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        <identifier>oai:figshare.com:article/33260582</identifier>
        <datestamp>2026-09-17T16:03:35Z</datestamp>
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          <dc:title>Flash Communication: Siloxides Promote the Iron-Catalyzed
Borylation of Aryl Chlorides</dc:title>
          <dc:creator>Patrick Daley-Dee (9970636)</dc:creator>
          <dc:creator>Luke Davies (13112628)</dc:creator>
          <dc:creator>Graham J. Tizzard (698749)</dc:creator>
          <dc:creator>Simon J. Coles (598079)</dc:creator>
          <dc:creator>Sebastien Monfette (1608055)</dc:creator>
          <dc:creator>Robin B. Bedford (1598683)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Science Policy</dc:subject>
          <dc:subject>Sociology</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>protracted induction period</dc:subject>
          <dc:subject>siloxide salts mosir</dc:subject>
          <dc:subject>aryl chloride substrates</dc:subject>
          <dc:subject>&lt;/ sup &gt;&lt;/</dc:subject>
          <dc:subject>3 &lt;/ sub</dc:subject>
          <dc:subject>2 &lt;/ sub</dc:subject>
          <dc:subject>aryl chlorides</dc:subject>
          <dc:subject>alkoxide salts</dc:subject>
          <dc:subject>&gt;&lt; sup</dc:subject>
          <dc:subject>siloxides promote</dc:subject>
          <dc:subject>precatalyst reduction</dc:subject>
          <dc:subject>obtained previously</dc:subject>
          <dc:subject>likely associated</dc:subject>
          <dc:subject>highly pyrophoric</dc:subject>
          <dc:subject>good effect</dc:subject>
          <dc:subject>flash communication</dc:subject>
          <dc:subject>catalyzed borylation</dc:subject>
          <dc:subject>also suggest</dc:subject>
          <dc:subject>activated species</dc:subject>
          <dc:description>In contrast to alkoxide salts, siloxide salts MOSiR&lt;sub&gt;3&lt;/sub&gt; (M = Na, Li) can be used to good effect as activators for B&lt;sub&gt;2&lt;/sub&gt;pin&lt;sub&gt;2&lt;/sub&gt; in the iron-catalyzed borylation of aryl chloride
substrates, in many cases giving results comparable to or better than
those obtained previously with highly pyrophoric &lt;i&gt;&lt;sup&gt;t&lt;/sup&gt;&lt;/i&gt;BuLi acting as an activator. Preliminary mechanistic investigations
reveal a protracted induction period, most likely associated with
precatalyst reduction, and these also suggest that the NaOSi&lt;i&gt;&lt;sup&gt;t&lt;/sup&gt;&lt;/i&gt;BuMe-activated B&lt;sub&gt;2&lt;/sub&gt;pin&lt;sub&gt;2&lt;/sub&gt; is
not as reducing as the equivalent &lt;i&gt;&lt;sup&gt;t&lt;/sup&gt;&lt;/i&gt;BuLi-activated
species.</dc:description>
          <dc:date>2026-09-14T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1021/acs.organomet.6c00235.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Flash_Communication_Siloxides_Promote_the_Iron-Catalyzed_Borylation_of_Aryl_Chlorides/33260582</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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