Dual mode detection of picric acid with fluorescence and smartphone colorimetry via AIE active tetraphenylethylene derivatives

苦味酸 荧光 光化学 四苯乙烯 光诱导电子转移 检出限 化学 猝灭(荧光) 双模 选择性 电子转移 材料科学 聚集诱导发射 色谱法 光学 有机化学 工程类 航空航天工程 催化作用 物理
作者
Ling Wang,Lingyu Zhai,Zhenyu Liang,Ruilong Zhang,Jiaxiang Yang,Lin Kong
出处
期刊:Dyes and Pigments [Elsevier BV]
卷期号:220: 111743-111743 被引量:1
标识
DOI:10.1016/j.dyepig.2023.111743
摘要

In this study, six tetraphenylethene (TPE) derivatives had been designed and synthesized, named as TPEH, TPEOMe, TPEtBu, TPEOH, TPECN and TPEPy, which exhibited intramolecular charge transfer (ICT) character and aggregation-induced emission (AIE) performance. Based on the electron-donating ability originated from the highly localized π electrons, electrons could be transferred from these TPE derivatives to electron-deficient nitroaromatic explosive picric acid (PA) resulting in quenched fluorescence emission. Thus, they had excellent sensitivity and selectivity for PA detection in aggregate states. The limits of detection (LOD) were 1.64, 0.50, 0.93, 1.48, 0.49 and 0.35 μM for them, respectively, captured from fluorescence signal. Moreover, a semi-quantitative detection method based on smartphone digital image was developed to detect PA with LOD of 490, 26.6, 69.1, 74.1, 3.57 and 100 μM, respectively. The dual-mode sensors had excellent detection character improving the accuracy of the detection result. The fluorescence quenching mechanism was explored as photoinduced electron transfer (PET) and energy transfer. This study provided a new strategy for the design of AIE active materials, expanded the application of smartphones in explosive detection which had practical potential in effective sensing.

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