| Project/Area Number |
22KF0396
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| Project/Area Number (Other) |
21F21337 (2021-2022)
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| Research Category |
Grant-in-Aid for JSPS Fellows
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| Allocation Type | Multi-year Fund (2023)
Single-year Grants (2021-2022) |
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| Section | 外国 |
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| Review Section |
Basic Section 35020:Polymer materials-related
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| Research Institution | Institute of Physical and Chemical Research |
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Principal Investigator |
相田 卓三 国立研究開発法人理化学研究所, 創発物性科学研究センター, グループディレクター (00167769)
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| Co-Investigator(Kenkyū-buntansha) |
SU ZEBIN 国立研究開発法人理化学研究所, 創発物性科学研究センター, 外国人特別研究員
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| Project Period (FY) |
2023-03-08 – 2024-03-31
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| Project Status |
Completed (Fiscal Year 2023)
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| Budget Amount *help |
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 2023: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2022: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2021: ¥900,000 (Direct Cost: ¥900,000)
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| Keywords | Supramolecular polymers / Self-assembly / Block copolymer / supramolecular polymers / self-assembly / block copolymers / Supramolecyular polymer / Phase seperation |
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| Outline of Research at the Start |
A library of novel molecules (or monomers) with thermodynamic incompatible side chains has been designed and synthesized. Supramolecular polymers are formed via “salt-bridge” interaction between. Multiple ordered nano-phase structures have been observed in the solid-state supramolecular polymers.
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| Outline of Annual Research Achievements |
I've successfully developed polymeric materials featuring sub-5nm periodic structures, utilizing solid-state supramolecular polymers. These polymers are assembled from supramolecular monomers, each comprising a carboxylate group, a guanidinium group, and two thermodynamically incompatible oligomers. Through 'salt-bridge' interactions between guanidinium and carboxylate, supramolecular polymerization is facilitated. Confirmation of nanoscale hierarchical structures was achieved via small-angle X-ray scattering and transmission electron microscopy. These polymeric materials, boasting hierarchical structures, exhibit a storage modulus over 26 times higher than their polymer-blending counterparts, which lack ordered structures.
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