journal article·2024-04-01Open access

Tunable Crystalline Organic Cage for Selective Sorting of Ortho-Monohalotoluene Isomers

Lukman O. Alimi, Basem Moosa, Weibin Lin, Niveen M. Khashab

ACS Materials Letters· Volume 6· Issue 4

Abstract

A highly flexible 4,4′-oxybis benzaldehyde-based imine cage ( Oba-cage ) has selectively adsorbed the ortho-isomer from all other monohalotoluene (X-toluene, X = F, Cl, and Br) isomers with moderate to excellent uptake 52%, 71%, and 93% for ortho-fluorotoluene (oFT), ortho-chlorotoluene (oCT), and ortho-bromotoluene (oBT), respectively. The structural changes demonstrated by the Oba-cage with different solvents appear to favor the discrimination of only the ortho-isomer from other monohalotoluene isomers through host–guest hydrogen bonding interactions. In addition, the uptake of these ortho isomers by the Oba-cage increases with the size of the halogen substituents. We believe that this work provides interesting insights for designing efficient molecular sieves for the selective separation of halo-toluene to lower the high energy bill of these industrial separations.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications · Chemical Synthesis and Characterization

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

Affiliations

Smart Hybrid Materials Laboratory (SHMs), Advanced Membranes and Porous Materials Center (AMPMC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia

Funding

King Abdullah University of Science and Technology

References (30)

Show source-provided references
1. 10.1016/j.apcata.2007.10.02710.1016/j.apcata.2007.10.027 ↗
2. 10.1021/ie50435a01210.1021/ie50435a012 ↗
3. 10.4028/www.scientific.net/AMR.781-784.18210.4028/www.scientific.net/AMR.781-784.182 ↗
4. 10.1023/A:100341290734710.1023/A:1003412907347 ↗
5. Di Bella, E. P.; Rochelle Park, N. J. Process for the Production of 2,4-Dichlorotoluene. U.S. Patent 3,366,698, 30 January 1968.
6. 10.1016/0926-860X(94)00293-210.1016/0926-860X(94)00293-2 ↗
7. 10.1016/S0926-860X(01)00577-410.1016/S0926-860X(01)00577-4 ↗
8. 10.1166/jnn.2015.1020310.1166/jnn.2015.10203 ↗
9. Chlorotoluene─Global Market Outlook (2020–2028). https://www.marketresearch.com/Stratistics-Market-Research-Consulting-v4058.
10. 10.1002/adma.20180508810.1002/adma.201805088 ↗
11. 10.1038/srep1398110.1038/srep13981 ↗
12. 10.1039/b802426j10.1039/b802426j ↗
13. 10.1021/jacs.0c1301910.1021/jacs.0c13019 ↗
14. 10.1039/D1CC03531B10.1039/D1CC03531B ↗
15. 10.1039/D1SC03509F10.1039/D1SC03509F ↗
16. 10.1039/D2CC03574J10.1039/D2CC03574J ↗
17. 10.1021/jacs.9b0998810.1021/jacs.9b09988 ↗
18. 10.1038/532435a10.1038/532435a ↗
19. 10.1038/nmat254510.1038/nmat2545 ↗
20. 10.1002/anie.20200778210.1002/anie.202007782 ↗
21. 10.1039/D1SC00440A10.1039/D1SC00440A ↗
22. 10.1002/anie.20210678410.1002/anie.202106784 ↗
23. 10.1021/cr200190s10.1021/cr200190s ↗
24. 10.1021/jacs.9b0431910.1021/jacs.9b04319 ↗
25. 10.1002/anie.20221259610.1002/anie.202212596 ↗
26. 10.1002/ange.20221259610.1002/ange.202212596 ↗
27. 10.1039/C8SC04598D10.1039/C8SC04598D ↗
28. 10.1021/jacs.5b1286010.1021/jacs.5b12860 ↗
29. 10.1021/jacs.0c1153010.1021/jacs.0c11530 ↗
30. 10.1002/jcc.2681210.1002/jcc.26812 ↗