Functionalizing metal-organic frameworks (MOFs) with amines is a commonly used strategy to enhance their performance in CO capture applications. As such, in this work, a two-step strategy to covalently functionalize NH-containing MOFs with short chain polyamines was developed. In the first step, the parent MOF, ZnO(NH-BDC), was exposed to bromoacetyl bromide (BrAcBr), which readily reacts with pendant -NH groups on the 2-amino-1,4-benzenedicarboxylate (NH-BDC) ligand. H NMR of the digested MOF sample revealed that as much as 90% of the MOF ligands could be functionalized in the first step. Next, the MOF samples 60% of the ligands functionalized with acetyl bromide, ZnO(NH-BDC)(BrAcNH-BDC), was exposed to several short chain amines including ethylenediamine (ED), diethylenetriamine (DETA), and tris(2-aminoethyl)amine (TAEA). Subsequent digested H NMR analysis indicated that a total of 30%, 28%, and 19% of the MOF ligands were successfully grafted to ED, DETA, and TAEA, respectively. Next, the CO adsorption properties of the amine grafted MOFs were studied. The best performing material, TAEA-appended-ZnO(NH-BDC)(BrAcNH-BDC), exhibits a zero-coverage isosteric heat of CO adsorption of -62.5 kJ/mol, a value that is considerably higher than the one observed for the parent framework, -21 kJ/mol. Although the boosted CO affinity only leads to a slight increase in the CO adsorption capacity in the low-pressure regime (0.15 bar), which is of interest in postcombustion carbon dioxide capture, the CO/N (15/85) selectivity at 313 K is 143, a value that is ∼35 times higher than the one observed for ZnO(NH-BDC), 4.1. Such enhancements are attributed to accessible primary amines, which were grafted to the MOF ligand. This hypothesis was further supported via DRIFTS measurements of TAEA-Ac-ZnO(NH-BDC)(BrAcNH-BDC) after exposure to CO, which revealed the chemisorption of CO via the formation of hydrogen bonded carbamates/carbamic acid and CO species; the latter are adducts formed between CO and [amineH]Br salts that are produced during the amine grafting step.
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http://dx.doi.org/10.1021/acs.inorgchem.1c01216 | DOI Listing |
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