<rss version="2.0" xmlns:a10="http://www.w3.org/2005/Atom"><channel><title>RSC - Polym. Chem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/PY</link><description>RSC - Polym. Chem. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Wed, 13 May 2026 10:08:50 Z</lastBuildDate><category>RSC - Polym. Chem. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - Polym. Chem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/PY</link></image><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00098C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00098C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00098C</link><title>Pyrrolidinium-based Gel Composites for Reprocessable, Flame-Retardant Electrolytes</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00098C, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Haobo Hong, Tshepiso L. Tema, Redoy Gazi Shuvo, Harald Rupp, Stephanie Krüger, Zviadi Katcharava, Anja Marinow, Wolfgang H. Binder&lt;br/&gt;Flame retardant and reprocessable gel composites composed of a pyrrolidinium-based poly(ionic liquid) were successfully prepared by incorporating surface-modified nanoparticles functionalized with ionic liquids or ureidopyrimidinone groups. Covalent functionalization was verified...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Haobo Hong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tshepiso L. Tema</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Redoy Gazi Shuvo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Harald Rupp</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephanie Krüger</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zviadi Katcharava</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anja Marinow</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wolfgang H. Binder</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00261G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00261G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00261G</link><title>Biomass-Derived Photocatalysts for Photocatalytic Atom Transfer Radical Polymerization</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00261G, Paper&lt;/div&gt;&lt;div&gt;Xiaoyu Guo, Xinrang  Wang, Chen Wang, Zhuo  Dang, Jiquan Liu, Lin Lei&lt;br/&gt;This study successfully developed a novel carbon-based photocatalyst (γ-CCD-r) using γ-cyclodextrin as the raw material. As a heterogeneous photocatalyst, it enables easy separation from the reaction mixture. Furthermore, it utilizes...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyu Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinrang  Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chen Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhuo  Dang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiquan Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lin Lei</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00214E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00214E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00214E</link><title>γ-Functionalized thioether, sulfoxide, and sulfone AB monomers for tunable aliphatic polyesters</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00214E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00214E, Paper&lt;/div&gt;&lt;div&gt;Hongqing Fu, Emma Mongkhoun, Nicolas Illy&lt;br/&gt;A modular strategy provides rare γ-functionalized thioether, sulfoxide and sulfone AB monomers for redox-tunable and recyclable polyesters.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hongqing Fu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Emma Mongkhoun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicolas Illy</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00204H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00204H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00204H</link><title>Programmable topological regulation of hierarchically organized crosslinked epoxy thermosets for improved dielectric and thermal properties</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00204H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00204H, Paper&lt;/div&gt;&lt;div&gt;Yiliang Gao, Lijia Liu, Wenchao Jiang, Longkai Jiao, Yawen Liu, Chao Wang, Chunhong Zhang, Yudan Wang&lt;br/&gt;A first-of-its-kind vinyl-functionalized active ester–epoxy system allows programmable regulation of a hierarchically organized crosslinked network, resulting in enhanced thermal robustness and low dielectric loss.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yiliang Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lijia Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenchao Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Longkai Jiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yawen Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chao Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunhong Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yudan Wang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90059C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90059C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90059C</link><title>Correction: Near-instantaneous volumetric printing of complex scaffolds comprised of tough PEG-based hydrogels</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY90059C, Correction&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Mahsa Ebrahimi, Ulrike Arickx, Mariana Arreguín-Campos, Quinten Thijssen, Antonio Jaén Ortega, Mugdha M. Joglekar, Ruth Cardinaels, Sandra Van Vlierberghe, Lorenzo Moroni, Matthew B. Baker, Louis M. Pitet&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mahsa Ebrahimi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrike Arickx</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mariana Arreguín-Campos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Quinten Thijssen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Jaén Ortega</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mugdha M. Joglekar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruth Cardinaels</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sandra Van Vlierberghe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lorenzo Moroni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew B. Baker</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Louis M. Pitet</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00258G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00258G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00258G</link><title>Investigating the synthesis, properties and Diels-Alder reactivity of diene-functional branched polyesters using copolymerisation of furfuryl methacrylate under transfer-dominated branching radical telomerisation (TBRT) conditions</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00258G, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Oliver Penrhyn-Lowe, Stephen Wright, Sarah Lomas, Steve P. Rannard, Andrew Slark, Andrew Dwyer&lt;br/&gt;Diels-Alder reactions have been of considerable interest for many years and strategies for polymeric diene synthesis have predominantly relied on controlled radical polymerisation techniques to avoid unwanted side reactions of...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Oliver Penrhyn-Lowe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephen Wright</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sarah Lomas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steve P. Rannard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew Slark</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew Dwyer</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00092D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00092D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00092D</link><title>Crown ether-based supramolecular elastomers exhibiting reversible and abundant shape programming</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00092D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00092D, Paper&lt;/div&gt;&lt;div&gt;Xinyi Quan, Rui Hu, Xiaohe Zhou, Qingyun Li, Xiaofan Ji&lt;br/&gt;Herein, thermo-responsive supramolecular elastomers were prepared through crown ether-based host–guest interactions, which showed abundant and reversible deformability and were applied in flexible robotic systems.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xinyi Quan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rui Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaohe Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qingyun Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaofan Ji</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00117C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00117C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00117C</link><title>Mechanochemical Strategies for the Catalytic Upcycling of Polyethylene via Transfer Hydrogenation</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00117C, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Antonio  Trimboli, Emilia Paone, Andrea  Donato, Riccardo Pellegrini, Elena Groppo, Maximilian Wohlgemuth, Sven Graetz, Francesco Mauriello, Lars Borchardt&lt;br/&gt;The development of innovative catalytic strategies is crucial to advance the sustainable upcycling of plastic waste. In this work, we present a mechanocatalytic approach for the selective depolymerization of low-density...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio  Trimboli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Emilia Paone</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrea  Donato</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Riccardo Pellegrini</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elena Groppo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maximilian Wohlgemuth</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sven Graetz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francesco Mauriello</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lars Borchardt</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00314A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00314A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00314A</link><title>Stereospecific polymerization of donor–acceptor cyclopropanes with C(sp3)–H bonds as the dormant species</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00314A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00314A, Paper&lt;/div&gt;&lt;div&gt;Yong-Le Tian, Yang-Yang Li, Lun-Heng Wei, Shu-Sen Chen, Ren-Rong Liu, Dian-Feng Chen&lt;br/&gt;MgBr&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;/DBU/C(sp&lt;small&gt;&lt;sup&gt;3&lt;/sup&gt;&lt;/small&gt;)–H bonds enable controlled stereospecific ring-opening polymerization of enantiopure donor–acceptor cyclopropane monomers.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-05T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yong-Le Tian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yang-Yang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lun-Heng Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shu-Sen Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ren-Rong Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dian-Feng Chen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00390G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00390G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00390G</link><title>Molecular design of silane-bridged phosphorus-containing compounds toward epoxy thermosets with flame retardancy, improved toughness, low water absorption and low dielectric constants</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00390G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00390G, Paper&lt;/div&gt;&lt;div&gt;Muhammad Salman, Rukhsana Ashraf, Ze-Tao Xiao, Hao-Jie Shi, Aksam Abdelkhalik, Yuan Hu, Xin Wang&lt;br/&gt;Three P/Si-containing flame retardants (FR&lt;small&gt;&lt;sub&gt;1&lt;/sub&gt;&lt;/small&gt;, FR&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;, and FR&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;) were synthesized &lt;em&gt;via&lt;/em&gt; simple addition reactions of bDMVSiB and TMDVSiO with DPPO and DOPO.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-28T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Muhammad Salman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rukhsana Ashraf</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ze-Tao Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hao-Jie Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aksam Abdelkhalik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuan Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xin Wang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00167J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00167J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00167J</link><title>Nanomicellization characteristics of amphiphilic block copolymer tricycles in various topologies</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00167J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1882-1891&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00167J, Paper&lt;/div&gt;&lt;div&gt;Brian J. Ree&lt;br/&gt;Nanomicellization characteristics of topologically-controlled tricyclic amphiphiles demonstrated the formation of micelles with narrow unimodal distributions in solutions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Brian J. Ree</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00267F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00267F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00267F</link><title>Catalyst- and additive-free light-induced oxidative polymerization of diphenyl disulfides for the facile synthesis of polyphenylene sulfides</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00267F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1789-1793&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00267F, Communication&lt;/div&gt;&lt;div&gt;Shan Hu, Xianyu Ying, Yong Wang, Mushou Cai, Hongjun Zhu&lt;br/&gt;A catalyst- and additive-free light-induced oxidative polymerization of diphenyl disulfides under an oxygen atmosphere is reported for the synthesis of polyphenylene sulfides.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-21T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shan Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xianyu Ying</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mushou Cai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongjun Zhu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00113K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00113K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00113K</link><title>Near-instantaneous volumetric printing of complex scaffolds comprised of tough PEG-based hydrogels</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00113K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1846-1860&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00113K, Paper&lt;/div&gt;&lt;div&gt;Mahsa Ebrahimi, Ulrike Arickx, Mariana Arreguín-Campos, Quinten Thijssen, Antonio Jaén Ortega, Mugdha V. Joglekar, Ruth Cardinaels, Sandra Van Vlierberghe, Lorenzo Moroni, Matthew B. Baker, Louis M. Pitet&lt;br/&gt;Mechanically robust hydrogels are printed &lt;em&gt;via&lt;/em&gt; light promoted crosslinking using volumetric additive manufacturing, leading to intricate 3-dimensional structures.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mahsa Ebrahimi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrike Arickx</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mariana Arreguín-Campos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Quinten Thijssen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Jaén Ortega</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mugdha V. Joglekar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruth Cardinaels</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sandra Van Vlierberghe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lorenzo Moroni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew B. Baker</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Louis M. Pitet</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00102E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00102E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00102E</link><title>Coupling shear-thickening and dynamic bonds in self-healing materials: synthesis, regulation and application</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00102E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1776-1788&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00102E, Minireview&lt;/div&gt;&lt;div&gt;Yuyang Meng, Xinxing Zhang, Xingchao Liu&lt;br/&gt;Coupling shear-thickening and dynamic bonds in self-healing materials enables STDB materials to play an increasingly important role in fields such as biomedical applications, aerospace, and intelligent wearable devices.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yuyang Meng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinxing Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xingchao Liu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00148C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00148C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00148C</link><title>Visible light responsive self-healing polyurea elastomers driven by dynamic coordination for underwater and low-temperature applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00148C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1873-1881&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00148C, Paper&lt;/div&gt;&lt;div&gt;Jingyi Liu, Hui Li, Yuanpeng Wu, Chunxia Zhao, Jinbo Cheng, Haoran Huang, Yijin Zhang&lt;br/&gt;Reversible trans–cis photoisomerization of PDB-Zn networks enables near 100% mechanical recovery in demanding aquatic and sub-zero conditions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jingyi Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuanpeng Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunxia Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinbo Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haoran Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yijin Zhang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00218H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00218H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00218H</link><title>Radical ring-opening polymerization-induced self-assembly for the synthesis of degradable particles incorporating ethyl lipoate</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00218H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1861-1872&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00218H, Paper&lt;/div&gt;&lt;div&gt;Fan Yang, Jacinta F. White, Yufu Wang, Yanting Gao, Daniel Yuen, Angus P. R. Johnston, Almar Postma, Lewis D. Blackman, Georgina K. Such&lt;br/&gt;Redox-degradable polymeric nanoparticles with tunable degradability were prepared &lt;em&gt;via&lt;/em&gt; a rROPISA approach by incorporating ethyl lipoate as a redox-responsive monomer.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-13T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fan Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jacinta F. White</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yufu Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanting Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel Yuen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Angus P. R. Johnston</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Almar Postma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lewis D. Blackman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Georgina K. Such</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01214G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01214G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01214G</link><title>Synthesis of well-defined and recyclable polyesters from ring opening polymerization of 1,5-dioxepan-2-one catalyzed by a Lewis acid–base pair</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01214G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1827-1836&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01214G, Paper&lt;/div&gt;&lt;div&gt;Zheng Li, Kai Li, Chengde Hu, Zhibo Li&lt;br/&gt;A ZnEt&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;/DMAP Lewis pair facilitates the controlled ring-opening polymerization of DXO to produce well-defined (co)polyesters. In addition, closed-loop chemical recycling of poly(1,5-dioxepan-2-one) (PDXO) has been successfully established.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zheng Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kai Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chengde Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhibo Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00309E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00309E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00309E</link><title>Carboxylic acid α-end-functionalized poly(2-oxazoline)s synthesized through benzylic CROP initiators</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00309E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1807-1818&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00309E, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Caroline T. Holick, Nora Engel, Nicole Fritz, Christine Weber, Ulrich S. Schubert&lt;br/&gt;Bromomethylbenzoates are suitable initiators for the polymerization of 2-oxazolines. They provide high end-group fidelity and enable access to heterotelechelic polyoxazolines and block copolymers with methyl ester or carboxylic acid end groups.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Caroline T. Holick</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nora Engel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicole Fritz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christine Weber</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrich S. Schubert</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00191B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00191B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00191B</link><title>Elucidating the molecular design principles of N-alkylated nylons for LCST-type phase separation through a systematic polymer library</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00191B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1819-1826&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00191B, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Akari Sugano, Keitaro Matsuoka, Kazuki Sada&lt;br/&gt;Hydrophilic polymers showing LCST-type phase separation are useful functional polymer materials.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Akari Sugano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Keitaro Matsuoka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kazuki Sada</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01210D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01210D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01210D</link><title>Degrafting reaction of polymer brushes: the determining role of molecular weight and grafting density</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01210D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1837-1845&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01210D, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Riccardo Chiarcos, Diego Antonioli, Luca Gabutti, Elo Marsengo, Michele Perego, Michele Laus&lt;br/&gt;The degrafting reaction rate in the presence of water increases when both the grafting density of the brush and the molecular weight of the grafted polymer increase.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Riccardo Chiarcos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Diego Antonioli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luca Gabutti</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elo Marsengo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michele Perego</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michele Laus</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00221H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00221H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00221H</link><title>Inner side-chain engineering of non-fullerene acceptors enables efficient thick-film all-polymer solar cells</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00221H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1794-1806&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00221H, Paper&lt;/div&gt;&lt;div&gt;Wenhao Peng, Xiaoman Gui, Shisong Sun, Zhenyu Wei, Panfeng Gao, Meixiu Wan, Lijun Huo&lt;br/&gt;Tuning acceptor alkyl spacer length controls H-aggregation in all-polymer solar cells. PM6:PY-EH yields 16.38% PCE, retains 14.24% at 410 nm—ideal thickness tolerance for roll-to-roll manufacturing.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-06T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wenhao Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoman Gui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shisong Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhenyu Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Panfeng Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Meixiu Wan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lijun Huo</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00229C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00229C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00229C</link><title>Trimethylamine N-oxide (TMAO)-grafted silicone hydrogels for anti-fibrosis</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00229C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00229C, Paper&lt;/div&gt;&lt;div&gt;Xiangyu Dang, Chongyu Zhu, Zhize Chen&lt;br/&gt;A trimethylamine &lt;em&gt;N&lt;/em&gt;-oxide (TMAO)-grafted silicone hydrogel was designed and prepared, which can effectively alleviate the foreign body reaction.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangyu Dang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chongyu Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhize Chen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00288A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00288A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00288A</link><title>Ultra-high molecular weight tanglemer hydrogels</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00288A, Paper&lt;/div&gt;&lt;div&gt;Saifur  Rahaman, Brett Leslie Pollard, Luke Andrew Connal&lt;br/&gt;Developing hydrogels that combine excellent mechanical strength with biocompatibility remains a challenge, particularly for designing materials for biomedical applications. We report the synthesis of ultra-high molecular weight poly(2-hydroxyethyl acrylate) hydrogels...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Saifur  Rahaman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Brett Leslie Pollard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luke Andrew Connal</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00222F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00222F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00222F</link><title>Binuclear Nickel Catalysts Enable One-Step Copolymerization of Ethylene with 2-Allylphenol to Phenol-Functionalized Branched Polyethylenes</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00222F, Paper&lt;/div&gt;&lt;div&gt;Yuan Lu, Yanshan Gao, Shuyang Yu, Yanan Zhao, Jie Yang, Xiuli Sun, Xiao-Yan Wang, Yong Tang&lt;br/&gt;One-step ethylene copolymerization with readily available short-chain alkenyl phenols is an attractive alternative to post-modification or the use of designed phenolic comonomers for preparing phenol-functionalized polyethylenes, yet prior examples have...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yuan Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanshan Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuyang Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanan Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jie Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiuli Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao-Yan Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yong Tang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00323K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00323K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00323K</link><title>Controlled Ring-Opening Polymerization of Xylose-derived Lactones towards Sustainable Polyesters</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00323K, Paper&lt;/div&gt;&lt;div&gt;Xiao-Yue Wang, Wei Wang, Wang-Long Wei, Wei-Min Ren, Xiaobing Lu, Hui Zhou&lt;br/&gt;Utilizing bio-resources to construct sustainable polymers offers a highly promising solution to address the global plastic waste crisis. Herein, a series of seven-membered biorenewable lactones were synthesized from D-/L-xyloses as...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao-Yue Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wang-Long Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei-Min Ren</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaobing Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Zhou</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01145K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01145K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01145K</link><title>Design and application of nanosilver hybridized fluorosilicone resin-modified epoxy coatings for SRB resistance in aviation fuel storage and transport equipment</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01145K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01145K, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Lanjiao Jiao, Xiaojuan Lai, Qiufeng An&lt;br/&gt;Microbiologically influenced corrosion threatens aviation fuel infrastructure. A nanosilver hybridized fluorosilicone resin-modified epoxy coating is designed to resist SRB and corrosion.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-05T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lanjiao Jiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaojuan Lai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiufeng An</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00293E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00293E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00293E</link><title>MWD of living polyacrylates fractionated by chromatography via chain-end modification</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00293E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00293E, Paper&lt;/div&gt;&lt;div&gt;Subin Choi, Eujin Bae, Suraj Aswale, Ye Rin Jang, Hong Y. Cho, Heung Bae Jeon, Hyun-jong Paik&lt;br/&gt;Living polyacrylates are synthesized and end-functionalized to enhance chain-end polarity, enabling selective separation of living and dead chains by solvent-gradient HPLC, confirming Poisson-distributed living fractions.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Subin Choi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eujin Bae</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Suraj Aswale</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ye Rin Jang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hong Y. Cho</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Heung Bae Jeon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyun-jong Paik</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00109B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00109B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00109B</link><title>Linkage effects of phenanthrene-based polymeric anodes for lithium-ion batteries</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00109B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00109B, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Yu-Ruei Kung, Huai-Sheng Chin, Santosh U. Sharma, Li Chen, Zi-Yun Ou, Hung-Ju Yen&lt;br/&gt;A systematic series of polyamides featuring aryloxy-phenanthrene backbones provides general design guidelines for the development of organic electrode materials. Image created with Adobe Firefly.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-27T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Ruei Kung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huai-Sheng Chin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Santosh U. Sharma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Li Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zi-Yun Ou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hung-Ju Yen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00121A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00121A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00121A</link><title>Achieving high lignin content and mechanical enhancement in biobased thermosets via a high-molecular-weight soybean oil skeleton</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00121A, Paper&lt;/div&gt;&lt;div&gt;Ying Lin, Kangyong  Xu, Puyou  Jia, Shenglong  Liao, Ye Sha, Qingping Song&lt;br/&gt;Developing sustainable thermosets from renewable resources that can rival their petroleum derived counterparts has attracted tremendous interest during recent years. Despite its prevalence as a reinforcement for thermosets, the utilization...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kangyong  Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Puyou  Jia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shenglong  Liao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ye Sha</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qingping Song</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00246C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00246C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00246C</link><title>AIE/CPL dual-functional poly(aryl isocyanide)s synthesized using (S,S)-bis(oxazolinylphenyl)amido-ligated palladium phenylethynyl complexes: high-security anti-counterfeiting and targeted cellular imaging</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00246C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00246C, Paper&lt;/div&gt;&lt;div&gt;Beiming Yu, Shuling Jia, Xuanren Zhu, Jiaojiao Li, Changguo Sun, Chao Ma, Shuangshuang Ma, Minjian Wu, Zhiyuan Hu, Xiaolu Wu, Guangpeng Gao, Xiaofang Li&lt;br/&gt;New (&lt;em&gt;S&lt;/em&gt;,&lt;em&gt;S&lt;/em&gt;)-bis(oxazolinylphenyl)amido palladium complexes act as catalysts for aryl isocyanide (co)polymerization, yielding AIE/CPL poly(aryl isocyanide)s for anti-counterfeiting and cellular imaging.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Beiming Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuling Jia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuanren Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiaojiao Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Changguo Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chao Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuangshuang Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minjian Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiyuan Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaolu Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guangpeng Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaofang Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00228E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00228E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00228E</link><title>Study on the Microstructure of Poly(Amide 6-Ether) Copolymers and Application in Elastic Fibers</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00228E, Paper&lt;/div&gt;&lt;div&gt;Yixiao  Yu, Weicheng  Yang, Yuhao Wu, Shengming Zhang, Chaosheng Wang, Huaping Wang, Peng Ji, Chengzhen Meng&lt;br/&gt;Fiber elasticity is an important property for achieving clothing comfort. The excellent resilience of poly (amide 6-ether) copolymers makes them a popular candidate material for preparing PA6-based elastic fibers. However,...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yixiao  Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Weicheng  Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuhao Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shengming Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chaosheng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huaping Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peng Ji</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chengzhen Meng</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00350H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00350H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00350H</link><title>Aminolysis of poly(ethylene terephthalate) to bis(2-hydroxy ethylene)terephthalamide with ethanolamine catalyzed by La(OAc)3</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00350H, Paper&lt;/div&gt;&lt;div&gt;Ye He, Zheyu Zhao, Jue Chen, Yunjie Luo&lt;br/&gt;Chemical recycling of PET waste is critically important for environmental preservation and resource conservation. While aminolysis of PET with ethanolamine to produce bis(2-hydroxyethyl)terephthalamide (BHETA) represents a promising approach, achieving efficient...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ye He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zheyu Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jue Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yunjie Luo</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00099A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00099A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00099A</link><title>A reusable visible light initiation system for radical polymerizations in water</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00099A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00099A, Paper&lt;/div&gt;&lt;div&gt;Yu-Chien Chen, Fu-Sheng Wang, Chi-How Peng&lt;br/&gt;A stable organic molecule, 4-nitrophenylacetylene, is used as a recyclable photo-initiator for the polymerization of aqueous monomers in water under ambient conditions.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-29T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Chien Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fu-Sheng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chi-How Peng</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00394J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00394J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00394J</link><title>Bifunctional Group Distribution and Gradient Structure Resulting from the Anionic Copolymerization of Styrene and Vinylbenzyl N,N-Allylmethylamine</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00394J, Paper&lt;/div&gt;&lt;div&gt;Kun Liu, Xupeng Han, Jiahao  Zhou, Yao Long, Min  Zhang, Yayan Wang, Jiaping  Tan, Meilin  Liu, Lijun Li, Yali  Li&lt;br/&gt;The synthesis of well-defined, functionalized polystyrene with controlled molecular weight and narrow molecular weight distribution by anionic polymerization under mild conditions poses certain challenges. In this study, a novel functionalized...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-06T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kun Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xupeng Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiahao  Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yao Long</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Min  Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yayan Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiaping  Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Meilin  Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lijun Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yali  Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00213G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00213G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00213G</link><title>Metal-free synthesis of terpene-derived polyester-block-polycarbonates and post-polymerization modification via thiol–ene click chemistry</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00213G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00213G, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Mikhailey D. S. Wheeler, Allison M. Clark, Andrew P. Kinsman, Megan L. Graham, Francesca M. Kerton&lt;br/&gt;Selective ring-opening copolymerization of bio-derived anhydrides with epoxides and terpolymerization with CO&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; under solvent free conditions was achieved; photoinitiated modification yielded thermally stable polymers with a range of properties.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mikhailey D. S. Wheeler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Allison M. Clark</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew P. Kinsman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Megan L. Graham</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francesca M. Kerton</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00203J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00203J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00203J</link><title>High-performance flame-retardant polyphosphate ester-based solid electrolyte via in situ ring-opening polymerization for safe Li metal batteries</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00203J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00203J, Paper&lt;/div&gt;&lt;div&gt;Linyuan Cui, Xinkai Zou, Chengliang Wang, Huiyu Zhao, Hairui Chen, Qiming Xu, Xuehong Sun, Jingjiang Sun, Qingfu Wang&lt;br/&gt;&lt;em&gt;In situ&lt;/em&gt; polymerized solid electrolyte with synergistic flame retardancy, high-voltage stability and fast Li&lt;small&gt;&lt;sup&gt;+&lt;/sup&gt;&lt;/small&gt; transport for safe lithium metal batteries.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Linyuan Cui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinkai Zou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chengliang Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huiyu Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hairui Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiming Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuehong Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingjiang Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qingfu Wang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00006A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00006A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00006A</link><title>Recent progress in bulk polymerization: spatiotemporally discontinuous change of polymerization accompanied by phase separation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00006A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1661-1674&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00006A, Review Article&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Yasuhito Suzuki, Akikazu Matsumoto&lt;br/&gt;Bulk polymerization converts liquid monomers into polymers &lt;em&gt;via&lt;/em&gt; an exothermic reaction, often leading to vitrification and spatiotemporal heterogeneity, which is closely linked to the sudden reaction acceleration known as the Trommsdorff effect.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yasuhito Suzuki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Akikazu Matsumoto</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00186F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00186F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00186F</link><title>Synthesis of optically active polymers containing a main-chain hydroxamic acid backbone via asymmetric polymerization</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00186F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1747-1754&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00186F, Paper&lt;/div&gt;&lt;div&gt;Naoya Kanbayashi, Kiyotaka Onitsuka&lt;br/&gt;Synthesis of an optically active polymer bearing a hydroxamic acid backbone.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Naoya Kanbayashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kiyotaka Onitsuka</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00180G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00180G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00180G</link><title>Palladium-catalyzed copolymerization to synthesize sulfur-containing polyethylene materials</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00180G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1701-1705&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00180G, Paper&lt;/div&gt;&lt;div&gt;Chuncai Zhao, Yuming Xu, Guifu Si, Dan Peng, Menghe Xu&lt;br/&gt;Sulfur-functionalized polyethylene materials were efficiently synthesized through phosphine–sulfonate palladium-catalyzed copolymerization of ethylene with norbornene-based sulfur-containing comonomers.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chuncai Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuming Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guifu Si</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dan Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Menghe Xu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00291A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00291A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00291A</link><title>Modulatable structural colors in rapid-curing high-performance hydrogels</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00291A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1755-1766&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00291A, Paper&lt;/div&gt;&lt;div&gt;Qiang Zhang, Xiao Yang, Zhaoyang Wu&lt;br/&gt;This study presents a rapid-curing methodology for fabricating high-performance hydrogels using a ternary copolymer system comprising 2-hydroxyethyl methacrylate (HEMA), &lt;em&gt;N&lt;/em&gt;-vinylpyrrolidone (NVP), and &lt;em&gt;N&lt;/em&gt;,&lt;em&gt;N&lt;/em&gt;-dimethylacrylamide (DMAA).&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Qiang Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhaoyang Wu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00075D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00075D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00075D</link><title>Synthesis and structure–property relationships of lipoic acid-based conductive elastomers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00075D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1694-1700&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00075D, Paper&lt;/div&gt;&lt;div&gt;Feng Chen, Fangjun Zhu, Weikun Xu, Yanpei Fei&lt;br/&gt;Crosslinked lipoic acid-based ionic conductive elastomers reveal how polymer network structure governs lithium salt compatibility and ionic transport.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Feng Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fangjun Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Weikun Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanpei Fei</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01024A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01024A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01024A</link><title>Organo-catalyzed deamination of polystyrene sulfonamide for diverse post-polymerization modification of styrenic polymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01024A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1721-1729&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01024A, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Tulaja Shrestha, Dan My Nguyen, Harrison Goehrig, Vidhika S. Damani, Caitlin M. Quinn, Laure V. Kayser&lt;br/&gt;Post-polymerization modification of polystyrene generates sulfinate intermediates that enable modular diversification to a wide range of functional groups.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tulaja Shrestha</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dan My Nguyen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Harrison Goehrig</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vidhika S. Damani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Caitlin M. Quinn</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laure V. Kayser</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00164E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00164E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00164E</link><title>Stereochemically purified trans-dihydroxy-substituted cage silsesquioxane-based bisurea supramolecular polymer materials enable metastable-to-thermodynamic phase evolution and enhanced modulus</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00164E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1740-1746&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00164E, Paper&lt;/div&gt;&lt;div&gt;Jinshiro Takeuchi, Takahiro Iwamoto, Naoki Watanabe, Hiroaki Imoto, Kensuke Naka&lt;br/&gt;Stereochemically purified &lt;em&gt;trans&lt;/em&gt;-dihydroxy-substituted cage silsesquioxane-based bisurea supramolecular polymer materials exhibit an effective metastable-to-thermodynamic phase transition upon heating.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-31T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jinshiro Takeuchi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takahiro Iwamoto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Naoki Watanabe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hiroaki Imoto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kensuke Naka</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00144K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00144K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00144K</link><title>Synthesis of macro-rotaxanes via direct trapping of multicyclic poly(n-butyl acrylate) in a cross-linked network</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00144K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1730-1739&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00144K, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Kotaro Ibe, Yamato Ebii, Minami Ebe, Kazushige Suzuki, Takayuki Kurokawa, Takuya Yamamoto, Feng Li, Takuya Isono, Toshifumi Satoh&lt;br/&gt;Macro-rotaxanes, in which both the linear and cyclic components are polymers, remain largely unexplored in terms of their formation and potential material applications due to the synthetic challenges associated with cyclic polymers.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-31T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kotaro Ibe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yamato Ebii</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minami Ebe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kazushige Suzuki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takayuki Kurokawa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takuya Yamamoto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Feng Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takuya Isono</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Toshifumi Satoh</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00118A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00118A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00118A</link><title>Double metal cyanide (DMC) catalysis: detailed in situ NMR kinetics studies on the copolymerization of propylene oxide with substituted epoxides</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00118A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1706-1720&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00118A, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Erik Kersten, Maximilian Kaiser, Jan Blankenburg, Kamil Maciol, Manfred Wagner, Sirus Zarbakhsh, Holger Frey&lt;br/&gt;The DMC-catalyzed copolymerization of PO with alkyl and aryl epoxides, glycidyl ethers and esters was investigated by &lt;em&gt;in situ&lt;/em&gt;&lt;small&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/small&gt;H NMR spectroscopy. With increasing steric demand at the oxirane ring, the reactivity difference to PO strongly increased.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-27T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Erik Kersten</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maximilian Kaiser</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jan Blankenburg</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kamil Maciol</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Manfred Wagner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sirus Zarbakhsh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Holger Frey</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01203A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01203A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01203A</link><title>Development and modification of porous polymer structures in the vicinity of cellulose fibers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01203A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1675-1693&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01203A, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Sebastian Pusse, Sebastian Heinz, Waranya Limprasart, Lea Gemmer, Suteera Witayakran, Samuel Schabel, Volker Presser, Torsten Gutmann, Markus Gallei&lt;br/&gt;Linear and branched amphiphilic block copolymers were synthesized &lt;em&gt;via&lt;/em&gt; anionic living polymerization to form porous structures on cellulose fibers. Surface properties were tuned at macro- and microscales &lt;em&gt;via&lt;/em&gt; post-modification with different agents.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastian Pusse</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastian Heinz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Waranya Limprasart</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lea Gemmer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Suteera Witayakran</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Samuel Schabel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Volker Presser</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Torsten Gutmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Markus Gallei</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00089D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00089D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00089D</link><title>Fluorescently labelled polypropylene as a model microplastic for cellular imaging</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00089D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00089D, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Alexander Evans, Ríona M. Devereux, Zoë R. Turner, Angela J. Russell, Dermot O'Hare&lt;br/&gt;The covalent functionalisation of polypropylene with the fluorescent label rhodamine B and its subsequent microplastic evaluation in a human embryonic kidney model cell line, enabling standardised polymer–cell studies in biological systems.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander Evans</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ríona M. Devereux</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zoë R. Turner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Angela J. Russell</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dermot O'Hare</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00172F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00172F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00172F</link><title>Creep-resistant, extrudable, and recyclable polyolefin covalent adaptable networks incorporating azine cross-links via reactive processing</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00172F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00172F, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Mathew J. Suazo, Stephanie M. Barbon, Hayley A. Brown, Evelyn Auyeung, Colin Li Pi Shan, John M. Torkelson&lt;br/&gt;Reprocessable and creep-resistant covalent adaptable networks were produced &lt;em&gt;via&lt;/em&gt; reactive processing of polyethylene and ethylene-based copolymers with an azine-based dynamic covalent cross-linker.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mathew J. Suazo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephanie M. Barbon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hayley A. Brown</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Evelyn Auyeung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Colin Li Pi Shan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">John M. Torkelson</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00184J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00184J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00184J</link><title>Thermoset meets thermoplastic: upcycling PLA in digital light processing 3D printing of dynamic thiol–ene composites</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00184J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00184J, Paper&lt;/div&gt;&lt;div&gt;Szymon Gaca, Daniel Bautista-Anguís, Milena Gleirscher, Michele Bonacina, Yves Leterrier, Véronique Michaud, Sandra Schlögl&lt;br/&gt;Thermoplastic microparticles are incoporporated into photocurable dynamic covalent networks to advance the circularity of 3D-printed photopolymers. Thiol–ene resins with up to 20 vol% PLA filler are successfully processed by DLP 3D printing.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Szymon Gaca</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel Bautista-Anguís</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Milena Gleirscher</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michele Bonacina</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yves Leterrier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Véronique Michaud</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sandra Schlögl</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00306K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00306K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00306K</link><title>Spiroorthoesters as promising comonomers for degradable polymer synthesis by cationic copolymerization with vinyl ethers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00306K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00306K, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Kota Yamamoto, Sadahito Aoshima, Arihiro Kanazawa&lt;br/&gt;Cationic copolymerization of vinyl ethers and spiroorthoesters successfully proceeded &lt;em&gt;via&lt;/em&gt; very frequent crossover reactions, resulting in pseudo-alternating copolymers with acid degradability.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kota Yamamoto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sadahito Aoshima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arihiro Kanazawa</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00256K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00256K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00256K</link><title>Robust, UV-resistant and transparent vitrimers from bio-based mercaptan via maleimide–thiol “click” chemistry for carbon fiber-reinforced polymer composites</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00256K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00256K, Paper&lt;/div&gt;&lt;div&gt;Yue Wang, Jialiang Zhong, Yanning Zeng&lt;br/&gt;Bio-based BMI vitrimers from glycerol/erythritol &lt;em&gt;via&lt;/em&gt; maleimide–thiol click chemistry offer high strength, thermal stability, UV resistance, self-healing, recyclability, and enable intact carbon fiber recovery in composites.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yue Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jialiang Zhong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanning Zeng</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00080K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00080K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00080K</link><title>Dynamic cross-linked latent accelerators featuring dual-dynamic urea bonds for one-component epoxy systems</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00080K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00080K, Paper&lt;/div&gt;&lt;div&gt;Xin Wang, Shaohe Qi, Siyu Cheng, Shanshan Dai, Shuaiqi Yang, Fengyuan Zhang, Songqi Ma&lt;br/&gt;Dynamic cross-linked accelerators were synthesized based on dual dynamic urea bonds to achieve high-performance one-component epoxy systems.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xin Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shaohe Qi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Siyu Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shanshan Dai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuaiqi Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fengyuan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Songqi Ma</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00298F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00298F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00298F</link><title>Antimicrobial amphiphilic random copolymers from bio-based methacrylates: effect of chemical composition on activity and selectivity</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00298F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00298F, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Zao Cheng, Erika Zaganelli, Theo van Kooten, Caterina Presutti, Bert Poolman, Laura Mazzocchetti, Patrizio Raffa&lt;br/&gt;Amphiphilic copolymers from bio-derived tetrahydrogeranyl methacrylate and amino acid methacrylates (Ala, Phe, Lys) were synthesized &lt;em&gt;via&lt;/em&gt; RAFT. Lys-based copolymers show superior antimicrobial activity and selectivity &lt;em&gt;via&lt;/em&gt; membrane disruption.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zao Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Erika Zaganelli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Theo van Kooten</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Caterina Presutti</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bert Poolman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laura Mazzocchetti</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Patrizio Raffa</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00241B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00241B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00241B</link><title>Synthesis of topologically controlled functional polyethylenes: combining C–H activation with copolymerization of ethylene and polar monomers using a scandium catalyst</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00241B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00241B, Paper&lt;/div&gt;&lt;div&gt;Yingzi Tan, Yang Yang, Zhaomin Hou, Haobing Wang&lt;br/&gt;By designing polar monomers with built-in C–H activation motifs (&lt;em&gt;e.g.&lt;/em&gt;, anisole or aniline derivatives), we prepare functionalized polyethylenes with programmable topologies (hyperbranched to linear, in-chain to end-functionalized structures).&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yingzi Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yang Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhaomin Hou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haobing Wang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00158K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00158K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00158K</link><title>Plasmonic enhancement of semiconducting double cable polythiophene–perylene diimide polymer performance in artificial photosynthesis of H2O2</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00158K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00158K, Paper&lt;/div&gt;&lt;div&gt;Faseeh Akbar, Shahryar Rasheed, Sana Iqbal, Shiza Basit, Sumera Siddique, Ishtiaq Ahmed, Ljiljana Fruk, Basit Yameen&lt;br/&gt;Solar to chemical energy conversion: Interfacing organic semiconducting polythiophene–perylene diimide double cable polymer with plasmonic AuNPs results in a hybrid exhibiting enhanced photocatalytic performance in artificial photosynthesis of H&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;O&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Faseeh Akbar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shahryar Rasheed</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sana Iqbal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shiza Basit</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sumera Siddique</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ishtiaq Ahmed</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ljiljana Fruk</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Basit Yameen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01084E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01084E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01084E</link><title>A fast emulsion polymerization in an open-to-air environment</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01084E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01084E, Paper&lt;/div&gt;&lt;div&gt;Uddhab Kalita, Vianna F. Jafari, Shubham Verma, Nikhil K. Singha, Greg G. Qiao&lt;br/&gt;This work employs emulsion polymerization of hydrophobic monomers using a “semi bio-Fenton initiation” strategy, enabling rapid polymer synthesis under open-to-air conditions and demonstrating its potential for industrial applications.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Uddhab Kalita</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vianna F. Jafari</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shubham Verma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nikhil K. Singha</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Greg G. Qiao</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00136J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00136J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00136J</link><title>Alternating copolymerization of ethylenesulfonyl fluoride and styrene for the synthesis of SuFEx modifiable polymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00136J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00136J, Communication&lt;/div&gt;&lt;div&gt;Chima Anyaegbu, Darsan Haridas, Joel F. Hooper&lt;br/&gt;This work investigates the copolymerization of ethenesulfonyl fluoride (ESF) and styrene, demonstrating this method as a practical approach to access highly functionalised sulfonyl fluoride-containing polymers.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chima Anyaegbu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Darsan Haridas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joel F. Hooper</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90046A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90046A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90046A</link><title>Correction: Fluorescent surface-grafted block copolymer brushes obtained in a versatile post-polymerization approach</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1652-1652&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY90046A, Correction&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Piotr Wieczorek, Tomasz Kuciel, Tomasz Uchacz, Szczepan Zapotoczny&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Piotr Wieczorek</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomasz Kuciel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomasz Uchacz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Szczepan Zapotoczny</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01170A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01170A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01170A</link><title>Zinc-based coordination exchange in epoxy networks cured via frontal polymerization</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01170A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1555-1561&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01170A, Communication&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Christoph Schmidleitner, Stefan Hirner, Elisabeth Rossegger&lt;br/&gt;Frontal polymerization meets dynamic chemistry: Zn&lt;small&gt;&lt;sup&gt;2+&lt;/sup&gt;&lt;/small&gt;-epoxy networks enable coordination-driven bond exchange. Zinc loading and counter anion tune front behavior, relaxation, and thermomechanical properties, enabling adjustable, weldable materials.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Christoph Schmidleitner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefan Hirner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elisabeth Rossegger</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00196C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00196C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00196C</link><title>Toward theta-shaped polymer composite particles by seeded emulsion polymerization</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00196C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1641-1651&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00196C, Paper&lt;/div&gt;&lt;div&gt;Zhongfu Ling, Xianhao Su, Yifeng Jiang, Hua Zou&lt;br/&gt;Theta-shaped (θ-shaped) polystyrene–poly(glycidyl methacrylate) (PS–PGMA) composite particles have been synthesized by seeded emulsion polymerization using PS seed particles pre-swollen with dibutyl phthalate (DBP) and glycidyl methacrylate (GMA).&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhongfu Ling</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xianhao Su</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yifeng Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hua Zou</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00219F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00219F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00219F</link><title>Solubility-limited depolymerization kinetics in the glycolysis of carbonyl-containing polymers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00219F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1569-1583&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00219F, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Shelby Watson-Sanders, Kendra Day Johnson, Sarah Barber, Alison Biery, Landri Wilcox, Nicholas J. Galan, Jackie Zheng, Tomonori Saito, Mark Dadmun&lt;br/&gt;Solubility-controlled phase behavior dictates depolymerization kinetics in heterogeneous polymer chemical recycling.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Shelby Watson-Sanders</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kendra Day Johnson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sarah Barber</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alison Biery</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Landri Wilcox</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicholas J. Galan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jackie Zheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomonori Saito</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mark Dadmun</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01190F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01190F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01190F</link><title>A novel approach to POx–chelate conjugates and a comparison of their antibacterial activity with POx systems containing amino groups</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01190F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1592-1602&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01190F, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Marcelina Bochenek, Barbara Mendrek, Agnieszka Kowalczuk, Karolina Olszowska, Łukasz Sieroń, Katarzyna Gawron, Natalia Oleszko-Torbus&lt;br/&gt;This study presents a novel synthetic strategy for the preparation of antibacterial poly(2-oxazoline)-based (POx) conjugates with chelating agents.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marcelina Bochenek</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Barbara Mendrek</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Agnieszka Kowalczuk</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Karolina Olszowska</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Łukasz Sieroń</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katarzyna Gawron</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Natalia Oleszko-Torbus</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00105J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00105J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00105J</link><title>Solution self-assembly of polycarbonate block copolymers containing crystalline side chains</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00105J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1584-1591&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00105J, Paper&lt;/div&gt;&lt;div&gt;Chen Liu, Lulu Liu, Jiarui Luan, Zaizai Tong&lt;br/&gt;Solution self-assembly of block copolymers containing crystalline side chains is currently a field of significant interest due to its well-documented capacity for morphological diversity and tunable order.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chen Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lulu Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiarui Luan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zaizai Tong</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00235H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00235H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00235H</link><title>Salinity-ultrasensitive hydrogels for high-performance salinity gradient energy conversion and harvesting</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00235H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1619-1627&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00235H, Paper&lt;/div&gt;&lt;div&gt;Yang Yang, Xiaocao Yan, Mukaddas Abliz, Xiaoying Zhao, Fang Xu, Yunxuan Weng, Hainan Gao&lt;br/&gt;This study presents a salinity-ultrasensitive hydrogel with a superior polyelectrolyte effect, enabling conversion of minor osmotic pressure gradients into substantial volumetric changes for highly efficient salinity gradient energy conversion.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yang Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaocao Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mukaddas Abliz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoying Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fang Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yunxuan Weng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hainan Gao</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00151C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00151C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00151C</link><title>3-Methylenephthalide derivatives enable degradation of vinyl (co)polymers via simultaneous main- and side-chain cleavage</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00151C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1562-1568&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00151C, Paper&lt;/div&gt;&lt;div&gt;Yota Chiba, Shoji Hirabayashi, Yasuhiro Kohsaka&lt;br/&gt;We report degradable vinyl (co)polymers with tunable properties. This (co)polymer design enables convergent decomposition into a single monomer precursor &lt;em&gt;via&lt;/em&gt; simultaneous hydrolysis of the main-chain and pendant groups.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-16T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yota Chiba</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shoji Hirabayashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yasuhiro Kohsaka</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00053C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00053C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00053C</link><title>Investigation of the dynamic behavior of metallopolymers by combined experimental and theoretical methods</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00053C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1603-1618&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00053C, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Milena Jäger, Michael Freduah Agyemang, Wanja T. Schulze, Julian Kimmig, Thomas Bätz, Chiara Wondraczek, Stefan Zechel, Alexander Croy, Michael Schmitt, Jürgen Popp, Stefanie Gräfe, Martin D. Hager, Ulrich S. Schubert&lt;br/&gt;This report studies the dynamic behavior of metallopolymers, by rheology, Raman spectroscopy and modelling. The observed changes are related to thermal-induced morphological changes of the polymer matrix in addition to changes of the metal complex.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Milena Jäger</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Freduah Agyemang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wanja T. Schulze</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Julian Kimmig</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas Bätz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chiara Wondraczek</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefan Zechel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander Croy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Schmitt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jürgen Popp</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefanie Gräfe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martin D. Hager</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrich S. Schubert</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01106J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01106J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01106J</link><title>Investigating an anisole/Cu(II)-macroligand-complex pair to broaden solubility scope and catalyst recycling for atom transfer radical polymerization</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01106J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1628-1640&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01106J, Paper&lt;/div&gt;&lt;div&gt;Richard Ngulube, Jiancheng Zhou, Huaiyuan Zhu, Zhiwei Fu, Naixu Li&lt;br/&gt;A thermoregulated phase-separable catalysis based on a highly soluble poly(ionic liquid)/anisole solvent system enables controlled ATRP at ppm CuBr&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; loadings, thereby supporting a sustainable, recyclable polymerization framework.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Richard Ngulube</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiancheng Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huaiyuan Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiwei Fu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Naixu Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00260A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00260A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00260A</link><title>Green transformation of fish-oil by-products into polysulfide-based nanocomposite adsorbents via coupled inverse vulcanization and exfoliation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00260A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00260A, Paper&lt;/div&gt;&lt;div&gt;Mohamed Boundor, Nadia Katir, Abdelkrim El Kadib&lt;br/&gt;Fish oil byproducts can be upcycled into porous foam composite adsorbents &lt;em&gt;via&lt;/em&gt; a one-step process combining reaction with elemental sulfur and &lt;em&gt;in situ&lt;/em&gt; exfoliation of montmorillonite or graphene oxide sheets.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mohamed Boundor</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nadia Katir</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Abdelkrim El Kadib</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01192B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01192B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01192B</link><title>Synthesis of a phosphorus-containing nickel(II) complex towards suppressing heat release and enhancing the fire safety of polyamide 6</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01192B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01192B, Paper&lt;/div&gt;&lt;div&gt;Yanlu Sun, Huazhao Zhang, Zhouzhou Du, Ke Liu, Wenxing Chen, Wangyang Lu&lt;br/&gt;A transition metal complex endows Polyamide (PA6) with enhanced flame retardancy and reduced heat release.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yanlu Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huazhao Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhouzhou Du</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ke Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenxing Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wangyang Lu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00150E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00150E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00150E</link><title>Perfectly alternating linear-dendritic polymers via dithiol–yne click chemistry</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00150E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00150E, Paper&lt;/div&gt;&lt;div&gt;Ashley V. Miles, Allycea Huskey, Anna Nuzzo, Scott M. Grayson&lt;br/&gt;A dithiol–yne reaction from a dendritic alkyne and a linear dithiol forms an alternating linear-dendritic copolymer.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ashley V. Miles</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Allycea Huskey</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Nuzzo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Scott M. Grayson</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00277C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00277C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00277C</link><title>Naphthalimide derivative-based photoinitiating systems for multi-wavelength visible light photopolymerization and 3D printing</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00277C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00277C, Paper&lt;/div&gt;&lt;div&gt;Jun Shen, Xiaotong Peng, Tong Gao, Penghui Fan, Haiwang Lai, Jing Zhang, Pu Xiao&lt;br/&gt;Naphthalimide derivative-based photoinitiating systems for versatile 3D printing across the 405–470 nm range are presented.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Shen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaotong Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tong Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Penghui Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haiwang Lai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pu Xiao</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00112B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00112B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00112B</link><title>Dynamic covalent polymer films formed by structural metamorphosis at nanoparticle surfaces</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00112B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00112B, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Matthew J. Priestley, David A. Fulton&lt;br/&gt;We report a structural metamorphosis approach to wrap nanoparticles within cross-linked polymer films.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew J. Priestley</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David A. Fulton</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00156D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00156D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00156D</link><title>Facile synthesis of quantitatively tertiary-amine functionalized poly(styrene-co-1,3-pentadiene) copolymers with controlled narrow composition distributions by LAP</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00156D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00156D, Paper&lt;/div&gt;&lt;div&gt;Yao Long, Xupeng Han, Jiahao Zhou, Yixin Xiang, Jingjiao Gui, Yi Xiao, Tingxuan Shang, Qiqi Dai, Kun Liu, Lijun Li&lt;br/&gt;Controlling the copolymer composition distribution (CCD) and achieving quantitative functionalization of polyolefins are essential for tailoring material properties.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yao Long</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xupeng Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiahao Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yixin Xiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingjiao Gui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tingxuan Shang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiqi Dai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kun Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lijun Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00189K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00189K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00189K</link><title>Single-chain level decoding of the conformational distribution in bisphenol A polycarbonate</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00189K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00189K, Paper&lt;/div&gt;&lt;div&gt;Yining Wang, Xinxin Bao, Wentao Yuan, Yuchen Wang, Hu-jun Qian, Zhong-yuan Lu, Yu Bao, Shuxun Cui&lt;br/&gt;Individual PC chains exist in two discrete conformational populations in a ∼1 : 1 ratio—chains with &lt;em&gt;cis&lt;/em&gt; content ≥90% and chains with &lt;em&gt;trans&lt;/em&gt; content of 65 ± 5%—yielding an overall &lt;em&gt;trans&lt;/em&gt; fraction of ∼30%.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yining Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinxin Bao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wentao Yuan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuchen Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hu-jun Qian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhong-yuan Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu Bao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuxun Cui</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90045C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90045C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY90045C</link><title>Correction: Determining the Q–e values of polymer radicals and monomers separately through the derivation of an intrinsic Q–e scheme for radical copolymerization</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1545-1545&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY90045C, Correction&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Susumu Kawauchi, Akinori Akatsuka, Yoshihiro Hayashi, Hidemine Furuya, Toshikazu Takata&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Susumu Kawauchi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Akinori Akatsuka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yoshihiro Hayashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hidemine Furuya</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Toshikazu Takata</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00086J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00086J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00086J</link><title>Enhancing the processability of polychlorotrifluoroethylene via copolymerization with perfluoropropyl vinyl ether</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00086J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1517-1528&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00086J, Paper&lt;/div&gt;&lt;div&gt;Xincheng Wang, Shuhui Li, Daixuan Gong, Bin Du, Wei Zhao, Yanqiu Guo, Meijie Qu, Yuezhen Bin&lt;br/&gt;A novel PCTFE-PPVE copolymer was successfully synthesized; PPVE incorporation reduces material crystallinity and melt viscosity, and the resulting copolymer shows enhanced processability.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-24T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xincheng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuhui Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daixuan Gong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Du</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanqiu Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Meijie Qu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuezhen Bin</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00003G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00003G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00003G</link><title>Preparation and characterization of low dielectric cross-linked polyimide containing fluorene group via post-polymerization cross-linking</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00003G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1507-1516&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00003G, Paper&lt;/div&gt;&lt;div&gt;Seong Hun Choi, Seonyoung Jo, Minki Choi, Jaeyoung Choi, Yun Ho Kim, Jongmin Park, Jong Chan Won&lt;br/&gt;Post-polymerization cross-linking to produce a free-volume developed aromatic polyimide matrix with advanced low dielectric performance and robust structural integrity.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Seong Hun Choi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Seonyoung Jo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minki Choi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jaeyoung Choi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yun Ho Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jongmin Park</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jong Chan Won</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00140H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00140H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00140H</link><title>Exploring thiol–ene and thiol–methacrylate reactions in the production of renewable materials from methacrylated eugenol</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00140H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1461-1474&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00140H, Paper&lt;/div&gt;&lt;div&gt;Gabriel Iago dos Santos, Caroline Gaglieri, Fernanda Barreto dos Santos, Sabrina Moises Moreno, Gilbert Bannach&lt;br/&gt;Methacrylated eugenol (ME) is a versatile biobased monomer for sustainable polymer networks, featuring reactive methacrylic and allylic carbon-carbon double bonds that enable both thiol-ene and thiol-methacrylate polymerization pathways.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Gabriel Iago dos Santos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Caroline Gaglieri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fernanda Barreto dos Santos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sabrina Moises Moreno</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gilbert Bannach</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00104A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00104A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00104A</link><title>Direct synthesis of porous organic polymers with protected ethyne monomers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00104A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1538-1544&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00104A, Paper&lt;/div&gt;&lt;div&gt;Bo Chen, Xinghua Guo, Yongdong Jin, Chuanqin Xia, Degao Wang&lt;br/&gt;A new synthetic method for alkynyl porous organic polymers using cheap protected ethyne as the monomer. This method was verified by a small molecular model reaction and 5 polymers.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bo Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinghua Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yongdong Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chuanqin Xia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Degao Wang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00054A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00054A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00054A</link><title>Ring-opening (co)polymerization of macrolactones catalyzed by a simple organoaluminum complex of MeAl(BHT)2</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00054A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1529-1537&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00054A, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Rui Han, Zheng Li, Zhibo Li&lt;br/&gt;Degradable aliphatic long-chain polyesters (ALCPEs), obtained from the ROP of macrolactones, have emerged as promising degradable polymers, as they combine the mechanical and thermal properties of polyethylene with the degradability of polyesters.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-16T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Rui Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zheng Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhibo Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01228G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01228G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01228G</link><title>A bio-based cellulose-supported photocatalyst enabling reversible complexation-mediated polymerization via energy transfer under white LED irradiation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01228G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1488-1497&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01228G, Paper&lt;/div&gt;&lt;div&gt;Huirong Li, Chen Zhou, Rui Zhao, Shumin Chen, Danni Tang, Longqiang Xiao, Linxi Hou&lt;br/&gt;Heterogeneous photocatalytic polymerization has emerged as a promising strategy for developing greener reversible complexation-mediated polymerization (RCMP) systems.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-16T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Huirong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chen Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rui Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shumin Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Danni Tang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Longqiang Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Linxi Hou</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01141H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01141H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01141H</link><title>Self-assembly of condensation homopolymers: with application in fractionation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5PY01141H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1498-1506&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01141H, Paper&lt;/div&gt;&lt;div&gt;Tielei Li, Kaini Yang, Baochen Wang, Yachun Su, Zhengqing Kong, Sanyang Li, Jin Zhu&lt;br/&gt;The self-assembly of condensation homopolymers is reported, presenting a distinct alternative to the conventional regime and showcasing their intriguing self-assembly into primary micelle and compound micelle constructs.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-16T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tielei Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kaini Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Baochen Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yachun Su</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhengqing Kong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sanyang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jin Zhu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00044D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00044D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00044D</link><title>Lignin-based non-isocyanate polyurethanes by transurethanisation: catalyst selection towards covalent adaptable networks</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00044D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Polym. Chem.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;17&lt;/b&gt;,1475-1487&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00044D, Paper&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Aline Rebejac, Nathan Wybo, Luc Avérous, Antoine Duval&lt;br/&gt;Lignin-based NIPUs synthesized by transurethanisation form covalent adaptable networks where catalysts can enhance recyclability by limiting side reactions during reprocessing.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Aline Rebejac</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nathan Wybo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luc Avérous</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antoine Duval</creator></item></channel></rss>