LiGe(SiMe₃)₃: A New Substituent for the Synthesis of Metalloid Tin Clusters from Metastable Sn(I) Halide Solutions

Molecules. 2018 Apr 26;23(5):1022. doi: 10.3390/molecules23051022.

Abstract

The most fruitful synthetic route to metalloid tin clusters applies the disproportionation reaction of metastable Sn(I) halide solutions, whereby Si(SiMe₃)₃ is mostly used as the stabilizing substituent. Here, we describe the synthesis and application of the slightly modified substituent Ge(SiMe₃)₃, which can be used for the synthesis of metalloid tin clusters to give the neutral cluster Sn10[Ge(SiMe₃)₃]₆ as well as the charged clusters {Sn10[Ge(SiMe₃)₃]₅} and {Sn10[Ge(SiMe₃)₃]₄}2−. The obtained metalloid clusters are structurally similar to their Si(SiMe₃)₃ derivatives. However, differences with respect to the stability in solution are observed. Additionally, a different electronic situation for the tin atoms is realized as shown by 119mSn Mössbauer spectroscopy, giving further insight into the different kinds of tin atoms within the metalloid cluster {Sn10[Ge(SiMe₃)₃]₄}2−. The synthesis of diverse derivatives gives the opportunity to check the influence of the substituent for further investigations of metalloid tin cluster compounds.

Keywords: Mössbauer spectroscopy; bulky substituents; co-condensation; disproportionation; germanium; metalloid clusters; nanoscaled clusters; tin.

MeSH terms

  • Crystallography, X-Ray
  • Germanium / chemistry*
  • Lithium / chemistry*
  • Molecular Structure
  • Organotin Compounds / chemical synthesis*
  • Organotin Compounds / chemistry

Substances

  • Organotin Compounds
  • Germanium
  • Lithium