<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>64(32)</volume><submitter>Perego J</submitter><pubmed_abstract>A novel class of ultra-microporous functionalized porous organic polymers (POPs) was developed starting from glyoxylic acid as a cross-linker and triflic acid as a catalyst on polyaromatic monomers, generating in situ methine bridges with carboxylic acids. This one-pot synthetic method generated functionalized POPs with high connectivity per each aromatic group and a high density of aliphatic carboxylic acids decorating the pore walls. Remarkably, the functional groups were transformed into esters, Na- and Li-carboxylates by post-synthetic modification with high yields, generating polyionic porous polymers. These porous polymers displayed excellent CO&lt;sub>2&lt;/sub> adsorption at 298 K and isosteric heat of adsorption with values as high as 50 kJ mol&lt;sup>-1&lt;/sup> for the Na-containing POP end</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pagination>e202507863</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12322657</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Direct Integration of Functionalized Bridges by One-Step Superacid-Catalyzed Reaction to Fabricate Porous Polymers for CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; Capture and Separation.</pubmed_title><pmcid>PMC12322657</pmcid><pubmed_authors>Perego J</pubmed_authors><pubmed_authors>Sozzani P</pubmed_authors><pubmed_authors>Piva S</pubmed_authors><pubmed_authors>Bezuidenhout CX</pubmed_authors><pubmed_authors>Comotti A</pubmed_authors><pubmed_authors>Bracco S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Direct Integration of Functionalized Bridges by One-Step Superacid-Catalyzed Reaction to Fabricate Porous Polymers for CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; Capture and Separation.</name><description>A novel class of ultra-microporous functionalized porous organic polymers (POPs) was developed starting from glyoxylic acid as a cross-linker and triflic acid as a catalyst on polyaromatic monomers, generating in situ methine bridges with carboxylic acids. This one-pot synthetic method generated functionalized POPs with high connectivity per each aromatic group and a high density of aliphatic carboxylic acids decorating the pore walls. Remarkably, the functional groups were transformed into esters, Na- and Li-carboxylates by post-synthetic modification with high yields, generating polyionic porous polymers. These porous polymers displayed excellent CO&lt;sub>2&lt;/sub> adsorption at 298 K and isosteric heat of adsorption with values as high as 50 kJ mol&lt;sup>-1&lt;/sup> for the Na-containing POP end</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-03-27T17:13:57.077Z</modification><creation>2025-08-30T03:09:34.782Z</creation></dates><accession>S-EPMC12322657</accession><cross_references><pubmed>40476516</pubmed><doi>10.1002/anie.202507863</doi></cross_references></HashMap>