Substituents Effects on the Addition of Silyllithium and Germyllithium to C_<60>
| Project/Area Number |
08454194
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Organic chemistry
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| Research Institution | University of Tsukuba |
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Principal Investigator |
ANDO Wataru Chemistry, University of Tsukuba, Professor, 化学系, 教授 (30008429)
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| Project Period (FY) |
1996 – 1997
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| Project Status |
Completed (Fiscal Year 1997)
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| Budget Amount *help |
¥6,100,000 (Direct Cost: ¥6,100,000)
Fiscal Year 1997: ¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1996: ¥3,800,000 (Direct Cost: ¥3,800,000)
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| Keywords | germyllithium / sillyllithium / C_<60> / C_<60>dimers / 1,16-adduct / 1,4-adduct / 1,2-付加 / 1,16-付加体 / シリルアニオン / 1.16-付加 / 電子移動 / ラジカル反応 / オクタフェニルシクロテトラシラン / オクタフェニルシクロテトラゲルマン / ジシラアントラセン / シリルリチウム |
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| Research Abstract |
Reactions of various substituted silyl and germyllithium with C_<60> were examined. Isopropylphenyl substituted silyllitiums react with C_<60> to give 1,2-silyl substituted adduct. Substituted tert-butylphenyl or trimethylsilyl substituted silyllithiums, on the other hand, react with C_<60> to give the di-adduct. On the basic spectroscopic and X-ray crystal structures of the product, the silyl substitutions are located at 1 and 16 position of C_<60>. Silyl substituted 1,4-adduct (SiHC_<60>) and C_<60> dimers are also obtained from tert-butylphenylsilyllithium reaction in the presence of biphenyl derivatives.
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Report
(3 results)
Research Products
(9 results)
