Synthesis and properties of a kinetically stabilized 9-silaphenanthrene

Norihiro Tokitoh*, Akihiro Shinohara, Takeshi Matsumoto, Takahiro Sasamori, Nobuhiro Takeda, Yukio Furukawa

*この研究の対応する著者

研究成果: Article査読

36 被引用数 (Scopus)

抄録

Reaction of 9-bromo-9,10-dihydro-9-silaphenanthrene (6) with lithium diisopropylamide (LDA) in THF at room temperature afforded kinetically stabilized 9-silaphenanthrene la bearing an efficient steric protection group, 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl (Tbt). 9-Silaphenanthrene la was isolated as pale yellow crystals, and the structure of la was completely determined by spectroscopic and X-ray crystallographic analyses. The 1H and 13C NMR chemical shifts corresponding to the 9-silaphenanthrene ring of la were observed in a typical aromatic region, while the central silicon atom showed the characteristic signal at 86.9 ppm in the 29Si NMR in C6D6. The 9-silaphenanthrene ring of la showed completely planar geometry, indicating that 9-silaphenanthrene has a delocalized 14π-electron system as an aromatic compound. In spite of its high thermal stability, la still has high reactivity at the 9,10position toward small reagents such as H2O.

本文言語English
ページ(範囲)4048-4053
ページ数6
ジャーナルOrganometallics
26
16
DOI
出版ステータスPublished - 2007 7月 30

ASJC Scopus subject areas

  • 物理化学および理論化学
  • 有機化学
  • 無機化学

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