<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>Tue, 30 Jun 2026 11:24:47 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/D6PY00173D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00173D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00173D</link><title>Foldamers: design principles, building blocks and 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=D6PY00173D" /&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/D6PY00173D, 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;Anna H. P. Cronjé, Rueben Pfukwa, Bert Klumperman&lt;br/&gt;This review article explores foldamers, a class of synthetic oligomers designed to mimic the structural and functional diversity of natural proteins.&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>2026-06-29T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anna H. P. Cronjé</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rueben Pfukwa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bert Klumperman</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00513F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00513F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00513F</link><title>Redox-regulated fusion and fission of Se/Te-containing polymer assemblies for compartmentalized reactions</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=D6PY00513F" /&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/D6PY00513F, Paper&lt;/div&gt;&lt;div&gt;Zhuoxin Ge, Muqing Cao, Huaping Xu&lt;br/&gt;Te–O–Te redox chemistry enables reversible Se/Te polymer assembly fusion–fission and oxidation-triggered compartmentalized fluorescence reactions.&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>2026-06-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhuoxin Ge</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Muqing Cao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huaping Xu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00329J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00329J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00329J</link><title>Dual-dynamic crosslinked polyurethanes with synergistic mechanical reinforcement, self-healing, recycling and photoluminescence</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=D6PY00329J" /&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/D6PY00329J, Paper&lt;/div&gt;&lt;div&gt;Haiyan Mao, Qi Zhou, Zhi Yu, Chenghui Zheng, Huanling Wu, Ling Lin&lt;br/&gt;Dual-dynamic crosslinked HIPUs exhibited excellent mechanical properties, self-healing and recycling capabilities, and distinct photoluminescent characteristics.&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>2026-06-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Haiyan Mao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qi Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhi Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chenghui Zheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huanling Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ling Lin</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00244G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00244G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00244G</link><title>Recycling Post-Consumer Polyesters Bottles and Fabrics to Photocurable Covalent Adaptable networks</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/D6PY00244G, 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;Sathiyaraj Subramaniyan, Amro Hindi, Federico Guerrero-Ruiz, Minna Hakkarainen&lt;br/&gt;Recycling aromatic polyester waste into UV curable covalent adaptable networks (CANs) offers a promising pathway toward more circular materials. Here, we present a straightforward strategy to convert post consumer polyethylene...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sathiyaraj Subramaniyan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Amro Hindi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Federico Guerrero-Ruiz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minna Hakkarainen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00565A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00565A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00565A</link><title>Deciphering the chain propagation mechanism in regioselective polymerization via alkene difunctionalization</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=D6PY00565A" /&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/D6PY00565A, Paper&lt;/div&gt;&lt;div&gt;R S Malavika, Rositha Kuniyil&lt;br/&gt;DFT calculations decode the competing chain propagation pathways, uncovering the electronic and steric origins of regioselectivity in the Nickel catalysed polymerisation &lt;em&gt;via&lt;/em&gt; alkene difunctionalisation.&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>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">R S Malavika</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rositha Kuniyil</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00380J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00380J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00380J</link><title>Engineering bio-based eutectogels from casein via 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=D6PY00380J" /&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/D6PY00380J, 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;Sebastián Locatelli, Gisela C. Luque, Ludmila I. Ronco, Oihane Varela, Xabier López de Pariza, David Mecerreyes, Roque J. Minari&lt;br/&gt;3D-printable bio-based eutectogels composed of casein and natural deep eutectic solvent with high ionic conductivity and good mechanical 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>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastián Locatelli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gisela C. Luque</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ludmila I. Ronco</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Oihane Varela</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xabier López de Pariza</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Mecerreyes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roque J. Minari</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00550K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00550K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00550K</link><title>Synthesis of Block Poly(carbonate-ether) Diol via Chain Transfer Copolymerization</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/D6PY00550K, Communication&lt;/div&gt;&lt;div&gt;Liqiang  Gan, Xinyu Liu, Xiaohan Cao, Chengjian Zhang, Xinghong Zhang&lt;br/&gt;Polycarbonate polyol is highly desired for making high-performance polyurethanes. This work reports a highly effective synthesis of a block diol with poly(carbonate-ether) and polyether blocks from the partially alternating copolymerization...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Liqiang  Gan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinyu Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaohan Cao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chengjian Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinghong Zhang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00368K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00368K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00368K</link><title>Rare earth metal ammonium tris(phenolate) catalysts for industrial poly(lactic acid) production</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=D6PY00368K" /&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/D6PY00368K, 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;Strachan N. McCormick, Gerrit Gobius du Sart, Wilko de Lang, Matthew D. Jones, Matthew G. Davidson&lt;br/&gt;In a kg-scale benchmarking study, zwitterionic rare earth (La, Y) ammonium tris(phenolate)s exhibit robustness and high catalytic activity suitable for the ring-opening polymerisation of lactide under challenging, industrially-relevant 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>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Strachan N. McCormick</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gerrit Gobius du Sart</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wilko de Lang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew D. Jones</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew G. Davidson</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00349D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00349D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00349D</link><title>Wet oxidation of polyethylene under elevated oxygen pressure: revisiting product selectivity</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/D6PY00349D, Paper&lt;/div&gt;&lt;div&gt;Vadim Zefirov, Polina S Kazaryan, Svetlana V Stakhanova, Elizaveta V Shmakova, Alexander V Dudkin, Ivan A. Godovikov, Elena Kharitonova, Marat Gallyamov, Alexei R. Khokhlov&lt;br/&gt;Wet oxidative upcycling of polyethylene is commonly discussed in terms of dicarboxylic-acid formation, yet the parameters of catalyst-free aqueous oxidation that ensure product selectivity remain poorly defined. Here we show...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Vadim Zefirov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Polina S Kazaryan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Svetlana V Stakhanova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elizaveta V Shmakova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander V Dudkin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ivan A. Godovikov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elena Kharitonova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marat Gallyamov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexei R. Khokhlov</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00492J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00492J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00492J</link><title>Three-step synthesis of a condensation polymer incorporating natural PHB fragments: structural and physicochemical characterization</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=D6PY00492J" /&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/D6PY00492J, Paper&lt;/div&gt;&lt;div&gt;Paweł Chaber, Paweł Gnida, Sebastian Jurczyk, Katarzyna Jelonek, Marta Musioł, Silke Andrä-Żmuda, Grażyna Adamus&lt;br/&gt;Introducing short-chain comonomer units into &lt;strong&gt;PHB&lt;/strong&gt; reduces crystallinity and improves thermal 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>2026-06-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Paweł Chaber</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paweł Gnida</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastian Jurczyk</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katarzyna Jelonek</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marta Musioł</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Silke Andrä-Żmuda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Grażyna Adamus</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00500D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00500D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00500D</link><title>Solid-state photoisomerization activating topology-mediated photoluminescence in a two-dimensional woven polymer</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=D6PY00500D" /&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/D6PY00500D, Paper&lt;/div&gt;&lt;div&gt;Jiawei Duan, Zhengbo Zhong, Yuhao Mi, Pengyu Guo, Zihe Xu, Junwei Zhang, Zhangkai Chen, Tianhui Ren, Zhipeng Li&lt;br/&gt;Photoisomerization activates PL in a two-dimensional woven polymer. Its topology drives lattice reorganization, weakening π–π and quenching. Reversible PL switching for optical storage and light-responsive devices.&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>2026-06-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jiawei Duan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhengbo Zhong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuhao Mi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pengyu Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zihe Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junwei Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhangkai Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tianhui Ren</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhipeng Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00425C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00425C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00425C</link><title>Thermoresponsive Fluorescent Polymers: Influence of Size, Composition, and Architecture</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/D6PY00425C, 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;Konpal Raheja, Sophia Beilharz, Ajitesh Lalam, Md Bablu Hasan, Divita Mathur, Metin Karayilan&lt;br/&gt;Thermoresponsive fluorescent polymers (TFPs) provide a versatile platform for optical temperature sensing by coupling phase transitions with changes in fluorescence. Here, we report TFPs based on poly(N-isopropylacrylamide) (PNIPAM) and poly(ethylene...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Konpal Raheja</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sophia Beilharz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ajitesh Lalam</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Md Bablu Hasan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Divita Mathur</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Metin Karayilan</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00436A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00436A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00436A</link><title>Tunable dynamic covalent networks from mechanochemical depolymerization of post-consumer 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=D6PY00436A" /&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/D6PY00436A, 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;Morgan E. Skala, Qian Ye, Ana Paula Kitos Vasconcelos, Katie A. Polich, Sridevi Narayan-Sarathy, Matthew R. Golder&lt;br/&gt;Ball mill grinding enables the sustainable aminolysis of PLA, PHBH, and an aliphatic polyester-based multilayer film packaging. Esterification of monomers with lipoic acid accesses dynamic and degradable photopolymer CANs from plastic waste.&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>2026-06-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Morgan E. Skala</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qian Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ana Paula Kitos Vasconcelos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katie A. Polich</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sridevi Narayan-Sarathy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew R. Golder</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00404K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00404K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00404K</link><title>Borane Lewis pair-mediated ring-opening polymerization of epoxides: direct access to α-acyl azide/ω-hydroxyl heterotelechelic polyethers and latent isocyanate-derived polyurethane</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=D6PY00404K" /&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/D6PY00404K, Paper&lt;/div&gt;&lt;div&gt;Xianhao Xin, Wenyan Wang, Hua-an Wang, Wu Gao, Xinhui Kou, Chuanli Ren, Xiaowu Wang&lt;br/&gt;Borane Lewis pair-mediated ROP of epoxides at 25 °C affords α-acyl azide/ω-hydroxyl heterotelechelic polyethers, which undergo Curtius rearrangement and self-polyaddition to yield latent-isocyanate-derived polyurethanes.&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>2026-06-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xianhao Xin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenyan Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hua-an Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wu Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinhui Kou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chuanli Ren</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaowu Wang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00464D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00464D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00464D</link><title>In situ reductive polymerization of bio-based α-lipoamides toward functional poly(β-hydroxy thioether)s</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=D6PY00464D" /&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/D6PY00464D, Paper&lt;/div&gt;&lt;div&gt;Zhengrong Zhang, Linlin Wang, Lei Li&lt;br/&gt;Bio-based cyclic disulfide α-lipoamide monomers undergo &lt;em&gt;in situ&lt;/em&gt; reductive step-growth polymerization to yield structurally diverse poly(β-hydroxy thioether)s.&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>2026-06-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhengrong Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Linlin Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00115G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00115G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00115G</link><title>Poly(butylene adipate-co-terephthalate) with synergistically enhanced mechanical, moisture/oxygen barrier, and degradation performance via embedding immobilized enzyme</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=D6PY00115G" /&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;,2638-2647&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00115G, Paper&lt;/div&gt;&lt;div&gt;Jing Yuan, Shitong Cui, Zixun Xu, Jun Xu, Jiaxin Shi, Jun Ge, Baohua Guo&lt;br/&gt;This work introduces a decoupled materials design strategy that integrates a high-crystallinity PBAT matrix with MOF-immobilized enzymes, enabling the simultaneous enhancement of service performance and biodegradability.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-29T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Yuan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shitong Cui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zixun Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiaxin Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Ge</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Baohua Guo</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00313C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00313C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00313C</link><title>Poly(chromenochromenedione) (PCCD): a structural isomer of poly(benzodifurandione) (PBDF)</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=D6PY00313C" /&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;,2539-2547&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00313C, 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;Uttam Pal, Reed M. Woolard, Priyanka Rout, Sanket Samal, Suman Kuila, Md Masudur Rahman Rahat, Guancheng Shen, Julia Laskin, Stephen Barlow, Seth R. Marder, Geoffrey R. Hutchison, Jianguo Mei&lt;br/&gt;Isomerization of poly(benzodifurandione) (PBDF) &lt;em&gt;via&lt;/em&gt; ring opening yields poly(chromenochromenedione) (PCCD), demonstrating how variations in backbone topology can affect n-type polymer properties.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-29T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Uttam Pal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Reed M. Woolard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Priyanka Rout</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sanket Samal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Suman Kuila</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Md Masudur Rahman Rahat</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guancheng Shen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Julia Laskin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephen Barlow</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Seth R. Marder</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Geoffrey R. Hutchison</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianguo Mei</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00299D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00299D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00299D</link><title>Stereocontrol as a tool for shaping abiotic, sequence-defined oligourethanes</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=D6PY00299D" /&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;,2619-2628&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00299D, 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;Sara Njoku, Ariel F. Perez Mellor, Johanna Brazard, Simone G. Giuffrida, Wojciech Dudziak, Céline Besnard, Thomas Bürgi, Takuji B. M. Adachi, Róża Szweda&lt;br/&gt;Stereochemistry controls oligourethane folding through backbone torsions, yielding helices and extended zig-zag structures formed by isotactic and syndiotactic motifs, respectively.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-28T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sara Njoku</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ariel F. Perez Mellor</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Johanna Brazard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Simone G. Giuffrida</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wojciech Dudziak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Céline Besnard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas Bürgi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takuji B. M. Adachi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Róża Szweda</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00292G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00292G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00292G</link><title>Ionic liquid [Bmim][Lac]-catalyzed melt polycondensation for bisphenol A-based polycarbonate synthesis</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=D6PY00292G" /&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;,2548-2558&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00292G, Paper&lt;/div&gt;&lt;div&gt;Sitong Chen, Pingjun Shao, Zhiqiang Ding, Guiqiu Ma, Zhe Ma, Bin Xiao, Zhiwei Liu, Yunzhong Gao, Bin Wang, Yuesheng Li&lt;br/&gt;The commercially available ionic liquid [Bmim][Lac] enables efficient synthesis of bisphenol A-based polycarbonates. Its excellent substrate generality and catalytic tolerance allow the chemical modification of bisphenol A-based polycarbonates.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sitong Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pingjun Shao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiqiang Ding</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guiqiu Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhe Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Xiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiwei Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yunzhong Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bin Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuesheng Li</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00139D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00139D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00139D</link><title>From low to high density: the effect of ionic modifications on permselectivity in biimidazole-based polyimides</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=D6PY00139D" /&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;,2603-2618&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00139D, Paper&lt;/div&gt;&lt;div&gt;Alain Tundidor-Camba, Ifeanyi S. Ibeto, Yennier Cruz, Fidel E. Rodriguez-Gonzalez, Pravin S. Shinde, Ana L. Montero-Alejo, Claudio A. Terraza, Sree Laxmi, Akhilesh Upasani, Sergey Vasenkov, Joshua D. Moon, Kathryn E. O'Harra, C. Heath Turner, Jason E. Bara&lt;br/&gt;Structural and thermal characterization confirm successful synthesis and reveal progressive densification of the polymer matrix upon quaternization and IL addition, as evidenced by reduced &lt;em&gt;d&lt;/em&gt;-spacing, fractional free volume, and mechanical stiffness.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alain Tundidor-Camba</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ifeanyi S. Ibeto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yennier Cruz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fidel E. Rodriguez-Gonzalez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pravin S. Shinde</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ana L. Montero-Alejo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Claudio A. Terraza</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sree Laxmi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Akhilesh Upasani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sergey Vasenkov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joshua D. Moon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kathryn E. O'Harra</creator><creator xmlns="http://purl.org/dc/elements/1.1/">C. Heath Turner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jason E. Bara</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00352D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00352D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00352D</link><title>Investigating the solubility of new branched polymers and copolymers synthesised using transfer-dominated branching radical telomerisation (TBRT) of dimethacrylates</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=D6PY00352D" /&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;,2569-2581&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00352D, 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;Bethany Linthwaite, Sean Flynn, Oliver B. Penrhyn-Lowe, Samuel Mckeating, Stephen Wright, Savannah R. Cassin, Steven L. Brown, Paul H. Findlay, Matthew Diable, Pierre Chambon, Andrew B. Dwyer, Steve P. Rannard&lt;br/&gt;Solubility is key to new (co)polymer applications and the 30 new TBRT synthesised macromolecules studied here show subtle effects and control directly relating to starting materials that affect backbone and side chain chemistries.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bethany Linthwaite</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sean Flynn</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Oliver B. Penrhyn-Lowe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Samuel Mckeating</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephen Wright</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Savannah R. Cassin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steven L. Brown</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul H. Findlay</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew Diable</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pierre Chambon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew B. Dwyer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steve P. Rannard</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00429F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00429F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00429F</link><title>Facile upcycling of poly(bisphenol A carbonate) via dynamic covalently cross-linked 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=D6PY00429F" /&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;,2582-2592&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00429F, Paper&lt;/div&gt;&lt;div&gt;Zeeshan Haider, Xiong Biao Xue, Xinliang Guo, Yufeng Song, Huan Yang, Yu Li, Xinli Jing&lt;br/&gt;PC was efficiently recycled through transesterification reaction with BPA followed by directly crosslinking with dynamic urethane bonds.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zeeshan Haider</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiong Biao Xue</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinliang Guo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yufeng Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huan Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinli Jing</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00073H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00073H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00073H</link><title>C
        2-Symmetric H-bonding benzene core motif promotes rapid growth of long supramolecular fibers from amphiphilic 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=D6PY00073H" /&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;,2593-2602&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00073H, 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 Städter, Hesam Makki, Ulrich Mansfeld, Stephanie Hoeppener, Albena Lederer, Johannes C. Brendel&lt;br/&gt;Benzene diurea monoamide (BDUA) is a synthetically accessible and scalable &lt;em&gt;C&lt;/em&gt;&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;-symmetric alternative to &lt;em&gt;C&lt;/em&gt;&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;-symmetric benzene core motifs that forms strong hydrogen bonds and rapidly assembles into well-defined helical supramolecular fibers in water.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastian Städter</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hesam Makki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrich Mansfeld</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephanie Hoeppener</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Albena Lederer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Johannes C. Brendel</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00250A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00250A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00250A</link><title>Vinylbenzenesulfonyl fluoride (VBSF)-based binary and ternary copolymers and selective post-polymerization modification via SuFEx 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=D6PY00250A" /&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;,2559-2568&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00250A, Paper&lt;/div&gt;&lt;div&gt;Meng Li, Ping Song, Shuiyuan Zhang, Xi Yan, Hui Shao, Hai-Chao Xu, Saihu Liao&lt;br/&gt;The good orthogonality of a sulfur(&lt;small&gt;VI&lt;/small&gt;) fluoride exchange (SuFEx) click reaction to active ester–amine chemistry enables efficient access to functionalized polymers from a single parent reactive polymer &lt;em&gt;via&lt;/em&gt; selective post-polymerization modification.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Meng Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ping Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuiyuan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xi Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Shao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hai-Chao Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Saihu Liao</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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00288A" /&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;,2629-2637&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00288A, Paper&lt;/div&gt;&lt;div&gt;Md Saifur Rahaman, Brett Leslie Pollard, Luke A. Connal&lt;br/&gt;Hydrogels are developed from ultra-high molecular weight polymers, the increased entanglements create new gels with enhanced properties.&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/">Md 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 A. Connal</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00263C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00263C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00263C</link><title>On-demand degradable thiol-maleimide PEG hydrogels as abrasion-free adhesives</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=D6PY00263C" /&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/D6PY00263C, Paper&lt;/div&gt;&lt;div&gt;Wachara Benchaphanthawee, Hui-Hui Yeo, Hung-Hsun Lu, Man-Hsuan Ku, Fu-Sheng Wang, Jian-Hua Lin, Yi-Ching Hung, Wei-Wen Liu, Hao-Chieh Chiu, Chi-How Peng&lt;br/&gt;We have synthesized on-demand degradable hydrogels that firmly attach to porcine skin and are easily removed by using &lt;small&gt;L&lt;/small&gt;-cysteine solution.&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>2026-06-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wachara Benchaphanthawee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui-Hui Yeo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hung-Hsun Lu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Man-Hsuan Ku</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fu-Sheng Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian-Hua Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi-Ching Hung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei-Wen Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hao-Chieh Chiu</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/D6PY00481D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00481D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00481D</link><title>Developing aggregation-induced emission vinyl ether polymers via cationic polymerization and tacticity regulation</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=D6PY00481D" /&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/D6PY00481D, Paper&lt;/div&gt;&lt;div&gt;Ziwei Yang, Shuai Zhou, Jie Chen, Yongji Hu, Yun Liao, Jianxu Chen, Hai-Chao Xu, Saihu Liao&lt;br/&gt;AIE vinyl ether polymers have been successfully developed &lt;em&gt;via&lt;/em&gt; cationic copolymerization, and stereoselective polymerization enables access to isotactic polymers, which exhibit stronger adhesion to glass and become visible under UV light.&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>2026-06-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ziwei Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shuai Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jie Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yongji Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yun Liao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianxu Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hai-Chao Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Saihu Liao</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00297H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00297H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00297H</link><title>Side-Group Effect of Poly(ε-caprolactone)-Based Polyurethane on Thermal, Surface-Wetting and Mechanical Properties</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/D6PY00297H, Paper&lt;/div&gt;&lt;div&gt;Zhuoyi  He, Benshun  Huang, Kangyu  Zhou, Jiayi  Luo, Xi  Yang, Zhen Wang, Limin  Ji, Yujun Chen, Jian  Chen, Yan  Cao, Yougen Chen&lt;br/&gt;To effectively optimize the physicochemical properties of polyurethanes for practical applications, we have designed and synthesized a series of poly(&lt;em&gt;ε&lt;/em&gt;-caprolactone)-based polyurethanes (PCL-based PUs) functionalized with five different side groups of...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhuoyi  He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Benshun  Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kangyu  Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiayi  Luo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xi  Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhen Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Limin  Ji</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yujun Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian  Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yan  Cao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yougen Chen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00437G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00437G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00437G</link><title>UV-curable 3D printing of polydimethylsiloxane elastomers for medical application</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/D6PY00437G, Review Article&lt;/div&gt;&lt;div&gt;Ying  Ren, Biao  Lv, Junru Yao, Xiaodong Liu, Rong  Zhao, Qiang Fu, Yang  Gao, Youyi Sun&lt;br/&gt;UV-curable 3D printing polydimethylsiloxane (PDMS) elastomers has attracted increasing attention due to their exceptional high-temperature resistance, stable chemical properties, and biocompatibility, making them suitable for a wide range of applications...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-17T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ying  Ren</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Biao  Lv</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junru Yao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaodong Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rong  Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qiang Fu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yang  Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Youyi Sun</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00347H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00347H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00347H</link><title>Post-polymerisation functionalisation of conjugated polymers: oligoether side-chain length governs exciton lifetime and dissociation for enhanced photocatalytic hydrogen evolution</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=D6PY00347H" /&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/D6PY00347H, Paper&lt;/div&gt;&lt;div&gt;Yidong Deng, Guoqing Tian, Rong Fan, Ningning Wang, Mingming Liu, Po Sun, Hua Sun&lt;br/&gt;This work demonstrates that oligoethylene glycol side-chain length on F8BT directly governs exciton lifetime and dipole moment, thereby systematically tuning photocatalytic hydrogen evolution performance.&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>2026-06-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yidong Deng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guoqing Tian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rong Fan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ningning Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mingming Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Po Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hua Sun</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00362A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00362A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00362A</link><title>Organocatalyzed ATRP meets nature: riboflavin-mediated synthesis of thick polymer brushes under visible light</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=D6PY00362A" /&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/D6PY00362A, Paper&lt;/div&gt;&lt;div&gt;Justyna Bała, Anna Kiełbasa, Piotr Wieczorek, Tomasz Uchacz, Małgorzata Klamut, Izabela Zaborniak, Szczepan Zapotoczny, Paweł Chmielarz, Karol Wolski&lt;br/&gt;Riboflavin derivatives enable sustainable, light-driven synthesis of polymer brushes &lt;em&gt;via&lt;/em&gt; organocatalyzed ATRP under mild conditions with a simple reaction setup.&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>2026-06-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Justyna Bała</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Kiełbasa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Piotr Wieczorek</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomasz Uchacz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Małgorzata Klamut</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Izabela Zaborniak</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Szczepan Zapotoczny</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paweł Chmielarz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Karol Wolski</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00311G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00311G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00311G</link><title>Integrated design of high-performance, recyclable, and antibacterial 3D-printing photopolymers from tannic acid</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=D6PY00311G" /&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/D6PY00311G, Paper&lt;/div&gt;&lt;div&gt;Yuxuan Que, Hang Zhou, Tianyi Tang, Xuehan Chen, Ying Li, Yi Tan, Zhengchun Cai, Yuanyuan Jiang, Jianfeng Yao, Ping Zhao, Chengguo Liu&lt;br/&gt;A biobased, chemically recyclable, and intrinsically antibacterial photo-curable resin was developed employing tannic acid as a rigid, multifunctional structural block.&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>2026-06-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yuxuan Que</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hang Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tianyi Tang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuehan Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ying Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yi Tan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhengchun Cai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuanyuan Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianfeng Yao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ping Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chengguo Liu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00353B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00353B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00353B</link><title>Mechanochromic polyurethane elastomers containing main-chain naphthalimide moieties</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=D6PY00353B" /&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/D6PY00353B, Paper&lt;/div&gt;&lt;div&gt;Tomoya Tada, Tetsuma Inaoka, Hiromitsu Sogawa, Fumio Sanda&lt;br/&gt;Naphthalimide-containing polyurethane elastomers showed a reversible fluorescence color change from green to blue upon stretching. Molecular simulations revealed that the mechanochromism originates from changes in naphthalimide aggregation.&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>2026-06-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tomoya Tada</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tetsuma Inaoka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hiromitsu Sogawa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fumio Sanda</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00344C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00344C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00344C</link><title>Thioamides on radical-chain growth monomers: post-polymerization transformation for tailored functional 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=D6PY00344C" /&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;,2437-2443&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00344C, 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;Selin Kinali-Demirci, Serkan Demirci, Brett VanVeller&lt;br/&gt;Thioamides cannot be easily incorporated into radical-chain growth polymerization schemes. Thioimidates provide a strategy to allow polymerization of protected thioamides that can be unveiled under mild conditions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Selin Kinali-Demirci</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Serkan Demirci</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Brett VanVeller</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00217J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00217J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00217J</link><title>Dynamic exchange in vinylogous urethane vitrimers: computational and experimental approaches to screen structure–property relationships of dynamic bonds</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=D6PY00217J" /&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;,2479-2490&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00217J, Paper&lt;/div&gt;&lt;div&gt;Jacopo Teotonico, Fernando Ruipérez, Nicholas Ballard&lt;br/&gt;Computational and experimental screening of vinylogous urethane vitrimers reveals how substituents tune dynamic bond exchange. DFT is combined with NMR experiments to link molecular structure to stress relaxation, enabling tailored performance.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jacopo Teotonico</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fernando Ruipérez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicholas Ballard</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00348F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00348F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00348F</link><title>Cellodextrin phosphorylase-catalyzed enzymatic polymerization from primers modified on poly(γ-glutamic acid) for the synthesis of moderate-molecular-weight celluloses</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=D6PY00348F" /&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;,2514-2521&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00348F, Paper&lt;/div&gt;&lt;div&gt;Kousuke Ohba, Mimi Tokunaga, Tao Takagaki, Masayasu Totani, Jun-ichi Kadokawa&lt;br/&gt;Moderate-molecular-weight cellulose graft chains were obtained by cellodextrin phosphorylase-catalyzed polymerization of α-&lt;small&gt;D&lt;/small&gt;-glucose 1-phosphate using primer-modified poly(γ-glutamic acid) (PGA), prepared by conjugation of cellobiosylamine onto PGA.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kousuke Ohba</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mimi Tokunaga</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Takagaki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Masayasu Totani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jun-ichi Kadokawa</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00266H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00266H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00266H</link><title>Influence of the nature of the Lewis acid on the AROP of epoxides initiated by 2,5-diketopiperazine</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=D6PY00266H" /&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;,2491-2504&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00266H, Paper&lt;/div&gt;&lt;div&gt;Valentin Puchelle, Sylvie Noinville, Philippe Guégan, Nicolas Illy&lt;br/&gt;Lewis acids enable controlled DKP-initiated epoxide AROP, suppressing side reactions and yielding well-defined bio-based polyethers with narrow dispersity.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Valentin Puchelle</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sylvie Noinville</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Philippe Guégan</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/D6PY00177G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00177G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00177G</link><title>Synthesis of a BC6 polymer via cyclotrimerization of alkynylborane and its application as a heterogeneous Lewis acid 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=D6PY00177G" /&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;,2473-2478&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00177G, 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;Naoki Takahashi, Kentaro Ohkura, Yuta Nishina&lt;br/&gt;We report the synthesis of a BC&lt;small&gt;&lt;sub&gt;6&lt;/sub&gt;&lt;/small&gt; polymer &lt;em&gt;via&lt;/em&gt; alkyne cyclotrimerization. The polymer acts as a recyclable catalyst and shows higher catalytic activity than small-molecule analogues due to its high boron content, stability, and enhanced Lewis acidity.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Naoki Takahashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kentaro Ohkura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuta Nishina</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00370B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00370B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00370B</link><title>A complementary DSC–NMR methodology for elucidating isocyanurate formation pathways in polyurethanes</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=D6PY00370B" /&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;,2505-2513&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00370B, 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;Ashok Ramakrishnan, Tobias Wagener, Oliver Welz, Berend Eling, Željko Tomović&lt;br/&gt;Combined DSC–NMR method investigating isocyanurate formation under solvent-free conditions with commercial catalysts, linking thermal events to composition changes and providing reaction mechanistic insights relevant to polyurethane systems.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ashok Ramakrishnan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tobias Wagener</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Oliver Welz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Berend Eling</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Željko Tomović</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00409A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00409A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00409A</link><title>Defining alternating sequences in polyurethanes: sequence-controlled photo-degradation in step 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=D6PY00409A" /&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;,2423-2436&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00409A, 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;Xaver Kneidl, Johannes Reeb-Begic, Tongtong Cui, Patrick Theato, Yosuke Akae&lt;br/&gt;In AA/BB-type step polymerization, the definition of a polymer sequence is inherently ambiguous. By introducing an AB-type monomer framework, alternating sequences become explicitly definable, giving rise to pronounced sequence–property relationship.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xaver Kneidl</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Johannes Reeb-Begic</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tongtong Cui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Patrick Theato</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yosuke Akae</creator></item><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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00098C" /&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;,2522-2530&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, Anja Marinow, Zviadi Katcharava, 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.&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/">Anja Marinow</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zviadi Katcharava</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/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 their application in elastic 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=D6PY00228E" /&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;,2456-2472&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, Chengzhen Meng, Peng Ji, Chaosheng Wang, Huaping Wang&lt;br/&gt;High-reactivity amide bonds are used to regulate the synthesis of nylon 6-based fibers that exhibit outstanding compatibility, mechanical properties, and elasticity.&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/">Chengzhen Meng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peng Ji</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></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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00394J" /&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;,2444-2455&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 route of VBAMA in this work.&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/D6PY00170J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00170J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00170J</link><title>A modular telechelic catechol platform for tunable Fe- and V-coordinated dynamic polymer gels</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=D6PY00170J" /&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/D6PY00170J, Paper&lt;/div&gt;&lt;div&gt;Ferley Orozco, Amy Hammett, Mahshad Karimi, Thomas E. Ericson, Lahiru Pasikku Hannadige, Joshua R. Fabian, Carol Korzeniewski, Anthony F. Cozzolino, Samantha L. Kristufek&lt;br/&gt;Dynamic metal–catechol coordination networks provide a powerful platform for bioinspired polymer gels, yet systematic molecular design rules connecting monomer structure to network mechanics and thermal behavior remain limited.&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>2026-06-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ferley Orozco</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Amy Hammett</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mahshad Karimi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas E. Ericson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lahiru Pasikku Hannadige</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joshua R. Fabian</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carol Korzeniewski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anthony F. Cozzolino</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Samantha L. Kristufek</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00257A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00257A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00257A</link><title>A synergistic compatibilization strategy for NBR/PA6 blends with ethylene–butadiene–fluorostyrene multiblock terpolymers</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=D6PY00257A" /&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/D6PY00257A, Paper&lt;/div&gt;&lt;div&gt;Biwei Sun, Xiaonan Xing, Huaqiang Zhang, Bo Liu, Chunji Wu, Shaojuan Wang, Shouke Yan, Dongmei Cui&lt;br/&gt;A synergistic compatibilization strategy for NBR/PA6 blends is developed using tailored E–BD–S&lt;small&gt;&lt;sup&gt;F&lt;/sup&gt;&lt;/small&gt; multiblock terpolymers, synthesized &lt;em&gt;via&lt;/em&gt; coordination polymerization. The resulting blends exhibit significantly enhanced 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>2026-06-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Biwei Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaonan Xing</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huaqiang Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bo Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chunji Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shaojuan Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shouke Yan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dongmei Cui</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00149A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00149A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00149A</link><title>Direct end-group modification of poly(Aib)-polymers: heterogeneous peptide coupling and chiral folding</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=D6PY00149A" /&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/D6PY00149A, 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;Sandipan Roy, Christian Hildebrand, Matthias Rohmer, Yishen Xie, Jitul Deka, Justus F. Thümmler, Wolfgang H. Binder&lt;br/&gt;The preparation of helical poly(α-aminoisobutyric acid) with defined endgroups on both sides is reported. Centro- and axial-chiral head-groups are combined with Au-binding thiols at the end to study the CISS effect.&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>2026-05-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sandipan Roy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christian Hildebrand</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthias Rohmer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yishen Xie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jitul Deka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Justus F. Thümmler</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/D6PY00399K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00399K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00399K</link><title>A crystalline supramolecular polymer constructed by the controlled self-assembly of clamparene and its application in photothermal conversion</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=D6PY00399K" /&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/D6PY00399K, Paper&lt;/div&gt;&lt;div&gt;Wen-Juan Qu, Wenjing Shi, Ke Wang, Wentao Hu, Hui Sun, Qi Lin, Tai-Bao Wei, Bingbing Shi&lt;br/&gt;We report the construction of a crystalline supramolecular polymer by the controlled self-assembly of clamparene and its application in photothermal conversion.&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>2026-06-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wen-Juan Qu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenjing Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ke Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wentao Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qi Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tai-Bao Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bingbing Shi</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00486E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00486E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00486E</link><title>From trees to 3D printing: “all-wood” photopolymer composites based on bisguiacol-F-diacrylate and methacrylated pinewood flour for digital light processing (DLP)</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=D6PY00486E" /&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/D6PY00486E, 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;Ettore Greco, Nicola Porcelli, Matteo Bergoglio, Niccolò Braidi, Fabrizio Roncaglia, Marco Sangermano, Minna Hakkarainen&lt;br/&gt;An all-wood photocurable resin based on lignin-derived monomers were used in 3D printing and Reinforced with methacrylated pinewood flour.&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>2026-06-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ettore Greco</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicola Porcelli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matteo Bergoglio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Niccolò Braidi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabrizio Roncaglia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marco Sangermano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minna Hakkarainen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00417B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00417B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00417B</link><title>Water stable perovskite nanocrystals for highly efficient photoinduced RAFT dispersion 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=D6PY00417B" /&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/D6PY00417B, Paper&lt;/div&gt;&lt;div&gt;Runqian Zhang, Wenjie Zhang, Chengli Wang, Xiaomeng Zhang, Zhe Cui, Peng Fu, Minying Liu, Zhibin Zhang, Yajing Chang, Yanjie He, Xinchang Pang&lt;br/&gt;Water-stable perovskite nanocrystals enable efficient photoinduced RAFT dispersion polymerization, yielding various uniform polymeric nano/microparticles, which are inaccessible to conventional catalysts.&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>2026-06-06T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Runqian Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wenjie Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chengli Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaomeng Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhe Cui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peng Fu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Minying Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhibin Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yajing Chang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanjie He</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xinchang Pang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01211B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01211B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01211B</link><title>CO2-derived functional polycarbonates as a sustainable platform for photosensitive polymeric materials</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/D5PY01211B, 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;Andreia C. S. Gonzalez, Rafael T. Aroso, Carla Cunha, Joao Sergio Seixas de Melo, M. Ermelinda S. Eusébio, Teresa Maria, Gabriela J. da Silva, Pedro F. Cruz, Rui M. M. Brito, Rui M. B. Carrilho, Mariette M. Pereira&lt;br/&gt;The development of CO2&lt;small&gt;&lt;sub /&gt;&lt;/small&gt;-based polymers integrating photo-responsiveness, synthetic versatility and processability remains an important challenge in polymer chemistry. Herein, a modular strategy was developed for multifunctional CO2&lt;small&gt;&lt;sub /&gt;&lt;/small&gt;-derived photosensitive polycarbonates. Catalytic...&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Andreia C. S. Gonzalez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rafael T. Aroso</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carla Cunha</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joao Sergio Seixas de Melo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M. Ermelinda S. Eusébio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Teresa Maria</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gabriela J. da Silva</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pedro F. Cruz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rui M. M. Brito</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rui M. B. Carrilho</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mariette M. Pereira</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00373G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00373G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00373G</link><title>Temperable dynamic polymeric glasses as tunable and rebondable adhesives</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=D6PY00373G" /&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/D6PY00373G, 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;Kexin Li, Nicholas R. Boynton, Joseph M. Dennis, Simon A. Fawcett, Stuart J. Rowan&lt;br/&gt;Thia-Michael-based dynamic polymer glasses have been designed that exhibit a range of room-temperature mechanical properties when subjected to varying temperatures during tempering, resulting in these materials acting as tunable adhesives.&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>2026-06-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kexin Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicholas R. Boynton</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joseph M. Dennis</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Simon A. Fawcett</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stuart J. Rowan</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00397D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00397D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00397D</link><title>Ring-opening copolymerization of (dihydro)levoglucosenone-derived spiro-epoxides and cyclic anhydrides</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=D6PY00397D" /&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/D6PY00397D, 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;Tianle Gao, Hiroto Ayakawa, Tatsuya Nishimura, Ayano Yoshida, Moeno Sugiyama, Takuya Yamamoto, Kenji Tajima, Kenji Takahashi, Feng Li, Takuya Isono, Katsuhiro Maeda, Toshifumi Satoh&lt;br/&gt;Ring-opening copolymerization of (dihydro)levoglucosenone-derived spiro-epoxides and cyclic anhydrides was developed to afford novel polyesters with rigid spirocyclic backbones, tunable thermal properties, and chiral conformations.&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>2026-06-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tianle Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hiroto Ayakawa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tatsuya Nishimura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ayano Yoshida</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Moeno Sugiyama</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takuya Yamamoto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kenji Tajima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kenji Takahashi</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/">Katsuhiro Maeda</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/D6PY00183A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00183A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00183A</link><title>Palladium-catalyzed direct preparation of highly branched ethylene oligomers and MA functionalized derivatives using dibenzhydryl pyrazine-imine ligands</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=D6PY00183A" /&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/D6PY00183A, Paper&lt;/div&gt;&lt;div&gt;Yusheng Han, Hui Wang, Shengyu Dai&lt;br/&gt;This study presents a highly efficient Pd(&lt;small&gt;II&lt;/small&gt;) catalytic system for direct synthesis of advanced polyolefin lubricants, correlating electronic structure with polymer topology and material performance.&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>2026-06-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yusheng Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shengyu Dai</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00295A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00295A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00295A</link><title>Dechlorination of poly(vinyl chloride): thermal benchmarks and complementary non-thermal pathways toward sustainable recycling</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=D6PY00295A" /&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;,2283-2315&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00295A, Review Article&lt;/div&gt;&lt;div&gt;Jinho Ko, Woojin Jeon, Daewhan Kim, Min Sang Kwon&lt;br/&gt;Emerging non-thermal strategies expand the mechanistic scope of PVC dechlorination beyond conventional thermal treatment, opening new pathways for chlorine management and polymer valorization.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-27T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jinho Ko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Woojin Jeon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daewhan Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Min Sang Kwon</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01149C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01149C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D5PY01149C</link><title>A new class of bio-elastomers based on β-myrcene and a glycomonomer: their application in sustainable adhesives</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=D5PY01149C" /&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;,2393-2402&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5PY01149C, Paper&lt;/div&gt;&lt;div&gt;Tuhin Subhra Pal, Uddhab Kalita, Suman Pradhan, Koushik Bhattacharya, Nikhil K. Singha&lt;br/&gt;A new class of bio-elastomers was synthesized &lt;em&gt;via&lt;/em&gt; emulsion copolymerization of β-myrcene and a glucose-based methacrylate glycomonomer, yielding biocompatible adhesives with enhanced performance through hydrolysis.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tuhin Subhra Pal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Uddhab Kalita</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Suman Pradhan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Koushik Bhattacharya</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nikhil K. Singha</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00273K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00273K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00273K</link><title>Synergistic short and long spacer fluorinated chain extenders for low refractive index waterborne polyurethane acrylate coatings</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=D6PY00273K" /&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;,2351-2366&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00273K, Paper&lt;/div&gt;&lt;div&gt;Haoxin Jing, Yuchao Yang, Lei Yang, Yupeng Zhang, Caiping Ma, Jianbing Wu, Baojun Wang, Yao Xu, Lixia Ling&lt;br/&gt;Synergistic incorporation of short spacer F-DEOA and long flexible spacer F-PETMP enables constraint release of fluorinated side chains, achieving low refractive index and high hydrophobicity in waterborne UV-curable polyurethane acrylate coatings.&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/">Haoxin Jing</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuchao Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yupeng Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Caiping Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianbing Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Baojun Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yao Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lixia Ling</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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00261G" /&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;,2403-2413&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;A novel bio-derived carbon photocatalyst (γ-CCD-r) enables controlled photo-ATRP under O&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; and visible light, yielding defined polymers with high recyclability, and was combined with heterogeneous catalyst and ATRPP to prepare polymer microspheres.&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/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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00258G" /&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;,2332-2339&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 B. Penrhyn-Lowe, Stephen Wright, Sarah Lomas, Andrew T. Slark, Andrew B. Dwyer, Steve P. Rannard&lt;br/&gt;Furfuryl methacrylate has been successfully incorporated, without side reactions, into branched TBRT polymers using free radical chemistries and are accessible for Diels-Alder coupling reactions&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 B. 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/">Andrew T. Slark</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew B. Dwyer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steve P. Rannard</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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00117C" /&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;,2340-2350&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 Cosimo Pio Trimboli, Emilia Paone, Andrea Donato, Riccardo Pellegrini, Elena Groppo, Maximilian Wohlgemuth, Sven Grätz, Francesco Mauriello, Lars Borchardt&lt;br/&gt;This work reports a mechanocatalytic strategy for the selective depolymerization of polyethylene using a Ru/Al&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;O&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; catalyst and 2-propanol as both hydrogen donor and liquid-assisted grinding medium across different mechanochemical platforms.&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 Cosimo Pio 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 Grätz</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/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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00222F" /&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;,2385-2392&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6PY00222F, Paper&lt;/div&gt;&lt;div&gt;Yuan Lu, Yanshan Gao, Shu-Yang Yu, Yanan Zhao, Jie Yang, Xiu-Li Sun, Xiaoyan Wang, Yong Tang&lt;br/&gt;A binuclear Ni/Et&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt;AlCl platform enables one-step ethylene/2-allylphenol copolymerization to afford phenol-functionalized branched polyethylenes with high activity, high molecular weight, and tunable incorporation.&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/">Shu-Yang 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/">Xiu-Li Sun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyan 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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00323K" /&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;,2377-2384&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, Xiao-Bing Lu, Hui Zhou&lt;br/&gt;The synthesis and controlled ring-opening polymerization of xylose-derived lactones were developed to construct a series of sustainable and functionalized polyesters.&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/">Xiao-Bing 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/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-hydroxyethyl)terephthalamide with ethanolamine catalyzed by La(OAc)3</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=D6PY00350H" /&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;,2367-2376&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;The rare-earth metal catalyst La(OAc)&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; enables the selective depolymerization of PET to bis(2-hydroxyethyl)terephthalamide (BHETA) with ethanolamine (EA) under mild conditions.&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/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, &lt;b&gt;17&lt;/b&gt;,2316-2331&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;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/D6PY00508J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00508J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00508J</link><title>A cleavage-type pyrrolyl enone photoinitiator enables photobleaching-regulated uniform thick-film photopolymerization</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=D6PY00508J" /&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/D6PY00508J, Paper&lt;/div&gt;&lt;div&gt;Jingfang Li, Wangwang Zhou, Shiqin Zhou, Luran Chun, Yuxuan Tang, Xiangqi Xu, Zhiceng Fu&lt;br/&gt;&lt;em&gt;N&lt;/em&gt;-Alkyl pyrrolyl enone C7-DPP-C7 enables cleavage-type photoinitiation, where slow photobleaching-driven crosslinking improves thermal and mechanical performance of thick films compared with rapid TPO polymerization.&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>2026-06-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jingfang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wangwang Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shiqin Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luran Chun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuxuan Tang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangqi Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiceng Fu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00239K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00239K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00239K</link><title>Polymers containing pendant lactone groups: synthesis and potential for sustainable 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=D6PY00239K" /&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/D6PY00239K, Minireview&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;Azra Kocaarslan, Baris Kumru&lt;br/&gt;Renewable plant resources provide a rich platform for the development of lactone-based monomers. This review highlights synthetic strategies for incorporating lactone motifs into side chains and discusses their potential sustainability implications.&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>2026-05-28T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Azra Kocaarslan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Baris Kumru</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00322B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00322B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00322B</link><title>A mild-temperature self-healing bio-based polyurethane film enabled by dual dynamic covalent bonds and segmental design</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=D6PY00322B" /&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/D6PY00322B, Paper&lt;/div&gt;&lt;div&gt;Yingcheng Han, Dingchuan Zhang, Junjiang Li, Yulei Qi, Zixuan Tao, Hang Yin, Panfang Lu&lt;br/&gt;Overcoming the trade-off between mechanics and healing, this work presents a bio-based polyurethane network synergizing oxime–urethane bonds and dynamic disulfide bonds.&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>2026-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yingcheng Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dingchuan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junjiang Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yulei Qi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zixuan Tao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hang Yin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Panfang Lu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00412A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00412A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00412A</link><title>Thermoresponsive alternating copolymers with tunable UCST behavior in an aqueous medium</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=D6PY00412A" /&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/D6PY00412A, Paper&lt;/div&gt;&lt;div&gt;Arya Karangat, Sreya Gain, Puja Poddar, Arnab Banerjee, Priyadarsi De&lt;br/&gt;This work reports the design of alternating polyelectrolytes with an upper critical solution temperature (UCST) in water as a function of polymer concentration, solution pH, salt, and molecular weight.&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>2026-05-28T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Arya Karangat</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sreya Gain</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Puja Poddar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arnab Banerjee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Priyadarsi De</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00382F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00382F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/PY/D6PY00382F</link><title>Rational design and synthesis of imine linked porous organic polymers: a bi-faceted approach towards customizing the acid–base properties for heterogeneous catalysis</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=D6PY00382F" /&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/D6PY00382F, Paper&lt;/div&gt;&lt;div&gt;Nandamol P. S., K. S. Sreelakshmi, Mintu Porel&lt;br/&gt;A bi-faceted approach for tailoring the acid-base properties of a porous organic framework with good crystallinity as well as thermal stability and effective utilization as a dual functional acid-base catalyst for synthesis of pyranochromenes.&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>2026-05-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nandamol P. S.</creator><creator xmlns="http://purl.org/dc/elements/1.1/">K. S. Sreelakshmi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mintu Porel</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, &lt;b&gt;17&lt;/b&gt;,2254-2264&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;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, &lt;b&gt;17&lt;/b&gt;,2208-2223&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;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/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, &lt;b&gt;17&lt;/b&gt;,2198-2207&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;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/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, &lt;b&gt;17&lt;/b&gt;,2180-2190&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;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/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;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6PY00121A" /&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;,2265-2274&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, Qingping Song, Ye Sha&lt;br/&gt;We developed sustainable thermosets with high lignin content (up to 50%) by constructing a flexible, ultra-high molecular weight soybean oil skeleton &lt;em&gt;via&lt;/em&gt; ring-opening metathesis polymerization (ROMP), achieving high strength and good toughness.&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/">Qingping Song</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ye Sha</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, &lt;b&gt;17&lt;/b&gt;,2247-2253&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;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/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, &lt;b&gt;17&lt;/b&gt;,2167-2179&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;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, &lt;b&gt;17&lt;/b&gt;,2191-2197&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;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/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, &lt;b&gt;17&lt;/b&gt;,2224-2246&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;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/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, &lt;b&gt;17&lt;/b&gt;,2153-2166&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;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></channel></rss>