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<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19944" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/19944</id>
  <updated>2026-10-09T23:24:55Z</updated>
  <dc:date>2026-10-09T23:24:55Z</dc:date>
  <entry>
    <title>Separation of gold and silver using a chelating resin - Thiosemicarbazide incorporated Amberlite IRC-50</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/20106" />
    <author>
      <name>Roy, Kamalika</name>
    </author>
    <author>
      <name>Basu, S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/20106</id>
    <updated>2013-07-29T16:40:29Z</updated>
    <published>2005-03-01T00:00:00Z</published>
    <summary type="text">Title: Separation of gold and silver using a chelating resin - Thiosemicarbazide incorporated Amberlite IRC-50
Authors: Roy, Kamalika; Basu, S
Abstract: A thiosemicarbazide group incorporated&#xD;
into a weakly acidic resin, Amberlite IRC-50 can selectively entrap two noble&#xD;
metals, gold and silver. The exchange capacity of the newly&#xD;
&#xD;
formed resin for Au(III) and Ag(I) is&#xD;
satisfactory. The resin can be utilized for the separation of these noble&#xD;
metals from different complex matrices.
Page(s): 531-534</summary>
    <dc:date>2005-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Pulse polarographic determination of organoisothiocyanates and a method for the analysis of Ditrapex</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/20105" />
    <author>
      <name>Verma, B C</name>
    </author>
    <author>
      <name>Chauhan, Chetan</name>
    </author>
    <author>
      <name>Thakur, Lata</name>
    </author>
    <author>
      <name>Sharma, D K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/20105</id>
    <updated>2013-08-05T16:42:27Z</updated>
    <published>2005-03-01T00:00:00Z</published>
    <summary type="text">Title: Pulse polarographic determination of organoisothiocyanates and a method for the analysis of Ditrapex
Authors: Verma, B C; Chauhan, Chetan; Thakur, Lata; Sharma, D K
Abstract: Pulse polarographic analysis shows that&#xD;
in acetonitrile medium, &lt;i&gt;n&lt;/i&gt;-butylamine transforms organoisothiocyanates&#xD;
quantitatively into the corresponding thiourea derivatives which&#xD;
&#xD;
yield well-defined diffusion controlled&#xD;
anodic waves in the presence of aqueous sulphuric acid (&lt;i&gt;p&lt;/i&gt;H 2-3) and&#xD;
potassium perchlorate (supporting electrolyte). The method has been&#xD;
&#xD;
successfully adapted for the analysis of&#xD;
Ditrapex, an insecticide formulation containing methyl isothiocyanate.
Page(s): 529-530</summary>
    <dc:date>2005-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Kinetic determination of traces of Al(III) ion by its catalytic effect on oxidation of 4-hydroxycoumarin by potassium permanganate</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/20104" />
    <author>
      <name>Igov, R P</name>
    </author>
    <author>
      <name>Simonovic, R M</name>
    </author>
    <author>
      <name>Pecev, T G</name>
    </author>
    <author>
      <name>Yeselinovic, B B</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/20104</id>
    <updated>2013-07-26T16:39:33Z</updated>
    <published>2005-03-01T00:00:00Z</published>
    <summary type="text">Title: Kinetic determination of traces of Al(III) ion by its catalytic effect on oxidation of 4-hydroxycoumarin by potassium permanganate
Authors: Igov, R P; Simonovic, R M; Pecev, T G; Yeselinovic, B B
Abstract: Oxidation of 4-hydroxycoumarin by&#xD;
potassium permanganate in acid media of acetate buffer is catalyzed by Al(III)&#xD;
ions, which is the basis of the proposed new homogenocaralytic&#xD;
&#xD;
method for determinati on of Al(III) in&#xD;
solutions. Under the optimum conditions, Al(III) has been determined at 525 nm&#xD;
in solutions containing analyte at 50-1000 ng/ml with probable relative error&#xD;
of 15.6-5.1 % and detect ion limit of 20 ng/ml. Appropriate kinetic equations&#xD;
for both catalytic and noncatalytic processes have been derived and the&#xD;
mechanism of catalytic effect of Al(III) investigated. Interference studies&#xD;
show that most of the common cat ions and anions do not interfere.
Page(s): 526-528</summary>
    <dc:date>2005-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Ruthenium complexes containing bridging dppm and benzene-1, 2-dithiolato ligands: X-ray crystal structure of [Ru&lt;sub&gt;2&lt;/sub&gt;(CO)&lt;sub&gt;4&lt;/sub&gt; {μ-S(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;)S} (μ-dppm)]</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/20103" />
    <author>
      <name>Begum, Noorjahan</name>
    </author>
    <author>
      <name>Hyder, Md Iqbal</name>
    </author>
    <author>
      <name>Kabir, Shariff E</name>
    </author>
    <author>
      <name>Kundu, Kalipada</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/20103</id>
    <updated>2013-07-27T16:39:38Z</updated>
    <published>2005-03-01T00:00:00Z</published>
    <summary type="text">Title: Ruthenium complexes containing bridging dppm and benzene-1, 2-dithiolato ligands: X-ray crystal structure of [Ru&lt;sub&gt;2&lt;/sub&gt;(CO)&lt;sub&gt;4&lt;/sub&gt; {μ-S(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;)S} (μ-dppm)]
Authors: Begum, Noorjahan; Hyder, Md Iqbal; Kabir, Shariff E; Kundu, Kalipada
Abstract: The reaction of benzene-1,2-dithiol with [Ru&lt;sub&gt;3&lt;/sub&gt;(CO)&lt;sub&gt;10&lt;/sub&gt;(μ-dppm)] &lt;b&gt;1&lt;/b&gt; in refluxing&#xD;
THF afforded two new compounds [Ru&lt;sub&gt;2&lt;/sub&gt;(CO)&lt;sub&gt;4&lt;/sub&gt; {μ-S(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;)S}(μ-dppm)] &lt;b&gt;2&lt;/b&gt;&#xD;
and [Ru&lt;sub&gt;3&lt;/sub&gt;(CO&lt;sub&gt;8&lt;/sub&gt;{μ-S(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;)S}(μ-dppm)] &lt;b&gt;3&lt;/b&gt; which&#xD;
were characterized by elemental analysis, infrared, &lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;31&lt;/sup&gt;P{&lt;sup&gt;1&lt;/sup&gt;H}&#xD;
NMR and mass spectra. The structure of &lt;b&gt;2&lt;/b&gt; was determined by single&#xD;
crystal X-ray diffraction analysis. The compound crystallizes in the monoclinic&#xD;
space group &lt;i&gt;P&lt;/i&gt;2&lt;sub&gt;1&lt;/sub&gt;/n, with &lt;i&gt;a= &lt;/i&gt;1 0.3133(2), &lt;i&gt;b= &lt;/i&gt;16.9806(3),&#xD;
&lt;i&gt;c= &lt;/i&gt;19.5605(3) Å, α=90, β=100.2298(11), γ=90°, &lt;i&gt;V&lt;/i&gt;=3371.10(10)&#xD;
Å&lt;sup&gt;3&lt;/sup&gt; and Z=4. Both Ru atoms are in distorted octahedral geometry. For&#xD;
each ruthenium, two CO groups in &lt;i&gt;cis &lt;/i&gt;positions, one bridged S atom and&#xD;
the other bonded Ru atom occupy the equatorial sites, and the other bridged S&#xD;
atom and a P atom of the bridging dppm ligand are in &lt;i&gt;trans&lt;/i&gt; positions on&#xD;
the meridional axis. Of the two S atoms, one lies in the Ru&lt;sub&gt;2&lt;/sub&gt;P&lt;sub&gt;2&lt;/sub&gt;&#xD;
plane while the other is perpendicular to this plane, thus making them&#xD;
nonequivalent but keeping the two P atoms of the bridging dppm ligand&#xD;
identical. The 50-electron compound &lt;b&gt;3&lt;/b&gt; contains a doubly briddging&#xD;
dithiolato and a bridging dppm ligand. Protonation of &lt;b&gt;2&lt;/b&gt; with&#xD;
trifluroacetic acid results in the formation of the cationic hydrido species [(μ-H)Ru&lt;sub&gt;2&lt;/sub&gt;(CO)&lt;sub&gt;4&lt;/sub&gt;&#xD;
{μ-S(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;)S} (μ-dppm)]&lt;sup&gt;+&lt;/sup&gt; which has been&#xD;
characterized by spectroscopic data.
Page(s): 521-525</summary>
    <dc:date>2005-03-01T00:00:00Z</dc:date>
  </entry>
</feed>

