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Published on: September 8, 2016
Disilene-Silylene Interconversion: A Synthetically Accessible Acyclic Bis(silyl)silylene
Dominik Reiter1, Richard Holzner1, Amelie Porzelt1
1Department of Chemistry, WACKER-Institute of Silicon Chemistry and Catalysis Research Center , Technische Universität München , Lichtenbergstraße 4 , 85748 Garching bei München , Germany.
Researchers isolated the first stable bis(silyl)silylene, a highly reactive compound. This novel silylene readily activates small molecules like hydrogen and ammonia, showing potential for future catalysis.
Area of Science:
- Organosilicon Chemistry
- Main Group Chemistry
- Catalysis
Background:
- Silylenes exhibit reactivity typically seen in transition-metal complexes.
- Highly reactive silylenes are potential economical alternatives for catalysis.
Purpose of the Study:
- To isolate and characterize a novel bis(silyl)silylene.
- To investigate the reactivity of this silylene in small molecule activation.
- To explore the disilene-silylene rearrangement mechanism.
Main Methods:
- Isolation of an equilibrium mixture of tetrasilyldisilene and bis(silyl)silylene.
- Small molecule activation studies (H2, NH3).
- Synthesis of donor-stabilized bis(silyl)silylenes.
- Theoretical calculations (DFT).
Main Results:
- First isolation of an isolable bis(silyl)silylene.
- Demonstrated facile small molecule activation (H2, NH3) under mild conditions.
- Gained insights into 1,2-silyl migration in disilene-silylene rearrangement.
Conclusions:
- The isolated bis(silyl)silylene is extremely reactive, enabling challenging small molecule activations.
- This work provides a new class of silylenes for potential catalytic applications.
- Understanding the rearrangement mechanism aids in designing future silicon-based catalysts.
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