Synthesis and structure of ethynylsilyllithiums

Mitsuo Kira, Tomoyuki Kadowaki, Dongzhu Yin, Kenkichi Sakamoto, Takeaki Iwamoto, Chizuko Kabuto

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7 Citations (Scopus)

Abstract

Ethynylsilyllithiums [R1R2CR3CC)SiLi: R1 = R2 = t-BuMe2Si, R3 = Me 3Si (5a); R1 = R2 = t-BuMe2-Si, R3 = Ph (5b); R1 = R2 = R3 = Me 3Si (5c); R1 = t-BuMe2Si, R2 = Ph, R3 = Me3Si (5d); R1 = t-BuMe2Si, R2 = Me3SiCC, R3 = Me3Si (5e)] were prepared by the sila-metalation reactions of the corresponding hydrosilanes using tert-butyllithium in THF and trapped by MeI, Me3SiCl, and i-Pr3SiCl in high yields. X-ray structural analysis of a single crystal of 5a has revealed that 5a adopts a dimer form (7a) containing one THF molecule per dimer. Dimer 7a is a syn dimer with a planar four-membered ring made by two lithium atoms and two anionic silicon atoms; one lithium atom is coordinated by two ethynyl π groups and the other by a THF molecule, indicative of the importance of the coordination of ethynyl π groups for the stabilization of the silyllithium. 7Li NMR analysis indicates that the dimeric structure of 5a (7a) is maintained in toluene, but 5a is monomelic in THF. Rates and activation parameters of facile intramolecular exchange of the two lithium atoms in 7a observed in toluene-d8 were determined by the dynamic 7Li NMR. The DFT calculations of a model ethynylsilyllithium [(H3Si)2(H3-SiCC)SiLi, 12] have shown mat dimer 13, with a similar geometry to 7a, is more stable than the monomelic form. The optimized monomeric form of 12 (12′) has an ethynylsilyllithium-type structure with a largely bent Si-CC skeleton, suggesting significant intramolecular π+ coordination to Li +.

Original languageEnglish
Pages (from-to)4890-4895
Number of pages6
JournalOrganometallics
Volume26
Issue number20
DOIs
Publication statusPublished - 2007 Sep 24

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

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    Kira, M., Kadowaki, T., Yin, D., Sakamoto, K., Iwamoto, T., & Kabuto, C. (2007). Synthesis and structure of ethynylsilyllithiums. Organometallics, 26(20), 4890-4895. https://doi.org/10.1021/om0611103