| Project/Area Number |
26888003
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| Research Category |
Grant-in-Aid for Research Activity Start-up
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| Allocation Type | Single-year Grants |
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| Research Field |
Functional solid state chemistry
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| Research Institution | University of Tsukuba |
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Principal Investigator |
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| Project Period (FY) |
2014-08-29 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Fiscal Year 2015: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
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| Keywords | 超分子化学 / ホストゲスト化学 / 金属錯体 / 環状分子 / 分子認識 / 動的共有結合 / 配位結合 / 双曲放物面 / 大環状配位子 |
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| Outline of Final Research Achievements |
We synthesized a macrocyclic hexamer with inward N,N,O tridentate coordination sites using a newly designed bifunctional monomer possessing aminophenol and pyridylcarbaldehyde units. A hexanuclear zinc complex of the macrocycle recognized two molecules of pimeric acid selectively among aliphatic dicarboxylic acids, and formed a host-guest complex with an uncommon stacked hyperbolic paraboloid shape. Following factors contributed to the formation of the unique structure: i) bridging of zinc atoms by carboxylate groups; ii) inter-macrocyclic coordination of the phenoxy oxygens to zinc atoms; iii) pi-pi interactions. This unique molecule with the hyperbolic paraboloid shape accumulates multiple labile metal centers in its cavity, and its application to the amplification of molecular signals or the fields for catalytic reactions is expected.
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