Construction of Anisotropic, Three-Dimensional, and Dynamic Molecular-Assembled Systems of Synthetic Double Helices and Development of Macroscopic Motional Functions
Project/Area Number |
15K18825
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Chemical pharmacy
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Research Institution | Tohoku University |
Principal Investigator |
SAITO Nozomi 東北大学, 薬学研究科, 助教 (40636411)
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Project Period (FY) |
2015-04-01 – 2017-03-31
|
Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2016: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2015: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
|
Keywords | ヘリセン / オリゴマー / 二重ラセン / 異方性 / 自己組織化 / 液晶 / 熱応答 / 超長鎖 / トリエチレングリコール / 水和 / 超長鎖アルカン |
Outline of Final Research Achievements |
Molecular properties of ethynylhelicene oligomers were controlled by taking advantage of molecular design. Then, construction of aniosotropic, three-dimensional, and dynamic molecular-assembled systems was examined by utilizing the self-assembly in order to integrate the molecular-level transition between double helices and random coils to a muscle-like macroscopic motion. (1) With regard to the oligomers which form anisotropic and fluidic thermotropic liquid crystals, reversibility of structural change was improved. (2) Details of the unique thermoresponse of the oligomers with TEG groups were revealed, such as the variety of applicable solvents and the dependence on the solvent composition. (3) A 1,ω-alkanediol with carbon number 128 was synthesized in order to align the oligomers in an anisotropic manner by taking advantage of the crystallinity of the superlong-chain alkane.
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Report
(3 results)
Research Products
(29 results)