Tang Lei, Wang Jiaoyun, Liu Yuan
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China.
Molecules. 2025 Feb 14;30(4):879. doi: 10.3390/molecules30040879.
A novel fluoride ion fluorescent probe is designed by introducing the strong electron-withdrawing triazine groups into the triarylboron/acridine conjugation system. The A-D-A' molecular configuration endows this molecule with multiple charge-transfer channels; upon reaction with F, the triazine groups act as primary acceptors within the molecule, facilitating charge transfer between the acridine units and the triazine groups. During fluoride ion detection, changes in the triarylboron moiety lead to a significant bathochromic-shift in fluorescence emission from green to yellow. Theoretical calculations attribute this phenomenon to a reduction in the molecular state energy level upon fluorination, resulting in a pronounced visible color change and chromogenic response during detection. Based on fluorescence intensity changes with varying degrees of F coordination, a detection limit as low as 10 M was determined for TB-1DMAc-2TRZ, demonstrating the high sensitivity of this probe.
通过将强吸电子的三嗪基团引入三芳基硼/吖啶共轭体系,设计了一种新型氟离子荧光探针。A-D-A'分子构型赋予该分子多个电荷转移通道;与F反应时,三嗪基团作为分子内的主要受体,促进吖啶单元与三嗪基团之间的电荷转移。在氟离子检测过程中,三芳基硼部分的变化导致荧光发射从绿色到黄色发生显著的红移。理论计算将此现象归因于氟化后分子态能级的降低,导致检测过程中出现明显的可见颜色变化和显色响应。基于不同程度F配位时荧光强度的变化,确定TB-1DMAc-2TRZ的检测限低至10 M,证明了该探针的高灵敏度。