2021
DOI: 10.1016/j.talanta.2021.122209
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A bi-functionalized metal-organic framework based on N-methylation and Eu3+ post-synthetic modification for highly sensitive detection of 4-Aminophenol (4-AP), a biomarker for aniline in urine

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Cited by 30 publications
(16 citation statements)
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“…In order to elucidate the possible sensing mechanism of 1 for monitoring of HT and HIAA, some experiments were systematically performed. First, PXRD patterns and IR spectra of 1 after immersion in HT and HIAA solutions are similar to those of the as-synthesized 1 (Figures S1 and S5), indicating that the luminescence quenching does not result from decomposition of the framework. , Second, to further understand the quenching mechanism of the luminescence sensor, the luminescence lifetimes of 1 at 546 nm with and without HT and HIAA were measured. As seen in Figure S20 and Table S5, the luminescentce lifetimes of 1 displayed different degrees of decay after HT and HIAA were added, suggesting a dynamic quenching process should be responsible for the quenching effect. ,, As is known to all, luminescence quenching may also be attributed to the competitive absorption of the excitation light between sensors and analytes. , It can be observed that the absorption spectra of HT and HIAA displayed an obvious overlap with the absorption band of 1 , indicating the occurrence of a competitive absorption between 1 and the biomarkers.…”
Section: Resultsmentioning
confidence: 65%
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“…In order to elucidate the possible sensing mechanism of 1 for monitoring of HT and HIAA, some experiments were systematically performed. First, PXRD patterns and IR spectra of 1 after immersion in HT and HIAA solutions are similar to those of the as-synthesized 1 (Figures S1 and S5), indicating that the luminescence quenching does not result from decomposition of the framework. , Second, to further understand the quenching mechanism of the luminescence sensor, the luminescence lifetimes of 1 at 546 nm with and without HT and HIAA were measured. As seen in Figure S20 and Table S5, the luminescentce lifetimes of 1 displayed different degrees of decay after HT and HIAA were added, suggesting a dynamic quenching process should be responsible for the quenching effect. ,, As is known to all, luminescence quenching may also be attributed to the competitive absorption of the excitation light between sensors and analytes. , It can be observed that the absorption spectra of HT and HIAA displayed an obvious overlap with the absorption band of 1 , indicating the occurrence of a competitive absorption between 1 and the biomarkers.…”
Section: Resultsmentioning
confidence: 65%
“…First, PXRD patterns and IR spectra of 1 after immersion in HT and HIAA solutions are similar to those of the as-synthesized 1 (Figures S1 and S5), indicating that the luminescence quenching does not result from decomposition of the framework. 42,43 Second, to further understand the quenching mechanism of the luminescence sensor, the luminescence lifetimes of 1 at 546 nm with and without HT and HIAA were measured. As seen in Figure S20 and Table S5, the luminescentce lifetimes of 1 displayed different degrees of decay after HT and HIAA were added, suggesting a dynamic quenching process should be responsible for the quenching effect.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
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“…As shown in Figure 3 a, the powder X-ray diffraction pattern of UA/Cu 2+ @Tb-MOFs collected from UA aqueous solution is in good agreement with that of Cu 2+ @Tb-MOFs and Tb-MOFs. This result not only indicates the structural stability of Cu 2+ @Tb-MOFs, but also excludes the possibility of fluorescence recovery caused by structural collapse or reorganization [ 48 , 49 ]. The luminescence lifetime is a very important parameter to explore the fluorescence recovery mechanism of Cu 2+ @Tb-MOFs; we determined the fluorescence lifetime of Tb-MOFs, Cu 2+ @Tb-MOFs and UA/Cu 2+ @Tb-MOFs samples.…”
Section: Resultsmentioning
confidence: 89%
“…Such materials have been used in the detection of analytes such as ionic species, [68] small molecules, [69] volatile organic molecules, [70] biomolecules [71] etc . For example, Yan ’s group has used lanthanide MOFs [72] to sense and detect molecules such as Levofloxacin, [73] pyrethroids, [74] nitrophenols, [75] mitoxantrone, [76] diphenyl phosphate, [77] 4‐aminophenol [78] and 5‐fluorouracil [79] . Hao et.…”
Section: Sensitized Lanthanide Emissive Mofs As Sensorsmentioning
confidence: 99%