step syntheses. We report on a straightforward access to soluble, polyhedral Si<sub>9</sub> clusters from the binary phase K<sub>12</sub>Si<sub>17</sub>, which contains both [Si<sub>4</sub>]<sup>4-</sup> and [Si<sub>9</sub>]<sup>4-</sup> clusters. [Si<sub>4</sub>]<sup>4-</sup> ions, characterised by a high charge per atom ratio, behave as strong reducing agents, preventing [Si<sub>9</sub>]<sup>4-</sup> from directed reactions. By the here reported separation of [Si<sub>4</sub>]<sup>4-</sup> by means of fractional crystallisation, Si<sub>9</sub> clusters of the precursor phase K<sub>12</sub>Si<sub>17</sub> are isolated as monoprotonated [Si<sub>9</sub>H]<sup>3-</sup> ions on a multi-gram scale and further crystallised as their 2.2.2-Cryptate salt. 20 grams of the product can be obtained through this two-step procedure - a new starting point for silicon Zintl chemistry, such as the isolation and structural characterisation of a trisilylated [<sup>Me</sup>Hyp<sub>3</sub>Si<sub>9</sub>]<sup>-</sup> cluster.