RESUMEN
The increasing degradation of ecosystems due to heavy metal residues has led to environment and food contamination, prompting the development of convenient platforms for monitoring heavy metals. Here, a new dual-emission fluorescent sensor CuNCs@Tb@UiO-66-(COOH)2 for the detection of copper ions (Cu2+ ) has been synthesized using one-pot encapsulation of Tb(III) and glutathione-stabilized copper nanoclusters (CuNCs) into metal-organic frameworks (MOFs) UiO-66-(COOH)2 . In this ratiometric sensor, the fluorescence intensity of Tb3+ decreased significantly upon the addition of Cu2+ , whereas that of CuNCs showed good stability, together with an apparent colour change. Therefore, ratiometric fluorescence detection of Cu2+ can be accomplished by measuring the ratio of the fluorescence intensity at the 450 nm (F450 ) wavelength of CuNCs to the 548 nm (F548 ) emission of Tb3+ in the fluorescence spectra of the CuNCs@Tb@UiO-66-(COOH)2 suspension. Moreover, the obtained fluorescent probe showed good results in the detection of actual samples. This work can provide the basis of method for the exploration of ratiometric fluorescence and visual sensors of trace pollutants analysis in complicated samples.
Asunto(s)
Contaminantes Ambientales , Estructuras Metalorgánicas , Cobre/química , Ecosistema , Colorantes Fluorescentes/química , Glutatión , Límite de Detección , Estructuras Metalorgánicas/química , Ácidos Ftálicos , Espectrometría de Fluorescencia/métodosRESUMEN
As an important trace element in the human body, the concentration of Cu2+ has an important impact on the environment and human health, and its quantitative determination is of great significance in the fields of environmental protection and food safety. Here, a ratiometric fluorescent probe based on Tb(III)-functionalized UiO-66-type MOFs has been synthesized via a facile post-synthetic modification method by employing mixed linkers containing terephthalic acid and 2,6-pyridinedicarboxylic acid for Cu2+ detection. The blue fluorescence intensity at 440 nm from the ligands of MOFs does not change much with increasing Cu2+ concentrations and can be used as a reference signal, while the green fluorescence of Tb3+ can be rapidly and selectively quenched, causing fluorescence intensity at 547 nm to decrease. The probe can be used as a ratiometric sensor for Cu2+ detection with a good linear response and low detection limit. The use of the probe for the determination of Cu2+ in real water samples and drinks shows good practicality. This method for Cu2+ detection is simple, specific and visualized to meet the needs of environmental monitoring and food analysis and provides a new strategy for the construction of new copper ion fluorescent sensors to analyze complex samples.
RESUMEN
A facile and efficient "bottle-around-ship" approach for preparing the ratiometric fluorescent probe has been developed by encapsulating the red-colored fluorescence CdTe quantum dots (QDs) and blue-colored fluorescence graphitic carbon nitride quantum dots (g-CNQDs) into the zeolitic imidazolate metal-organic frameworks (ZIF-8) in one step. At a single excitation of 360 nm, the obtained probe ZIF-8@g-CNQD/CdTe shows the dual-emission peaked at 450 and 633 nm, respectively. The red emission of CdTe QDs is selectively quenched by the Hg2+, whereas the blue fluorescence of g-CNQDs as an internal reference is insensitive, resulting in an apparent color transformation from pink to blue for special recognition of Hg2+. By this approach, the relative fluorescence intensity ratio (F633/F450) decreased linearly with increasing Hg2+ concentration in the 0.2-3.5 µM range with a low limit of detection (LOD) of ~ 46 nM. Therefore, we demonstrate that this "bottle-around-ship" process provides a new strategy for the construction of ratiometric fluorescent Hg2+ probes with good simplicity, high efficiency, and excellent stabilities. Moreover, the obtained Hg2+ fluorescent probe shows good results in the detection of actual samples.