journal article·2024-03-22

Fabrication of Nanoporous 3D Carbon Nitride from Poly(ionic liquid)s for Regiospecific Synthesis of Benzimidazole Frameworks

Javad Safaei Ghomi, Zahra Elyasi, Gholam Reza Najafi, Abdollatif Shafaie Douk, Majid Farsadrooh, Marzieh Gharaei

ACS Applied Nano Materials· Volume 7· Issue 6
Publisher page

Abstract

The traditional form of carbon nitride materials poses limitations, particularly in catalysis, due to a limited number of active sites and low surface area. In response to these challenges, two porous carbon nitride tubes (CNTs) with diverse properties were designed and fabricated by introducing different poly(ionic liquid)s (PILs) as templates. Imidazolium-based PILs were synthesized with different ion pairs, including halogen (Br) and chiral amino acid ( l -phenylalanine). The results indicate that the morphology and properties of CNTs are influenced by the nature of PIL ion pairs. Synthesized CNT, assisted by PIL-Br (designated as CNT1), demonstrated superior characteristics in terms of thermal stability (up to 640 °C), specific surface area (73.5 m 2 /g), and recoverability (six runs without a significant decrease in reaction yield), which are the key factors of a high-performance catalyst. In the following, CNT architectures were employed as heterogeneous catalysts, and their catalytic efficiencies were compared in the regiospecific synthesis of benzimidazole ring systems. As expected, CNT1 demonstrates superfast synthesis (8–12 min) of various pharmaceutical benzimidazole scaffolds with excellent yields (up to 95%) under ultrasound irradiation. In a groundbreaking achievement, this is the first report that presents the preparation of a superactive catalyst through the integration of two distinct categories of advanced materials, including ionic polymers and graphite carbon nitrides, for regiospecific multicomponent reactions. This study offers a fresh perspective on enhancing the catalytic activity of graphitic carbon nitride by changing ion pairs of PILs for advanced technological applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications

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

Affiliations

Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan 51167, I. R. Iran

Department of Chemistry, Qom Branch, Islamic Azad University, Qom 37491-13191, I. R. Iran

Renewable Energies Research Laboratory, Department of Chemistry, Faculty of Science, University of Sistan and Baluchestan, Zahedan 98135 674, I. R. Iran

References (55)

Show source-provided references
1. 10.1002/anie.20150178810.1002/anie.201501788 ↗
2. 10.1021/acsami.3c1010410.1021/acsami.3c10104 ↗
3. 10.1002/adfm.20170269510.1002/adfm.201702695 ↗
4. 10.1016/j.carbon.2019.04.10410.1016/j.carbon.2019.04.104 ↗
5. 10.1039/C8TA08464E10.1039/C8TA08464E ↗
6. 10.1039/C9NR04568F10.1039/C9NR04568F ↗
7. 10.1039/d0ra05580h10.1039/d0ra05580h ↗
8. 10.1038/natrevmats.2017.3010.1038/natrevmats.2017.30 ↗
9. 10.1016/j.cej.2020.12817810.1016/j.cej.2020.128178 ↗
10. 10.1016/j.nanoen.2022.10803210.1016/j.nanoen.2022.108032 ↗
11. 10.1016/j.ijhydene.2023.05.06610.1016/j.ijhydene.2023.05.066 ↗
12. 10.1002/admt.20210099310.1002/admt.202100993 ↗
13. 10.1016/j.carbon.2020.10.07310.1016/j.carbon.2020.10.073 ↗
14. 10.1016/j.apcatb.2020.11882810.1016/j.apcatb.2020.118828 ↗
15. 10.1021/am405076b10.1021/am405076b ↗
16. 10.1016/j.carbon.2017.10.03310.1016/j.carbon.2017.10.033 ↗
17. 10.1016/j.apcatb.2020.11862410.1016/j.apcatb.2020.118624 ↗
18. 10.1016/j.cej.2013.10.07610.1016/j.cej.2013.10.076 ↗
19. 10.1038/srep0194310.1038/srep01943 ↗
20. 10.1016/j.cclet.2023.10830610.1016/j.cclet.2023.108306 ↗
21. 10.1002/cctc.20190103810.1002/cctc.201901038 ↗
22. 10.1002/aenm.20170150310.1002/aenm.201701503 ↗
23. 10.1016/j.matpr.2017.10.04510.1016/j.matpr.2017.10.045 ↗
24. 10.1016/j.cej.2022.13562510.1016/j.cej.2022.135625 ↗
25. 10.1021/acssuschemeng.9b0154410.1021/acssuschemeng.9b01544 ↗
26. 10.1016/j.progpolymsci.2013.04.00210.1016/j.progpolymsci.2013.04.002 ↗
27. 10.1016/j.cej.2021.12852810.1016/j.cej.2021.128528 ↗
28. 10.1039/C4QO00088A10.1039/C4QO00088A ↗
29. 10.1016/j.ejmech.2009.04.03710.1016/j.ejmech.2009.04.037 ↗
30. 10.1002/ardp.20170004010.1002/ardp.201700040 ↗
31. 10.1002/cmdc.20160004110.1002/cmdc.201600041 ↗
32. 10.1007/s11094-019-01976-310.1007/s11094-019-01976-3 ↗
33. 10.1016/j.cclet.2012.04.02010.1016/j.cclet.2012.04.020 ↗
34. 10.3390/ph1407066310.3390/ph14070663 ↗
35. 10.1021/acsinfecdis.0c0091010.1021/acsinfecdis.0c00910 ↗
36. 10.1016/j.ejmech.2015.03.05010.1016/j.ejmech.2015.03.050 ↗
37. 10.2174/138955752066620110209440110.2174/1389557520666201102094401 ↗
38. 10.1039/D0RA08647A10.1039/D0RA08647A ↗
39. 10.1016/j.mtchem.2022.10094310.1016/j.mtchem.2022.100943 ↗
40. 10.1007/s12274-018-2003-210.1007/s12274-018-2003-2 ↗
41. 10.1021/acsomega.0c0160710.1021/acsomega.0c01607 ↗
42. 10.1021/ja01134a02610.1021/ja01134a026 ↗
43. 10.1016/j.saa.2015.06.07010.1016/j.saa.2015.06.070 ↗
44. 10.1016/j.jece.2021.10549810.1016/j.jece.2021.105498 ↗
45. 10.1021/acs.chemmater.5b0041110.1021/acs.chemmater.5b00411 ↗
46. 10.1021/jo500776210.1021/jo5007762 ↗
47. 10.1080/10406638.2019.162506510.1080/10406638.2019.1625065 ↗
48. 10.1016/j.tetlet.2018.05.00510.1016/j.tetlet.2018.05.005 ↗
49. 10.1021/am502925j10.1021/am502925j ↗
50. 10.1021/acssuschemeng.8b0331810.1021/acssuschemeng.8b03318 ↗
51. 10.1039/d1qm00650a10.1039/d1qm00650a ↗
52. 10.1016/j.ijbiomac.2023.12658910.1016/j.ijbiomac.2023.126589 ↗
53. 10.1016/j.ultsonch.2021.10561410.1016/j.ultsonch.2021.105614 ↗
54. 10.1016/j.molliq.2021.11780010.1016/j.molliq.2021.117800 ↗
55. 10.1021/ol101568d10.1021/ol101568d ↗