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Design amphiphilic dipolar π-systems for stimuli-responsive luminescent materials using metastable states

Author

Listed:
  • Shiki Yagai

    (Graduate School of Engineering, Chiba University
    Japan Science and Technology Agency (JST), Core Research for Evolutional Science and Technology (CREST))

  • Satoru Okamura

    (Graduate School of Engineering, Chiba University)

  • Yujiro Nakano

    (Graduate School of Engineering, Chiba University)

  • Mitsuaki Yamauchi

    (Graduate School of Engineering, Chiba University)

  • Keiki Kishikawa

    (Graduate School of Engineering, Chiba University)

  • Takashi Karatsu

    (Graduate School of Engineering, Chiba University)

  • Akihide Kitamura

    (Graduate School of Engineering, Chiba University)

  • Akira Ueno

    (Microjet Corporation)

  • Daiki Kuzuhara

    (Graduate School of Material Science, Nara Institute of Science and Technology (NAIST))

  • Hiroko Yamada

    (Japan Science and Technology Agency (JST), Core Research for Evolutional Science and Technology (CREST)
    Graduate School of Material Science, Nara Institute of Science and Technology (NAIST))

  • Tomohiro Seki

    (Graduate School of Engineering, Hokkaido University)

  • Hajime Ito

    (Graduate School of Engineering, Hokkaido University)

Abstract

π-Conjugated compounds that exhibit tunable luminescence in the solid state under external mechanical stimuli have potential applications in sensors and imaging devices. However, no rational designs have been proposed that impart these mechano-responsive luminescent properties to π-conjugated compounds. Here we demonstrate a strategy for mechano-responsive luminescent materials by imparting amphiphilic and dipolar characteristics to a luminescent π-conjugated system. The oligo(p-phenylenevinylene) luminophore with a didodecylamino group at one end and a tri(ethylene glycol) ester group at the other end yields segregated solid structures by separately aggregating its hydrophobic and hydrophilic moieties. The segregated structures force the molecules to align in the same direction, thereby generating a conflict between the side-chain aggregation and dipolar stabilization of the π-system. Consequently, these metastable solid structures can be transformed through mechanical stimulation to a more stable structure, from a π–π stacked aggregate to a liquid crystal and further to a crystalline phase with variable luminescence.

Suggested Citation

  • Shiki Yagai & Satoru Okamura & Yujiro Nakano & Mitsuaki Yamauchi & Keiki Kishikawa & Takashi Karatsu & Akihide Kitamura & Akira Ueno & Daiki Kuzuhara & Hiroko Yamada & Tomohiro Seki & Hajime Ito, 2014. "Design amphiphilic dipolar π-systems for stimuli-responsive luminescent materials using metastable states," Nature Communications, Nature, vol. 5(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms5013
    DOI: 10.1038/ncomms5013
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    Cited by:

    1. Shuang Tong & Jianhong Dai & Jiangman Sun & Yuanyuan Liu & Xiaoli Ma & Zhehong Liu & Teng Ma & Jiao Tan & Zhen Yao & Shanmin Wang & Haiyan Zheng & Kai Wang & Fang Hong & Xiaohui Yu & Chunxiao Gao & Xi, 2022. "Fluorescence-based monitoring of the pressure-induced aggregation microenvironment evolution for an AIEgen under multiple excitation channels," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    2. Dan Li & Yujie Yang & Jie Yang & Manman Fang & Ben Zhong Tang & Zhen Li, 2022. "Completely aqueous processable stimulus responsive organic room temperature phosphorescence materials with tunable afterglow color," Nature Communications, Nature, vol. 13(1), pages 1-8, December.

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