<?xml version="1.0" encoding="UTF-8"?>
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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/41211" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/41211</id>
  <updated>2026-10-08T19:51:20Z</updated>
  <dc:date>2026-10-08T19:51:20Z</dc:date>
  <entry>
    <title>Molecular topology 27: A Schultz-type index based on the Wiener matrix</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/41330" />
    <author>
      <name>Diudea, Mircea V</name>
    </author>
    <author>
      <name>Pop, Corina M</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/41330</id>
    <updated>2017-04-19T10:09:56Z</updated>
    <published>1996-04-01T00:00:00Z</published>
    <summary type="text">Title: Molecular topology 27: A Schultz-type index based on the Wiener matrix
Authors: Diudea, Mircea V; Pop, Corina M
Abstract: A novel Schultz analogous index, denoted WI, is defined on the basis of Wiener matrix and the matrix algebra initiated by Schultz. It is compared with the well known indices such as molecular topological index, MTI, Wiener index, W, hyper-Wiener index, R, and the recently introduced indices DI and HI, within the set of octane isomers and other selected graphs.
Page(s): 257-261</summary>
    <dc:date>1996-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Reactions of ethene over silica, &lt;img src='/image/spc_char/gamma2.gif' border=0&gt;-alumina, YBa&lt;sub&gt;2&lt;/sub&gt;Cu&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;6.9&lt;/sub&gt; perovskite and ZSM-5 zeolite: Thermal versus catalytic processes</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/41329" />
    <author>
      <name>Shete, B S</name>
    </author>
    <author>
      <name>Belapurkar, A D</name>
    </author>
    <author>
      <name>Kamble, V S</name>
    </author>
    <author>
      <name>Gupta, N M</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/41329</id>
    <updated>2017-04-19T10:08:28Z</updated>
    <published>1996-04-01T00:00:00Z</published>
    <summary type="text">Title: Reactions of ethene over silica, &lt;img src='/image/spc_char/gamma2.gif' border=0&gt;-alumina, YBa&lt;sub&gt;2&lt;/sub&gt;Cu&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;6.9&lt;/sub&gt; perovskite and ZSM-5 zeolite: Thermal versus catalytic processes
Authors: Shete, B S; Belapurkar, A D; Kamble, V S; Gupta, N M
Abstract: The reaction products formed during the flow of ethene at temperatures above 500°C over silica, YBa&lt;sub&gt;2&lt;/sub&gt;Cu&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;6.9&lt;/sub&gt; perovskite and through an empty quartz reactor have been found to be similar to those obtained during its reaction over ZSM-5 zeolite and &lt;img src='/image/spc_char/gamma2.gif' border=0&gt;-alumina samples at lower temperatures. The prominent reaction products consisted of methane, propane, butane, propene, butene, pentene, methylpentane, cyclohexene, hexene, benzene and toluene. The product distribution, however, varies with the nature of the sample and the reaction temperature. The addition of oxygen in ethene leads to higher yields of almost all the reaction products, particularly at sample temperatures above 500°C. The enhancement increases progressively with the increase in oxygen content, the effect being more pronounced on the lower hydrocarbons containing odd number of carbon atoms, e.g., propene and pentene. It is suggested that at reaction temperatures above 500°C, the free radicals such as CH&lt;sub&gt;3&lt;/sub&gt;, CH&lt;sub&gt;2&lt;/sub&gt; and CH, formed during thermal dissociation or self hydrogenation of C&lt;sub&gt;2&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt; molecules, help in the hydrocarbon chain growth. The formation of the highly unstable epoxy species, viz. &lt;img src='http://www.niscair.res.in/jinfo/equation41.gif' border=0&gt; in the presence of oxygen facilitates this process. In the case of catalytic reactions over ZSM-5 or &lt;img src='/image/spc_char/gamma2.gif' border=0&gt;-alumina, the lewis acid sites rather than the Bronsted hydroxyl groups are proposed to be the reaction sites where ethene adsorbed in the form of a cyclic complex transforms to the similar transient surface species at lower temperatures.
Page(s): 262-269</summary>
    <dc:date>1996-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Transfer energetics of some nucleosides in aqueous mixtures of urea and glycerol</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/41326" />
    <author>
      <name>Ganguly, Sonali</name>
    </author>
    <author>
      <name>Kundu, Kiron K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/41326</id>
    <updated>2017-04-19T09:48:07Z</updated>
    <published>1996-04-01T00:00:00Z</published>
    <summary type="text">Title: Transfer energetics of some nucleosides in aqueous mixtures of urea and glycerol
Authors: Ganguly, Sonali; Kundu, Kiron K
Abstract: Standard free energies (&lt;img src='/image/spc_char/delta.gif' border=0&gt;&lt;i&gt;G&lt;/i&gt;&lt;img src='http://www.niscair.res.in/jinfo/zerot.gif' border=0&gt;) and entropies (&lt;img src='/image/spc_char/delta.gif' border=0&gt;&lt;i&gt;S&lt;/i&gt;&lt;img src='http://www.niscair.res.in/jinfo/zerot.gif' border=0&gt;) of transfer of some nucleosides viz. adenosine (ado), guanosine (guo) and xanthosine (xao) from water to aqueous mixtures of urea (UH) and glycerol (GL) have been evolved from solubilities measured at different temperatures. The observed &lt;img src='/image/spc_char/delta.gif' border=0&gt;&lt;i&gt;G-&lt;/i&gt;&lt;img src='http://www.niscair.res.in/jinfo/zerot.gif' border=0&gt; composition profiles show increasing stabilization for the nucleosides in both the cosolvent systems. The &lt;i&gt;T&lt;/i&gt;&lt;img src='/image/spc_char/delta.gif' border=0&gt;S&lt;img src='http://www.niscair.res.in/jinfo/zerot.gif' border=0&gt;-composition profiles are, however, complicated. So, after the elimination of various interaction effects, viz. cavity, dipole-dipole, dipole-induced dipole and dispersion interactions, the results have been discussed in the light of the hydrophilic-hydrophobic hydration effect. The solvation behaviour of the nucleosides in UH-water and GL-water mixtures help understand the relative stability of the double stranded nucleic acid helix in these. two cosolvent systems.
Page(s): 270-280</summary>
    <dc:date>1996-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Electrochemical oxidation of 2-mercaptobenzoxazole</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/41325" />
    <author>
      <name>Goyal, Rajendra N</name>
    </author>
    <author>
      <name>Verma, Madhu Shri</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/41325</id>
    <updated>2017-04-19T09:42:04Z</updated>
    <published>1996-04-01T00:00:00Z</published>
    <summary type="text">Title: Electrochemical oxidation of 2-mercaptobenzoxazole
Authors: Goyal, Rajendra N; Verma, Madhu Shri
Abstract: Electrochemical oxidation of 2-mercaptobenzoxazole has been studied in the phosphate buffers of &lt;i&gt;p&lt;/i&gt;H 2.5-10.3 at solid electrodes. In the entire &lt;i&gt;p&lt;/i&gt;H range a well-defined oxidation peak (I&lt;sub&gt;a&lt;/sub&gt;) was observed. The peak potential of this peak is linearly dependent on &lt;i&gt;p&lt;/i&gt;H and the &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;p&lt;/sub&gt;&lt;i&gt;-p&lt;/i&gt;H plot shows a break around &lt;i&gt;p&lt;/i&gt;H 7.8, corresponding to the &lt;i&gt;pk&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; of the species. At &lt;i&gt;p&lt;/i&gt;H ≥ 7.0 an additional oxidation peak (II&lt;sub&gt;a&lt;/sub&gt;) has been noticed. The electrode process is found to involve adsorption complications at PGE and the change in &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;p&lt;/sub&gt; with log v indicated radical radical coupling. The products of oxidation have been separated and characterized by using m.p., &lt;sup&gt;1&lt;/sup&gt;H NMR and mass spectra.
Page(s): 281-287</summary>
    <dc:date>1996-04-01T00:00:00Z</dc:date>
  </entry>
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