<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kawamoto M</submitter><funding>JST, PRESTO</funding><funding>Toshiaki Ogasawara Memorial Foundation</funding><pagination>e70572</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12817154</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(2)</volume><pubmed_abstract>Conjugated diene polymers cross-linked with boronic acid functionalities were synthesized via free-radical copolymerization of styrylboronic acid and isoprene or myrcene. The polymerization proceeded with an identical boron incorporation to the comonomer feed in a 1,4-specific manner. The molecular weight (M&lt;sub>n&lt;/sub>) of the copolymer reached 46,000-110,000 g/mol, guaranteeing an adequate number of boronic acids in one polymer chain for cross-linking. To obtain a soluble copolymer, the concentration of styrylboronic acid monomer in THF/H&lt;sub>2&lt;/sub>O mixture solvent is important to prevent dehydrative boroxine formation during polymerization. The cross-linking driven by thermal dehydration-condensation of boronic acid moieties was confirmed by the increase in tensile modulus of the mold</pubmed_abstract><journal>Chemistry, an Asian journal</journal><pubmed_title>Synthesis of Boronic Acid-Cross-Linked Diene-Based Polymers via Free-Radical Copolymerization.</pubmed_title><pmcid>PMC12817154</pmcid><funding_grant_id>JPMJPR22N8</funding_grant_id><pubmed_authors>Dolui S</pubmed_authors><pubmed_authors>Nakayama Y</pubmed_authors><pubmed_authors>Tanaka R</pubmed_authors><pubmed_authors>Shiono T</pubmed_authors><pubmed_authors>Kawamoto M</pubmed_authors><pubmed_authors>Kihara SI</pubmed_authors><pubmed_authors>Nishizono M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis of Boronic Acid-Cross-Linked Diene-Based Polymers via Free-Radical Copolymerization.</name><description>Conjugated diene polymers cross-linked with boronic acid functionalities were synthesized via free-radical copolymerization of styrylboronic acid and isoprene or myrcene. The polymerization proceeded with an identical boron incorporation to the comonomer feed in a 1,4-specific manner. The molecular weight (M&lt;sub>n&lt;/sub>) of the copolymer reached 46,000-110,000 g/mol, guaranteeing an adequate number of boronic acids in one polymer chain for cross-linking. To obtain a soluble copolymer, the concentration of styrylboronic acid monomer in THF/H&lt;sub>2&lt;/sub>O mixture solvent is important to prevent dehydrative boroxine formation during polymerization. The cross-linking driven by thermal dehydration-condensation of boronic acid moieties was confirmed by the increase in tensile modulus of the mold</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-06T19:41:33.009Z</modification><creation>2026-06-04T03:11:48.014Z</creation></dates><accession>S-EPMC12817154</accession><cross_references><pubmed>41556157</pubmed><doi>10.1002/asia.70572</doi></cross_references></HashMap>