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![The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F54498.jpg&w=3840&q=50)
The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique
Published on: November 28, 2016
A Step in Between: [Sn3Bi3](5-) and Its Structural Relationship to [Sn3Bi5](3-) and [Sn4Bi4](4.)
Ute Friedrich1, Nikolaus Korber1
1Fakultät für Chemie und Pharmazie Universität Regensburg Universitätsstraße 31 93053 Regensburg Germany.
Abstract:
Extraction of "RbSnBi" in liquid ammonia yielded the cluster anion [Sn3Bi5](3-), which could be crystallized in the compound [Rb@[2.2.2]crypt]3[Sn3Bi5]⋅8.87 NH3. This anion is found to be derived from the formerly reported [Sn4Bi4](4-) by the formal substitution of one tin atom by bismuth. In contrast, the extraction of "RbSn2/Rb3Bi2" in liquid ammonia yielded the anion [Sn3Bi3](5-) in the compound Rb6[Sn3Bi3][Sn4]1/4⋅6.75 NH3. The structural correlation of the two novel clusters indicates that [Sn3Bi3](5-) might be an intermediate of the reaction pathway to [Sn3Bi5](3-) and [Sn4Bi4](4-). Each cluster is investigated by means of the electron localization function and further characterization was performed by using ESI-MS.
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