| Project/Area Number |
07640707
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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 |
Organic chemistry
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| Research Institution | University of Tsukuba |
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Principal Investigator |
KABE Yoshio University of Tsukuba, Institute of Chemistry Lecturer, 化学系, 講師 (40214506)
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| Project Period (FY) |
1995 – 1997
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| Project Status |
Completed (Fiscal Year 1997)
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| Budget Amount *help |
¥2,400,000 (Direct Cost: ¥2,400,000)
Fiscal Year 1997: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1996: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1995: ¥1,100,000 (Direct Cost: ¥1,100,000)
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| Keywords | Silicon Compounds / Metathesis / 1,2-Disilacyclobutanes / Zirconocene Complex / 1,2-ジシラシクロブタン / 環状ケイ素化合物 / Si-Siメタテシス / トランスメタル化 / 環化付加 |
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| Research Abstract |
We found that cyclic disilanes such as 1,2-Disilacyclobutanes underwent palladium-catalyzed Si-Si metathesis to from a dimer (Organometallics, 14,2556(1995)). It was considered which types of cyclic disilanes lead to the Si-Si metathesis reaction as well as a new versatile snthetic method of cyclic disilanes. For the preparation of 1.2-disilacyclobutane, new zirconocene promoted alkyne-coupling reaction of 1,2-alkynyldisilane have been discolsed. However bulky alkoxy groups as erminal substituents of alkynes, which is essential for the zirconocene cpoupling reaction, disturbed the Si-Si metathesis reaction with Pd(PPh3)4 and Pd(CNtBu)2 to afford bissilylpalladium complexes respectively. Furthermore, bissilylpalladium complex react with activated acetylene to give bissilylation products, while the reaction with CpPdAllyl led to the intramolecular sily Heck reaction
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