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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15894" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/15894</id>
  <updated>2026-10-16T02:36:22Z</updated>
  <dc:date>2026-10-16T02:36:22Z</dc:date>
  <entry>
    <title>Catalytic effect of CTAB reverse micelles on the reduction of toluidine blue  by ascorbic acid</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15922" />
    <author>
      <name>Padma, M</name>
    </author>
    <author>
      <name>Shyamala, P</name>
    </author>
    <author>
      <name>Satyanarayana, A</name>
    </author>
    <author>
      <name>Rao, P V Subba</name>
    </author>
    <author>
      <name>Mathew, Asha</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/15922</id>
    <updated>2016-07-20T04:55:13Z</updated>
    <published>2013-02-01T00:00:00Z</published>
    <summary type="text">Title: Catalytic effect of CTAB reverse micelles on the reduction of toluidine blue  by ascorbic acid
Authors: Padma, M; Shyamala, P; Satyanarayana, A; Rao, P V Subba; Mathew, Asha
Abstract: &lt;span style="font-size:9.0pt;mso-bidi-font-size:&#xD;
12.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-US"&gt;The&#xD;
kinetics of the reduction of toluidine blue by ascorbic acid has been studied&#xD;
in the presence of CTAB/CHCl&lt;sub&gt;3&lt;/sub&gt;/hexane/water reverse micelles. In the&#xD;
absence of added acid, the reaction obeys simple first order kinetics with&#xD;
respect to both the reactants. &#xD;
The second order rate constant in the presence of reverse micelles, &#xD;
&lt;i style="mso-bidi-font-style:normal"&gt;k&lt;/i&gt;&lt;sub&gt;w &lt;/sub&gt;(0.027 &lt;i style="mso-bidi-font-style:normal"&gt;M&lt;/i&gt;&lt;sup&gt; -1&lt;/sup&gt; s&lt;sup&gt;-1&lt;/sup&gt;) was&#xD;
found to be about sixty times greater than that in aqueous medium, &lt;i style="mso-bidi-font-style:normal"&gt;k&lt;/i&gt;&lt;sub&gt;o&lt;/sub&gt; (4.50×10&lt;sup&gt;-4&lt;/sup&gt; &lt;i style="mso-bidi-font-style:normal"&gt;M&lt;/i&gt;&lt;sup&gt; -1&lt;/sup&gt; s&lt;sup&gt;-1&lt;/sup&gt;) under&#xD;
identical experimental conditions. The significant increase is attributed to&#xD;
the concentration effect in the reverse micelles, and, lower &#xD;
micro-polarity due to the reverse micelles, which facilitates the reaction&#xD;
between oppositely charged ions. The effect of variation of &lt;i style="mso-bidi-font-style:normal"&gt;W&lt;/i&gt; (= [H&lt;sub&gt;2&lt;/sub&gt;O]/[CTAB]) at&#xD;
constant [CTAB] and variation of [CTAB] at fixed &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;W&lt;/i&gt; has been studied. The kinetics at &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;W &lt;/i&gt;&lt; 6 is explained on the basis of the special properties of the&#xD;
entrapped water, while the kinetics at &lt;i style="mso-bidi-font-style:normal"&gt;W&lt;/i&gt;&#xD;
&gt; 10 is explained on the basis of ionic strength.&lt;/span&gt;
Page(s): 221-225</summary>
    <dc:date>2013-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB"&gt;Electrocatalytic oxidation of hydroquinone with Cu&lt;sup&gt;2+&lt;/sup&gt; modified gold-L-cysteine self-assembled monolayer electrodes&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15921" />
    <author>
      <name>Barman, Kaushik</name>
    </author>
    <author>
      <name>Jasimuddin, Sk</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/15921</id>
    <updated>2016-07-20T04:54:13Z</updated>
    <published>2013-02-06T09:04:05Z</published>
    <summary type="text">Title: &lt;span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB"&gt;Electrocatalytic oxidation of hydroquinone with Cu&lt;sup&gt;2+&lt;/sup&gt; modified gold-L-cysteine self-assembled monolayer electrodes&lt;/span&gt;
Authors: Barman, Kaushik; Jasimuddin, Sk
Abstract: &lt;span style="font-size:11.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-bidi-font-family:="" mangal;mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:="" hi"="" lang="EN-GB"&gt;Electrocatalytic activity of a new catalyst towards the oxidation reaction&#xD;
of hydroquinone as a model compound is described. The catalyst is formed by&#xD;
immobilizing Cu(II) ion on the top side of a gold-L-cysteine self assembled&#xD;
monolayer electrode. Preparation steps and the electrocatalytic activity of&#xD;
Au-L-cysteine-Cu&lt;sup&gt;2+&lt;/sup&gt; have been studied by cyclic voltammetry and&#xD;
electrochemical impedance spectroscopy. The Au-L-cysteine-Cu&lt;sup&gt;2+&lt;/sup&gt;&#xD;
electrode exhibits better electrocatalytic activity than &#xD;
Au-L-cysteine and bare Au electrode for the oxidation of hydroquinone.&lt;/span&gt;
Page(s): 217-220</summary>
    <dc:date>2013-02-06T09:04:05Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB"&gt;Excimer formation in inclusion complexes of antihypertensive drugs with HP-α- and HP-β-cyclodextrins&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15920" />
    <author>
      <name>Jenita, M Jude</name>
    </author>
    <author>
      <name>Venkatesh, G</name>
    </author>
    <author>
      <name>Subramanian, V K</name>
    </author>
    <author>
      <name>Rajendiran, N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/15920</id>
    <updated>2016-07-20T04:48:43Z</updated>
    <published>2013-02-06T09:03:27Z</published>
    <summary type="text">Title: &lt;span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB"&gt;Excimer formation in inclusion complexes of antihypertensive drugs with HP-α- and HP-β-cyclodextrins&lt;/span&gt;
Authors: Jenita, M Jude; Venkatesh, G; Subramanian, V K; Rajendiran, N
Abstract: The inclusion complexation behavior of three&#xD;
antihypertensive drugs, viz., salbutamol, sotalol and atenolol with &lt;span style="mso-bidi-font-size:14.0pt;mso-bidi-font-weight:bold" lang="EN-GB"&gt;hydroxypropyl-α-cyclodextrin (HP-α-CD) &lt;span style="mso-bidi-font-size:14.0pt;mso-bidi-font-weight:bold" lang="EN-GB"&gt;and&#xD;
hydroxypropyl-β-cyclodextrin&#xD;
(HP-β-CD) is investigated by UV-visible, steady state/time&#xD;
resolved fluorescence and PM3 methods and compared with complexation with α-CD&#xD;
and β-CD. In the presence of any of the CDs, dual emission is observed in these&#xD;
drugs, whereas in the absence of CDs, single emission is seen. Addition of CD to aqueous solutions of the drugs&#xD;
results in excimer emission. In CD solutions, the monomer emission intensity&#xD;
decreases regularly while excimer emission intensity increases. The excimer&#xD;
emission is concluded to be due to a &#xD;
1:2 inclusion complex between the CD and the drugs.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;
Page(s): 207-216</summary>
    <dc:date>2013-02-06T09:03:27Z</dc:date>
  </entry>
  <entry>
    <title>Oxidation of glycine by diperiodatocuprate(III) in aqueous alkaline medium</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15919" />
    <author>
      <name>Gowda, Jayant I</name>
    </author>
    <author>
      <name>Hanabaratti, Rohini M</name>
    </author>
    <author>
      <name>Pattanashetti, Nandini A</name>
    </author>
    <author>
      <name>Nandibewoor, Sharanappa T</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/15919</id>
    <updated>2016-07-20T04:43:40Z</updated>
    <published>2013-02-06T09:02:21Z</published>
    <summary type="text">Title: Oxidation of glycine by diperiodatocuprate(III) in aqueous alkaline medium
Authors: Gowda, Jayant I; Hanabaratti, Rohini M; Pattanashetti, Nandini A; Nandibewoor, Sharanappa T
Abstract: Oxidation of&#xD;
the amino acid, glycine, by diperiodatocuprate(III) is studied spectrophotometrically&#xD;
in alkaline medium at constant ionic strength (0.20 mol dm&lt;sup&gt;-3&lt;/sup&gt;) and at&#xD;
varying temperatures (298-318 K). The reaction between diperiodatocuprate(III) and glycine in aqueous alkaline medium exhibits 1:4 stoichiometry.&#xD;
Intervention of free radicals is observed in the reaction. Mechanism involving&#xD;
monoperiodatocuprate(III) as the reactive oxidant species, proceeding through&#xD;
the formation of a complex is proposed. The reaction constants involved in the&#xD;
different steps of the mechanism and activation parameters with respect to the&#xD;
slow step of the mechanism are computed and discussed. The thermodynamic&#xD;
quantities are also determined for the various equilibrium steps. The&#xD;
isokinetic temperature is found to be 381 K.
Page(s): 200-206</summary>
    <dc:date>2013-02-06T09:02:21Z</dc:date>
  </entry>
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