ArticleChemical science2019
Polymorph selectivity of an AIE luminogen under nano-confinement to visualize polymer microstructures.
Article in Chemical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Mechanically Twisting-Induced Top-Down Chirality Transfer for Tunable Full-Color Circularly Polarized Luminescent Fibers.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Chiral assembly of organic luminogens with aggregation-induced emission.Chemical science · 2022Review
- Solid-state intramolecular motions in continuous fibers driven by ambient humidity for fluorescent sensors.National science review · 2021Article
- Functional Polymer Systems with Aggregation-Induced Emission and Stimuli Responses.Topics in current chemistry (Cham) · 2021Review
- The endeavor of vibration-induced emission (VIE) for dynamic emissions.Chemical science · 2020Review
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Despite the huge progress of luminescent molecular assemblies over the past decade, it is still challenging to understand their confined behavior in semi-crystalline polymers for constrained space recognition. Here, we report a polymorphic luminogen with aggregation-induced emission (AIE), capable of selective growth in polymer amorphous and crystalline phases with distinct color. The polymorphic behaviors of the AIE luminogen embedded within the polymer network are dependent on the size of nano-confinement: a thermodynamically stable polymorph of the AIE luminogen with green emission is stabilized in the amorphous phase, while a metastable polymorph with yellow emission is confined in the crystalline phase. The information on polymer crystalline and amorphous phases is transformed into distinct fluorescence colors, allowing a single AIE luminogen as a fluorescent marker for visualization of polymer microstructures in terms of amorphous and crystalline phase distribution, quantitative polymer crystallinity measurement, and spatial morphological arrangement. Our findings demonstrate that confinement of the AIE luminogen in the polymer network can achieve free space recognition and also provide a correlation between microscopic morphologies and macroscopic optical signals. We envision that our strategy will inspire the development of other materials with spatial confinement to incorporate AIE luminogens for various applications.
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Registered trials
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