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A (4,6)-c copper–organic framework constructed from triazole-inserted dicarboxylate linker with CO2 selective adsorption
Angular ligands are a class of important linkers to design and construct new metal–organic frameworks (MOFs). Herein, solvothermal reaction of 4,4′-(4H-1,2,4-triazole-3,5-diyl)dibenzoic acid (TZDB), a triazole-inserted dicarboxylate, acetate, and Cu(NO3)2·3H2O afforded a copper(ii)-organic framework...
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Published in: | CrystEngComm 2024-02, Vol.26 (9), p.1204-1208 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Angular ligands are a class of important linkers to design and construct new metal–organic frameworks (MOFs). Herein, solvothermal reaction of 4,4′-(4H-1,2,4-triazole-3,5-diyl)dibenzoic acid (TZDB), a triazole-inserted dicarboxylate, acetate, and Cu(NO3)2·3H2O afforded a copper(ii)-organic framework of Cu-TZDB. Structural analysis shows that Cu-TZDB displays an unusual (4,6)-c topological network concomitant with the generation of metalloligand [Cu(TZDB)(H2O)2] in situ. Due to its bi-channel cavities replete with triazolate, coordinated water and methyl groups, Cu-TZDB exhibits CO2 selective adsorption over N2 and CH4, which was not only predicted by ideal adsorption solution theory (IAST), but also verified by dynamic column breakthrough tests. |
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ISSN: | 1466-8033 |
DOI: | 10.1039/d3ce01217d |