<p>In this work, an anthracene and triphenylamine functionalized <i>E</i>-cyanostilbene derivative (EN-TPA) was designed, synthesized and characterized. EN-TPA possessed excellent dual-state emission (DSE) property, possessing highly efficient emission both in solution and solid state. Meanwhile, the EN-TPA displayed obviously solvatochromic effect due to the intermolecular charge transfer, as confirmed by the Lippert–Mataga equation and quantum chemistry theoretical calculations. In aggregation state, EN-TPA was bright emissive with the solid fluorescence quantum yield (<i>Φ</i><sub><i>f</i></sub>) of 52.2%. Notably, the solid fluorescence of EN-TPA showed a 20&#xa0;nm red shift after grinding, accompanied by a 4-fold decrease in <i>Φ</i><sub><i>f</i></sub>, attributed to the transition of crystalline to amorphous phase under grinding. Leveraging the reversible mechanochromic, the storage paper device of EN-TPA was fabricated and exhibited a distinct fluorescence change from green to yellow upon mechanical stimulation. Single-crystal X-ray diffraction analysis revealed that the twisted molecular structure of EN-TPA inhibited the π-π stacking and induced the molecule to form loose packing arrangements to achieve bright solid emission and stimulus response property. This work provides a new perspective for designing high-performing DSE molecules.</p> Graphical abstract <p></p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Dual-state emission of anthracene and triphenylamine functionalized E-cyanostilbene derivative with mechanochromic property

  • Gaobin Zhang,
  • Shuyi Yao,
  • Mengjie Miao,
  • Jianli Yan,
  • Fangjie Chen,
  • Jiaxiang Yang

摘要

In this work, an anthracene and triphenylamine functionalized E-cyanostilbene derivative (EN-TPA) was designed, synthesized and characterized. EN-TPA possessed excellent dual-state emission (DSE) property, possessing highly efficient emission both in solution and solid state. Meanwhile, the EN-TPA displayed obviously solvatochromic effect due to the intermolecular charge transfer, as confirmed by the Lippert–Mataga equation and quantum chemistry theoretical calculations. In aggregation state, EN-TPA was bright emissive with the solid fluorescence quantum yield (Φf) of 52.2%. Notably, the solid fluorescence of EN-TPA showed a 20 nm red shift after grinding, accompanied by a 4-fold decrease in Φf, attributed to the transition of crystalline to amorphous phase under grinding. Leveraging the reversible mechanochromic, the storage paper device of EN-TPA was fabricated and exhibited a distinct fluorescence change from green to yellow upon mechanical stimulation. Single-crystal X-ray diffraction analysis revealed that the twisted molecular structure of EN-TPA inhibited the π-π stacking and induced the molecule to form loose packing arrangements to achieve bright solid emission and stimulus response property. This work provides a new perspective for designing high-performing DSE molecules.

Graphical abstract