<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Li C</submitter><pubmed_abstract>The p-π conjugated polymers have garnered considerable interest owing to their distinctive electronic structures, which arise from the interaction between p orbitals and π electrons. Currently, the p-π conjugated polymers with charged side chains have been extensively studied, those featuring charged backbones are rare due to the synthetic difficulties. In this work, we developed a spontaneous amino-yne click polymerization utilizing pyridinium-activated alkyne and aromatic primary amine monomers, enabling the efficient synthesis of p-π conjugated ionic polymers with high weight-average molecular weights (&lt;i>M&lt;/i> &lt;sub>w&lt;/sub>, up to 44 100) and excellent yields (up to 98%). The resultant polymers are emissive, but demonstrate remarkable photothermal properties. Upon irradiation with an 80</pubmed_abstract><journal>Chemical science</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12394897</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Spontaneous amino-yne click polymerization enabled by pyridinium-activated alkynes toward p-π conjugated ionic polymers.</pubmed_title><pmcid>PMC12394897</pmcid><pubmed_authors>Zhang G</pubmed_authors><pubmed_authors>Qin A</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Zhang K</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Tang BZ</pubmed_authors><pubmed_authors>Wei L</pubmed_authors><pubmed_authors>Liu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Spontaneous amino-yne click polymerization enabled by pyridinium-activated alkynes toward p-π conjugated ionic polymers.</name><description>The p-π conjugated polymers have garnered considerable interest owing to their distinctive electronic structures, which arise from the interaction between p orbitals and π electrons. Currently, the p-π conjugated polymers with charged side chains have been extensively studied, those featuring charged backbones are rare due to the synthetic difficulties. In this work, we developed a spontaneous amino-yne click polymerization utilizing pyridinium-activated alkyne and aromatic primary amine monomers, enabling the efficient synthesis of p-π conjugated ionic polymers with high weight-average molecular weights (&lt;i>M&lt;/i> &lt;sub>w&lt;/sub>, up to 44 100) and excellent yields (up to 98%). The resultant polymers are emissive, but demonstrate remarkable photothermal properties. Upon irradiation with an 80</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-29T17:53:43.577Z</modification><creation>2026-04-08T05:44:03.832Z</creation></dates><accession>S-EPMC12394897</accession><cross_references><pubmed>40896324</pubmed><doi>10.1039/d5sc03991f</doi></cross_references></HashMap>