Covalent organic framework supported palladium catalysts
- Author
- Hadi Salemi (UGent) , Maarten Debruyne (UGent) , Veronique Van Speybroeck (UGent) , Pascal Van Der Voort (UGent) , Matthias D'hooghe (UGent) and Christian Stevens (UGent)
- Organization
- Abstract
- Covalent organic frameworks (COFs), as highly porous crystalline structures, are newly emerging materials designed with tuneable features. They have a high potential to be a host to immobilize metal catalysts. The unique property of these materials, such as their high surface area, oriented channels, and heteroatom enrichment, make them promising materials to improve some disadvantages of heterogeneous metal catalysts. In this review, the fabrication and application of Pd anchored COFs as one of the most critical transition-metal catalysts that play a crucial role in a wide range of reactions is summarized.
- Keywords
- EFFICIENT HETEROGENEOUS CATALYST, PD NANOPARTICLES, METAL NANOPARTICLES, COUPLING REACTIONS, CONSTRUCTION, ULTRAFINE, HYDROGENATION, PERFORMANCE, PD(OAC)(2), NANOSHEETS
Downloads
-
d2ta05234b.pdf
- full text (Published version)
- |
- open access
- |
- |
- 3.55 MB
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-01GM39M0X6JF0GN2BF10PQ6TDN
- MLA
- Salemi, Hadi, et al. “Covalent Organic Framework Supported Palladium Catalysts.” JOURNAL OF MATERIALS CHEMISTRY A, vol. 10, no. 39, 2022, pp. 20707–29, doi:10.1039/d2ta05234b.
- APA
- Salemi, H., Debruyne, M., Van Speybroeck, V., Van Der Voort, P., D’hooghe, M., & Stevens, C. (2022). Covalent organic framework supported palladium catalysts. JOURNAL OF MATERIALS CHEMISTRY A, 10(39), 20707–20729. https://doi.org/10.1039/d2ta05234b
- Chicago author-date
- Salemi, Hadi, Maarten Debruyne, Veronique Van Speybroeck, Pascal Van Der Voort, Matthias D’hooghe, and Christian Stevens. 2022. “Covalent Organic Framework Supported Palladium Catalysts.” JOURNAL OF MATERIALS CHEMISTRY A 10 (39): 20707–29. https://doi.org/10.1039/d2ta05234b.
- Chicago author-date (all authors)
- Salemi, Hadi, Maarten Debruyne, Veronique Van Speybroeck, Pascal Van Der Voort, Matthias D’hooghe, and Christian Stevens. 2022. “Covalent Organic Framework Supported Palladium Catalysts.” JOURNAL OF MATERIALS CHEMISTRY A 10 (39): 20707–20729. doi:10.1039/d2ta05234b.
- Vancouver
- 1.Salemi H, Debruyne M, Van Speybroeck V, Van Der Voort P, D’hooghe M, Stevens C. Covalent organic framework supported palladium catalysts. JOURNAL OF MATERIALS CHEMISTRY A. 2022;10(39):20707–29.
- IEEE
- [1]H. Salemi, M. Debruyne, V. Van Speybroeck, P. Van Der Voort, M. D’hooghe, and C. Stevens, “Covalent organic framework supported palladium catalysts,” JOURNAL OF MATERIALS CHEMISTRY A, vol. 10, no. 39, pp. 20707–20729, 2022.
@article{01GM39M0X6JF0GN2BF10PQ6TDN,
abstract = {{Covalent organic frameworks (COFs), as highly porous crystalline structures, are newly emerging materials designed with tuneable features. They have a high potential to be a host to immobilize metal catalysts. The unique property of these materials, such as their high surface area, oriented channels, and heteroatom enrichment, make them promising materials to improve some disadvantages of heterogeneous metal catalysts. In this review, the fabrication and application of Pd anchored COFs as one of the most critical transition-metal catalysts that play a crucial role in a wide range of reactions is summarized.}},
author = {{Salemi, Hadi and Debruyne, Maarten and Van Speybroeck, Veronique and Van Der Voort, Pascal and D'hooghe, Matthias and Stevens, Christian}},
issn = {{2050-7488}},
journal = {{JOURNAL OF MATERIALS CHEMISTRY A}},
keywords = {{EFFICIENT HETEROGENEOUS CATALYST,PD NANOPARTICLES,METAL NANOPARTICLES,COUPLING REACTIONS,CONSTRUCTION,ULTRAFINE,HYDROGENATION,PERFORMANCE,PD(OAC)(2),NANOSHEETS}},
language = {{eng}},
number = {{39}},
pages = {{20707--20729}},
title = {{Covalent organic framework supported palladium catalysts}},
url = {{http://dx.doi.org/10.1039/d2ta05234b}},
volume = {{10}},
year = {{2022}},
}
- Altmetric
- View in Altmetric
- Web of Science
- Times cited: