journal article·2021-07

Achieving Multifunctional Detection of Th4+ and UO22+ in the Post‐Synthetically Modified Metal–Organic Framework and Application of Functional MOF Membrane

Jin Xiao Li, Qing Lin Guan, Zi Xin You, Yu Wang, Zhan Shi, Yong Heng Xing, Feng Ying Bai, Li Xian Sun

Advanced Materials Technologies· Volume 6· Issue 7
Publisher page

Abstract

Abstract The field of post‐synthesis modification has aroused widespread concern from diverse perspectives, including chemistry, biology, and material science. Post‐synthesis modification can introduce rich functionality into metal–organic frameworks (MOFs) without destroying the main structure of MOFs. Based on this research status, a series of lanthanide metal–organic frameworks ([Ln2(NH2‐BDC)2.5(CH3COO)(DMA)(H2O)]•DMA, Ln = Pr, Nd, Sm, Eu, Gd and Tb, NH2‐BDC = 2‐aminoterephthalic acid, DMA = N,N‐Dimethylacetamide) with 3D network structures, are synthesized by hydrothermal synthesis. Due to the presence of uncoordinated amino groups in the ligands, a series of post‐synthesis modified compounds are successfully synthesized through aldimine condensation reaction. Based on the good fluorescence properties and stable structure of coordination polymers and post‐synthesis modified compounds in water or organic solvents, they are able to be used as potential fluorescence sensor for the detection of Th4+, UO22+, and Cr2O72−, and the calculation result shows that the post‐synthesis modified compounds are more sensitive to the detection of analytes (Th4+, UO22+ and Cr2O72−) than coordination polymers. In addition, the MOF membrane prepared by self‐assembly of [Eu2(NH2‐BDC)2.5(CH3COO)(DMA)(H2O)]•DMA and ternary soap‐free copolymer (VAc‐AA‐BA) emulsion can be used first for detecting aldehyde vapors.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Lanthanide and Transition Metal Complexes · Molecular Sensors and Ion Detection

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Chemistry and Chemical Engineering Liaoning Normal University Dalian 116029 P. R. China

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P. R. China

Guangxi Key Laboratory of Information Materials Guilin University of Electronic Technology Guilin 541004 P. R. China

Funding

National Natural Science Foundation of China · Guilin University of Electronic Technology

References (65)

Show source-provided references
1. 10.1021/cr990043210.1021/cr9900432 ↗
2. 10.1021/ic100867w10.1021/ic100867w ↗
3. 10.1021/acs.cgd.7b0013110.1021/acs.cgd.7b00131 ↗
4. 10.1021/acs.accounts.5b0053010.1021/acs.accounts.5b00530 ↗
5. 10.1021/ja805884310.1021/ja8058843 ↗
6. 10.1039/C4TA04396K10.1039/C4TA04396K ↗
7. 10.1002/anie.20170091910.1002/anie.201700919 ↗
8. 10.1021/acs.est.8b0472810.1021/acs.est.8b04728 ↗
9. 10.1021/ja206029a10.1021/ja206029a ↗
10. 10.1021/acs.est.6b0630510.1021/acs.est.6b06305 ↗
11. 10.1039/b802426j10.1039/b802426j ↗
12. 10.1039/b807080f10.1039/b807080f ↗
13. 10.1039/b807083k10.1039/b807083k ↗
14. 10.1021/cr200179u10.1021/cr200179u ↗
15. 10.1039/C0CS00031K10.1039/C0CS00031K ↗
16. 10.1039/b802258p10.1039/b802258p ↗
17. 10.1021/ja074366o10.1021/ja074366o ↗
18. 10.1039/b802258p10.1039/b802258p ↗
19. 10.1039/C4CS00089G10.1039/C4CS00089G ↗
20. 10.1016/j.poly.2018.08.06910.1016/j.poly.2018.08.069 ↗
21. 10.1039/C9CC08206A10.1039/C9CC08206A ↗
22. 10.1039/C1CS15276A10.1039/C1CS15276A ↗
23. 10.1080/0306731890802686910.1080/03067318908026869 ↗
24. 10.1021/acs.iecr.5b0343010.1021/acs.iecr.5b03430 ↗
25. 10.1002/pc.2067610.1002/pc.20676 ↗
26. 10.1039/C6TA10513K10.1039/C6TA10513K ↗
27. 10.1021/jf300387q10.1021/jf300387q ↗
28. 10.1002/anie.20170091910.1002/anie.201700919 ↗
29. 10.1021/acs.est.8b0472810.1021/acs.est.8b04728 ↗
30. 10.1021/cm503767r10.1021/cm503767r ↗
31. 10.1021/acs.inorgchem.6b0021710.1021/acs.inorgchem.6b00217 ↗
32. 10.1039/C5NJ03419A10.1039/C5NJ03419A ↗
33. 10.1039/C9NJ05175A10.1039/C9NJ05175A ↗
34. 10.1021/acsomega.6b0048910.1021/acsomega.6b00489 ↗
35. 10.1021/cr980101410.1021/cr9801014 ↗
36. 10.1039/b809631g10.1039/b809631g ↗
37. 10.1039/c3sc00016h10.1039/c3sc00016h ↗
38. 10.1038/nature0133310.1038/nature01333 ↗
39. 10.1016/j.cattod.2011.08.01710.1016/j.cattod.2011.08.017 ↗
40. 10.1021/ar000034b10.1021/ar000034b ↗
41. 10.1039/C4CS00135D10.1039/C4CS00135D ↗
42. 10.1038/nchem.44410.1038/nchem.444 ↗
43. 10.1021/acscentsci.8b0007310.1021/acscentsci.8b00073 ↗
44. 10.1039/C4MH00210E10.1039/C4MH00210E ↗
45. 10.1016/j.snb.2012.10.02310.1016/j.snb.2012.10.023 ↗
46. 10.1021/acsami.7b1973810.1021/acsami.7b19738 ↗
47. 10.1039/b400314d10.1039/b400314d ↗
48. 10.1016/0039-9140(92)80063-J10.1016/0039-9140(92)80063-J ↗
49. 10.1107/S010876730704393010.1107/S0108767307043930 ↗
50. Sheldrick G. M. · 1996
51. Sheldrick G. M. · 1997 · 107
52. 10.1107/S002188980202211210.1107/S0021889802022112 ↗
53. 10.1039/C6NJ01503D10.1039/C6NJ01503D ↗
54. 10.1021/cr200205j10.1021/cr200205j ↗
55. 10.1021/ja805222x10.1021/ja805222x ↗
56. 10.1039/C4TA06828A10.1039/C4TA06828A ↗
57. 10.1039/C0PY00046A10.1039/C0PY00046A ↗
58. 10.1021/am502567610.1021/am5025676 ↗
59. 10.1002/anie.20120888510.1002/anie.201208885 ↗
60. 10.1039/C4AY01941E10.1039/C4AY01941E ↗
61. 10.1021/ma051584y10.1021/ma051584y ↗
62. 10.1002/slct.20160207610.1002/slct.201602076 ↗
63. 10.1039/c2an35512d10.1039/c2an35512d ↗
64. 10.1021/ol203123t10.1021/ol203123t ↗
65. 10.1039/b718367d10.1039/b718367d ↗