Shi Heng, Chen Hongjin, Li Xiangguo, Xing Jieni, Zhang Gang, Zhang Rui, Liu Jian
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Jiangsu Key Lab of Biomass-based Green Fuels and Chemicals, College of Chemical Engineering, Nanjing Forestry University Nanjing 210037 China
RSC Adv. 2020 Dec 21;11(1):1-6. doi: 10.1039/d0ra06782b.
Two colorimetric and ratiometric fluoride ion probes SHJ-1 and SHJ-2 based on the acylhydrazone skeleton have been developed. Among the eight anions (F, Cl, Br, I, ClO , HPO , HSO , CHCOO), the present probes showed high selectivity and sensitivity toward fluoride ion detection with obvious color change. Notably, the probe SHJ-1 exhibited a red shift of 145 nm upon fluoride sensing, which is the largest value among fluoride ion probes based on acylhydrazone derivates to date. HNMR titration study and theoretical calculations suggested that the strong binding of the probe SHJ-1 to fluoride as well as the further deprotonation may facilitate the intramolecular charge transfer transition. These two probes are 1 : 1 complexed with fluoride ions, and the detection limits were calculated to be 1.24 μM for SHJ-1 and 15.73 μM for SHJ-2.
基于酰腙骨架的两种比色和比率型氟离子探针SHJ-1和SHJ-2已被开发出来。在八种阴离子(F、Cl、Br、I、ClO 、HPO 、HSO 、CHCOO)中,目前的探针在氟离子检测方面表现出高选择性和灵敏度,伴有明显的颜色变化。值得注意的是,探针SHJ-1在氟离子传感时表现出145 nm的红移,这是迄今为止基于酰腙衍生物的氟离子探针中的最大值。核磁共振氢谱滴定研究和理论计算表明,探针SHJ-1与氟离子的强结合以及进一步的去质子化可能促进分子内电荷转移跃迁。这两种探针与氟离子形成1:1配合物,计算得出SHJ-1的检测限为1.24 μM,SHJ-2的检测限为15.73 μM。