Organic materials exhibiting mechanoluminescence (ML) are promising for usage in displays, lighting and sensing. However, the mechanism for ML generation remains unclear, and the light-emitting performance of organic ML materials in the solid state has been severely limited by an aggregation-caused quenching (ACQ) effect. Herein, we present two strongly photoluminescent polymorphs (i.e., C g and C b) with distinctly different ML activities based on a tetraphenylethene derivative P 4 TA. As an aggregation-induced emission (AIE) emitter, P 4 TA perfectly surmounted the ACQ, making the resultant block-like crystals in the C g phase exhibit brilliant green ML under daylight at room temperature. The ML-inactive prism-like crystals C b can also have their ML turned on by transitioning toward C g with the aid of dichloromethane vapor. Moreover, the C g polymorph shows ML and mechanochromism simultaneously and respectively without and with UV irradiation under a force stimulus, thus suggesting a feasible design direction for the development of efficient and multifunctional ML materials.
CITATION STYLE
Xu, B., He, J., Mu, Y., Zhu, Q., Wu, S., Wang, Y., … Xu, J. (2015). Very bright mechanoluminescence and remarkable mechanochromism using a tetraphenylethene derivative with aggregation-induced emission. Chemical Science, 6(5), 3236–3241. https://doi.org/10.1039/c5sc00466g
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