Chemistry of Functionality of Expanded Porphyrin Metal Complexes
| Project/Area Number |
17350017
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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 |
Organic chemistry
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| Research Institution | Kyoto University |
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Principal Investigator |
OSUKA Atsuhiro Kyoto University, Graduate School of Science, Professor, 大学院理学研究科, 教授 (80127886)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥14,500,000 (Direct Cost: ¥14,500,000)
Fiscal Year 2006: ¥4,100,000 (Direct Cost: ¥4,100,000)
Fiscal Year 2005: ¥10,400,000 (Direct Cost: ¥10,400,000)
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| Keywords | Porphyrin / expanded porphyrin / anion recognition / nonlinear optical properties / two-photon absorption / aromaticity / anti-aromaticity / 金属錯体 |
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| Research Abstract |
Various new reactions and new metal coordination behaviors were revealed for mesa-aryl expanded porphyrins. Representative results are synthesis of novel heptaphyrins bearing direct pyrrole-pyrrole linkage in aqueous phase, extensive synthesis of meso-trifluoromethyl-substituted expanded porphyrins, sequential N-fusion reactions of heptaphyrin. Through these studies, we found that meso-aryl substituted hexaphyrins can take two types of stable conformations in solution depending on the meso-substituents. From 5,20-di(2-thienyl)-substituted hexaphyrin, we obtained new bis palladium complex formed via C-H bond activation of the 5-thienyl position.
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Report
(3 results)
Research Products
(24 results)
