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Polyyne bridged AIE luminogens with red emission: design, synthesis, properties and applications

  • Zheng Zhao
  • , Huifang Su
  • , Pengfei Zhang
  • , Yuanjing Cai
  • , Ryan T.K. Kwok
  • , Yuncong Chen
  • , Zikai He
  • , Xinggui Gu
  • , Xuewen He
  • , Herman H.Y. Sung
  • , Ian D. Willimas
  • , Jacky W.Y. Lam
  • , Zhenfeng Zhang*
  • , Ben Zhong Tang
  • *Corresponding author for this work

Research output: Contribution to journal › Journal Article › peer-review

Abstract

Construction of a donor-acceptor (D-A) structure and extension of π-conjugation are the commonly used strategies to shift the emission of luminophores to the red region. However, molecules with high conjugation and a strong D-A effect tend to show weak emission due to the severe π-π interactions and twisted intramolecular charge transfer (TICT) effects. The turn-on characteristic of AIE luminogens (AIEgens) will also be lost due to the conjugation-enhanced emission in the solution state. Herein, a polyyne-bridged AIE luminogen (2TPE-4E) with long wavelength absorption and red emission has been afforded. Despite its large π-conjugation, 2TPE-4E suffers from no emission quenching resulted from strong π-π interactions and twisted intramolecular charge transfer effects. The strong red emission and the high photostability of 2TPE-4E inspired us to use it for targeted-imaging of cancer cells and monitoring the receptor mediated endocytosis process.

Original languageEnglish
Pages (from-to)1650-1657
Number of pages8
JournalJournal of Materials Chemistry B
Volume5
Issue number8
DOIs
Publication statusPublished - 2017

Bibliographical note

Publisher Copyright:
© The Royal Society of Chemistry.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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