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Rapid and reversible photoinduced switching of a rotaxane crystal

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  • Kai-Jen Chen

    (Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University)

  • Ya-Ching Tsai

    (Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University)

  • Yuji Suzaki

    (Chemical Resources Laboratory, Tokyo Institute of Technology)

  • Kohtaro Osakada

    (Chemical Resources Laboratory, Tokyo Institute of Technology)

  • Atsushi Miura

    (Faculty of Science, Graduate School of Chemical Sciences and Engineering, Hokkaido University)

  • Masaki Horie

    (Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University)

Abstract

Crystalline phase transitions caused by external stimuli have been used to detect physical changes in the solid-state properties. This study presents the mechanical switching of crystals of ferrocene-containing rotaxane controlled by focused laser light. The expansion and contraction of the crystals can be driven by turning on and off laser light at 445 nm. The irradiation-induced expansion of the crystal involves elongation along the a, b and c axes at 30 °C, whereas heating of the crystal at 105 °C causes the shortening of c axis. The expansions reversibly occur and have the advantage of a rapid relaxation (reverse) process. Single-crystal X-ray crystallography reveals the detailed structural changes of the molecules, corresponding to a change in the size of the crystals on laser irradiation. This molecular crystal behaviour induced by laser irradiation, is demonstrated for the remote control of objects, namely, microparticle transport and microswitching in an electric circuit.

Suggested Citation

  • Kai-Jen Chen & Ya-Ching Tsai & Yuji Suzaki & Kohtaro Osakada & Atsushi Miura & Masaki Horie, 2016. "Rapid and reversible photoinduced switching of a rotaxane crystal," Nature Communications, Nature, vol. 7(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13321
    DOI: 10.1038/ncomms13321
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