<rss version="2.0" xmlns:a10="http://www.w3.org/2005/Atom"><channel><title>RSC - RSC Mechanochem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/MR</link><description>RSC - RSC Mechanochem. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Tue, 30 Jun 2026 11:42:32 Z</lastBuildDate><category>RSC - RSC Mechanochem. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - RSC Mechanochem. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/MR</link></image><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00048G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00048G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00048G</link><title>Liquid-assisted ball-milling synthesis of organic carbonates as aroma compounds</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=D6MR00048G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00048G, 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;Can Bozdemir, Mehmet Efe Çelik, Mehmet Mart, Aydın Alemdar, Ahmet Baydar, Cagatay Dengiz&lt;br/&gt;This manuscript explores the synthesis of aroma compounds using a solvent-free ball milling method, yielding nine new carbonate compounds. This approach offers an alternative to traditional methods, eliminating the use of low-odor-threshold bases.&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/">Can Bozdemir</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mehmet Efe Çelik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mehmet Mart</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aydın Alemdar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ahmet Baydar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cagatay Dengiz</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR90014C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR90014C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR90014C</link><title>Moving mechanochemistry forward: tribochemistry</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=D6MR90014C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR90014C, Editorial&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;James Batteas, Wilfred Tysoe, Judith A. Harrison&lt;br/&gt;Editor-in-Chief James Batteas, Wilfred Tysoe and Judith A. Harrison examine important advances in tribochemistry.&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/">James Batteas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wilfred Tysoe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Judith A. Harrison</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR90015A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR90015A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR90015A</link><title>Outstanding Reviewers for RSC Mechanochemistry in 2025</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=D6MR90015A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR90015A, Editorial&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;&lt;br/&gt;We would like to take this opportunity to highlight the Outstanding Reviewers for &lt;em&gt;RSC Mechanochemistry&lt;/em&gt; in 2025, as selected by the editorial team for their significant contribution to the journal.&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></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00044D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00044D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00044D</link><title>Energy-efficient mechanochemical synthesis of MgWO4 phase materials: (micro)-structural, thermal, and optical 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=D6MR00044D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00044D, 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;S. A. Ashika, S. Balamurugan&lt;br/&gt;A simple, energy-efficient mechanochemical milling method for achieving phase formation of monoclinic MgWO&lt;small&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;/small&gt; materials using a mixture of MgO and WO&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt; without the need for additional thermal treatment.&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/">S. A. Ashika</creator><creator xmlns="http://purl.org/dc/elements/1.1/">S. Balamurugan</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00053C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00053C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00053C</link><title>One-sequence mechanochemical synthesis-deracemisation of a levetiracetam intermediate</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=D6MR00053C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00053C, 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;Guillaume Wery, Tom Leyssens&lt;br/&gt;Mechanochemistry allows for a one-sequence synthesis-deracemization process for the synthesis of an enantioenriched intermediate of levetiracetam.&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/">Guillaume Wery</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tom Leyssens</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00052E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00052E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00052E</link><title>Unlocking the reversibility of the mechanochemical synthesis of a pharmaceutical cocrystal</title><description>&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Accepted Manuscript&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00052E, 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;Artem Golomolzin, Evgeniy A. Losev, Elena Boldyreva&lt;br/&gt;Opposite transformations (synthesis or decomposition of the cocrystal) in the system “piroxicam (P) – succinic acid (S) – their 2:1 cocrystal (P2S)” are documented depending on the protocol of mechanical...&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/">Artem Golomolzin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Evgeniy A. Losev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elena Boldyreva</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00055J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00055J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00055J</link><title>Resonant acoustic mixing-induced polymorphic transformation of glycine observed by solid-state NMR</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=D6MR00055J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00055J, Communication&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/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;Simon Sinn, Elizabeth Brown, Téodor Iftemie, David L. Bryce&lt;br/&gt;Carbon-13 magic-angle spinning solid-state NMR is used to monitor the real-time resonant acoustic mixing-induced polymorphic transformation of α-glycine to γ-glycine. Stepped JMAK kinetics are found to depend on the RAM vial filling factor.&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/">Simon Sinn</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elizabeth Brown</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Téodor Iftemie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David L. Bryce</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00034G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00034G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00034G</link><title>When breaking heterojunctions unlocks a reactive compromise in photomechanocatalytic phenol degradation over P25-TiO2</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=D6MR00034G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00034G, 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;Guillaume Demily, Nicolas Kania, Anne Ponchel, Stéphane Menuel&lt;br/&gt;Mechanical activation disrupts TiO₂ heterojunctions, unlocking dark oxidative reactivity while compromising optimal UV photocatalysis, establishing a reactive compromise for sustainable environmental remediation.&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/">Guillaume Demily</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nicolas Kania</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anne Ponchel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stéphane Menuel</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00040A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00040A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00040A</link><title>Mechanistic insights into mechanochemical oxidation of 1,1-disubstituted alkenes mediated by polymer-derived mechanoradicals</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=D6MR00040A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00040A, 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;Akira Kodaka, Takumi Yamamoto, Hajime Sugita, Akira Takahashi, Hideyuki Otsuka&lt;br/&gt;Mechanochemical polymer radicals enable solvent-free oxidative cleavage of 1,1-disubstituted alkenes using molecular oxygen in the solid state.&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/">Akira Kodaka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Takumi Yamamoto</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hajime Sugita</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Akira Takahashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hideyuki Otsuka</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00024J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00024J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00024J</link><title>Making and breaking Si–Si bonds under mechanochemical 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=D6MR00024J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00024J, 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;Thomas Lainer, Michael Haas&lt;br/&gt;Mechanochemistry offers a sustainable alternative to solution-based synthesis, yet its potential in main-group chemistry remains largely untapped.&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/">Thomas Lainer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Haas</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D5MR00134J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D5MR00134J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D5MR00134J</link><title>Interfacial mechano-nanoarchitectonics for chemical, materials and biological processes</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=D5MR00134J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5MR00134J, 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;Katsuhiko Ariga&lt;br/&gt;This review discusses interfacial mechano-nanoarchitectonics in chemical, materials and biological processes, suggesting that interfaces are essential for combining mechanical manipulation of functional material systems with nanoarchitectonics.&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>2026-05-22T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Katsuhiko Ariga</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00036C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00036C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00036C</link><title>Sonochemistry- and mechanochemistry-driven one-pot synthesis of polyfunctionalised 5-iodo-1H-1,2,3-triazoles through copper(I)-catalysed 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=D6MR00036C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00036C, 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;Koushik Pal, Pintu Karmakar, Goutam Brahmachari&lt;br/&gt;Straightforward, rapid, and practical alternative dual synthetic strategies to access 5-iodo-1&lt;em&gt;H&lt;/em&gt;-1,2,3-triazoles, using ultrasound and a high-speed ball mill as green energy tools.&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/">Koushik Pal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pintu Karmakar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Goutam Brahmachari</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00032K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00032K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00032K</link><title>Mechanochemistry-directed ligand design for enhanced reactivity and enantioselectivity in solve-less palladium-catalyzed conjugate arylations</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=D6MR00032K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00032K, 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;Keisuke Kondo, Hina Shoji, Koji Kubota, Hajime Ito&lt;br/&gt;We have developed the first mechanochemical protocol for a solvent-less palladium-catalyzed conjugate arylation, which was enabled by designing new mechanochemistry-directed bipyridine and chiral pyridine–oxazoline ligands.&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/">Keisuke Kondo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hina Shoji</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Koji Kubota</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hajime Ito</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00028B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00028B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/MR/D6MR00028B</link><title>Amano-PS-IM-catalyzed mechanochemical enzymatic acylative kinetic resolution of secondary alcohols</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=D6MR00028B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;RSC Mechanochem.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6MR00028B, 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;Koji Kubota, Yuri Kamakura, Taiga Takeda, Hajime Ito&lt;br/&gt;An appropriate choice of milling conditions as well as a liquid-assisted grinding additive enable the Amano-PS-IM-catalyzed highly efficient acylative kinetic resolution of secondary alcohols under mechanochemical 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>2026-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Koji Kubota</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuri Kamakura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Taiga Takeda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hajime Ito</creator></item></channel></rss>