<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Aoki K</submitter><funding>Iketani Science and Technology Foundation</funding><funding>Tokai Foundation for Technology</funding><funding>Asahi Glass Foundation</funding><funding>Foundation of Kinoshita Memorial Enterprise</funding><pagination>10396-10401</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10683071</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(46)</volume><pubmed_abstract>Sol-gel transitions of polymers are pivotal phenomena in material science, yet the critical phenomenon of structure during gelation has remained unclear. Here, we investigated the sol-gel transition of a fluorous polymer, poly(vinylidene fluoride-&lt;i>co&lt;/i>-hexafluoropropylene), in a blend of two ionic liquids. This system features a quite high amount of cross-linker and binding sites with ion-dipole interactions between the cation and C-F dipoles, thereby facilitating easy exchange of the cross-links. Changing the mixing ratio of the two ionic liquids enabled tuning the ion-dipole interactions and inducing sol-gel transition. Notably, the correlation length and molar mass, obtained by small-angle X-ray scattering, diverged at the gelation point. Moreover, the derived critical exponents (ν = 0.85 ± 0.05) aligns remarkably well with the prediction from percolation theory (ν = 0.88). To our knowledge, this is the first report on the evident divergence during polymeric gelation by small-angle scattering and the verification of the critical exponents of the percolation theory.</pubmed_abstract><journal>The journal of physical chemistry letters</journal><pubmed_title>Polymeric Sol-Gel Transition with the Diverging Correlation Length Verified by Small-Angle X-ray Scattering.</pubmed_title><pmcid>PMC10683071</pmcid><funding_grant_id>0341186-A</funding_grant_id><pubmed_authors>Takahashi R</pubmed_authors><pubmed_authors>Aoki K</pubmed_authors><pubmed_authors>Sugawara-Narutaki A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Polymeric Sol-Gel Transition with the Diverging Correlation Length Verified by Small-Angle X-ray Scattering.</name><description>Sol-gel transitions of polymers are pivotal phenomena in material science, yet the critical phenomenon of structure during gelation has remained unclear. Here, we investigated the sol-gel transition of a fluorous polymer, poly(vinylidene fluoride-&lt;i>co&lt;/i>-hexafluoropropylene), in a blend of two ionic liquids. This system features a quite high amount of cross-linker and binding sites with ion-dipole interactions between the cation and C-F dipoles, thereby facilitating easy exchange of the cross-links. Changing the mixing ratio of the two ionic liquids enabled tuning the ion-dipole interactions and inducing sol-gel transition. Notably, the correlation length and molar mass, obtained by small-angle X-ray scattering, diverged at the gelation point. Moreover, the derived critical exponents (ν = 0.85 ± 0.05) aligns remarkably well with the prediction from percolation theory (ν = 0.88). To our knowledge, this is the first report on the evident divergence during polymeric gelation by small-angle scattering and the verification of the critical exponents of the percolation theory.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-18T13:12:46.491Z</modification><creation>2025-04-06T22:45:27.72Z</creation></dates><accession>S-EPMC10683071</accession><cross_references><pubmed>37955630</pubmed><doi>10.1021/acs.jpclett.3c02631</doi></cross_references></HashMap>