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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22016</link>
    <description />
    <items>
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        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22114" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22113" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22112" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22111" />
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    <dc:date>2026-10-05T11:53:44Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22114">
    <title>Synthesis and antifungal activities of ω-(5-arylamino-1,3,4-thiadiazol-2-thio)-ω-(1&lt;i&gt;H&lt;/i&gt;-1,2,4-triazol-1-yl)acetophenones</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22114</link>
    <description>Title: Synthesis and antifungal activities of ω-(5-arylamino-1,3,4-thiadiazol-2-thio)-ω-(1&lt;i&gt;H&lt;/i&gt;-1,2,4-triazol-1-yl)acetophenones
Authors: Chu, Chang-Hu; Hui, Xin-Ping; Xu, Peng-Fei; Zhang, Zi-Yi; Li, Zhi-Chun; Liao, Ren-An
Abstract: Several ω-(5-arylamino-1,3,4-thiadiazol-2-thio)-ω-(1&lt;i&gt;H&lt;/i&gt;-1,2,4-triazol-1-yl)acetophenones&#xD;
&#xD;
&lt;b&gt;4a-i&lt;/b&gt; have been synthesized. The&lt;i&gt;&#xD;
&lt;/i&gt;representative compounds exhibit some antifungal and plant&lt;i&gt; &lt;/i&gt;growth regulatory&#xD;
activities. The structures of these compounds&lt;i&gt; &lt;/i&gt;have been confirmed by elemental&#xD;
analyses, &lt;sup&gt;1&lt;/sup&gt;H NMR, IR and MS spectra.
Page(s): 2436-2438</description>
    <dc:date>2002-11-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22113">
    <title>Do chromium(VI) complexes oxidize &lt;i&gt;via &lt;/i&gt;a common mechanism?</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22113</link>
    <description>Title: Do chromium(VI) complexes oxidize &lt;i&gt;via &lt;/i&gt;a common mechanism?
Authors: Karunakaran, C; Latha, K; Venkataramanan, R; Velan, S Senthil
Abstract: Oxidation of 2-propanol by twelve chromium(VI)&#xD;
reagents exhibit identical kinetic behaviour; first order in chromium(VI) and alcohol,&#xD;
second order in H&lt;sup&gt;+&lt;/sup&gt; and inhibited by Mn(II). The activation free energies&#xD;
do not differ significantly. Also, the energy of activation correlates with the&#xD;
logarithm o f frequency factor and so is the enthalpy of activation with the entropy&#xD;
of activation.
Page(s): 2432-2435</description>
    <dc:date>2002-11-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22112">
    <title>Crystal structure of &lt;i&gt;N&lt;/i&gt;[(2'-hydroxy)benzylidene]-3-chloro-4-fluoroaniline</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22112</link>
    <description>Title: Crystal structure of &lt;i&gt;N&lt;/i&gt;[(2'-hydroxy)benzylidene]-3-chloro-4-fluoroaniline
Authors: Gowda, K V Aijuna; Kokila, M K; Puttaraja; Kulkarni, M V; Prakash, N C Shiva
Abstract: &lt;span style="font-size:12.0pt;line-height:115%;&#xD;
font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:hi"=""&gt;The crystal&#xD;
structure of &lt;i&gt;N&lt;/i&gt;[(2'-hydroxy)benzylidene]-3-chloro-4-fluoroaniline has been&#xD;
de termined by X-ray methods. The compound crystallizes under monoclinic system&#xD;
with cell parameters a = 3.878(2)Å, b = 10.809(1)Å, c = 26.262(2)Å and &lt;span style="font-size:12.0pt;line-height:115%;font-family:" times="" new="" roman";="" mso-fareast-font-family:hiddenhorzocr;mso-ansi-language:en-in;mso-fareast-language:="" en-in;mso-bidi-language:hi"=""&gt;β= &lt;span style="font-size:12.0pt;line-height:&#xD;
115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:hi"=""&gt;94.17(7)&lt;sup&gt;o&lt;/sup&gt;.&#xD;
The entire molecule is planar. The torsional angle of C1-N-C7-C1' is 178° which&#xD;
indicates an anti periplanar arrangement. In view of the importance of weak interactions&#xD;
like Cl....Cl, H....Cl and F... H stabilizing the crystal structure it is pertinent&#xD;
to note some of such observations during the present study.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 2428-2431</description>
    <dc:date>2002-11-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22111">
    <title>Oxidation of urazoles to triazolinediones under solvent-free conditions using permanganate and alumina-supported permanganate</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22111</link>
    <description>Title: Oxidation of urazoles to triazolinediones under solvent-free conditions using permanganate and alumina-supported permanganate
Authors: Hajipour, Abdol R; Mallakpour, Shadpour E; Zolfigol, Mohammad A; Adibi, H
Abstract: Treatment of urazoles with potassium permanganate leads to a simple and mild oxidation reaction, which produces triazolinediones. The reaction is conducted under solvent-free conditions and triazoline diones can be isolated in good to high yields by a simple work-up procedure. The reaction with alumina-supported permanganate enhances the rate and yield.
Page(s): 2425-2427</description>
    <dc:date>2002-11-01T00:00:00Z</dc:date>
  </item>
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