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The Variance of Photophysical Properties of Tetraphenylethene and Its Derivatives During Their Transitions from Dissolved States to Solid States

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Publisher MDPI
Date 2022 Jul 27
PMID 35890656
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Abstract

The study of aggregation-induced emission luminogens (AIEgens) shows promising perspectives explored in lighting, optical sensors, and biological therapies. Due to their unique feature of intense emissions in aggregated solid states, it smoothly circumvents the weaknesses in fluorescent dyes, which include aggregation-caused quenching of emission and poor photobleaching character. However, our present knowledge of the AIE phenomena still cannot comprehensively explain the mechanism behind the substantially enhanced emission in their aggregated solid states. Herein, to systematically study the mechanism, the typical AIEgens tetraphenylethene (TPE) was chosen, to elucidate its photophysical properties, the TPE in THF/HO binary solvents, TPE in THF solvents depending on concentration, and the following direct conversion from a dissolved state to a precipitated solid state were analyzed. Moreover, the TPE derivatives were also investigated to supply more evidence to better decipher the generally optical behaviors of TPE and its derivatives. For instance, the TPE derivative was homogeneously dispersed into tetraethyl orthosilicate to monitor the variance of photophysical properties during sol-gel processing. Consequently, TPE and its derivatives are hypothesized to abide by the anti-Kasha rule in dissolved states. In addition, the factors primarily influencing the nonlinear emission shifting of TPE and its derivatives are also discussed.

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References
1.
Yang W, Ling B, Hu B, Yin H, Mao J, Walsh P . Synergistic N-Heterocyclic Carbene/Palladium-Catalyzed Umpolung 1,4-Addition of Aryl Iodides to Enals. Angew Chem Int Ed Engl. 2019; 59(1):161-166. DOI: 10.1002/anie.201912584. View

2.
Hu F, Xu S, Liu B . Photosensitizers with Aggregation-Induced Emission: Materials and Biomedical Applications. Adv Mater. 2018; 30(45):e1801350. DOI: 10.1002/adma.201801350. View

3.
Hu F, Mao D, Kenry , Cai X, Wu W, Kong D . A Light-Up Probe with Aggregation-Induced Emission for Real-Time Bio-orthogonal Tumor Labeling and Image-Guided Photodynamic Therapy. Angew Chem Int Ed Engl. 2018; 57(32):10182-10186. DOI: 10.1002/anie.201805446. View

4.
Peng Q, Ma H, Shuai Z . Theory of Long-Lived Room-Temperature Phosphorescence in Organic Aggregates. Acc Chem Res. 2020; 54(4):940-949. DOI: 10.1021/acs.accounts.0c00556. View

5.
Gao Y, Chang X, Liu X, Li Q, Cui G, Thiel W . Excited-State Decay Paths in Tetraphenylethene Derivatives. J Phys Chem A. 2017; 121(13):2572-2579. PMC: 5385518. DOI: 10.1021/acs.jpca.7b00197. View