Electron-Rich π-Extended Diindolotriazatruxene-Based Chemosensors with Highly Selective and Rapid Responses to Nitroaromatic Explosives

被引:6
|
作者
Li, Xiangchun [1 ]
Wang, Chunyu [1 ]
Song, Wan [1 ]
Meng, Cheng [1 ]
Zuo, Chao [1 ]
Xue, Yibo [1 ]
Lai, Wen-Yong [1 ,2 ]
Huang, Wei [1 ,2 ]
机构
[1] Nanjing Univ Posts & Telecommun, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, IAM, KLOEID, 9 Wenyuan Rd, Nanjing 210023, Jiangsu, Peoples R China
[2] NPU, SIFE, 127 West Youyi Rd, Xian 710072, Shaanxi, Peoples R China
来源
CHEMPLUSCHEM | 2019年 / 84卷 / 10期
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
diindolotriazatruxene; explosives; photoinduced electron transfer; polycyclic aromatic hydrocarbons; sensors; AGGREGATION-INDUCED EMISSION; CONJUGATED POLYMERS; PICRIC ACID; RECENT PROGRESS; FLUORESCENT; SENSORS; FLUOROPHORES; SENSITIVITY; DERIVATIVES; MOLECULES;
D O I
10.1002/cplu.201900347
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of electron-rich pi-extended diindolotriazatruxene-based compounds DIT, 4Py-DIT (bearing pyrene units) and 4PyF-DIT (bearing fluorene units) have been explored and investigated as fluorescence chemosensors. Quantitative analysis through fluorescence titrations showed that the resulting DIT molecules exhibited highly selective response to electron-deficient nitroaromatic explosives. The calculated Stern-Volmer quenching constants (>4.0x10(3) M-1) revealed that these sensors were much more sensitive in solution compared to most of the existing small-molecule fluorescence chemosensors based on pyrene, triphenylene, triphenylamine, and triazatruxene skeletons. Fluorescence quenching showed that the sensors adsorbed on paper were sensitive to explosives in the solid, solution, and vapor phases, with fast response times of about 10 s. Moreover, these chemosensors are reusable for the detection of nitroaromatic compounds as they recover their fluorescence intensity after quenching.
引用
收藏
页码:1623 / 1629
页数:7
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