2011 Fiscal Year Final Research Report
Exploration of Dynamic (Arene)chromium Complex for the Development from Novel Catalytic Reaction to Molecular Computing.
Project/Area Number |
21200054
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Research Category |
Grant-in-Aid for Scientific Research on Innovative Areas (Research a proposed research project)
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Allocation Type | Single-year Grants |
Research Field |
Organic chemistry
Functional materials/Devices
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Research Institution | Osaka Prefecture University |
Principal Investigator |
KAMIKAWA Ken 大阪府立大学, 理学系研究科, 准教授 (40316021)
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Project Period (FY) |
2009 – 2011
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Keywords | 反応有機化学 / 分子素子 / 合成化学 |
Research Abstract |
We have developed axial chirality induction utilizing chromium tricarbonyl migration of N-arylacridane chromium complex, which has a pro-chiral N-C bond. We also succeeded to control the slippage reaction of chromium tricarbonyl group in conjugated aromatic compound. It was found that the introduction of TES group at the edge of carbazole and naphthalene compound could induce the reversible chromium tricarbonyl migration by external stimuli i.e. light or heat. In addition, it was confirmed that the electron density of the aromatic ring was largely changed due to the migration of electron withdrawing chromium tricarbonyl group. On the other hand, the chromium tricarbonyl group in a non-conjugated axially chiral biaryl chromium complex with a hydroxymethyl directing group could migrate to the another arene face of biaryl stereoselectively. In addition, axially chiral teraryl chromium complex also was synthesized and second migration reaction to the newly introduced arene could be achieved to give a migrated complex.
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