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Experimental and computational investigation of a DNA-shielded 3D metal–organic framework for the prompt dual sensing of Ag(+) and S(2−)
We herein report an efficient Ag(+) and S(2−) dual sensing scenario by a three-dimensional (3D) Cu-based metal–organic framework [Cu(Cdcbp)(bpea)](n) (MOF 1, H(3)CdcbpBr = 3-carboxyl-(3,5-dicarboxybenzyl)-pyridinium bromide, bpea = 1,2-di(4-pyridinyl)ethane) shielded with a 5-carboxytetramethylrhoda...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064208/ https://www.ncbi.nlm.nih.gov/pubmed/35514810 http://dx.doi.org/10.1039/c9ra02028d |
Sumario: | We herein report an efficient Ag(+) and S(2−) dual sensing scenario by a three-dimensional (3D) Cu-based metal–organic framework [Cu(Cdcbp)(bpea)](n) (MOF 1, H(3)CdcbpBr = 3-carboxyl-(3,5-dicarboxybenzyl)-pyridinium bromide, bpea = 1,2-di(4-pyridinyl)ethane) shielded with a 5-carboxytetramethylrhodamine (TAMRA)-labeled C-rich single-stranded DNA (ss-probe DNA, P-DNA) as a fluorescent probe. The formed MOF-DNA probe, denoted as P-DNA@1, is able to sequentially detect Ag(+) and S(2−) in one pot, with detection limits of 3.8 nM (for Ag(+)) and 5.5 nM (for S(2−)), which are much more lower than the allowable Ag(+) (0.5 μM) and S(2−) (0.6 μM) concentration in drinking water as regulated by World Health Organization (WHO). The detection method has been successfully applied to sense Ag(+) and S(2−) in domestic, lake, and mineral water with satisfactory recoveries ranging from 98.2 to 107.3%. The detection mechanism was further confirmed by molecular simulation studies. |
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