| Project/Area Number |
15350012
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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 |
Physical chemistry
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| Research Institution | Kyoto University |
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Principal Investigator |
SAKAKI Shigeyoshi Kyoto University, Graduate School of Engineering, Professor, 工学研究科, 教授 (20094013)
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| Co-Investigator(Kenkyū-buntansha) |
SATO Hirofumi Kyoto University, Graduate School of Engineering, Associate Professor, 工学研究科, 助教授 (70290905)
NAKAO Yoshihide Kyoto University, Graduate School of Engineering, Research Associate, 工学研究科, 助手 (40362462)
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| Project Period (FY) |
2003 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥14,200,000 (Direct Cost: ¥14,200,000)
Fiscal Year 2005: ¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2004: ¥5,300,000 (Direct Cost: ¥5,300,000)
Fiscal Year 2003: ¥5,700,000 (Direct Cost: ¥5,700,000)
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| Keywords | Electronic Structure Theory / Transition Metal Complexes / Reaction Mechanism / Bonding Nature / Structure / Electron correlation effects / Reaction control / Function control / 混合原子価錯体 / 錯体触媒反応 / 遷移状態 / 触媒サイクル / 電子状態制御 / 遷移金属元素 / 複合電子系 / ヘテロ元素 / 理論的研究 / 触媒反応機構 / σ結合活性化 / シスプラテイン |
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| Research Abstract |
Theoretical Studies with electronic structure theory were carried out about hydrosilylation of alkene, hydrogenation of carbon dioxide, and Stille coupling reaction, which are typical transition-metal-catalyzed reaction. The hydrosilylation of alkene by Cp_2Zr takes place not only through alkene insertion into Zr-H bond but also coupling reaction between Zr-alkene species and hydrosilane. The product release step is not simple C-H and Si-C reductive elimination but alkene-assisted reductive eliminations and metathesis with hydrosilane. These differences from the late-transition-metal catalyzed hydrosilylation arise from the d orbital energy difference. Reaction mechanism of Ru-catalyzed hydrogenation of carbon dioxide was also theoretically elucidated in the presence of water molecule ; not the insertion of carbon dioxide into Ru-H but nucleophilic attack of hydride to carbon center of CO_2 takes place in the presence of water molecule, of which activation barrier is much smaller than usual CO_2 insertion. Stille coupling reaction takes place through oxidative addition of iodobenzene, transmetallation, and reductive elimination. Transmetallation is rate-determining step, which is accelerated by the presence of fluoride anion. The reason was discussed on the basis of bond energy.
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