Pyrazine-Based Covalent Organic Frameworks for Effective Iodine and Carbon Dioxide Capture
Source abstract
Abstract
Covalent organic frameworks (COFs) possess good porosity, uniform channels, and tunable skeletons, as well as excellent stability, which are well-suited for gas adsorption. In this study, we developed two pyrazine-based COFs, namely, TFPPz–MPA–COF and TFPPz–BD(OMe) 2 –COF, by condensation reaction of C 4 and C 2 axisymmetric monomers. Both COFs exhibited good crystallinity, well-defined pore structures, and outstanding thermal and chemical stability. TFPPz–MPA–COF and TFPPz–BD(OMe) 2 –COF demonstrated high iodine adsorption capabilities of up to 5.41 and 5.18 g g –1 in iodine vapor, and 95.42 and 98.04 mg g –1 in n -hexane, respectively. In addition, TFPPz–MPA–COF and TFPPz–BD(OMe) 2 –COF exhibited good CO 2 uptake capacities of 1.48 and 1.34 mmol g –1 at 273 K, respectively.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry, Zhengzhou University, Zhengzhou 450001, China
Funding
Natural Science Foundation of Henan Province · National Natural Science Foundation of China
References (42)
Show source-provided references
1. 10.1039/C2CS35072F10.1039/C2CS35072F ↗
2. 10.1038/natrevmats.2016.6810.1038/natrevmats.2016.68 ↗
3. 10.1039/D2MA00143H10.1039/D2MA00143H ↗
4. 10.1039/D2CP03044F10.1039/D2CP03044F ↗
5. 10.1016/S1872-2067(18)63057-810.1016/S1872-2067(18)63057-8 ↗
6. 10.1016/j.ccr.2021.21415210.1016/j.ccr.2021.214152 ↗
7. 10.3389/fchem.2022.94381310.3389/fchem.2022.943813 ↗
8. 10.1016/j.chemosphere.2020.12952310.1016/j.chemosphere.2020.129523 ↗
9. 10.1016/j.jnucmat.2015.11.03810.1016/j.jnucmat.2015.11.038 ↗
10. 10.1002/aic.1713710.1002/aic.17137 ↗
11. 10.1021/acsami.0c0315510.1021/acsami.0c03155 ↗
12. 10.1039/C9TA04408F10.1039/C9TA04408F ↗
13. 10.1016/j.micromeso.2019.10984210.1016/j.micromeso.2019.109842 ↗
14. 10.1021/acsanm.2c0174110.1021/acsanm.2c01741 ↗
15. 10.3390/molecules2724904510.3390/molecules27249045 ↗
16. 10.1039/C8MH01656A10.1039/C8MH01656A ↗
17. 10.3390/ma1604163010.3390/ma16041630 ↗
18. 10.1039/C9CS00827F10.1039/C9CS00827F ↗
19. 10.1021/acsami.2c1767210.1021/acsami.2c17672 ↗
20. 10.1039/C8CE01397G10.1039/C8CE01397G ↗
21. 10.1039/D2PY00329E10.1039/D2PY00329E ↗
22. 10.1021/acsanm.2c0465210.1021/acsanm.2c04652 ↗
23. 10.1038/nchem.235210.1038/nchem.2352 ↗
24. 10.1039/C9RA01904A10.1039/C9RA01904A ↗
25. 10.1039/C7RA09414K10.1039/C7RA09414K ↗
26. 10.1039/D2TA09448G10.1039/D2TA09448G ↗
27. 10.1039/D0RA10587B10.1039/D0RA10587B ↗
28. 10.1021/acsmaterialslett.3c0021310.1021/acsmaterialslett.3c00213 ↗
29. 10.1002/anie.20210852210.1002/anie.202108522 ↗
30. 10.1021/acs.chemmater.7b0512110.1021/acs.chemmater.7b05121 ↗
31. 10.1039/D1CC00737H10.1039/D1CC00737H ↗
32. 10.1016/j.cclet.2022.03.05310.1016/j.cclet.2022.03.053 ↗
33. 10.1021/jacs.2c0395910.1021/jacs.2c03959 ↗
34. 10.1039/D1TA03879F10.1039/D1TA03879F ↗
35. 10.1007/s10570-022-04476-y10.1007/s10570-022-04476-y ↗
36. 10.1021/acsanm.2c0494110.1021/acsanm.2c04941 ↗
37. 10.1039/C7CC01045A10.1039/C7CC01045A ↗
38. 10.1016/j.cclet.2022.03.00110.1016/j.cclet.2022.03.001 ↗
39. 10.1016/j.micromeso.2021.11135110.1016/j.micromeso.2021.111351 ↗
40. 10.1002/chem.20150120610.1002/chem.201501206 ↗
41. 10.1016/j.cej.2022.13555510.1016/j.cej.2022.135555 ↗
42. 10.1016/j.micromeso.2022.11241910.1016/j.micromeso.2022.112419 ↗