TY - JOUR
T1 - Pyrazine-Based Chiral AIE Electronic Acceptors for Real-Time Monitoring Hierarchical Self-Assembly and Tuning Emissions through Intermolecular Charge-Transfer Effects
AU - He, Xiang
AU - Xie, Meizhu
AU - Hong, Yingjuan
AU - Zheng, Canze
AU - Deng, Xin
AU - Qiu, Siyuan
AU - Li, Kai
AU - Chen, Ming
AU - Tang, Ben Zhong
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/1/14
Y1 - 2025/1/14
N2 - Development of chiral aggregation-induced emission (AIE) materials toward hierarchical self-assembly is crucial to reveal the origin and evolution of life. In this work, a pair of chiral AIE enantiomers is fabricated by attaching the typical AIE units to the chiral binaphthyl core via a single bond linkage. The AIE behavior is inherited from the introduced AIE unit while the binaphthyl unit can not only improve the photo-physical properties but also provide the whole molecules with chirality. Moreover, as driven by the dipolar structure and chirality of the AIEgens, the hierarchical self-assembly with different morphologies such as spheres, ribbons or fibers, flowers, and even bigger structures with various sizes can be dynamically monitored with the assembled time, which provided a favorable evidence to study the structural evolution from molecular level to a higher-level structure. On the other hand, these AIEgens can act strong electronic acceptors due to the introduced AIE unit. By complexing them with strong electronic donors, the resulting intermolecular charge transfer can induce remarkable red emissions with the tunable properties which is much different from their individuals. This enabled it as a facile, economic, and flexible approach to develop organic photoelectric materials.
AB - Development of chiral aggregation-induced emission (AIE) materials toward hierarchical self-assembly is crucial to reveal the origin and evolution of life. In this work, a pair of chiral AIE enantiomers is fabricated by attaching the typical AIE units to the chiral binaphthyl core via a single bond linkage. The AIE behavior is inherited from the introduced AIE unit while the binaphthyl unit can not only improve the photo-physical properties but also provide the whole molecules with chirality. Moreover, as driven by the dipolar structure and chirality of the AIEgens, the hierarchical self-assembly with different morphologies such as spheres, ribbons or fibers, flowers, and even bigger structures with various sizes can be dynamically monitored with the assembled time, which provided a favorable evidence to study the structural evolution from molecular level to a higher-level structure. On the other hand, these AIEgens can act strong electronic acceptors due to the introduced AIE unit. By complexing them with strong electronic donors, the resulting intermolecular charge transfer can induce remarkable red emissions with the tunable properties which is much different from their individuals. This enabled it as a facile, economic, and flexible approach to develop organic photoelectric materials.
KW - aggregation-induced emission
KW - chirality
KW - electronic acceptor
KW - intermolecular charge transfer
KW - self-assembly
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001324771200001
UR - https://www.scopus.com/pages/publications/85205497568
U2 - 10.1002/adom.202402037
DO - 10.1002/adom.202402037
M3 - Journal Article
SN - 2195-1071
VL - 13
JO - Advanced Optical Materials
JF - Advanced Optical Materials
IS - 2
M1 - 2402037
ER -