Engineering Pyrazine Units in Vinylene‐Linked Covalent Organic Frameworks for Efficient C 2 H 2 /CO 2 Separation
Source abstract
Abstract
ABSTRACT Effective separation of C 2 H 2 /CO 2 is a daunting challenge due to their close molecular sizes and physical properties. Covalent organic frameworks (COFs) have recently attracted widespread attention in the fields of gas adsorption and separation owing to their high surface area and pore designability. In this work, three nitrogen‐rich vinylene‐linked isostructural COFs were constructed via Aldol condensation between tetratopic monomers containing pyrazine (PZ) groups and terephthalaldehyde. All three PZ‐COFs exhibited high specific surface area and decent chemical/thermal stability. Intriguingly, both their adsorption capacity of C 2 H 2 (from 57.7 to 107.2 cm 3 g −1 ) and the separation efficiency of C 2 H 2 /CO 2 increased along with the growing amount of PZ units within the three frameworks. Dynamic experimental breakthrough results and theoretical calculations further demonstrated that the high‐density nitrogen sites along the one‐dimensional channels of these COFs played the pivotal role in the C─H···N bond interactions toward C 2 H 2 molecules, which subsequently regulated their separation performance of C 2 H 2 /CO 2 mixtures.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Covalent Organic Framework Applications · Carbon Dioxide Capture Technologies · Metal-Organic Frameworks: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Materials Science and Engineering Fuzhou University Fuzhou 350108 P. R. China
Key Laboratory of Green and High‐end Utilization of Salt Lake Resources Qinghai Institute of Salt Lakes Chinese Academy of Sciences Qinghai Provincial Key Laboratory of Resources and Chemistry of Salt Lakes Xining 810008 P. R. China
Funding
Natural Science Foundation of Fujian Province
References (59)
Show source-provided references
1. 10.1021/cr400276u10.1021/cr400276u ↗
2. 10.1126/science.aax866610.1126/science.aax8666 ↗
3. 10.1002/adma.20190827510.1002/adma.201908275 ↗
4. 10.1039/C7CS00153C10.1039/C7CS00153C ↗
5. 10.1002/anie.20201667310.1002/anie.202016673 ↗
6. 10.1038/s44286‐025‐00185‐y10.1038/s44286‐025‐00185‐y ↗
7. 10.1002/adfm.20221488710.1002/adfm.202214887 ↗
8. 10.1038/s41467‐022‐33271‐310.1038/s41467‐022‐33271‐3 ↗
9. 10.1021/accountsmr.3c0014110.1021/accountsmr.3c00141 ↗
10. 10.1039/D0CS01347A10.1039/D0CS01347A ↗
11. 10.1038/532435a10.1038/532435a ↗
12. 10.1126/science.aam723210.1126/science.aam7232 ↗
13. 10.1002/adfm.20170555310.1002/adfm.201705553 ↗
14. 10.1016/j.gee.2022.12.01010.1016/j.gee.2022.12.010 ↗
15. 10.1021/acsnano.2c1277410.1021/acsnano.2c12774 ↗
16. 10.1002/anie.20211648310.1002/anie.202116483 ↗
17. 10.1002/anie.20221152310.1002/anie.202211523 ↗
18. 10.1126/science.112041110.1126/science.1120411 ↗
19. 10.1126/science.aat767910.1126/science.aat7679 ↗
20. 10.1038/natrevmats.2016.6810.1038/natrevmats.2016.68 ↗
21. 10.1021/jacs.2c1107110.1021/jacs.2c11071 ↗
22. 10.1039/D0CS00199F10.1039/D0CS00199F ↗
23. 10.1021/acs.chemrev.9b0055010.1021/acs.chemrev.9b00550 ↗
24. 10.1126/science.aal158510.1126/science.aal1585 ↗
25. 10.1002/adma.20150500410.1002/adma.201505004 ↗
26. 10.1021/jacs.8b0132010.1021/jacs.8b01320 ↗
27. 10.1038/s41467‐023‐39126‐910.1038/s41467‐023‐39126‐9 ↗
28. 10.1002/anie.20221326810.1002/anie.202213268 ↗
29. 10.1038/s41467‐024‐47377‐310.1038/s41467‐024‐47377‐3 ↗
30. 10.1002/anie.20221667510.1002/anie.202216675 ↗
31. 10.1002/anie.20201250410.1002/anie.202012504 ↗
32. 10.1021/jacs.2c0105810.1021/jacs.2c01058 ↗
33. 10.1002/smll.20230368410.1002/smll.202303684 ↗
34. 10.1038/s41467‐024‐46942‐010.1038/s41467‐024‐46942‐0 ↗
35. 10.1021/jacs.3c0739310.1021/jacs.3c07393 ↗
36. 10.1002/anie.20221874210.1002/anie.202218742 ↗
37. 10.1021/jacs.7b0230310.1021/jacs.7b02303 ↗
38. 10.1021/jacs.3c0875510.1021/jacs.3c08755 ↗
39. 10.1021/accountsmr.1c0001710.1021/accountsmr.1c00017 ↗
40. 10.1126/science.aan020210.1126/science.aan0202 ↗
41. 10.1039/D1QM00015B10.1039/D1QM00015B ↗
42. 10.1002/anie.20241889510.1002/anie.202418895 ↗
43. 10.1002/smll.20240929210.1002/smll.202409292 ↗
44. 10.1038/s41467-021-22288-910.1038/s41467-021-22288-9 ↗
45. 10.1002/anie.20201185210.1002/anie.202011852 ↗
46. 10.1002/anie.20190119410.1002/anie.201901194 ↗
47. Fully Conjugated Benzobisoxazole‐Bridged Covalent Organic Frameworks for Boosting Photocatalytic Hydrogen Evolution
48. 10.1021/jacs.3c0722410.1021/jacs.3c07224 ↗
49. 10.1021/acsami.2c0833810.1021/acsami.2c08338 ↗
50. 10.1021/jacs.0c0199010.1021/jacs.0c01990 ↗
51. 10.1021/acs.jpcc.2c0515910.1021/acs.jpcc.2c05159 ↗
52. 10.1021/jacs.2c0530910.1021/jacs.2c05309 ↗
53. 10.1021/jacs.1c0373910.1021/jacs.1c03739 ↗
54. 10.1007/s11426‐022‐1224‐310.1007/s11426‐022‐1224‐3 ↗
55. 10.1021/jacs.1c0719110.1021/jacs.1c07191 ↗
56. 10.1002/anie.20230063810.1002/anie.202300638 ↗
57. 10.1021/jacs.3c0313010.1021/jacs.3c03130 ↗
58. Frisch M. J. · 2016
59. 10.1016/0263‐7855(96)00018‐510.1016/0263‐7855(96)00018‐5 ↗