Acta Chim. Sinica ›› 2016, Vol. 74 ›› Issue (4): 351-355.DOI: 10.6023/A16010001 Previous Articles     Next Articles


取代基效应对喹啉腈AIE荧光性能的研究 2016 Awarded

夏志清, 邵安东, 李强, 朱世琴, 朱为宏   

  1. 华东理工大学精细化工研究所 科技信息研究所 上海 200237
  • 投稿日期:2016-01-03 发布日期:2016-03-03
  • 通讯作者: 朱为宏
  • 基金资助:

    项目受国家自然科学基金(No. 21325625, 21476076)资助.

Substituent Effect on Quinoline-Malononitrile AIE Fluorescent Properties

Xia Zhiqing, Shao Andong, Li Qiang, Zhu Shiqin, Zhu Weihong   

  1. Institute of Fine Chemicals, Institute of Science and Technology Information, East China University of Science & Technology, Shanghai 200237
  • Received:2016-01-03 Published:2016-03-03
  • Supported by:

    Project supported by the National Natural Science Foundation of China (Nos. 21325625, 21476076).

As well-known, traditional luminescent dyes such as dicyanomethylene-4H-pyran (DCM) luminogens used in biological diagnosis and therapy still exit several limitations due to their inherent molecular structures. One of the most notorious phenomena is "aggregation caused quenching" (ACQ), namely that the fluorescence can be easily observed in dilute solution, but quenched in high concentration or aggregated state. Therefore, how to understand the aggregation environment formed by dye molecules and further utilize the aggregate itself as a potential pattern for biomedical application is highly desirable. Since the intriguing discovery of the aggregation-induced emission (AIE) phenomenon, much effort has been paid to exploration of AIE systems and their applications. These AIE chromophores exhibit highly bright fluorescence when aggregated, and weak fluorescence when dissolved in solution, making them beneficial for improving the sensitivity of biosensors and bioimaging in situ or in vivo. Herein we set out to construct a novel AIE-active quinoline-malononitrile (QM) building block, by merely replacing the oxygen atom in DCM moiety with N-ethyl group, thoroughly solving the fluorescence quenching problems of DCM derivatives in aggregation. Five QM derivatives (QM-H, QM-F, QM-Br, QM-I and QM-N) with different substituent groups have been successfully synthesized by Knoevenagel reaction, extending the AIE wavelength from 528 to 614 nm in the aggregated state. A series of experiments were performed to examine the photoluminescence properties of QM-H, QM-F, QM-Br, QM-I and QM-N. As expected, all these AIE-active compounds show weak or no fluorescence in molecular state when dissolved in THF solution, but enhanced emission in solid or aggregate state along with an increasing volume fraction of water in tetrahydrofuran/water (THF/H2O) mixtures. Moreover, their AIE-active fluorescent properties are dependent upon the different aggregated microenvironment affected by substituent groups of QM derivatives. Notably, the halogen atoms of QM-F, QM-Br and QM-I play important role in AIE quantum yield, while introducing electron donor group shifts the solid fluorescence of QM-N into red emission. The substituent effect of QM derivatives with excellent AIE properties can provide a platform to develop NIR AIE materials.

Key words: aggregation-induced emission, quinoline-malononitrile, substituent effect, luminescent quantum yield