Utilizing d–pπ Bonds for Ultralong Organic Phosphorescence

  • Shuai Tian
  • , Huili Ma
  • , Xuan Wang
  • , Anqi Lv
  • , Huifang Shi
  • , Yun Geng
  • , Jie Li
  • , Fushun Liang
  • , Zhong Min Su
  • , Zhongfu An
  • , Wei Huang

Research output: Contribution to journalArticlepeer-review

186 Scopus citations

Abstract

Developing pure organic materials with ultralong lifetimes is attractive but challenging. Here we report a concise chemical approach to regulate the electronic configuration for phosphorescence enhancement. After the introduction of d–pπ bonds into a phenothiazine model system, a phosphorescence lifetime enhancement of up to 19 times was observed for DOPPMO, compared to the reference PPMO. A record phosphorescence lifetime of up to 876 ms was obtained in phosphorescent phenothiazine. Theoretical calculations and single-crystal analysis reveal that the d–pπ bond not only reduces the (n, π*) proportion of the T1 state, but also endows the rigid molecular environment with multiple intermolecular interactions, thus enabling long-lived phosphorescence. This finding makes a valuable contribution to the prolongation of phosphorescence lifetimes and the extension of the scope of phosphorescent materials.

Original languageEnglish
Pages (from-to)6645-6649
Number of pages5
JournalAngewandte Chemie - International Edition
Volume58
Issue number20
DOIs
StatePublished - 13 May 2019

Keywords

  • crystal engineering
  • d–pπ bonds
  • excited states
  • organic phosphorescence
  • phenothiazines

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