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              <creatorName>Raby Buck, Sarah</creatorName>
              <givenName>Sarah</givenName>
              <familyName>Raby Buck</familyName>
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            <creator>
              <creatorName>Browne, Duncan L.</creatorName>
              <givenName>Duncan L.</givenName>
              <familyName>Browne</familyName>
              <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="http://orcid.org">0000-0002-8604-229X</nameIdentifier>
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            <creator>
              <creatorName>Ingram, Katherine</creatorName>
              <givenName>Katherine</givenName>
              <familyName>Ingram</familyName>
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            <creator>
              <creatorName>Mattioli, Renan Rodini</creatorName>
              <givenName>Renan Rodini</givenName>
              <familyName>Mattioli</familyName>
              <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="http://orcid.org">0000-0001-5952-1941</nameIdentifier>
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            <creator>
              <creatorName>Pastre, Julio</creatorName>
              <givenName>Julio</givenName>
              <familyName>Pastre</familyName>
              <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="http://orcid.org">0000-0001-9972-425X</nameIdentifier>
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            <creator>
              <creatorName>Bolt, Robert</creatorName>
              <givenName>Robert</givenName>
              <familyName>Bolt</familyName>
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          <titles>
            <title><![CDATA[Analytical data for: <b>Nickel-Catalyzed Cross-Coupling of Aryl Chlorides by Heated Mechanochemistry: Scalable Suzuki-Miyaura Reactions via Twin-Screw Extrusion</b>]]></title>
          </titles>
          <subjects>
            <subject>Organic chemical synthesis</subject>
            <subject>Organic green chemistry</subject>
            <subject>Mechanochemistry</subject>
            <subject>Nickel catalysed Suzuki-Miyaura cross coupling</subject>
            <subject>Reactive Extrusion</subject>
            <subject>cross-coupling</subject>
            <subject>nickel catalysis</subject>
            <subject>twin-screw extrusion</subject>
            <subject>aryl chlorides</subject>
          </subjects>
          <dates>
            <date dateType="Created">2025-07-07</date>
            <date dateType="Updated">2025-07-07</date>
          </dates>
          <resourceType resourceTypeGeneral="Dataset">Dataset</resourceType>
          <publicationYear>2025</publicationYear>
          <publisher>University College London</publisher>
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            <description descriptionType="Abstract"><![CDATA[<p dir="ltr"><i>The direct use of aryl chlorides in Suzuki–Miyaura cross-coupling remains a long-standing challenge due to the inert nature of the C–Cl bond. Herein, we report the first nickel-catalyzed Suzuki–Miyaura cross-coupling of aryl chlorides under solvent-minimized, heated mechanochemical conditions. Employing liquid-assisted grinding (LAG) and thermal input, a broad range of electron-deficient and electron-rich aryl chlorides were successfully coupled with aryl boronic acids in under 1 hour. The methodology was translated to a twin-screw extrusion (TSE) process, enabling continuous production at scales up to 400 mmol and 65 g isolated product. This work demonstrates a sustainable, scalable strategy for C–C bond formation using readily available feedstocks, highlighting the synergy between nickel catalysis, mechanochemistry, and continuous flow processing.</i></p>]]></description>
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