Robust Hydrogen-Bonded Organic Framework with Four-Fold Interpenetration for Adsorptive Separation of C2H6/C2H4 and Xe/Kr

• Published in: Precision Chemistry Vol. 1; no. 9; pp. 524 - 529
• Main Authors: Guo, Fu-An, Zhou, Kang, Liu, Jiaqi, Wang, Hao, Li, Jing
• Format: Journal Article
• Language: English
• Published: University of Science and Technology of China and American Chemical Society 27.11.2023; American Chemical Society
• Subjects: Letter; Hydrogen-Bonded Organic Frameworks; Selectivity; Separation; Interpenetration; Adsorption
• ISSN: 2771-9316; 2771-9316
• DOI: 10.1021/prechem.3c00040

Hydrogen-bonded organic frameworks (HOFs) are an emerging class of porous materials that hold promise for the adsorptive separation of industrially relevant gas mixtures. However, developing HOFs with high thermal stability and resistance to water remains a daunting challenge. We report here a microporous HOF (HIAM-103) assembled from a hexacarboxylate linker (2,4,6-trimethylbenzene-1,3,5-triylisophthalic acid, H6TMBTI). The compound crystallizes in the trigonal crystal system, and its structure is a four-fold interpenetrated network. Upon thermal activation, the single crystals remain intact, allowing for precise determination of the activated structure. HIAM-103 exhibits remarkable thermal and hydrothermal stability. Its microporous channels demonstrate selective adsorption of C2H6 over C2H4 and Xe over Kr, and its separation capability toward mixed gases has been validated by column breakthrough experiments under dry and humid conditions. The preferential gas adsorption sites and separation mechanisms have been uncovered through DFT analysis, which suggests that the methyl group decorated 1D channels are the primary reason for the selective adsorption.