Article

Artificial muscle-like function from hierarchical supramolecular assembly of photoresponsive molecular motors

  • Nature Chemistry volume 10, pages 132138 (2018)
  • doi:10.1038/nchem.2887
  • Download Citation
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Abstract

A striking feature of living systems is their ability to produce motility by amplification of collective molecular motion from the nanoscale up to macroscopic dimensions. Some of nature's protein motors, such as myosin in muscle tissue, consist of a hierarchical supramolecular assembly of very large proteins, in which mechanical stress induces a coordinated movement. However, artificial molecular muscles have often relied on covalent polymer-based actuators. Here, we describe the macroscopic contractile muscle-like motion of a supramolecular system (comprising 95% water) formed by the hierarchical self-assembly of a photoresponsive amphiphilic molecular motor. The molecular motor first assembles into nanofibres, which further assemble into aligned bundles that make up centimetre-long strings. Irradiation induces rotary motion of the molecular motors, and propagation and accumulation of this motion lead to contraction of the fibres towards the light source. This system supports large-amplitude motion, fast response, precise control over shape, as well as weight-lifting experiments in water and air.

  • Compound

    11,11'-((9-(5-(dodecyloxy)-2-methyl-2,3-dihydro-1H-benzo[f]thiochromen-1-ylidene)-9H-thioxanthene-4,5-diyl)bis(oxy))diundecanoic acid

  • Compound

    (R)-(M)-11,11'-((9-(5-(dodecyloxy)-2-methyl-2,3-dihydro-1H-benzo[f]thiochromen-1-ylidene)-9H-thioxanthene-4,5-diyl)bis(oxy))diundecanoic acid

  • Compound

    (R)-(P)-11,11'-((9-(5-(dodecyloxy)-2-methyl-2,3-dihydro-1H-benzo[f]thiochromen-1-ylidene)-9H-thioxanthene-4,5-diyl)bis(oxy))diundecanoic acid

  • Compound

    5-hydroxy-2-methyl-2,3-dihydro-1H-benzo[f]thiochromen-1-one

  • Compound

    4,5-dihydroxy-9H-thioxanthen-9-one

  • Compound

    5-(dodecyloxy)-2-methyl-2,3-dihydro-1H-benzo[f]thiochromen-1-one

  • Compound

    dimethyl 11,11'-((9-oxo-9H-thioxanthene-4,5-diyl)bis(oxy))diundecanoate

  • Compound

    (Z)-(5-(dodecyloxy)-2-methyl-2,3-dihydro-1H-benzo[f]thiochromen-1-ylidene)hydrazine

  • Compound

    1-diazo-5-(dodecyloxy)-2-methyl-2,3-dihydro-1H-benzo[f]thiochromene

  • Compound

    dimethyl 11,11'-((9-thioxo-9H-thioxanthene-4,5-diyl)bis(oxy))diundecanoate

  • Compound

    dimethyl 11,11'-((5-(dodecyloxy)-2-methyl-2,3-dihydrodispiro[benzo[f]thiochromene-1,2'-thiirane-3',9''-thioxanthene]-4'',5''-diyl)bis(oxy))diundecanoate

  • Compound

    dimethyl 11,11'-((9-(5-(dodecyloxy)-2-methyl-2,3-dihydro-1H-benzo[f]thiochromen-1-ylidene)-9H-thioxanthene-4,5-diyl)bis(oxy))diundecanoate

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Acknowledgements

This work was supported financially by the Netherlands Organization for Scientific Research (NWO-CW), the European Research Council (ERC, advanced grant no. 694345 to B.L.F.), the Ministry of Education, Culture and Science (Gravitation Program no. 024.001.035) and a Grant-in-Aid for Scientific Research on Innovative Areas ‘π-Figuration’ (nos. 26102008 and 15K21721) of The Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan. The synchrotron XRD experiments were performed at BL45XU in SPring-8 with the approval of the RIKEN SPring-8 Center (proposal no. 20160027).

Author information

Author notes

    • Jiawen Chen
    •  & Franco King-Chi Leung

    These authors contributed equally to this work.

Affiliations

  1. Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747AG Groningen, The Netherlands

    • Jiawen Chen
    • , Franco King-Chi Leung
    • , Marc C. A. Stuart
    •  & Ben L. Feringa
  2. Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8503, Japan

    • Franco King-Chi Leung
    • , Takashi Kajitani
    •  & Takanori Fukushima
  3. RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo, Hyogo 679-5148, Japan

    • Takashi Kajitani
  4. Zernike Institute for Advanced Materials, University of Groningen, 9747AG Groningen, The Netherlands

    • Erik van der Giessen

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Contributions

B.L.F., F.K.-C.L. and J.C. conceived the research. J.C. and F.K.-C.L. carried out the synthesis of 1. J.C. characterized the motion of the molecular motor. M.C.A.S. performed the cryo-TEM. F.K.-C.L. prepared the string and carried out POM and SEM analysis. F.K.-C.L. and T.K. performed all XRD measurements and structural analysis. J.C. and F.K.-C.L. carried out the actuation experiments. J.C. and E.v.d.G. analysed and calculated the mechanical work. J.C., F.K.-C.L., T.K., T.F. and B.L.F. co-wrote the paper. All authors discussed the results and commented on the manuscript.

Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to Ben L. Feringa.

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