| Project/Area Number |
06640761
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
物質変換
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| Research Institution | Niigata University (1996)
University of Tsukuba (1994-1995) |
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Principal Investigator |
AKASAKA Takeshi Graduats School of Sci.& Tech Niigata University, Professor, 自然科学研究科, 教授 (60089810)
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| Project Period (FY) |
1994 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1996: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1995: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1994: ¥800,000 (Direct Cost: ¥800,000)
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| Keywords | C_<60> / Fullerene / Silylation / Bissily lation / Disilirane / Digermiraue / C_<70> / Endohedral Metallofullerenes / C60 / C70 / シリレン / ジシラン / シラシクロプロパン |
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| Research Abstract |
Much attention has been drawn to the chemical derivatization of buckminsterfullerene, C_<60> in recent years. Among various reactions to be used for the functionalization of C_<60>, [2+1], [2+2], [2+3], [2+4] and [2+8] cycloaddition reactions have been successfully employed for preparation of the ring-fused C_<60> derivatives. In all cases, C_<60> acts as a dienophile. Meanwhile, photo-excited C_<60> is a strong electron acceptor and strained Si-Si and Ge-Ge s bonds can act as an electron donor. During the course of our research on chemical derivatization of fullerenes with organosilicon and -germanium compounds, we found that photochemical [2+3] cycloaddition of C_<60> and C_<70> with a disilirane and a digermirane take place and can demonstrate the intermediacy of an exciplex.
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