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<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18205" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/18205</id>
  <updated>2026-10-09T20:39:09Z</updated>
  <dc:date>2026-10-09T20:39:09Z</dc:date>
  <entry>
    <title>A new single pulse method for the measurements of photosensitized singlet oxygen quantum yield</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18229" />
    <author>
      <name>Venkatesan, R</name>
    </author>
    <author>
      <name>Tamijselvy, S</name>
    </author>
    <author>
      <name>Periasamy, N</name>
    </author>
    <author>
      <name>Rajendiran, T M</name>
    </author>
    <author>
      <name>Rao, P S</name>
    </author>
    <author>
      <name>Srivastava, T S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18229</id>
    <updated>2016-07-20T04:57:59Z</updated>
    <published>2002-02-01T00:00:00Z</published>
    <summary type="text">Title: A new single pulse method for the measurements of photosensitized singlet oxygen quantum yield
Authors: Venkatesan, R; Tamijselvy, S; Periasamy, N; Rajendiran, T M; Rao, P S; Srivastava, T S
Abstract: A new&#xD;
simpler relative method for estimating photosensitized singlet oxygen quantum&#xD;
yield has been developed. In this method a strong depletion signal is observed&#xD;
when porphyrin (2μ&lt;i&gt;M) &lt;/i&gt;and l,3-diphenylisobenzofuran (DPBF, 500 μ &lt;i&gt;M) &lt;/i&gt;are&#xD;
irradiated using second harmonic 532 nm Nd-YAG laser pulse and monitored at 410&#xD;
or 415 nm by a ultraviolet filtered white light. The observed&#xD;
&#xD;
depletion is&#xD;
attributed to the reaction of DPBF with sensitized singlet oxygen. The&#xD;
amplitude of the depletion signal is related directly to the singlet oxygen&#xD;
sensitization yield. Appropriate kinetic equations have been derived to relate&#xD;
the change in the absorbance of DPBF and singlet oxygen quantum yield. The&#xD;
&#xD;
singlet&#xD;
oxygen quantum yields of fifteen porphyrins and metalloporphyrins have been&#xD;
investigated in dimethylformamide solution. The results are compared with the&#xD;
quantum yields obtained by the usual kinetic run experiments. The results are found&#xD;
to match exceedingly well in the two methods.
Page(s): 346-349</summary>
    <dc:date>2002-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and characterization of chlorodibenzyltin(IV) complexes with N,N-dialkyl dithiocarbamate ligands and crystal structure of (PhCH&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;SnCl(S&lt;sub&gt;2&lt;/sub&gt;CNMe&lt;sub&gt;2&lt;/sub&gt;)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18228" />
    <author>
      <name>Yin, Handong</name>
    </author>
    <author>
      <name>Ma, Chunlin</name>
    </author>
    <author>
      <name>Wang, Yong</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18228</id>
    <updated>2016-07-20T05:06:44Z</updated>
    <published>2002-02-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and characterization of chlorodibenzyltin(IV) complexes with N,N-dialkyl dithiocarbamate ligands and crystal structure of (PhCH&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;SnCl(S&lt;sub&gt;2&lt;/sub&gt;CNMe&lt;sub&gt;2&lt;/sub&gt;)
Authors: Yin, Handong; Ma, Chunlin; Wang, Yong
Abstract: Thirteen&#xD;
chlorodibenzyltin(IV) complexes with N,N-dialkyl dithiocarbamate ligands have&#xD;
been synthesized by the reaction of dibenzyltin dichloride with N,N-dialkyl&#xD;
dithiocarbamates in 1:1 stoichiometry and characterized by elemental analysis,&#xD;
UV, I R and &lt;sup&gt;1&lt;/sup&gt;H NMR. The crystal structure of (PhCH&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;SnCl(S&lt;sub&gt;2&lt;/sub&gt;CNMe&lt;sub&gt;2&lt;/sub&gt;)&#xD;
has been determined by X-ray single crystal diffraction. The crystallographic&#xD;
data are as follows: triclinic, space group P-1,&#xD;
&#xD;
&lt;i&gt;a&lt;/i&gt;=7.5750(15)&#xD;
Å, &lt;i&gt;b&lt;/i&gt;= 10.615(2) Å, &lt;i&gt;c&lt;/i&gt;= 12.059(2) Å, α=95.053(3)&lt;sup&gt;o&lt;/sup&gt;,&#xD;
&#xD;
β=95.539(4)&lt;sup&gt; o&lt;/sup&gt;, γ=99.113(4)&lt;sup&gt; o&lt;/sup&gt;, Z=2, &lt;i&gt;V=&lt;/i&gt;947.6(3)&lt;i&gt;&#xD;
&lt;/i&gt;Å, &lt;i&gt;Dx= &lt;/i&gt;1.600&lt;i&gt;g/&lt;/i&gt;cm&lt;sup&gt;-3&lt;/sup&gt;, μ= 1.705mm&lt;sup&gt;-1&lt;/sup&gt;, &lt;i&gt;F&lt;/i&gt;(000)&lt;i&gt;=&lt;/i&gt;456&lt;i&gt;,&#xD;
R&lt;/i&gt;&lt;sub&gt;1&lt;/sub&gt;&lt;i&gt;=&lt;/i&gt;0.0409,  &lt;i&gt;w&lt;/i&gt;R&lt;sub&gt;2&lt;/sub&gt;=0. 1194(I≥ ~2σ(I). The&#xD;
&#xD;
structures&#xD;
consist of discrete molecules containing five-coordinate tin atoms in a&#xD;
seriously distorted trigonal bipyramidal configuration. The molecules are&#xD;
packed in the unit cell as weakly-bridged dimers.
Page(s): 342-345</summary>
    <dc:date>2002-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis, magnetic and spectral studies of some new mixed-ligand nitrosyl complexes of chromium(I)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18227" />
    <author>
      <name>Maurya, R C</name>
    </author>
    <author>
      <name>Pandey, A</name>
    </author>
    <author>
      <name>Verma, R</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18227</id>
    <updated>2016-07-20T04:51:15Z</updated>
    <published>2002-02-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis, magnetic and spectral studies of some new mixed-ligand nitrosyl complexes of chromium(I)
Authors: Maurya, R C; Pandey, A; Verma, R
Abstract: The&#xD;
synthesis and characterization of some new mixed-ligand nitrosyl chromium(I)&#xD;
complexes (having (CrNO}&lt;sup&gt;5*&lt;/sup&gt; electron configuration) of the general&#xD;
formula [Cr(NO)(acac)&lt;sub&gt;2&lt;/sub&gt;(L)] , [where L = benzothiazole (BZT),&#xD;
2-(2'-pyridyl)benzimidazole (PBZL), 2- hydroxymethylpyridine (2-HMP),&#xD;
3-hydroxymetlylpyridine (3-HMP), &lt;i&gt;o&lt;/i&gt;-anisidine (ANS) or&#xD;
N,N'-dimethylanilinc (NNDA)] have been carried out. The compounds having&#xD;
chromium(I) in a lowspin &lt;i&gt;d&lt;/i&gt;&lt;sup&gt;5&lt;/sup&gt;&lt;i&gt; &lt;/i&gt;configuration have been&#xD;
characterized by elemental analyses, molar conductance. TGA, magnetic&#xD;
measurements, elcctron spin resonance and infrared spectral studies.
Page(s): 339-341</summary>
    <dc:date>2002-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and characterization of epoxy resin in the presence of &lt;i&gt;p&lt;/i&gt;-acetylbenylidene triphenylarsoniumylide-mercuric chloride complex</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18226" />
    <author>
      <name>Pandey, Saurabh</name>
    </author>
    <author>
      <name>Srivastava, A K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18226</id>
    <updated>2016-07-20T04:55:37Z</updated>
    <published>2002-02-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and characterization of epoxy resin in the presence of &lt;i&gt;p&lt;/i&gt;-acetylbenylidene triphenylarsoniumylide-mercuric chloride complex
Authors: Pandey, Saurabh; Srivastava, A K
Abstract: &lt;i&gt;p&lt;/i&gt;-Acetylbenylidene&#xD;
triphenylarsoniumylide-mercuric chloride complex modifies and also has&#xD;
autocatalytic curing properties for epoxy resin. The degree of cure (αʹ),&#xD;
percentage crystallinity and glass transition temperature (Tg) of the modified&#xD;
resin, investigated by differential scanning calorimetry, are 1.03, 91 % and&#xD;
298°C respectively. The TGA technique has been used to&#xD;
&#xD;
calculate&#xD;
the activation energy and the order of reaction, which are 97 kJ/mol and one&#xD;
respectively. The SEM analysis shows presence of Hg (40%) in the epoxy resin.
Page(s): 333-338</summary>
    <dc:date>2002-02-01T00:00:00Z</dc:date>
  </entry>
</feed>

