Photoexcitation‐Induced Chiral Self‐Assembly for Phosphorescence‐to‐Thermally Activated Delayed Fluorescence Transformation

Phosphorescence and thermally activated delayed fluorescence are currently two important photophysical pathways that have greatly promoted the development of display, sensing, and bioimaging. However, achieving in situ conversion of these two photophysical pathways within the same molecule is extremely challenging. In this study, we covalently bond chiral donor-acceptor-donor' structures into a photoexcitation-induced aggregated molecule, specifically hexathiobenzene, to achieve this goal through light irradiation. Initially, the target molecules predominantly exhibit phosphorescent properties. Upon photoirradiation, chiral self-assembly occurs within the target molecules, which gives rise to a thermally activated delayed fluorescence (TADF)-dominant emission behavior. This TADF emission relies on a self-assembly structure that can effectively prevent oxygen from quenching triplet excitons, resulting in stronger signal intensity and longer photoluminescence lifetime. Consequently, a real time improvement of time-resolved bioimaging can be achieved with the utilization of our strategy, rendering selectively dynamic control of imaging parameters at the desired time- and spatial resolution.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-10-29
DOI
https://doi.org/10.1002/anie.202516591
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Photoexcitation‐Induced Chiral Self‐Assembly for Phosphorescence‐to‐Thermally Activated Delayed Fluorescence Transformation

Danfeng Ye, Yunhui Wan, Shan Li, Ziran Tang et al.
Angewandte Chemie International Edition
Luminescence and Fluorescent Materials
article

Photoexcitation‐Induced Chiral Self‐Assembly for Phosphorescence‐to‐Thermally Activated Delayed Fluorescence Transformation

Danfeng Ye, Yunhui Wan, Shan Li, Ziran Tang, Smruti Ranjan Sahoo, Hans Ågren, Zhensheng Tao, Glib Baryshnikov, Haiyan Yang, Xudong Wang, Yulong Shi, Rui Jiang, Liangliang Zhu
article en

Abstract

Phosphorescence and thermally activated delayed fluorescence are currently two important photophysical pathways that have greatly promoted the development of display, sensing, and bioimaging. However, achieving in situ conversion of these two photophysical pathways within the same molecule is extremely challenging. In this study, we covalently bond chiral donor-acceptor-donor' structures into a photoexcitation-induced aggregated molecule, specifically hexathiobenzene, to achieve this goal through light irradiation. Initially, the target molecules predominantly exhibit phosphorescent properties. Upon photoirradiation, chiral self-assembly occurs within the target molecules, which gives rise to a thermally activated delayed fluorescence (TADF)-dominant emission behavior. This TADF emission relies on a self-assembly structure that can effectively prevent oxygen from quenching triplet excitons, resulting in stronger signal intensity and longer photoluminescence lifetime. Consequently, a real time improvement of time-resolved bioimaging can be achieved with the utilization of our strategy, rendering selectively dynamic control of imaging parameters at the desired time- and spatial resolution.

Angewandte Chemie International EditionVol. 64(52)
Linköping University (SE), Ningbo University (CN), Wrocław University of Science and Technology (PL), Uppsala University (SE), Ningbo University of Technology (CN), Shenzhen University (CN), Fudan University (CN), First People's Hospital of Yunnan Province (CN), State Key Laboratory of Surface Physics, AGH University of Krakow (PL)
European Commission, National Science Council, Linköpings Universitet, Vetenskapsrådet, Tianjin University, National Supercomputer Centre, Linköpings Universitet
Openalex Percentile: Top 75%
Luminescence and Fluorescent Materials
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