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Excited-state relaxation processes of three newly synthesized multi-branched alkyl-triphenylamine end-capped triazines

  • Xiang Li
  • , Zhiquan Wang
  • , Yuting Gao
  • , Zhengjun Shang
  • , Minghao Ni
  • , Jianli Hua
  • , Bo Li*
  • , Ye Chen
  • *此作品的通讯作者
  • East China Normal University
  • East China University of Science and Technology

科研成果: 期刊稿件文章同行评审

摘要

The excited-state relaxation processes of three newly synthesized multi-branched alkyl-triphenylamine end-capped triazines ATT-(1–3) are characterized in different solvents by steady-state and time-resolved spectroscopy. In toluene, a weakly polar solvent, the emission originates from the intramolecular charge transfer (ICT) state; in tetrahydrofuran (THF), a strongly polar solvent, the existence of a nonradiative channel from ICT to twisted intramolecular charge transfer (TICT) accelerates the relaxation rate of the ICT state. The rate of the evolution process of ATT-(1–3) increases with increasing number of donor branches, which could ascribed to enhancements in the electron donor and acceptor abilities of the triazines.

源语言英语
文章编号136800
期刊Chemical Physics Letters
736
DOI
出版状态已出版 - 12月 2019

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