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            <name>Title</name>
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    <name>Article</name>
    <description>Faculty Publications -Articles</description>
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          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>Crystal structure of 4-{(E)-[2-(pyridin-4-ylcarbonyl)hydrazin-1-ylidene]methyl}-phenyl acetate monohydrate</text>
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          <name>Subject</name>
          <description>The topic of the resource</description>
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              <text>Aroyl hydrazone; Crystal structure; Hydrazone; Hydrogen bonding</text>
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          <name>Description</name>
          <description>An account of the resource</description>
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              <text>The asymmetric unit of the title compound, C15H13N3O3H2O, comprises a 4-{(E)-[2-(pyridin-4-ylcarbonyl)hydrazinyl-idene]methyl}phenyl acetate molecule and a solvent water molecule linked by O - H?O and O - H?N hydrogen bonds from the water molecule and a C - H?O contact from the organic molecule. The compound adopts an E conformation with respect to the azomethine bond and the dihedral angle between the pyridine and benzene rings is 21.90 (7). The azomethine bond [1.275 (2)  distance is very close to the formal C=N bond length, which confirms the azomethine bond formation. An extensive set of O - H?O, O - H?N, N - H?O and C - H?O hydrogen bonds builds a two-dimensional network progressing along the c axis.</text>
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          <name>Creator</name>
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              <text>Datta R.; Ramya V.; Sithambaresan M.; Prathapachandra Kurup M.R.; Simpson J.</text>
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          <name>Source</name>
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              <text>Acta Crystallographica Section E: Structure Reports Online, Vol-71, No. 2, pp. o79-o80.</text>
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          <name>Publisher</name>
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              <text>International Union of Crystallography</text>
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          <name>Date</name>
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              <text>2015-01-01</text>
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          <name>Identifier</name>
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              <text>&lt;a href="https://doi.org/10.1107/S2056989014027819" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1107/S2056989014027819&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-84928164138&amp;amp;doi=10.1107%2FS2056989014027819&amp;amp;partnerID=40&amp;amp;md5=1fe96ca4704d511d4cbf99da1d6abba7" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-84928164138&amp;amp;doi=10.1107%2fS2056989014027819&amp;amp;partnerID=40&amp;amp;md5=1fe96ca4704d511d4cbf99da1d6abba7&lt;/a&gt;</text>
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          <name>Rights</name>
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            <elementText elementTextId="138040">
              <text>All Open Access; Gold Open Access; Green Open Access</text>
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          <name>Relation</name>
          <description>A related resource</description>
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              <text>ISSN: 16005368</text>
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          <name>Format</name>
          <description>The file format, physical medium, or dimensions of the resource</description>
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              <text>Online</text>
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          <name>Language</name>
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              <text>English</text>
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          <name>Type</name>
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              <text>Article</text>
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          <name>Coverage</name>
          <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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              <text>Datta R., Department of Chemistry, Christ University, Hosur Road, Bangalore, 560 029, India; Ramya V., Department of Chemistry, Christ University, Hosur Road, Bangalore, 560 029, India; Sithambaresan M., Department of Chemistry, Faculty of Science, Eastern University, Sri Lanka, Chenkalady, Sri Lanka; Prathapachandra Kurup M.R., Department of Applied Chemistry, Cochin University of Science and Technology, Kochi, 682 022, India; Simpson J., University of Otago, New Zealand</text>
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