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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/46583</link>
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    <pubDate>Sun, 11 Oct 2026 12:10:42 GMT</pubDate>
    <dc:date>2026-10-11T12:10:42Z</dc:date>
    <item>
      <title>Determination of inductive effect parameter of methyl group from gas-phase charge transfer bands of molecular complexes of N-phenyl-tetrachlorophthalimide with methyl substituted benzenes</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46786</link>
      <description>Title: Determination of inductive effect parameter of methyl group from gas-phase charge transfer bands of molecular complexes of N-phenyl-tetrachlorophthalimide with methyl substituted benzenes
Authors: Roy, M; Mukherjee, A K; Seal, B K
Abstract: The charge transfer absorption bands of electron donor-acceptor (EDA) complexes of N-phenyltetrachlorophthalimide as acceptor with a series of methyl substituted benzenes as donors have been studied in dioxan, chloroform, dichloromethane and dimethylformamide as solvents. The absorption maxima (v&lt;sub&gt;CT&lt;/sub&gt;) of the complexes in these solvents deviate greatly from Mulliken's equation when plotted against donor ionisation potentials but the gas-phase values of v&lt;sub&gt;CT&lt;/sub&gt;, determined from the CT transition energies in the first three weakly polar solvents, give a reasonable fit to Mulliken type plot with the donor ionisation potentials. The energies of the HOMOs of methyl substituted benzenes, obtained as functions of the inductive effect PMO parameter (h&lt;sub&gt;Me&lt;/sub&gt;) of the methyl group by Coulson-Longuet- Higgins perturbation technique, give a linear correlation with the gas-phase hv&lt;sub&gt;CT&lt;/sub&gt; values of the complexes. From the slope of this plot, h&lt;sub&gt;Me&lt;/sub&gt; is found to be -0.1843, a value in fair agreement with that (-0.21) obtained by Lepley from studies of CT complexes of TCNE with a series of methyl substituted benzenes and naphthalenes.
Page(s): 635-638</description>
      <pubDate>Tue, 01 Aug 1989 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46786</guid>
      <dc:date>1989-08-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Charge-transfer complexation reaction in the solid state - reaction between p-chloranil and 8-hydroxyquinoline</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46785</link>
      <description>Title: Charge-transfer complexation reaction in the solid state - reaction between p-chloranil and 8-hydroxyquinoline
Authors: Singh, N B; Singh, R J; Singh, N N
Abstract: &lt;em&gt;p&lt;/em&gt;-Chloranil forms 1:2 charge transfer complex with 8-hydroxyquinoline both in solid state and solution. It is found that during solid state reaction, 8-hydroxyquinoline diffuses towards &lt;em&gt;p&lt;/em&gt;-chloranil. The diffusion is a vapour phase dominated process although surface migration also occurs. Initial reaction starts at the point of defect present in the crystal lattice of &lt;em&gt;p&lt;/em&gt;-chloranil.
Page(s): 639-644</description>
      <pubDate>Tue, 01 Aug 1989 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46785</guid>
      <dc:date>1989-08-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Thermal reactions of CdC12 and CdBr2 in NaNO3-KNO3 eutectic melt</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46784</link>
      <description>Title: Thermal reactions of CdC12 and CdBr2 in NaNO3-KNO3 eutectic melt
Authors: Singh, N B; Kumar, P; Pandey, S P
Abstract: CdCl&lt;sub&gt;2&lt;/sub&gt; and CdBr&lt;sub&gt;2&lt;/sub&gt;, dissolve in NaNO&lt;sub&gt;3&lt;/sub&gt;-KNO&lt;sub&gt;3&lt;/sub&gt; eutectic melt. When these melts are heated, cadmium halides undergo decomposition reaction, CdBr&lt;sub&gt;2&lt;/sub&gt; reacting with a faster rate as compared with CdCl&lt;sub&gt;2&lt;/sub&gt;. The two reactions obey second order kinetics. In the case of CdCl&lt;sub&gt;2&lt;/sub&gt;, eutectic system, CdO, NaCl, KCl, NO&lt;sub&gt;2&lt;/sub&gt; and O&lt;sub&gt;2&lt;/sub&gt;, are obtained as the end products. However, in the case of CdBr&lt;sub&gt;2&lt;/sub&gt;-eutectic system, CdO, NaBr, KBr, Br, NO&lt;sub&gt;2&lt;/sub&gt; and O&lt;sub&gt;2&lt;/sub&gt; are obtained as the reaction products. The kinetics of the reactions have been followed by isothermal thermogravimetry and the solid residues identified by X-ray diffraction technique. The gaseous products have been analysed in the usual manner. Mechanisms of reactions have been explored by DTA technique also.
Page(s): 645-648</description>
      <pubDate>Tue, 01 Aug 1989 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46784</guid>
      <dc:date>1989-08-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Thermal stability of doped γ-ferric oxide</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46783</link>
      <description>Title: Thermal stability of doped γ-ferric oxide
Authors: Bhat, Ramachandra; Anantharaman, M R; Keer, H V
Abstract: The thermal stablity of &amp;gamma;-ferric oxide doped with magnesium (II), cobalt (II), nickel (II) and copper (has been studied. The dopant cations get substituted in the &amp;gamma;-ferric oxide lattice. The Madelung constant and the Coulomb energy have also been evaluated. The dopants such as magnesium (II), cobalt (II), nickel (II) and copper (II) stabilize the &amp;gamma;-Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; lattice, as revealed by the increase in the temperature of onset of the phase transition (conversion into ɑ- Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;) as compared to that of pure maghemite.
Page(s): 649-652</description>
      <pubDate>Tue, 01 Aug 1989 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46783</guid>
      <dc:date>1989-08-01T00:00:00Z</dc:date>
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