4.8 Article

Enhancing the Operability of Photoexcitation-Controlled Aggregation-Induced Emissive Molecules in the Organic Phase

期刊

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 12, 期 26, 页码 6182-6189

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.1c01535

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资金

  1. NSFC [21975046, 21905075]
  2. China Postdoctoral Science Foundation [2020M682283]
  3. National Key Research and Development Program of China [2017YFA0207700]
  4. Shanghai Pujiang Program [20PJ1404500]
  5. Natural Science Foundation of Shanghai [20ZR1421700]
  6. Swedish Research Council [2018-05973, 2020-04600]
  7. Swedish National Infrastructure [SNIC 2020-3-29]

向作者/读者索取更多资源

This study investigates the control of photoexcitation-induced AIEgens using hexathiobenzene as a prototype phosphorescent group, exploring factors such as light intensity, dissolved oxygen content, and solvent polarity. An organogel strategy is developed to minimize interference factors and improve practical application ability, providing new insights for further development of functional materials based on photoexcitation.
Controllable aggregation-induced emission luminogens (AIEgens) by photoexcitation can be conducted within a single solvent, thus opening new opportunities for preparing and processing smart materials. However, undesired side-reactions like photooxidation that can easily occur in the organic phase remain, limiting their applications. To enhance the operability of photoexcitation-controlled AIEgens (to specifically produce a phosphorescence characteristic) in the organic phase, in this work, we employ a typical prototype, hexathiobenzene, usually as the specific phosphorescent group, and investigate a series of physical and chemical factors, such as light intensity, dissolved oxygen content, and solvent polarity, to explore ways to control the photoexcitation-controllable AIEgens against the impurities from side-reactions. An organogel strategy was also developed to minimize interference factors and improve the practical application ability. We believe that the presented results provide new insights into the further development of the photoexcitation-based functional materials and the promotion of their practical usage.

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