Difluoroboron β‐Diketonate Systems: Large Transformation of Photophysical Mechanism Induced by Tiny Structural Modification or Isomerization

Author:

Chen Xuefeng1,Wang Guangming1,Li Junbo1,Chen Xiuzheng1,Zhao Xiaoya1,Zeng Ying1,Su Yuming1,Zhang Kaka1ORCID

Affiliation:

1. Key Laboratory of Synthetic and Self‐Assembly Chemistry for Organic Functional Molecules Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences Chinese Academy of Sciences 345 Lingling Road Shanghai 200032 P. R. China

Abstract

AbstractLiving system involves a plenty of delicate processes where a tiny structural variation of biological substance may lead to drastic change of the fate of the living system. Inspired by this, in artificial photofunctional systems, if tiny structural variation changes the fate of excited states, a new class of advanced material would emerge for optical analysis, sensing, and next‐generation display is reasoned. However, such delicate processes remain rarely explored in photofunctional systems, especially in room temperature organic afterglow systems. Here the attachment/detachment of methoxy group can switch off/on twisted intramolecular charge transfer property in difluoroboron β‐diketonate systems is reported. In addition, structural isomerization triggers afterglow transformation from room temperature phosphorescence to thermally activated delayed fluorescence. These observations are helpful for better photophysical understanding on luminescence systems and advanced material design.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Ningbo Municipality

Publisher

Wiley

Subject

Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials

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