材料科学
分子内力
发光
部分
激发态
光电子学
化学物理
光化学
相(物质)
光学
荧光
立体化学
有机化学
原子物理学
物理
化学
作者
Qingkai Qi,Jingyu Qian,Xiao Tan,Jibo Zhang,Lijuan Wang,Bin Xu,Bo Zou,Wenjing Tian
标识
DOI:10.1002/adfm.201501224
摘要
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.
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