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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/18241" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/18240" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/18239" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/18238" />
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/18241">
    <title>Studies on the determination of palladium(II) by fluorescence quenching method with meso-tetra[ 4-(carboxymethy lenoxy)phenyl]porphyrin</title>
    <link>http://nopr.niscair.res.in/handle/123456789/18241</link>
    <description>Title: Studies on the determination of palladium(II) by fluorescence quenching method with meso-tetra[ 4-(carboxymethy lenoxy)phenyl]porphyrin
&lt;br/&gt;
&lt;br/&gt;Authors: Fang, Yan-jun; Chen, Hui; Gao, Zhi-xian; Jin, Xiao-yong
&lt;br/&gt;
&lt;br/&gt;Abstract: The&#xD;
spectrofluorimetric determination of Pd(II) using&#xD;
meso-tetra[4-(carboxymethylenoxy)phenyl]porphyrin (TCMOPPH&lt;sub&gt;2&lt;/sub&gt;) as an&#xD;
emission reagent has been investigated by measuring the decrease of its&#xD;
fluorescence intensity of the complexation of Pd(II)-TCMOPP. An emission peak of TCMOPPH&lt;sub&gt;2&lt;/sub&gt;, which is decreased&#xD;
linearly by adding of Pd(II), occurs at 394 nm in aqueous solution with&#xD;
excitation at 306 nm. The fluorescence intensity vary linearly with the&#xD;
concentration of palladium(II) in the range 3.754×10&lt;sup&gt;-3 &lt;/sup&gt;~0.3625 μg/mL&#xD;
(SD = 0.034 for 10 times measurements) and the detection limit down to 2.715×10&lt;sup&gt;-4&lt;/sup&gt;&#xD;
μg/mL. The interference of other noble metals and some of inorganic ions have&#xD;
been described, and the quenching mechanism has also been investigated&#xD;
according to the Stern-Volmer equation.
&lt;br/&gt;
&lt;br/&gt;Page(s): 521-524</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/18240">
    <title>Structural studies on some trifluoro-β-diketonates of tin (IV) and lead(II)</title>
    <link>http://nopr.niscair.res.in/handle/123456789/18240</link>
    <description>Title: Structural studies on some trifluoro-β-diketonates of tin (IV) and lead(II)
&lt;br/&gt;
&lt;br/&gt;Authors: Singh, Sudha; Gupta, Vishnu D
&lt;br/&gt;
&lt;br/&gt;Abstract: Organotin(IV),&#xD;
tin(IV) and lead(II) trifluoro-β-diketonates have been prepared and&#xD;
characterized on the basis of IR, &lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;13&lt;/sup&gt;C NMR data.&#xD;
All the organotin(IV) complexes are thermally stable liquids. SnCl&lt;sub&gt;2&lt;/sub&gt;(CF&lt;sub&gt;3&lt;/sub&gt;COCHCOPh)&lt;sub&gt;2&lt;/sub&gt;&#xD;
(&lt;b&gt;7&lt;/b&gt;) is characterized by X-ray crystallography which reveals a distorted &lt;i&gt;cis&lt;/i&gt;-octahedral&#xD;
structure. X- ray diffraction analysis of Pb(CF&lt;sub&gt;3&lt;/sub&gt;COCHCOC&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;-&lt;i&gt;p&lt;/i&gt;-Cl)&lt;sub&gt;2&lt;/sub&gt;&#xD;
(&lt;b&gt;8&lt;/b&gt;) shows a highly distorted trigonal bipyramidal structure.
&lt;br/&gt;
&lt;br/&gt;Page(s): 513-520</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/18239">
    <title>Synthesis and characterization of azaphosphole complexes of ruthenium and rhodium</title>
    <link>http://nopr.niscair.res.in/handle/123456789/18239</link>
    <description>Title: Synthesis and characterization of azaphosphole complexes of ruthenium and rhodium
&lt;br/&gt;
&lt;br/&gt;Authors: Jain, Vimal K; Hemrajani, Leena; Bansal, Raj K
&lt;br/&gt;
&lt;br/&gt;Abstract: Reaction of&#xD;
azaphospholes (&lt;b&gt;L&lt;/b&gt;) [2-phosphaindolizines (&lt;b&gt;1&lt;/b&gt;) and&#xD;
1,3-azaphospholo[5, 1-a]isoquinolines (&lt;b&gt;2&lt;/b&gt;)] with [η&lt;sup&gt;5&lt;/sup&gt;-Cp*RhCl&lt;sub&gt;2&lt;/sub&gt;]&lt;sub&gt;2&lt;/sub&gt;&#xD;
(Cp* = pentamethylcyclopentadienyl) and [Ru(η&lt;sup&gt;6&lt;/sup&gt;-cymene)Cl&lt;sub&gt;2&lt;/sub&gt;]&lt;sub&gt;2&lt;/sub&gt;&#xD;
in 2:1 molar ratio in dichloromethane yields mononuclear complexes of the type&#xD;
[Cp*RhCl&lt;sub&gt;2&lt;/sub&gt;(L)] .H&lt;sub&gt;2&lt;/sub&gt;O and [Ru(cymene) Cl&lt;sub&gt;2&lt;/sub&gt;(L)] .H&lt;sub&gt;2&lt;/sub&gt;O.&#xD;
These complexes have been&#xD;
&#xD;
characterized&#xD;
by elemental analysis, FAB mass, IR and NMR (&lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;31&lt;/sup&gt;P)&#xD;
spectral data. Stereochemistry of these complexes has been discussed based on &lt;span style="mso-bidi-font-weight:bold"&gt;NMR data. &lt;span style="mso-bidi-font-weight:&#xD;
bold"&gt;NMR studies reveal a dynamic equilibrium between covalent and&#xD;
ionic forms of the complexes derived from &lt;b&gt;1&lt;/b&gt; in solution.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 506-512</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/18238">
    <title>Exchange kinetic studies on zirconium antimonophosphate</title>
    <link>http://nopr.niscair.res.in/handle/123456789/18238</link>
    <description>Title: Exchange kinetic studies on zirconium antimonophosphate
&lt;br/&gt;
&lt;br/&gt;Authors: Mittal, S K; Singh, Pritpal
&lt;br/&gt;
&lt;br/&gt;Abstract: Exchange&#xD;
kinetics of the alkaline earth metal ions with labile protons of the synthetic&#xD;
ion exchanger zirconium anti monophosphate has been studied, using the limited&#xD;
bath technique. Effect of concentration, particle size and temperature on the extent&#xD;
of exchange at the solution-solid in terrace are reported. The Boyd method for&#xD;
studing the kinetics of spherical particles is used to explain the results.&#xD;
Distinction between particle diffusion and film diffusion has been made by interruption&#xD;
test. The overall studies indicate that the effective diffusion coefficient&#xD;
consists of two components, an initial&#xD;
fast exchange and later a slow exchange, representing the&#xD;
inter-diffusion of counter ions through the pores of the exchanger matrix, with&#xD;
increase in temperature. The contribution of the faster component decreases,&#xD;
probably because the metal ions diffuse as dehydrated ions and the dehydration&#xD;
of the metal ions is easy at lower temperature. The effect of concentration and&#xD;
particle size on the exchange rate are also discussed.
&lt;br/&gt;
&lt;br/&gt;Page(s): 500-505</description>
  </item>
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