journal article·2025-11-25

Construction of MOF-on-MOF Heterojunctions for the Highly Efficient Catalytic Nitroarene Hydrogenation under Mild Conditions

Zuxian Cai, Ju Wang, Zhaoxu Wang, Ruirui Yun, Hu Zhou, Baishu Zheng

Langmuir· Volume 41· Issue 46
Publisher page

Abstract

High Resolution Image Download MS PowerPoint Slide Precise modulation of the electronic structure of the catalyst is critical for generating highly active sites in targeted catalytic transformations. We report a strategy to regulate the electronic properties of metal–organic frameworks (MOFs) by constructing functional-group-modified MOF-on-MOF heterojunctions for selective nitroarene hydrogenation. As a representative heterostructure, the ZIF-67-on-NH 2 -UiO-66 heterostructure is fabricated by epitaxially growing Co-based ZIF-67 on NH 2 -UiO-66. Combining experimental studies and first-principles calculations demonstrates that the electron-donating substituent (−NH 2 ) group elevates the d-band center of the heterojunction, facilitating electron transfer compared to the unfunctionalized ZIF-67-on-UiO-66 analog. Consequently, ZIF-67-on-NH 2 -UiO-66 exhibits exceptional reactivity and chemoselectivity for hydrogenating diverse functionalized nitroarenes under mild conditions, surpassing most reported catalysts under comparable settings. This work establishes ZIF-on-MOF functionalization as an effective strategy to engineer electronic structures at catalytic interfaces for advanced selective hydrogenations.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Nanomaterials for catalytic reactions · Covalent Organic Framework Applications

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

Affiliations

School of Chemistry and Chemical Engineering

Hunan University of Science and Technology, Key Laboratory of Theoretical Organic Chemistry and Function Molecule, Ministry of Education, Key Laboratory of Molecular Design and Green Chemistry of Hunan Provincial Universities, Hunan Provincial Key Laboratory of Controllable Preparation and Functional Application of Fine Polymers

School of Materials and Chemical Engineering

Xuzhou University of Technology

The Key Laboratory of Functional Molecular Solids Ministry of Education, College of Chemistry and Materials Science

Anhui Normal University

Funding

Natural Science Foundation of Hunan Province · National Natural Science Foundation of China · Hunan Provincial Key Laboratory of Controllable Preparation and Functional Application of Fine Polymers

References (58)

Show source-provided references
1. 10.1021/es400422k10.1021/es400422k ↗
2. 10.1021/acs.est.6b0073010.1021/acs.est.6b00730 ↗
3. 10.1039/D3QI01847D10.1039/D3QI01847D ↗
4. 10.1007/s12274-023-5750-710.1007/s12274-023-5750-7 ↗
5. 10.6023/A2308037410.6023/A23080374 ↗
6. 10.1039/D1GC01439K10.1039/D1GC01439K ↗
7. 10.1007/s12274-022-4294-610.1007/s12274-022-4294-6 ↗
8. 10.1039/D0GC01835J10.1039/D0GC01835J ↗
9. 10.1021/acsanm.2c0468910.1021/acsanm.2c04689 ↗
10. 10.1039/D1TA04415J10.1039/D1TA04415J ↗
11. 10.1021/acs.oprd.3c0014410.1021/acs.oprd.3c00144 ↗
12. 10.1039/D2QI01451C10.1039/D2QI01451C ↗
13. 10.1021/acs.inorgchem.1c0274010.1021/acs.inorgchem.1c02740 ↗
14. 10.1039/D1TA06006F10.1039/D1TA06006F ↗
15. 10.1039/D3MH01645E10.1039/D3MH01645E ↗
16. 10.1021/acs.analchem.3c0190510.1021/acs.analchem.3c01905 ↗
17. 10.1002/anie.20190170710.1002/anie.201901707 ↗
18. 10.1016/j.ccr.2020.21374310.1016/j.ccr.2020.213743 ↗
19. 10.1002/bkcs.1233510.1002/bkcs.12335 ↗
20. 10.1016/j.bios.2019.11153610.1016/j.bios.2019.111536 ↗
21. 10.1021/jacs.3c1027710.1021/jacs.3c10277 ↗
22. 10.1016/j.seppur.2023.12490310.1016/j.seppur.2023.124903 ↗
23. 10.1021/jacs.3c0051510.1021/jacs.3c00515 ↗
24. 10.1016/j.bios.2018.09.07910.1016/j.bios.2018.09.079 ↗
25. 10.1002/anie.20190777210.1002/anie.201907772 ↗
26. 10.1021/acsanm.0c0156610.1021/acsanm.0c01566 ↗
27. 10.1021/acs.nanolett.3c0165010.1021/acs.nanolett.3c01650 ↗
28. 10.1002/advs.20210437410.1002/advs.202104374 ↗
29. 10.1039/D4QI02293A10.1039/D4QI02293A ↗
30. 10.1002/adfm.20221462710.1002/adfm.202214627 ↗
31. 10.1021/acs.accounts.4c0046910.1021/acs.accounts.4c00469 ↗
32. 10.1002/smll.20210060710.1002/smll.202100607 ↗
33. 10.1002/smll.20230873210.1002/smll.202308732 ↗
34. 10.1039/c0cs00163e10.1039/c0cs00163e ↗
35. 10.1039/C5GC02615F10.1039/C5GC02615F ↗
36. 10.1039/C8GC03868F10.1039/C8GC03868F ↗
37. 10.1021/acsami.0c0608010.1021/acsami.0c06080 ↗
38. 10.1039/D2TA09999C10.1039/D2TA09999C ↗
39. 10.1021/acsami.4c0136510.1021/acsami.4c01365 ↗
40. 10.1039/C9QI00172G10.1039/C9QI00172G ↗
41. 10.1039/C8QI01279B10.1039/C8QI01279B ↗
42. 10.1002/anie.20170973810.1002/anie.201709738 ↗
43. 10.1016/j.jhazmat.2024.13601710.1016/j.jhazmat.2024.136017 ↗
44. 10.1039/c3cc46105j10.1039/c3cc46105j ↗
45. 10.1016/j.apcatb.2017.01.04010.1016/j.apcatb.2017.01.040 ↗
46. 10.1016/j.seppur.2024.12827310.1016/j.seppur.2024.128273 ↗
47. 10.1038/s41467-020-18776-z10.1038/s41467-020-18776-z ↗
48. 10.1016/j.cej.2018.10.04310.1016/j.cej.2018.10.043 ↗
49. 10.1016/j.seppur.2022.12109910.1016/j.seppur.2022.121099 ↗
50. 10.1002/smll.20220719810.1002/smll.202207198 ↗
51. 10.1002/anie.20160437210.1002/anie.201604372 ↗
52. 10.1016/j.cej.2020.12402310.1016/j.cej.2020.124023 ↗
53. 10.1021/acscatal.2c0625510.1021/acscatal.2c06255 ↗
54. 10.1016/j.micromeso.2021.11143310.1016/j.micromeso.2021.111433 ↗
55. 10.1016/j.cej.2021.13018410.1016/j.cej.2021.130184 ↗
56. 10.1021/acs.jpcc.1c0187710.1021/acs.jpcc.1c01877 ↗
57. 10.1021/acs.inorgchem.3c0310610.1021/acs.inorgchem.3c03106 ↗
58. 10.1021/acscatal.2c0237310.1021/acscatal.2c02373 ↗