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One-Step Multicomponent Polymerizations for the Synthesis of Multifunctional AIE Polymers

Journal

MACROMOLECULAR RAPID COMMUNICATIONS
Volume 42, Issue 6, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.202000471

Keywords

aggregation-induced emission; functional polymers; multicomponent polymerization

Funding

  1. National Natural Science Foundation of China [21905176, 21788102]
  2. Research Grants Council of Hong Kong [C6009-17G]
  3. Innovation of Technology Commission [ITC-CNERC14SC01]
  4. National Key Research and Development Program of China [2018YFE0190200]
  5. Science and Technology Plan of Shenzhen [JCYJ20190808142403590]

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AIE polymers, as a new class of functional luminescent materials, have attracted much attention for their efficient solid-state fluorescence, excellent processability, and multifunctionalities. Among various methods for preparing AIE polymers, multicomponent polymerizations (MCPs) stand out for their simplicity, high atom economy, good polymerization efficiency, and broad functional-group tolerance. This feature article highlights the recent progress in one-step MCPs for the synthesis of AIE polymers and discusses the challenges and future development directions in this field.
As a new class of functional luminescent materials, polymers with aggregation-induced emission (AIE) feature attract much attention because of their advantages of efficient solid-state fluorescence, excellent processability, structural diversity, and multifunctionalities. Among all polymerization methods toward AIE polymers, multicomponent polymerizations (MCPs) exhibit the merits of simple operation, good atom economy, high polymerization efficiency, broad functional-group tolerance, etc. In this feature article, the recent progress on the development of one-step MCPs for the synthesis of AIE polymers is highlighted. The representative functionalities of the resulting AIE polymers are illustrated. Perspectives on the challenges and future development directions of this field are also discussed.

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