Lighting Up Nonemissive Azobenzene Derivatives by Pressure

Pressure-induced emission (PIE) is a compelling phenomenon that can activate luminescence within nonemissive materials. However, PIE in nonemissive organic materials has never been achieved. Herein, we present the first observation of PIE in an organic system, specifically within nonemissive azobenzene derivatives. The emission of 1,2-bis(4-(anthracen-9-yl)phenyl)diazene was activated at 0.52 GPa, primarily driven by local excitation promotion induced by molecular conformational changes. Complete photoisomerization suppression of the molecule was observed at 1.5 GPa, concurrently accelerating the emission enhancement to 3.53 GPa. Differing from the key role of isomerization inhibition in conventional perception, our findings demonstrate that the excited-state constituent is the decisive factor for emission activation, providing a potentially universal approach for high-efficiency azobenzene emission. Additionally, PIE was replicated in the analogue 1,2-bis(4-(9<i>H</i>-carbazol-9-yl)phenyl)diazene, confirming the general applicability of our findings. This work marks a significant breakthrough within the PIE paradigm and paves the novel high-pressure route for crystalline-state photoisomerization investigation.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-09-16
DOI
https://doi.org/10.1021/jacs.4c09784
Citations
17
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
1.99

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article

Lighting Up Nonemissive Azobenzene Derivatives by Pressure

Haiyan Li, Dong Yao, Mingguang Yao, Shuhe Hu et al.
17 citations
Journal of the American Chemical Society
Luminescence and Fluorescent Materials
1.99
article

Lighting Up Nonemissive Azobenzene Derivatives by Pressure

Haiyan Li, Dong Yao, Mingguang Yao, Shuhe Hu, Bo Zou, Ruiyang Zhao, Min Wu, Jiahui Mu, Yuguang Ma, Ran Liu, Haichao Liu, Qiuyan Cen, Guangtian Zou, Long Lv, Xiu Yin, Yuye Yan, Shuang Liu
article en
17 citations

Abstract

Pressure-induced emission (PIE) is a compelling phenomenon that can activate luminescence within nonemissive materials. However, PIE in nonemissive organic materials has never been achieved. Herein, we present the first observation of PIE in an organic system, specifically within nonemissive azobenzene derivatives. The emission of 1,2-bis(4-(anthracen-9-yl)phenyl)diazene was activated at 0.52 GPa, primarily driven by local excitation promotion induced by molecular conformational changes. Complete photoisomerization suppression of the molecule was observed at 1.5 GPa, concurrently accelerating the emission enhancement to 3.53 GPa. Differing from the key role of isomerization inhibition in conventional perception, our findings demonstrate that the excited-state constituent is the decisive factor for emission activation, providing a potentially universal approach for high-efficiency azobenzene emission. Additionally, PIE was replicated in the analogue 1,2-bis(4-(9<i>H</i>-carbazol-9-yl)phenyl)diazene, confirming the general applicability of our findings. This work marks a significant breakthrough within the PIE paradigm and paves the novel high-pressure route for crystalline-state photoisomerization investigation.

Journal of the American Chemical SocietyVol. 146(42)
Qingdao University of Science and Technology (CN), Jilin University (CN), Liaocheng University (CN), State Key Laboratory of Supramolecular Structure and Materials, State Key Laboratory of High Pressure and Superhard Materials (CN), South China University of Technology (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Affordable and clean energy
Openalex Percentile: Top 9%
Luminescence and Fluorescent Materials
1.99
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