<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0">
  <channel>
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/45960</link>
    <description />
    <pubDate>Fri, 09 Oct 2026 16:16:43 GMT</pubDate>
    <dc:date>2026-10-09T16:16:43Z</dc:date>
    <item>
      <title>Contrasting isomer stabilities of silaboranes and carboranes : Si2B3H5 and C2B3H5 isomers</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46210</link>
      <description>Title: Contrasting isomer stabilities of silaboranes and carboranes : Si2B3H5 and C2B3H5 isomers
Authors: Jemmis, Eluvathingal D; Subramanian, G
Abstract: The relative stabilities of the isomers of closo- Si&lt;sub&gt;2&lt;/sub&gt;B&lt;sub&gt;3&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt; have been calculated at the MNDO, HF/6- 31G* and MP2/6-3IG* levels. Contrary to the results for the corresponding carborane C&lt;sub&gt;2&lt;/sub&gt;B&lt;sub&gt;3&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt; reported earlier, Si&lt;sub&gt;2&lt;/sub&gt;B&lt;sub&gt;3&lt;/sub&gt;H&lt;sub&gt;5 &lt;/sub&gt;is predicted to be the most stable. The concept of the compatibility of orbitals in overlap is used to rationalize our observation of this reversal of trends in isomer stabilities.
Page(s): 645-646</description>
      <pubDate>Tue, 01 Sep 1992 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46210</guid>
      <dc:date>1992-09-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Cyclic conjugation in benzo-annelated polyacenes</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46209</link>
      <description>Title: Cyclic conjugation in benzo-annelated polyacenes
Authors: Gutman, Ivan; Petrovic, Vesna
Abstract: Conjugation along a particular ring in a polycyclic conjugated molecule can be measured by means&#xD;
of the effect of the ring on total π-electron energy. Using this approach, we have studied cyclic conjugation&#xD;
in mono-, di-, tri- and tetra-benzo polyacenes. The main conclusion of our research is that the Clar&#xD;
aromatic sextet formulas of the benzo-annelated polyacenes provide a reasonable description of their&#xD;
conjugation modes. A few refinements are, however, possible. The extent of cyclic conjugation is found&#xD;
to be minimal in the central region of the polyacene molecule and it monotonically increases towards its&#xD;
two termini. Geminal annelation has an extra increasing effect on cyclic conjugation. Isoarithmic systems&#xD;
are shown to have practically coinciding conjugation modes.
Page(s): 647-650</description>
      <pubDate>Tue, 01 Sep 1992 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46209</guid>
      <dc:date>1992-09-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Hot atom chemistry in oxyanion targets: Part V―Pre-activation heat treatment study of recoil 56Mn in permanganates</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46208</link>
      <description>Title: Hot atom chemistry in oxyanion targets: Part V―Pre-activation heat treatment study of recoil 56Mn in permanganates
Authors: Mishra, Shuddhodan P; Singh, (Miss) Jyoti
Abstract: The effect of pre-heat treatment on the fate of &lt;sup&gt;56&lt;/sup&gt;Mn recoil atoms originating from (n, γ) reaction in KMnO&lt;sub&gt;4&lt;/sub&gt;, Ba(MnO&lt;sub&gt;4&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt; and NH&lt;sub&gt;4&lt;/sub&gt;MnO&lt;sub&gt;4&lt;/sub&gt; targets results in a slight increase in the initial &lt;sup&gt;56&lt;/sup&gt;Mn retention and decrease in the extent of subsequent thermal annealing. Fletcher-Brown model has been utilized to deduce the kinetic behaviour of the annealing phenomenon which consists of two apparent first order processes for both the pre-heated and untreated permanganates. The implications of the results are explained on the basis of competitive participation of oxidising/reducing inherent crystal defects.
Page(s): 651-657</description>
      <pubDate>Tue, 01 Sep 1992 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46208</guid>
      <dc:date>1992-09-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Effect of 3-fluoro-4-cyano substituted benzoates in the formation of induced smectic phases with N-[4-ethoxybenzylidene]-4'-&lt;em&gt;n&lt;/em&gt;-butylaniline</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46207</link>
      <description>Title: Effect of 3-fluoro-4-cyano substituted benzoates in the formation of induced smectic phases with N-[4-ethoxybenzylidene]-4'-&lt;em&gt;n&lt;/em&gt;-butylaniline
Authors: Sharma, N K; Charak, Anila; Ostereicher, F
Abstract: Diagrams of state of the binary liquid crystalline systems, in which one component is a 4-cyano-3-fluoro&#xD;
substituted benzoates and the other component is N-[4-ethoxybenzylidene]-4'-&lt;i&gt;n&lt;/i&gt;-butylaniline, have been&#xD;
investigated. The nematic phase shows uninterrupted miscibility in ali the binary systems. Induced smectic. A&#xD;
phase is observed in all but one diagram of state. The effect of 4-cyano-3-f1uoro substitution on induced&#xD;
phases is discussed on the basis of dipole moments.
Page(s): 658-660</description>
      <pubDate>Tue, 01 Sep 1992 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46207</guid>
      <dc:date>1992-09-01T00:00:00Z</dc:date>
    </item>
  </channel>
</rss>

