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Assembling Molecular Shuttles Powered by Reversibly Attached Kinesins
Published on: January 26, 2019
Synthetic molecular machine based on reversible end-to-interior and end-to-end loop formation triggered by
Jae Wook Lee1, Ilha Hwang, Woo Sung Jeon
1National Creative Research Initiative Center for Smart Supramolecules and Department of Chemistry, Pohang University of Science and Technology, San 31 Hyojadong, Pohang 790-784, Korea.
Abstract:
We have designed and synthesized a novel [2]pseudorotaxane-based molecular machine in which the interconversion between end-to-interior and end-to-end loop structures is reversibly controlled by electrochemical stimuli. Cucurbit[8]uril (CB[8]) and the thread molecule 3(4+) with an electron-rich hydroxynaphthalene unit and two electron-deficient viologen units form the 1:1 complex 4(4+) with an end-to-interior loop structure, which is reversibly converted into an end-to-end structure upon reduction. Large changes in shape and size of the molecule accompany the reversible redox process. The key feature of the machine-like behavior is the reversible interconversion between an intramolecular charge-transfer complex and viologen cation radical dimer inside CB[8] triggered by electrochemical stimuli.
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