化学
荧光
选择性
检出限
光诱导电子转移
光化学
激发态
肉眼
分析物
猝灭(荧光)
席夫碱
离子
甲醇
电子转移
催化作用
结晶学
色谱法
有机化学
物理
量子力学
核物理学
标识
DOI:10.1016/j.snb.2022.132837
摘要
Naphthalene-grafted zirconium-organic framework UiO-66 ([email protected]2) was synthesized via the Schiff base reaction. [email protected]2 retained the original crystal structure of UiO-66 and high thermal stability. [email protected]2 exhibited fluorescence sensing ability in two modes, “turn-off” response to Fe3+ in methanol and “turn-on” response to ClO4- in ethanol with high selectivity and sensitivity accompanied by obvious changes of fluorescence color. Its fluorescence intensity presented linear changes with the concentrations of Fe3+ and ClO4- with low detection limits (LOD) were 0.911 μM for Fe3+ and 1.44 μM for ClO4-. In addition, [email protected]2 can simply identified Fe3+ and ClO4- in the test paper mode with naked eyes. The photoinduced electron transfer (PET) from excited [email protected]2 to Fe3+ ion and the absorption competition quenching (ACQ) were responsible for the fluorescence quenching, the fluorescence enhancement of [email protected]2 induced by ClO4- was attributed to the hydrogen bond formation between [email protected]2 and ClO4-. The satisfying accuracy in detection of Fe3+ in serum and the good recovery of [email protected]2 in detection of Fe3+ and ClO4- in water samples confirmed the practical application capability. This work paved a way to fabricate the fluorescent sensing materials for the simple, accurate and instantaneous detection and recognition of the different analytes.
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