journal article·2017-09-20

Ratiometric Luminescent Detection of Organic Amines Due to the Induced Lactam–Lactim Tautomerization of Organic Linker in a Metal–Organic Framework

Wen-Qiang Zhang, Qiu-Yan Li, Jun-Yan Cheng, Ke Cheng, Xinyu Yang, Yinwei Li, Xinsheng Zhao, Xiao-Jun Wang

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Abstract

Here we demonstrate that a fluorescent benzothiadiazole (BTD)-conjugated terphenyldicarboxylate (TPDC) linker (denoted as H 2 -ostpdc) has been hybridized by a quinoxaline-2,3-(1 H,4 H )-dione (QD) moiety possessing lactam-lactim tautomerism, which was further integrated into a robust and porous UiO-68 type zirconium metal–organic framework (MOF UiO-68-osdm) by utilizing the mixed two dicarboxylate struts with the same ligand lengths. The resultant MOF UiO-68-osdm can work as a ratiometric luminescent sensor for visual and selective detection of alkyl amines. Furthermore, it can discriminate secondary alkylamines from other type amine species.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Molecular Sensors and Ion Detection · Luminescence and Fluorescent Materials

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Affiliations

College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan 250014, P. R. China

Funding

National Natural Science Foundation of China · Top-notch Academic Programs Project of Jiangsu Higher Education Institutions · Priority Academic Program Development of Jiangsu Higher Education Institutions

References (30)

Show source-provided references
1. 10.1021/cr300014x10.1021/cr300014x ↗
2. 10.1021/acs.accounts.6b0057710.1021/acs.accounts.6b00577 ↗
3. 10.1016/j.ccr.2016.11.00810.1016/j.ccr.2016.11.008 ↗
4. 10.1016/j.chempr.2016.12.00210.1016/j.chempr.2016.12.002 ↗
5. 10.1002/adma.20170113910.1002/adma.201701139 ↗
6. 10.1021/cr200324t10.1021/cr200324t ↗
7. 10.1021/ic402194c10.1021/ic402194c ↗
8. 10.1039/C6CS00930A10.1039/C6CS00930A ↗
9. 10.1002/advs.20150043410.1002/advs.201500434 ↗
10. 10.1021/acs.inorgchem.5b0220010.1021/acs.inorgchem.5b02200 ↗
11. 10.1002/chem.20140221110.1002/chem.201402211 ↗
12. 10.1002/cplu.20160013710.1002/cplu.201600137 ↗
13. 10.1021/ja508962m10.1021/ja508962m ↗
14. 10.1039/C7TA01546A10.1039/C7TA01546A ↗
15. 10.1021/jacs.5b1345810.1021/jacs.5b13458 ↗
16. 10.1007/s11426-015-5498-310.1007/s11426-015-5498-3 ↗
17. 10.1021/acssensors.6b0082910.1021/acssensors.6b00829 ↗
18. 10.1016/j.snb.2016.01.12410.1016/j.snb.2016.01.124 ↗
19. 10.1002/anie.20140443910.1002/anie.201404439 ↗
20. 10.1021/ja509058u10.1021/ja509058u ↗
21. 10.1039/C4SC03224A10.1039/C4SC03224A ↗
22. 10.1021/acs.inorgchem.6b0025210.1021/acs.inorgchem.6b00252 ↗
23. 10.1039/C6CC10278F10.1039/C6CC10278F ↗
24. 10.1039/C5TC01287B10.1039/C5TC01287B ↗
25. 10.1021/acs.inorgchem.7b0078710.1021/acs.inorgchem.7b00787 ↗
26. 10.1021/acsami.7b0705510.1021/acsami.7b07055 ↗
27. 10.1021/acs.inorgchem.5b0262610.1021/acs.inorgchem.5b02626 ↗
28. 10.1021/ja805795310.1021/ja8057953 ↗
29. 10.1039/C5CS00837A10.1039/C5CS00837A ↗
30. 10.6023/A1609049610.6023/A16090496 ↗