分子内力
分子间力
戒指(化学)
荧光
光化学
氢键
荧光光谱法
光谱学
材料科学
化学
立体化学
有机化学
光学
分子
量子力学
物理
作者
Nan Li,Yarong Gu,Yaping Chen,Long Zhang,Qing‐Xin Zeng,Ting Geng,Lianwei Wu,Lina Jiang,Guanjun Xiao,Kai Wang,Bo Zou
标识
DOI:10.1021/acs.jpcc.9b00670
摘要
Pressure-induced emission enhancement (PIEE) is a new phenomenon that has attracted widespread attention in the past few years for improving the solid-state emission efficiency of fluorophores. However, a thorny issue still remains in the study of PIEE. Thus, it is urgent and important to discover and design more PIEE systems for further enhancing the efficiency. In this paper, we found that triphenylethylene (TriPE) showed both conspicuous emission enhancement within the pressure range of 0.0–0.8 GPa and piezochromism behavior upon compression. More interestingly, infrared (IR) analysis indicated that ring-opening reaction of the phenyl ring occurred when pressure was beyond 14.2 GPa. Also, the ring-opening reaction of the phenyl ring led to irreversible optical changes. In situ high-pressure IR spectroscopy and angle-dispersive X-ray diffraction analysis demonstrated that the PIEE of TriPE was attributed to the related C–H···π and C–H···C hydrogen bonds that could inhibit or restrict the movement of aromatic parts remarkably, restraining the energy loss by intramolecular motion. Our study provides insights into the significant effect of intermolecular interactions on fluorescence emission properties.
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