A new post-synthetic route to graft amino groups in porous organic polymers for CO2 capture

Abstract

Herein, we report the development of a post-synthetic modification approach to introduce a high loading of formyl groups onto porous aromatic framework (PAF)-5 via Friedel–Crafts alkylation followed by hydrolysis. Rigorous characterization by NMR, X-ray photoelectron spectroscopy, and Fourier-transform infrared spectroscopy authenticated the successful integration of aldehyde moieties into PAF-5, affording PAF-5-CHO. Subsequent functionalization of PAF-5-CHO with various amines produced three amine-functionalized PAF derivatives. Notably, PAF-5-C[double bond, length as m-dash]N-EDA exhibited a 78% enhancement in carbon dioxide (CO2) adsorption capacity, reaching 3.78 mmol g−1 at 1 bar and 298 K relative to PAF-5-CHO. Breakthrough experiments demonstrated that PAF-5-C[double bond, length as m-dash]N-EDA could effectively separate CO2 from simulated flue gas (CO2/N2 = 15 : 85, v/v; 10 mL min−1). In situ infrared spectroscopy, density functional theory calculations and temperature-programmed desorption studies provided insights into the CO2 adsorption mechanism.

Graphical abstract: A new post-synthetic route to graft amino groups in porous organic polymers for CO2 capture

Supplementary files

Article information

Article type
Edge Article
Submitted
15 Jan 2025
Accepted
24 Jun 2025
First published
01 Jul 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2025, Advance Article

A new post-synthetic route to graft amino groups in porous organic polymers for CO2 capture

Q. Wang, L. Lin, L. Jiang, Z. Wang, Y. Zhang, Q. Han, X. Huang, C. Zhu, J. Jia, Z. Bian and G. Zhu, Chem. Sci., 2025, Advance Article , DOI: 10.1039/D5SC00355E

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