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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18289" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/18289</id>
  <updated>2026-10-09T21:55:25Z</updated>
  <dc:date>2026-10-09T21:55:25Z</dc:date>
  <entry>
    <title>Adsorption of oxine and its derivatives on granular activated carbon</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18456" />
    <author>
      <name>Mustoor, Ms Veena</name>
    </author>
    <author>
      <name>Natarajan, G S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18456</id>
    <updated>2016-07-20T04:28:18Z</updated>
    <published>2002-12-01T00:00:00Z</published>
    <summary type="text">Title: Adsorption of oxine and its derivatives on granular activated carbon
Authors: Mustoor, Ms Veena; Natarajan, G S
Abstract: The adsorption&#xD;
of 8-hydroxyquinoline and some of its derivatives on granular activated carbon.&#xD;
F-400 sample, has been studied. The adsorption isotherms have been determined&#xD;
and tested for adherance to Freundlich and Langmuir theories. The surface area&#xD;
calculated on the basis of monolayer formation of&#xD;
&#xD;
these adsorbates&#xD;
has been correlated with structure of the oxines.
Page(s): 2551-2554</summary>
    <dc:date>2002-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Trace level determination of bromide in presence of large concentration of chloride by differential pulse polarography</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18455" />
    <author>
      <name>Sharma, P</name>
    </author>
    <author>
      <name>Sharma, Rakesh</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18455</id>
    <updated>2016-07-20T04:27:40Z</updated>
    <published>2002-12-01T00:00:00Z</published>
    <summary type="text">Title: Trace level determination of bromide in presence of large concentration of chloride by differential pulse polarography
Authors: Sharma, P; Sharma, Rakesh
Abstract: The optimum conditions&#xD;
for the determination of bromide at low concentrations has been developed employing&#xD;
differential pulse polarography. A detection limit of 0.3 &lt;i&gt;μ&lt;/i&gt;g/ml has been&#xD;
achieved. The method has been successfully applied for  the analysis of bromide content in underground&#xD;
waters and food&#xD;
&#xD;
products.
Page(s): 2548-2550</summary>
    <dc:date>2002-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and characterization of lanthanide complexes of 1-phenyl-3-methyl-5- hydroxy-4-pyrazolyl-phenyl ketone-2ʹ-picolinoyl hydrazone</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18454" />
    <author>
      <name>Thaker, B T</name>
    </author>
    <author>
      <name>Modi, Chetan K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18454</id>
    <updated>2016-07-20T04:23:59Z</updated>
    <published>2002-12-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and characterization of lanthanide complexes of 1-phenyl-3-methyl-5- hydroxy-4-pyrazolyl-phenyl ketone-2ʹ-picolinoyl hydrazone
Authors: Thaker, B T; Modi, Chetan K
Abstract: The &amp;nbsp;ligand, 1-phenyl-3-methyl-5-hydroxy-4-pyrazolyl-phenyl&#xD;
ketone-2ʹ-picolinoyl hydrazone (HL) is prepared by condensation of 1-phenyl-3-methyl&#xD;
-4-ben zoyl-5-pyrazolone with 2-picolinic acid hydrazide. Seven complexes of&#xD;
lanthanides with HL of the type [Ln&#xD;
(HL)&lt;sub&gt;3&lt;/sub&gt;].2 H&lt;sub&gt;2&lt;/sub&gt;O (where Ln=trivalent lanthanides&#xD;
such as La, Ce, Nd, Sm, Gd, Dy and Er) have been synthesized and&#xD;
&#xD;
characterized&#xD;
by complexometric titration of lanthanoid ions,elemental analysis, molar condudance,&#xD;
IR, &lt;sup&gt;1&lt;/sup&gt;H NMR, electronic spectral studies, and TGA analysis, IR spectra&#xD;
and thermogram shows the presence of two water moieties outside the coordination&#xD;
sphere and are non-electrolytic in nature. The complexes appear to be nine -coordinated&#xD;
and ligand act as a tridentate ligand.
Page(s): 2544-2547</summary>
    <dc:date>2002-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and spectroscopic characterization of molybdenum(0) and molybdenum(II) carbonyl benzophenoneazine complexes</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18453" />
    <author>
      <name>Affan, M A</name>
    </author>
    <author>
      <name>Hitam, Ramli bin</name>
    </author>
    <author>
      <name>Shamsuddin, Mustaffa bin</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18453</id>
    <updated>2016-07-20T04:27:04Z</updated>
    <published>2002-12-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and spectroscopic characterization of molybdenum(0) and molybdenum(II) carbonyl benzophenoneazine complexes
Authors: Affan, M A; Hitam, Ramli bin; Shamsuddin, Mustaffa bin
Abstract: A chelating&#xD;
2-methylpyridylbenzophenoneazinc ligand has been prepared by the condensation of&#xD;
2-acetylpyridine with benzophenone hydrazone. Reaction of the ligand with Mo(CO)&lt;sub&gt;6&lt;/sub&gt;&#xD;
gives 12-methylpyridylbenzophenoneazine) tetracarbonylmolybdenum(0) complex where&#xD;
the ligand is bidentate N, N. Oxidative-addition of the tetracarbonyl complex with&#xD;
1 mol equivalent of&#xD;
&#xD;
bromine, yields&#xD;
the neutral seven-coordinated dibromotricarbonylmolybdenum(&#xD;
&#xD;
II) azine complex.&#xD;
Treatment of the tetracarbonyl complex with 1 mol equivalent of PPh&lt;sub&gt;3&lt;/sub&gt;&#xD;
gives the expected tri -carbnonylmolybdenum(0)-azine tri phenylphosphine substituted&#xD;
complex.
Page(s): 2540-2543</summary>
    <dc:date>2002-12-01T00:00:00Z</dc:date>
  </entry>
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