Porous imine-linked networks (PINs) have been prepared by catalyst-free Schiff base condensation of 2,4,6-(4-aminophenyl)1,3,5-triazine with 9,10-anthracene-dicarboxaldehyde (PIN1 and PIN1_2) and with 4,4′,4′′,4′′′-methanetetrakis-benzaldehyde (PIN2). Even after synthesis optimisation, only with DMSO (PIN1 and PIN2) microporous frameworks were obtained, whereas DMF (PIN1_2) and other solvents led to nonporous systems, estimated by argon measurements. Furthermore, ¹⁵N solid state NMR and IR spectroscopy reveal the influence of the decomposition products of DMSO leading to protonation of the imine linkage and resulting in an ionic structure with an incorporated sulfonic counterion. Until now, protonation of an imine function due to the usage of DMSO as solvent has not been discussed in the literature. In contrast, for PIN1_2 the imine linkage remains neutral. Argon sorption isotherms for PIN1 and PIN2 exhibit surface areas of 458 m² g⁻¹ and 325 m² g⁻¹ and the pore structure displays micro- and small mesopores with pore diameters from 0.6 to 5 nm. Additionally, CO₂ isotherms at 273 K demonstrate ultramicropores for all three polymers with similar pore size distributions. Despite their different network structures, similar CO₂ uptakes (1.8–1.06 mmol g⁻¹ at 273 K at 1.0 bar) and heat of adsorption Q_st values of 30 kJ mol⁻¹ were obtained. In line with the polyionic character of PIN1 and PIN2, both compounds adsorb three times more water than the more hydrophobic, neutral PIN1_2 at room temperature indicating two different adsorption mechanisms. IAST selectivity calculations show good CO₂/N₂ (30–31) and CO₂/CH₄ (8–12) selectivity factors. Despite their moderate BET-surface areas, the PINs show good CO₂ uptakes and selectivity factors.