4.8 Article

Halogen Bond-Driven Aggregation-Induced Emission Skeleton: N-(3-(Phenylamino)allylidene) Aniline Hydrochloride

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 15, Issue 7, Pages 9751-9763

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c21073

Keywords

AIEgens; molecular skeleton; fluorescence; halogen bond; luminescent substances; self-assembly; luminescent film; light-emitting diodes

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Aggregation-induced emission (AIE) is a unique phenomenon that revolutionizes luminescence. However, the research on AIE has been limited to a few molecular structures, hindering in-depth studies and exploitation of their potential values. In this study, a novel dumbbell AIE skeleton is reported, which overcomes the challenges of difficult modification and low luminous efficiency. The skeleton exhibits strong solid-state emission and diverse modification possibilities, making it applicable in various scenarios.
Aggregation-induced emission (AIE) is a unique photophysical process, and its emergence brings a revolutionary change in luminescence. However, AIE-based research has been limited to a few classical molecular skeletons, which is unfavorable for in-depth studies of the photophysical characteristics of AIE and the full exploitation of their potential values. There is an urgent need to develop new skeletons to rise to the challenges of an insufficient number of AIE core structures and difficult modification. Here, we report a novel dumbbell AIE skeleton, in which two phenyls are connected through (E)-3-iminoprop-1-en-1-amine. This skeleton shows extremely strong solid-state emission with an absolute quantum yield up to 69.5%, a large Stokes shift, and typical AIE characteristics, which well resolves the challenge of difficult modification and low luminous efficiency of the traditional AIE skeletons. One-step reaction, high yield, and diversified modification endow the skeleton with great scalability from simple to complicated, or from symmetrical to asymmetrical structures, which establishes the applicability of the skeleton in various scenarios. These molecules self-assemble into highly ordered layer-, rod-, petal-, hollow pipe-, or helix-like nanostructures, which contribute to strong AIE emission. Crystallographic data reveal the highly ordered layer structures of the aggregates with different substituents, and a novel halogen bond-driven self-assembly mechanism that restricts intramolecular motion is clearly discovered. Taking advantage of these merits, a full-band emission system from green to red is successfully established, which displays great potential in the construction of light-emitting films and advanced light-emitting diodes. The discovery of this AIE skeleton may motivate a huge potential application value in luminescent materials and lead to hitherto impossible technological innovations.

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