journal article·2026-02

Utility of a Triazine‐Based Imine‐Linked Donor–Acceptor COF (TAPT–TP) for the Synthesis of 2‐Oxazolidinone Derivatives and CO 2 Photoreduction Under Visible Light Irradiation

Biddyut Das, Jhumur Seth, Amitesh Roy, Bipasha Banerjee, Anil Chandra Kothari, Subhas Chandra Debnath, Sk. Manirul Islam

ChemNanoMat· Volume 12· Issue 2
Publisher page

Abstract

Carbon dioxide (CO 2 ) emission represents a critical environmental challenge that has garnered increasing attention in recent years. This nontoxic, readily available gas can be utilized to produce important chemicals along with the main energy source, fossil fuels. But the efficient utilization of CO 2 is highly demanding due to its thermodynamic stability as well as kinetic inertness. Over the last few decades, covalent organic frameworks (COFs) owing designable structures have shown promising performance to convert CO 2 to important chemicals or fuels. Herein, we have synthesized TAPT–TP COF in a simple method. This material has shown its superior photocatalytic activities to synthesize 2‐oxazolidinone from propargylic acid and amine, using atmospheric CO 2 under mild reaction condition. Also, it has shown its excellent photocatalytic performance for the photoreduction of CO 2 to formic acid. The photocatalyst exhibited excellent stability and reusability over multiple cycles. These results highlight a promising strategy for environmentally friendly CO 2 conversion using metal‐free catalyst. This work provides a new and excellent protocol for metal‐free synthesis of 2‐oxazolidinone and formic acid through a one‐pot reaction method.
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Research context

OpenAlex topics: Covalent Organic Framework Applications · Carbon dioxide utilization in catalysis · Advanced Photocatalysis Techniques

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

Affiliations

Department of Chemistry University of Kalyani Kalyani India

Light Stock Processing Division CSIR Indian Institute of Petroleum Dehradun India

Academy of Scientific and Innovative Research (AcSIR) Ghaziabad India

References (95)

Show source-provided references
1. 10.1039/C5CS00023H10.1039/C5CS00023H ↗
2. 10.1039/C5CS00859J10.1039/C5CS00859J ↗
3. 10.1039/C5CS00859J10.1039/C5CS00859J ↗
4. 10.1039/C7QI00651A10.1039/C7QI00651A ↗
5. 10.1038/s41467-018-08208-410.1038/s41467-018-08208-4 ↗
6. 10.1002/chem.20170241810.1002/chem.201702418 ↗
7. 10.1016/j.molcata.2006.01.00810.1016/j.molcata.2006.01.008 ↗
8. 10.1016/j.ccr.2019.04.00210.1016/j.ccr.2019.04.002 ↗
9. 10.1039/C8QI00543E10.1039/C8QI00543E ↗
10. 10.1002/smll.20160299610.1002/smll.201602996 ↗
11. 10.1021/acscatal.5b0249010.1021/acscatal.5b02490 ↗
12. 10.1002/chem.20160115110.1002/chem.201601151 ↗
13. 10.1039/B715660J10.1039/B715660J ↗
14. 10.1039/c4nj00053f10.1039/c4nj00053f ↗
15. 10.1021/cs200131g10.1021/cs200131g ↗
16. 10.1002/adma.20170758210.1002/adma.201707582 ↗
17. 10.1039/C7CS00033B10.1039/C7CS00033B ↗
18. 10.1002/adma.20150500410.1002/adma.201505004 ↗
19. 10.1002/chem.20150120610.1002/chem.201501206 ↗
20. 10.1002/anie.20190961310.1002/anie.201909613 ↗
21. 10.1039/C9CS00299E10.1039/C9CS00299E ↗
22. 10.1021/jacs.9b0995610.1021/jacs.9b09956 ↗
23. 10.1021/jacs.5b1349010.1021/jacs.5b13490 ↗
24. 10.1039/C6CS00528D10.1039/C6CS00528D ↗
25. 10.1021/jacs.8b0629110.1021/jacs.8b06291 ↗
26. 10.1038/s41467-018-02889-710.1038/s41467-018-02889-7 ↗
27. 10.1021/jacs.9b0244810.1021/jacs.9b02448 ↗
28. 10.1002/anie.20180199810.1002/anie.201801998 ↗
29. 10.1002/chem.20160119910.1002/chem.201601199 ↗
30. 10.1039/C6CC00853D10.1039/C6CC00853D ↗
31. 10.1039/C9NJ03015H10.1039/C9NJ03015H ↗
32. 10.1002/cptc.20190008910.1002/cptc.201900089 ↗
33. 10.1016/j.mtchem.2021.10050910.1016/j.mtchem.2021.100509 ↗
34. Opportunities of Covalent Organic Frameworks for Advanced Applications
35. 10.1002/chem.20130208410.1002/chem.201302084 ↗
36. 10.1002/asia.20190152710.1002/asia.201901527 ↗
37. 10.1038/s43586-022-00181-z10.1038/s43586-022-00181-z ↗
38. 3D Covalent Organic Frameworks from Design, Synthesis to Applications in Optoelectronics
39. 10.1021/jacs.2c1107110.1021/jacs.2c11071 ↗
40. 10.1002/anie.20230699910.1002/anie.202306999 ↗
41. 10.1016/j.apcatb.2023.12321610.1016/j.apcatb.2023.123216 ↗
42. 10.1126/sciadv.adk856410.1126/sciadv.adk8564 ↗
43. 10.1039/D2CS00289B10.1039/D2CS00289B ↗
44. 10.1002/adma.20220947510.1002/adma.202209475 ↗
45. 10.1021/acsami.0c0001310.1021/acsami.0c00013 ↗
46. 10.1016/j.ccr.2022.21477410.1016/j.ccr.2022.214774 ↗
47. 10.1039/C9CC01047E10.1039/C9CC01047E ↗
48. 10.1002/adma.20210500210.1002/adma.202105002 ↗
49. 10.1016/j.apcatb.2021.12014910.1016/j.apcatb.2021.120149 ↗
50. 10.1016/j.jcat.2020.12.01310.1016/j.jcat.2020.12.013 ↗
51. 10.1021/acsami.0c1467810.1021/acsami.0c14678 ↗
52. 10.1002/adma.20120118510.1002/adma.201201185 ↗
53. 10.1002/adma.20211026610.1002/adma.202110266 ↗
54. 10.1038/s41467-021-26817-410.1038/s41467-021-26817-4 ↗
55. 10.1002/anie.20220232810.1002/anie.202202328 ↗
56. Design and Synthesis of a Triazine‐Based sp2 Carbon‐Conjugated Covalent Organic Framework for Blue Light Photocatalysis
57. Review of Solutions to Global Warming, Air Pollution, and Energy Security
58. 10.1016/j.rser.2016.09.11310.1016/j.rser.2016.09.113 ↗
59. 10.1039/C7GC00199A10.1039/C7GC00199A ↗
60. 10.1002/cssc.20170128310.1002/cssc.201701283 ↗
61. 10.1039/C7CY02094E10.1039/C7CY02094E ↗
62. 10.1016/j.jcou.2019.05.01710.1016/j.jcou.2019.05.017 ↗
63. 10.1002/chem.20180007510.1002/chem.201800075 ↗
64. 10.1039/C8CC01461B10.1039/C8CC01461B ↗
65. 10.1016/j.jcat.2025.11593810.1016/j.jcat.2025.115938 ↗
66. 10.1039/D5GC02137E10.1039/D5GC02137E ↗
67. 10.1016/j.cclet.2025.11195310.1016/j.cclet.2025.111953 ↗
68. Emerging Applications of Metal–Organic Frameworks and Covalent Organic Frameworks10.1021/acs.chemmater.6b04677 ↗
69. 10.1039/C4CS00094C10.1039/C4CS00094C ↗
70. 10.1021/cr200190s10.1021/cr200190s ↗
71. 10.1021/acs.chemrev.6b0062610.1021/acs.chemrev.6b00626 ↗
72. 10.1016/j.ccr.2019.02.00110.1016/j.ccr.2019.02.001 ↗
73. 10.1002/chem.20170338410.1002/chem.201703384 ↗
74. Petroleum B. · Statistical Review of World Energy · 2020
75. 10.1039/C4CS00122B10.1039/C4CS00122B ↗
76. 10.1021/acs.chemrev.7b0043510.1021/acs.chemrev.7b00435 ↗
77. 10.1063/1.498562410.1063/1.4985624 ↗
78. 10.1002/anie.20241771210.1002/anie.202417712 ↗
79. Regulating Exciton Dynamics in Organic Polymer Photocatalysts with Dual‐Polarization Structure
80. 10.1021/acsami.7b0587010.1021/acsami.7b05870 ↗
81. 10.1002/smll.20220012910.1002/smll.202200129 ↗
82. 10.1002/anie.20220148210.1002/anie.202201482 ↗
83. 10.1016/j.apcatb.2019.05.03310.1016/j.apcatb.2019.05.033 ↗
84. 10.1039/C7TA08629F10.1039/C7TA08629F ↗
85. 10.1021/jacs.6b0978710.1021/jacs.6b09787 ↗
86. Adsorption Pore Volume Distribution Heterogeneity of Middle and High Rank Coal Reservoirs and Determination of Its Influencing Factors
87. 10.1039/C9SC03052B10.1039/C9SC03052B ↗
88. 10.1021/acsami.9b0862510.1021/acsami.9b08625 ↗
89. 10.1021/acs.chemrev.0c0048710.1021/acs.chemrev.0c00487 ↗
90. 10.1038/nchem.244410.1038/nchem.2444 ↗
91. 10.1021/jacs.1c1011010.1021/jacs.1c10110 ↗
92. Fabrication of Efficient Au@ TiO2/rGO Heterojunction Nanocomposite: Boosted Photocatalytic Activity Under Ultraviolet and Visible Light Irradiation
93. 10.1002/cctc.20250023210.1002/cctc.202500232 ↗
94. 10.1002/cctc.20240092010.1002/cctc.202400920 ↗
95. 10.1002/cssc.20190354510.1002/cssc.201903545 ↗