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Updated: Dec 8, 2025
![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
MeSi(CH2 SnRO)3 (R=Ph, Me3 SiCH2 ): Building Blocks for Triangular-Shaped Diorganotin Oxide Macrocycles
Jihed Ayari1, Christian R Göb2, Iris M Oppel2
1Fakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Straße 6, 44227, Dortmund, Germany.
Researchers synthesized novel silicon-bridged organotin compounds and their halogenated derivatives. These compounds formed exceptionally large, belt-like molecular diorganotin oxides, the largest reported to date.
Area of Science:
- Organometallic Chemistry
- Materials Science
- Supramolecular Chemistry
Background:
- Organotin compounds are versatile in synthesis and have diverse applications.
- The construction of large, well-defined molecular architectures remains a significant challenge in chemistry.
Purpose of the Study:
- To synthesize novel silicon-bridged tris(tetraorganotin) compounds and their halogenated derivatives.
- To investigate the formation and structural characterization of high-nuclearity molecular diorganotin oxides.
Main Methods:
- Synthesis of novel organotin precursors.
- Reactions with di-t-butyltin oxide and sodium hydroxide to form macrocyclic structures.
- Characterization using elemental analysis, ESI-MS, NMR (including 1H DOSY), IR spectroscopy, and single-crystal X-ray diffraction.
Main Results:
- Successful synthesis of silicon-bridged tris(tetraorganotin) compounds and halogenated derivatives.
- Formation of unprecedented 18-nuclear and 30-nuclear molecular diorganotin oxides (compounds 7 and 8).
- Elucidation of belt-like, ladder-type macrocyclic structures for compounds 7 and 8 via X-ray diffraction.
Conclusions:
- The study reports the synthesis of novel organotin compounds and the creation of the largest molecular diorganotin oxides to date.
- The belt-like macrocyclic structures represent a significant advancement in supramolecular assembly of organotin compounds.
- The characterized compounds offer new possibilities for exploring the chemistry and applications of large organometallic architectures.
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