Remarkable Turn-On and Color-Tuned Piezochromic Luminescence: Mechanically Switching Intramolecular Charge Transfer in Molecular Crystals

The molecular crystals of acridonyl‐tetraphenylethene (AD‐TPE) exhibit an intriguing turn‐on and color‐tuned luminescence in response to mechanical grinding and hydrostatic compression. On the basis of in‐depth experimental and computational studies, it is hypothesized that the origin of the piezoch...

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Published inAdvanced functional materials Vol. 25; no. 26; pp. 4005 - 4010
Main Authors Qi, Qingkai, Qian, Jingyu, Tan, Xiao, Zhang, Jibo, Wang, Lijuan, Xu, Bin, Zou, Bo, Tian, Wenjing
Format Journal Article
LanguageEnglish
Published Blackwell Publishing Ltd 01.07.2015
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Abstract The molecular crystals of acridonyl‐tetraphenylethene (AD‐TPE) exhibit an intriguing turn‐on and color‐tuned luminescence in response to mechanical grinding and hydrostatic compression. On the basis of in‐depth experimental and computational studies, it is hypothesized that the origin of the piezochromic behavior from the D‐phase to the B‐phase is the change of the intramolecular geometrical conformation, especially for the torsion angle between the TPE and AD moiety. The different molecular conformation in the two distinctive solid phases causes the substantial switching of the intra­molecular charge transfer (ICT) process, which can be directly correlated with the subsequent fluorescence from locally excited (LE) state and ICT state in both phases. The AD‐TPE molecular system presents a very rare example of high‐contrast reversible fluorescence tuning driven by a switching of the excited state in the solid state under the mechanical stimuli, and thus provides a novel mechanism of the piezochromic behavior. Tuning the solid state luminescence of organic materials under mechanical stimuli is an attractive subject for both the fundamental research and practical application in the optical recording and sensing. Herein, a structurally well‐defined molecule, acridonyl‐tetraphenylethene is reported, whose molecular crystals exhibit an intriguing turn‐on and color‐tuned luminescence with high contrast in response to the mechanical stimuli such as grinding and hydrostatic pressure.
AbstractList The molecular crystals of acridonyl‐tetraphenylethene (AD‐TPE) exhibit an intriguing turn‐on and color‐tuned luminescence in response to mechanical grinding and hydrostatic compression. On the basis of in‐depth experimental and computational studies, it is hypothesized that the origin of the piezochromic behavior from the D‐phase to the B‐phase is the change of the intramolecular geometrical conformation, especially for the torsion angle between the TPE and AD moiety. The different molecular conformation in the two distinctive solid phases causes the substantial switching of the intra­molecular charge transfer (ICT) process, which can be directly correlated with the subsequent fluorescence from locally excited (LE) state and ICT state in both phases. The AD‐TPE molecular system presents a very rare example of high‐contrast reversible fluorescence tuning driven by a switching of the excited state in the solid state under the mechanical stimuli, and thus provides a novel mechanism of the piezochromic behavior. Tuning the solid state luminescence of organic materials under mechanical stimuli is an attractive subject for both the fundamental research and practical application in the optical recording and sensing. Herein, a structurally well‐defined molecule, acridonyl‐tetraphenylethene is reported, whose molecular crystals exhibit an intriguing turn‐on and color‐tuned luminescence with high contrast in response to the mechanical stimuli such as grinding and hydrostatic pressure.
The molecular crystals of acridonyl‐tetraphenylethene (AD‐TPE) exhibit an intriguing turn‐on and color‐tuned luminescence in response to mechanical grinding and hydrostatic compression. On the basis of in‐depth experimental and computational studies, it is hypothesized that the origin of the piezochromic behavior from the D‐phase to the B‐phase is the change of the intramolecular geometrical conformation, especially for the torsion angle between the TPE and AD moiety. The different molecular conformation in the two distinctive solid phases causes the substantial switching of the intra­molecular charge transfer (ICT) process, which can be directly correlated with the subsequent fluorescence from locally excited (LE) state and ICT state in both phases. The AD‐TPE molecular system presents a very rare example of high‐contrast reversible fluorescence tuning driven by a switching of the excited state in the solid state under the mechanical stimuli, and thus provides a novel mechanism of the piezochromic behavior.
The molecular crystals of acridonyl-tetraphenylethene (AD-TPE) exhibit an intriguing turn-on and color-tuned luminescence in response to mechanical grinding and hydrostatic compression. On the basis of in-depth experimental and computational studies, it is hypothesized that the origin of the piezochromic behavior from the D-phase to the B-phase is the change of the intramolecular geometrical conformation, especially for the torsion angle between the TPE and AD moiety. The different molecular conformation in the two distinctive solid phases causes the substantial switching of the intra-molecular charge transfer (ICT) process, which can be directly correlated with the subsequent fluorescence from locally excited (LE) state and ICT state in both phases. The AD-TPE molecular system presents a very rare example of high-contrast reversible fluorescence tuning driven by a switching of the excited state in the solid state under the mechanical stimuli, and thus provides a novel mechanism of the piezochromic behavior. Tuning the solid state luminescence of organic materials under mechanical stimuli is an attractive subject for both the fundamental research and practical application in the optical recording and sensing. Herein, a structurally well-defined molecule, acridonyl-tetraphenylethene is reported, whose molecular crystals exhibit an intriguing turn-on and color-tuned luminescence with high contrast in response to the mechanical stimuli such as grinding and hydrostatic pressure.
Author Xu, Bin
Tan, Xiao
Zou, Bo
Tian, Wenjing
Zhang, Jibo
Qian, Jingyu
Qi, Qingkai
Wang, Lijuan
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– sequence: 2
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  organization: State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry Jilin University, 130012, Changchun, P. R. China
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  surname: Tan
  fullname: Tan, Xiao
  organization: State Key Laboratory of Superhard Materials, Jilin University, 130012, Changchun, P. R. China
– sequence: 4
  givenname: Jibo
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  fullname: Zhang, Jibo
  organization: State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry Jilin University, 130012, Changchun, P. R. China
– sequence: 5
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  organization: State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry Jilin University, 130012, Changchun, P. R. China
– sequence: 6
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  email: xubin@jlu.edu.cn
  organization: State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry Jilin University, 130012, Changchun, P. R. China
– sequence: 7
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  organization: State Key Laboratory of Superhard Materials, Jilin University, 130012, Changchun, P. R. China
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  givenname: Wenjing
  surname: Tian
  fullname: Tian, Wenjing
  email: xubin@jlu.edu.cn
  organization: State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry Jilin University, 130012, Changchun, P. R. China
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Snippet The molecular crystals of acridonyl‐tetraphenylethene (AD‐TPE) exhibit an intriguing turn‐on and color‐tuned luminescence in response to mechanical grinding...
The molecular crystals of acridonyl-tetraphenylethene (AD-TPE) exhibit an intriguing turn-on and color-tuned luminescence in response to mechanical grinding...
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SubjectTerms Charge transfer
Crystals
Excitation
Fluorescence
high contrast
ICT switch
Luminescence
mechanical stimuli
molecular crystals
piezochromic luminescence
Stimuli
Switching
Tuning
Title Remarkable Turn-On and Color-Tuned Piezochromic Luminescence: Mechanically Switching Intramolecular Charge Transfer in Molecular Crystals
URI https://api.istex.fr/ark:/67375/WNG-80TFV6CW-8/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadfm.201501224
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