<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(41)</volume><submitter>Li J</submitter><pubmed_abstract>The chemical stability of the anion exchange membranes (AEMs) is determinative towards the engineering applications of anion exchange membrane fuel cells (AEMFCs) and other AEM-based electrochemical devices, yet remains a challenge due to deficiencies in the structural design of cations. In this work, an effective design strategy for ultra-stable piperidinium cations is presented based on the systematic investigation of the chemical stability of piperidinium in harsh alkaline media. Firstly, benzyl-substituted piperidinium was degraded by about 23% in a 7 M KOH solution at 100 °C after 1436 h, which was much more stable than pyrrolidinium due to its lower ring strain. The introduction of substituent effects at the α-C position was proved to be an effective strategy for enhancing the chemic</pubmed_abstract><journal>RSC advances</journal><pagination>26542-26549</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9486533</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chemically stable piperidinium cations for anion exchange membranes.</pubmed_title><pmcid>PMC9486533</pmcid><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Xia Z</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Sun G</pubmed_authors><pubmed_authors>Yang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chemically stable piperidinium cations for anion exchange membranes.</name><description>The chemical stability of the anion exchange membranes (AEMs) is determinative towards the engineering applications of anion exchange membrane fuel cells (AEMFCs) and other AEM-based electrochemical devices, yet remains a challenge due to deficiencies in the structural design of cations. In this work, an effective design strategy for ultra-stable piperidinium cations is presented based on the systematic investigation of the chemical stability of piperidinium in harsh alkaline media. Firstly, benzyl-substituted piperidinium was degraded by about 23% in a 7 M KOH solution at 100 °C after 1436 h, which was much more stable than pyrrolidinium due to its lower ring strain. The introduction of substituent effects at the α-C position was proved to be an effective strategy for enhancing the chemic</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-26T00:59:04.823Z</modification><creation>2025-04-06T09:54:42.604Z</creation></dates><accession>S-EPMC9486533</accession><cross_references><pubmed>36275149</pubmed><doi>10.1039/d2ra02286a</doi></cross_references></HashMap>