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A Novel Selective “Turn-On” Fluorescent Chemosensor Based on Thiophene Appended Cyclotriphosphazene Schiff Base for Detection of Ag+ Ions

机译:基于硫芬附加的硫氰酸磷酸苯基基地的一种新型的选择性“转旋”荧光化学传感器,用于检测Ag+离子

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摘要

The salicylaldehyde-functionalized cyclotriphosphazene (1) and thiophene appended cyclotriphosphazene based Schiff base (2) were designed and synthesized. The characterizations were carried out via MALDI-TOF, FTIR, 13 C, 31 P and 1 H NMR. The photophysical behavior of compound 2 was evaluated by UV- Vis absorption, time-resolved fluorescence, excitation-emission matrix (EEM) analysis, steady-state fluorescence, and 3D- fluorescence spectroscopies. Compound 2 demonstrated selec- tive fluorescence “turn-on” response at 427 nm towards to Ag+ ion when the tested competitive species did not affect fluorescence signal. The binding and sensing mechanisms were evaluated by DFT calculations which approved that the PET process between C=N and fluorophore groups was inhibited, and the fluorescence “turn-on” response was obtained with the contribution of CHEF after 1:1 coordination of compound 2 with Ag+ ion.
机译:设计并合成了基于环磷酸的Schiff碱(2)的水杨醛官能化环磷酸(1)和硫苯甲醛。 通过Maldi-TOF,FTIR,13 C,31 P和1 H NMR进行表征。 通过紫外线吸收,时间分辨荧光,激发发射矩阵(EEM)分析,稳态荧光和3D-荧光光谱评估化合物2的光物理行为。 当测试竞争性物种不影响荧光信号时,化合物2在427 nm处显示出427 nm处的荧光“转到”响应。 通过DFT计算评估了结合和感应机制,该计算批准抑制C = N和荧光团基团之间的PET过程,并在1:1的化合物配位后通过厨师的贡献获得了荧光“转交”响应。 与Ag+离子。

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