Abstract

Controlled synthesis of two-dimensional covalent organic frameworks (2D COFs), including stoichiometric and sub-stoichiometric variations, is a topic of growing interest due to its potential in gas separation applications. In this study, we successfully synthesized three distinct 2D COFs by carefully adjusting solvent compositions and monomer ratios during the synthesis of [4 + 4] type COFs. These included a stoichiometric [4 + 4] type COF and two sub-stoichiometric [4 + 2] type COFs, featuring unreacted amino or formyl groups. The resulting COFs exhibit different gas adsorption and separation properties. Specifically, sub-stoichiometric COF-DA with residual amino groups shows comparable adsorption capacity for C2H2, C2H4, and CO2 to stoichiometric COF-DAPy. In contrast, sub-stoichiometric COF-Py with residual formyl groups displays enhanced adsorption selectivity for C2H2/C2H4 and C2H2/CO2 separation, with the C2H2/C2H4 selectivity being the highest among reported COFs, attributed to increased pore polarity resulting from the presence of formyl groups. This study not only offers an additional example of sub-stoichiometric COF synthesis but also advocates for further exploration of sub-stoichiometric COF materials, particularly in the field of gas adsorption and separation.

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