The DOI matches its Crossref record; 76 of the 76 references it cites were found in a registry or an index.
Bipyridine- and Phenanthroline-Based Metal–Organic Frameworks for Highly Efficient and Tandem Catalytic Organic Transformations via Directed C–H Activation
Abstract
We report here the synthesis of a series of robust and porous bipyridyl- and phenanthryl-based metal-organic frameworks (MOFs) of UiO topology (BPV-MOF, mBPV-MOF, and mPT-MOF) and their postsynthetic metalation to afford highly active single-site solid catalysts. While BPV-MOF was constructed from only bipyridyl-functionalized dicarboxylate linker, both mBPV- and mPT-MOF were built with a mixture of bipyridyl- or phenanthryl-functionalized and unfunctionalized dicarboxylate linkers. The postsynthetic metalation of these MOFs with [Ir(COD)(OMe)]2 provided Ir-functionalized MOFs (BPV-MOF-Ir, mBPV-MOF-Ir, and mPT-MOF-Ir), which are highly active catalysts for tandem hydrosilylation of aryl ketones and aldehydes followed by dehydrogenative ortho-silylation of benzylicsilyl ethers as well as C-H borylation of arenes using B2pin2. Both mBPV-MOF-Ir and mPT-MOF-Ir catalysts displayed superior activities compared to BPV-MOF-Ir due to the presence of larger open channels in the mixed-linker MOFs. Impressively, mBPV-MOF-Ir exhibited high TONs of up to 17,000 for C-H borylation reactions and was recycled more than 15 times. The mPT-MOF-Ir system is also active in catalyzing tandem dehydrosilylation/dehydrogenative cyclization of N-methylbenzyl amines to azasilolanes in the absence of a hydrogen acceptor. Importantly, MOF-Ir catalysts are significantly more active (up to 95 times) and stable than their homogeneous counterparts for all three reactions, strongly supporting the beneficial effects of active site isolation within MOFs. This work illustrates the ability to increase MOF open channel sizes by using the mixed linker approach and shows the enormous potential of developing highly active and robust single-site solid catalysts based on MOFs containing nitrogen-donor ligands for important organic transformations.
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Covalent Chemistry beyond Molecules
Jiang, J., Zhao, Y., & Yaghi, O. M. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.5b10666 · Cited by 448
MOF-enabled confinement and related effects for chemical catalyst presentation and utilization
Liu, J., Goetjen, T. A., Wang, Q., Knapp, J. G., Wasson, M. C., Yang, Y., Syed, Z. H., Delferro, M., Notestein, J. M., Farha, O. K., et al. (2022) · Chemical Society Reviews · doi:10.1039/d1cs00968k · Cited by 386
Nanoscale Metal–Organic Frameworks for Ratiometric Oxygen Sensing in Live Cells
Xu, R., Wang, Y., Duan, X., Lu, K., Micheroni, D., Hu, A., & Lin, W. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.5b13458 · Cited by 319
Self-citationXia, Q., Li, Z., Tan, C., Liu, Y., Gong, W., & Cui, Y. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b03113 · Cited by 265
Metadata
- Authors
- Manna, K., Zhang, T., Greene, F. X., & Lin, W.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2015-02-16
- Volume
- 137
- Issue
- 7
- Pages
- 2665-2673
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2080326204
- Cited by
- 289
- References
- 76
- FWCI
- 19.08
- Type
- journal article
- Language
- en
- Open access
- closed
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