期刊
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
卷 223, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2019.117283
关键词
Dual-emission; Fluorescence sensor; Metal-organic framework; Metal ions; DMA; Nitro-based molecules
类别
资金
- National Natural Science Foundation of China [21671169, 21573192]
- Top-notch Academic Programs Project of Jiangsu Higher Education Institutions
A novel multifunctional Pb(II)-based MOF, [Pb-1.5(DBPT)](2)center dot(DMA)(3)(H2O)(4) (1), with excellent chemical stability, was successfully assembled by connecting {Pb2O10) unit with a multi-topic polycarboxylate ligand of 3-(3,5-dicarboxylphenyl)-5-(4-carboxylphenyl)-1-H-1,2,4-triazole (H3DBPT). It exhibits dual fluorescence emissions at 380 nm (lambda(ex) = 280 nm) and 540 nm (lambda(ex) = 380 nm), respectively. Through the adjustable dual fluorescence emissions, it could act as a turn-off and turn-on switch for detecting N.N-dimethylacetamide (DMA) molecule. Moreover, Fe3+ ions exert luminescence quenching role on compound 1 at both excitation lengths in water, among which the quenching at lambda(ex) = 280 nm is of high sensitivity (K-SV = 12 x 10(5)), and the quenching at lambda(ex) = 380 nm is of wide-range. The sensing for metal ions of In3+, Zr4+, and Al3+ is also effective at lambda(ex) = 280 nm, with the K-SV constants of 1.6 x 10(5), 1.6 x 10(5), and 43 x 10(4), respectively. More importantly, a series of nitroaromatic compounds (TNP, 2,4,6-trinitrophenol; 4-NA, 4-nitroaniline; NB, nitrobenzene) and nitro-based drugs (MNZ, metronidazole; DMZ, dimetridazole) could be detected at both excitation lengths, demonstrating the advantage of broad range response of fluorescence sensing. Thanks to the excellent chemical stability and unusual dual emission luminescence properties for chemical detection of various metal ions, nitro-based molecules and DMA solvent, the Pb-based MOF reported in this work is, therefore, a very promising multi-response sensor. (C) 2019 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据