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        <identifier>oai:figshare.com:article/33758200</identifier>
        <datestamp>2026-09-14T20:45:28Z</datestamp>
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          <dc:title>Data for An expanded MIL-53-type coordination polymer with a reactive pendant ligand</dc:title>
          <dc:creator>Hannah Kunicki (24901027)</dc:creator>
          <dc:creator>Thomas W. Chamberlain (1355565)</dc:creator>
          <dc:creator>Guy J. Clarkson (1301127)</dc:creator>
          <dc:creator>Reza J. Kashtiban (1423762)</dc:creator>
          <dc:creator>Joseph E. Hooper (8486937)</dc:creator>
          <dc:creator>Daniel M. Dawson (1328457)</dc:creator>
          <dc:creator>Sharon E. Ashbrook (1328460)</dc:creator>
          <dc:creator>Richard I. Walton (1328463)</dc:creator>
          <dc:subject>Coordination polymers</dc:subject>
          <dc:subject>Organometallic compounds</dc:subject>
          <dc:subject>Ligands</dc:subject>
          <dc:subject>Migrated from ePrints</dc:subject>
          <dc:description>A coordination polymer with a structure isoreticular to MIL-53, but containing a divalent metal cation (Co2+ or Mg2+) and a coordinating 4-styrylpyridine-N-oxide ligand, crystallises under solvothermal conditions; the pendant ligand can be brominated, with evidence from powder X-ray diffraction, element mapping and 81Br solid-state NMR for this post-synthesis modification.&lt;br&gt;&lt;br&gt;Crystal structure are available from the CCDC using the information provided in the paper.  Thermogravimetric analysis (TGA-DSC in Figure 3a) is provded in an ascii file in x,y1,y2 format: temperature, percentage mass, heat flow  Measured powder XRD (Figure 4a) is provided in acsii files in x,y format: angle, intensity.</dc:description>
          <dc:date>2018-07-03T00:00:00Z</dc:date>
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          <dc:type>Dataset</dc:type>
          <dc:identifier>10.82444/warw.33758200.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_for_An_expanded_MIL-53-type_coordination_polymer_with_a_reactive_pendant_ligand/33758200</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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