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Assembling Molecular Shuttles Powered by Reversibly Attached Kinesins
Published on: January 26, 2019
A light-operated pillar[6]arene-based molecular shuttle.
Tomoki Ogoshi1, Daisuke Kotera2, Shixin Fa3
1Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan. ogoshi@sbchem.kyoto-u.ac.jp and WPI Nano Life Science Institute, Kanazawa University, Kakuma-machi, Kanazawa, 920-1192, Japan.
Researchers developed a molecular shuttle using pillar[6]arene and an azobenzene axle. Light control over the azobenzene unit allows reversible switching of the pillar[6]arene ring
Area of Science:
- Supramolecular Chemistry
- Molecular Machines
- Photochemistry
Background:
- Molecular shuttles are crucial for developing advanced molecular machines.
- Controlling molecular motion is key to designing functional nanomaterials.
Purpose of the Study:
- To synthesize and characterize a novel molecular shuttle.
- To demonstrate light-induced control over the shuttle's motion.
Main Methods:
- Synthesis of a pillar[6]arene macrocycle and an azobenzene-containing axle.
- Utilizing UV irradiation to induce photoisomerization of the azobenzene unit.
- Observing the shuttling behavior of the macrocycle on the axle.
Main Results:
- A molecular shuttle was successfully synthesized, featuring a pillar[6]arene ring and an azobenzene axle with two stations.
- The E-isomer of azobenzene acted as an 'open gate', permitting rapid bidirectional movement of the pillar[6]arene ring.
- UV irradiation converted the azobenzene to its Z-isomer, functioning as a 'closed gate' and halting the ring's movement.
Conclusions:
- The synthesized molecular shuttle exhibits light-controllable motion.
- Photoisomerization of azobenzene provides a mechanism for switching the shuttle's state between 'open' and 'closed'.
- This work contributes to the field of molecular machines and light-responsive materials.
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