Construction of highly efficient and highly selective catalytic oxidation systems based on proton-coupled electron transfer
Project/Area Number |
21350035
|
Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Inorganic chemistry
|
Research Institution | University of Tsukuba |
Principal Investigator |
|
Project Period (FY) |
2009 – 2011
|
Project Status |
Completed (Fiscal Year 2011)
|
Budget Amount *help |
¥19,500,000 (Direct Cost: ¥15,000,000、Indirect Cost: ¥4,500,000)
Fiscal Year 2011: ¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2010: ¥6,110,000 (Direct Cost: ¥4,700,000、Indirect Cost: ¥1,410,000)
Fiscal Year 2009: ¥8,190,000 (Direct Cost: ¥6,300,000、Indirect Cost: ¥1,890,000)
|
Keywords | ルテニウム錯体 / 高原子価オキソ錯体 / プロトン共役電子移動 / 環境/エネルギー / 外部基質酸化触媒系 / 基質酸化反応機構 / スピン状態 / 速度論的考察 / 光触媒反応 / 環境・エネルギー |
Research Abstract |
We have established highly efficient and highly selective catalytic oxidation systems for organic substrates using Ru(II)-pyridylamine-aqua complexes as catalysts in aqueous buffer solutions. In those reactions, Ru(IV)-oxo complexes were formed via proton-coupled electron transfer and their characterization were made by spectroscopic and crystallographic methods and DFT calculations. In this research, we have clarified that the spin states of Ru(IV)-oxo complexes do not affect their reactivity. We have also succeeded in the direct observation of the oxygen-rebound mechanism in C-H hydroxylation for the first time and elucidated the reaction mechanism of C-H oxidation in the light of kinetic analysis.
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Report
(4 results)
Research Products
(120 results)
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[Journal Article] Supramolecular Structures and Photoelectronic Properties of the Inclusion Complex of a Cyclic Free-Base Porphyrin Dimerand C602010
Author(s)
H.Nobukuni, Y.Shimazaki, H.Uno, Y.Naruta, K.Ohkubo, T.Kojima, S.Fukuzumi, S.Seki, H.Sakai, T.Hasobe, F.Tani
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Journal Title
Chemistry-A European Journal
Volume: 16
Pages: 11611-11623
Related Report
Peer Reviewed
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