{Sn<sub>9</sub>[Si(SiMe<sub>3</sub>)<sub>3</sub>]<sub>3</sub>}<sup>−</sup> and {Sn<sub>8</sub>Si[Si(SiMe<sub>3</sub>)<sub>3</sub>]<sub>3</sub>}<sup>−</sup>: Variations of the
E<sub>9</sub> Cage of Metalloid Group 14 Clusters
posted on 2012-04-02, 00:00authored byClaudio Schrenk, Marco Neumaier, Andreas Schnepf
The disproportionation reaction of the subvalent metastable
halide
SnBr proved to be a powerful synthetic method for the synthesis of
metalloid cluster compounds of tin. Hence, the neutral metalloid cluster
compound Sn<sub>10</sub>[Si(SiMe<sub>3</sub>)<sub>3</sub>]<sub>6</sub> (<b>3</b>) was synthesized from the reaction of SnBr with
LiSi(SiMe<sub>3</sub>)<sub>3</sub>. In the course of the reaction
anionic clusters might also be present, and we now present the first
anionic cluster compound {Sn<sub>8</sub>E[Si(SiMe<sub>3</sub>)<sub>3</sub>]<sub>3</sub>}<sup>−</sup> (E = Si, Sn), where one
position in the cluster core is occupied by a silicon or a tin atom,
giving further insight into structural variations of E<sub>9</sub> cages in metalloid group 14 cluster compounds.