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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/20567</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 21:09:26 GMT</pubDate>
    <dc:date>2026-10-10T21:09:26Z</dc:date>
    <item>
      <title>Thermodynamics of ternary mixtures: Excess isentropic compressibilities</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20648</link>
      <description>Title: Thermodynamics of ternary mixtures: Excess isentropic compressibilities
Authors: Sharma, V K; Kalra, K C; Romi; Katoch, Ashma
Abstract: Ultrasonic velocity data for&#xD;
nitrobenzene(i) + benzene(j) + toluene, or + &lt;i&gt;o&lt;/i&gt;-xylene, or + &lt;i&gt;p&lt;/i&gt;-xylene&#xD;
(k) ternary mixtures have been determined as a function of composition at 298.15K.&#xD;
The observed data have been utilized to evaluate excess isentroic&#xD;
compressibilities, K&lt;img src='http://www.niscair.res.in/jinfo/es.gif' border=0&gt;, K&lt;img src='http://www.niscair.res.in/jinfo/es.gif' border=0&gt; values have also been&#xD;
computed using Flory theory. It has been observed that K&lt;img src='http://www.niscair.res.in/jinfo/es.gif' border=0&gt; values evaluated from Flory theory make&#xD;
qualitative agreement with the values evaluated from experimental data.
Page(s): 292-294</description>
      <pubDate>Sat, 01 Feb 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20648</guid>
      <dc:date>2003-02-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>A novel magnetic exchange mechanism in&lt;b&gt; &lt;/b&gt;bridged copper (II) coordinations of naturally occurring spin carriers viz. &lt;i&gt;ortho-&lt;/i&gt;functionalized&lt;i&gt; p&lt;/i&gt;-naphthoquinones</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20647</link>
      <description>Title: A novel magnetic exchange mechanism in&lt;b&gt; &lt;/b&gt;bridged copper (II) coordinations of naturally occurring spin carriers viz. &lt;i&gt;ortho-&lt;/i&gt;functionalized&lt;i&gt; p&lt;/i&gt;-naphthoquinones
Authors: Rane, Sandhya; Gawali, Sunita; Padhye, Subhash; Date, Sadgopal; Bakare, Pramod
Abstract:      Magnetic exchange and&#xD;
charge transfer mechanisms in dimeric (&lt;b&gt;1&lt;/b&gt;) [Cu(Lw)&lt;sub&gt;2&lt;/sub&gt;H&lt;sub&gt;2&lt;/sub&gt;O]&#xD;
and&#xD;
monomeric (&lt;b&gt;2&lt;/b&gt;), [Cu(phth)&lt;sub&gt;2&lt;/sub&gt;] complexes of lawsone (2-hydroxy-1,4-naphthoquinone)&#xD;
and phthiocol (3-methyl-2-hydroxy 1,4-naphthoquinone) are described. Magnetic&#xD;
susceptibility measurements of (&lt;b&gt;1&lt;/b&gt;) are fitted to Heisenberg's isotropic&#xD;
spin pair (S' = 1,1) model and&#xD;
&#xD;
tetranuclear (S' = ½, ½,½, ½) spins in a&#xD;
two dimensional model. Both models result in intradimer antiferromagnetic&#xD;
coupling (&lt;i&gt;J&lt;/i&gt; = -44.4 cm&lt;sup&gt;-1&lt;/sup&gt;) between [Cu(NSQ)]&lt;sub&gt;2&lt;/sub&gt; units&#xD;
and ferromagnetic coupling (&lt;i&gt;zJ&lt;/i&gt;&lt;sub&gt;1&lt;/sub&gt; = 28.5 cm&lt;sup&gt;-1&lt;/sup&gt;)&#xD;
between one Cu(II)NSQ coordinated unit (where NSQ = naphtho-semiquinone).&lt;br&gt; &#xD;
&#xD;
        Latter interaction leads&#xD;
to a triplet ground state and triplet-triplet intradimer interaction governs&#xD;
the ‘‘quintet state’’ at room temperature, as detected from X- and Q-band EPR&#xD;
studies. The zero- field split interaction (0.024 cm&lt;sup&gt;-1&lt;/sup&gt;) exhibits&#xD;
&#xD;
contributions from D&lt;sub&gt;pd&lt;/sub&gt; (-0.071&#xD;
cm&lt;sup&gt;-1&lt;/sup&gt;) and combined D&lt;sub&gt;d&lt;/sub&gt; and D&lt;sub&gt;anti&lt;/sub&gt; (+0.095 cm&lt;sup&gt;-1&lt;/sup&gt;)&#xD;
interactions. The intradimer exchange is due to a stacked (S' = 1,1) spin pair&#xD;
with r = 3.04Å. The monomeric complex (2) is devoid of such interactions due to&#xD;
the bulky methyl group at C3 position of quinonoid ring.&lt;br&gt; &#xD;
&#xD;
        Cyclic voltammograms of&#xD;
(&lt;b&gt;1&lt;/b&gt;) and (&lt;b&gt;2&lt;/b&gt;) show an anodic peak at +0.22 V, assigned to Cu(0) →&#xD;
Cu(II) charge transfer. Only one redox couple at E&lt;sub&gt;1/2 &lt;/sub&gt;= -0.687 V due&#xD;
to NSQ CAT (catechol) charge transfer leads to radical coordination in (1).&#xD;
However, quarsireversible NQ NSQ redox couple at E&lt;sub&gt;1/2&lt;/sub&gt; = -0.525 V&#xD;
together with an irreversible NSQ → CAT reduction peak in (2) at E&lt;sub&gt;1/2 &lt;/sub&gt;=&#xD;
-0.75 V indicate fully the presence of oxidized (NQ) i.e. naphthoquinone&#xD;
ligation in (2).
Page(s): 255-261</description>
      <pubDate>Sat, 01 Feb 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20647</guid>
      <dc:date>2003-02-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>A rapid spectrophotometric method for the determination of trichloromethane sulphenyl chloride derivatives and commercial fungicides</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20593</link>
      <description>Title: A rapid spectrophotometric method for the determination of trichloromethane sulphenyl chloride derivatives and commercial fungicides
Authors: Sharma, D K; Sood, Sunita; Kumar, Ramesh; Verma, B C
Abstract: A new, simple and rapid&#xD;
spectrophotometric method for the microdetermination of trichloromethane&#xD;
sulphenyl chloride derivatives (RSCCl&lt;sub&gt;3&lt;/sub&gt;) based on their reaction with&#xD;
thiophenol in acetonitrile in the presence of triethylamine is described. The&#xD;
yellow colour, which develops instantaneously on mixing the reagents in&#xD;
acetonitrile, is stable for atleast 6 h and is measured at 450 nm. Beer's law is&#xD;
applicable upto 200 &lt;i&gt;μ&lt;/i&gt;g ml&lt;sup&gt;-1&lt;/sup&gt; of each derivative concentration.&#xD;
The method has been successfully adapted to the analysis of captan and folpet&#xD;
fungicides based on these derivatives in their commercial formulations for the&#xD;
purpose of quality control.
Page(s): 331-332</description>
      <pubDate>Sat, 01 Feb 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20593</guid>
      <dc:date>2003-02-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>One-dimensional chain crown ether complexes: Synthesis and crystal structure of [Na(18-crown-6)]&lt;sub&gt;2&lt;/sub&gt;[M(mnt)&lt;sub&gt;2&lt;/sub&gt;](M = Zn, Cd)</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20592</link>
      <description>Title: One-dimensional chain crown ether complexes: Synthesis and crystal structure of [Na(18-crown-6)]&lt;sub&gt;2&lt;/sub&gt;[M(mnt)&lt;sub&gt;2&lt;/sub&gt;](M = Zn, Cd)
Authors: Yu, Qingjiang; Dou, Jianmin; Li, Dacheng; Wang, Daqi; Zhong, Baoyun; Wei, Yong; Zheng, Peiju
Abstract: The reactions of IR-crown-6 with Na&lt;sub&gt;2&lt;/sub&gt;[Zn(mnt)&lt;sub&gt;2&lt;/sub&gt;]&#xD;
and Na&lt;sub&gt;2&lt;/sub&gt;[Cd(mnt)&lt;sub&gt;2&lt;/sub&gt;] have been studied and the complexes&#xD;
[Na(18-crown-6)]&lt;sub&gt;2&lt;/sub&gt;[M(mnt)&lt;sub&gt;2&lt;/sub&gt;](M = Zn, Cd), are characterized&#xD;
by elemental&#xD;
&#xD;
analysis, IR spectrum and X-ray&#xD;
diffraction analysis. &lt;b&gt;1&lt;/b&gt; and &lt;b&gt;2&lt;/b&gt; belong to monoclinic, space group&#xD;
c2/c&lt;i&gt; &lt;/i&gt;with cell dimensions, &lt;b&gt;1&lt;/b&gt;: a = 2.2418(6), b = 1.1359(3), c =&#xD;
1.9887(6) nm,&#xD;
&#xD;
β= 120.391 (4)&lt;sup&gt;o&lt;/sup&gt;, V = 4.368(2),&#xD;
nm&lt;sup&gt;3&lt;/sup&gt;, Z = 4, Dcalcd = 1.399 Mg/m&lt;sup&gt;3&lt;/sup&gt;,&lt;i&gt; &lt;/i&gt;F(000) = 1920, R&lt;sub&gt;1&lt;/sub&gt;&#xD;
= 0.0302, wR&lt;sub&gt;2&lt;/sub&gt; = 0.0560 and &lt;b&gt;2&lt;/b&gt;: a = 2.2547(6),&lt;i&gt; &lt;/i&gt;b =&#xD;
1.1412(3), c = 1.9938(6) nm, β=119.715(4)°, V = 4.455 nm&lt;sup&gt;3&lt;/sup&gt;,&lt;i&gt; &lt;/i&gt;Z&#xD;
= 4, Dcalcd = 1.442 Mg/m&lt;sup&gt;3 &lt;/sup&gt;, F(000)= 1992, R&lt;sub&gt;1&lt;/sub&gt; = 0.0384,&lt;i&gt;&#xD;
&lt;/i&gt;wR&lt;sub&gt;2&lt;/sub&gt; = 0.0575. Two complexes display a one-dimensional chain of [Na(18C6)]&lt;sup&gt;+&lt;/sup&gt;(complex&#xD;
cations and [M(mnt)&lt;sub&gt;2&lt;/sub&gt;]&lt;sup&gt;2-&lt;/sup&gt; (M = Zn, Cd) complex anion bridged&#xD;
by Na-O interactions between adjacent&amp;nbsp; [Na(18C6)]&lt;sup&gt;+&#xD;
&lt;/sup&gt;units respectively.
Page(s): 327-330</description>
      <pubDate>Sat, 01 Feb 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20592</guid>
      <dc:date>2003-02-01T00:00:00Z</dc:date>
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