期刊
INORGANIC CHEMISTRY
卷 57, 期 3, 页码 1417-1425出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.7b02827
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资金
- National Natural Science Foundation of China [21571005]
- High School Leading Talent Incubation Program of Anhui Province [gxbjZD2016010]
- Innovation Foundation of Anhui Normal University [2017xjj104]
- Recruitment Program for Leading Talent Team of Anhui Province
Tb3+-doped zinc-based coordination polymer nanospindle bundles (Zn-PDC/Tb3+, or [Zn(2,5-PDC)(H2O)(2)]center dot H2O/Tb3+) were synthesized by a simple solution precipitation route at room temperature, employing Zn(NO3)(2), Tb(NO3)(3), and 2,5-Na2PDC as the initial reactants, and a mixture of water and ethanol with the volume ratio of 10:10 as the solvent. The as-obtained nanostructures presented strong fluorescent emission under the excitation of 298 nm light, which was attributed to the characteristic emission of the Tb3+ ion. It was found that the above-mentioned strong fluorescence of the nanostructures could be selectively quenched by cefixime (CFX) in aqueous solution. The other common antibiotics hardly interfered. Thus, as-obtained Zn-PDC/Tb3+ nanostructures could be prepared as a highly sensitive fluorescence probe for selective detection of CFX in an aqueous system. The corresponding detection limit reached 72 ppb. The theoretic calculation and UV-vis absorption experiments confirmed that the fluorescence quenching of Zn-PDC/Tb3+ nanostructures toward CFX should be attributed to the electron transfer and the fluorescence inner filter effect between the fluorescent matter and the analyte. In addition, the strong fluorescence of the nanostructures could also be selectively quenched by acetone in the water system.
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