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  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/33763">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33763</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/33773" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/33772" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/33771" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/33770" />
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    <dc:date>2026-10-11T13:38:46Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/33773">
    <title>&lt;span style="font-size:11.0pt;font-family: "Times New Roman","serif";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;Kinetics and mechanism of oxidation of aliphatic and aromatic alcohols by &lt;i&gt;in situ&lt;/i&gt; generated bromine in reaction between oxone and bromide ion&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33773</link>
    <description>Title: &lt;span style="font-size:11.0pt;font-family: "Times New Roman","serif";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;Kinetics and mechanism of oxidation of aliphatic and aromatic alcohols by &lt;i&gt;in situ&lt;/i&gt; generated bromine in reaction between oxone and bromide ion&lt;/span&gt;
Authors: Thombare, Malharrao R; Gokavi, Gavisiddappa S
Abstract: &lt;span style="mso-ansi-language:EN-US;mso-bidi-language:&#xD;
AR-SA" lang="EN-US"&gt;Oxidation of aliphatic and aromatic alcohols by oxone catalyzed by&#xD;
bromide ions has been studied in acidic medium, to avoid formation of alkoxide.&#xD;
Since no prior protonation equilibrium is involved, the rate of the reaction is&#xD;
independent of &lt;i&gt;p&lt;/i&gt;H. The reaction is initiated by the oxidation of bromide&#xD;
to bromine, which abstracts a hydride ion from the alcohol in a rate&#xD;
determining step to form R&lt;sub&gt;1&lt;/sub&gt;R&lt;sub&gt;2&lt;/sub&gt;COH&lt;sup&gt;+&lt;/sup&gt; cation. This&#xD;
cation loses a proton to give the corresponding carbonyl compound in a fast&#xD;
step. A mechanism for the bromide ion mediated oxidation is proposed and the&#xD;
rate law is derived based on the mechanism. Effect of relative permittivity,&#xD;
ionic strength and temperature is also studied; these effects also support the&#xD;
proposed mechanism.&#xD;
&#xD;
&lt;/span&gt;
Page(s): 182-186</description>
    <dc:date>2016-02-15T17:50:35Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/33772">
    <title>&lt;span style="font-size:11.0pt;font-family: "Times New Roman","serif";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;Oxygen reduction reaction of manganese oxide/graphene oxide nanocomposite&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33772</link>
    <description>Title: &lt;span style="font-size:11.0pt;font-family: "Times New Roman","serif";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;Oxygen reduction reaction of manganese oxide/graphene oxide nanocomposite&lt;/span&gt;
Authors: Pravinkumar, K; Balaji, S; Manichandran, T; Anandakumar, M; Kumaraguruparan, G
Abstract: &lt;span style="font-size:11.0pt;font-family:&#xD;
" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";mso-bidi-font-family:="" mangal;letter-spacing:-.3pt;mso-ansi-language:en-gb;mso-fareast-language:en-us;="" mso-bidi-language:hi"="" lang="EN-GB"&gt;MnO&lt;sub&gt;2&lt;/sub&gt;/graphene oxide composite coating has been&#xD;
prepared by electrochemical anodic deposition method. Optimization of current&#xD;
density and deposition efficiency is reported. The formation of &#xD;
α-MnO&lt;sub&gt;2&lt;/sub&gt;/graphene oxide nanocomposite is elucidated through X ray&#xD;
diffraction and infrared reflection measurements. Morphological studies reveal&#xD;
the increase in porosity and exfoliation of graphene oxide by MnO&lt;sub&gt;2&lt;/sub&gt;&#xD;
particles. The extent of oxygen reduction reaction occurring at the surface of&#xD;
MnO&lt;sub&gt;2&lt;/sub&gt;/graphene oxide composite coating have been analyzed by cyclic&#xD;
voltammetry and electrochemical impedance spectroscopy in aqueous 1 &lt;i&gt;M&lt;/i&gt; Li&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;&#xD;
solution. The composite coating is observed to possess better catalytic&#xD;
properties towards oxygen reduction.&lt;/span&gt;
Page(s): 177-181</description>
    <dc:date>2016-02-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/33771">
    <title>&lt;span style="font-size:13.0pt;font-family: "Times New Roman","serif";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;Tetraaquabis(4-methoxyphenylacetato-O') magnesium(II) dihydrate and catena-poly[[(diaqua)manganese(II)]- bis(μ&lt;sub&gt;2&lt;/sub&gt;-4-methoxyphenylacetato-O,O')]: A monomeric and a two-dimensional coordination polymer based on 4-methoxyphenylacetic acid&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33771</link>
    <description>Title: &lt;span style="font-size:13.0pt;font-family: "Times New Roman","serif";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;Tetraaquabis(4-methoxyphenylacetato-O') magnesium(II) dihydrate and catena-poly[[(diaqua)manganese(II)]- bis(μ&lt;sub&gt;2&lt;/sub&gt;-4-methoxyphenylacetato-O,O')]: A monomeric and a two-dimensional coordination polymer based on 4-methoxyphenylacetic acid&lt;/span&gt;
Authors: Dhavskar, Kiran T; Srinivasan, Bikshandarkoil R
Abstract: &lt;span style="font-size:11.0pt;font-family:&#xD;
" times="" new="" roman","serif";mso-fareast-font-family:"times="" roman";mso-bidi-font-family:="" mangal;letter-spacing:-.2pt;mso-ansi-language:en-gb;mso-fareast-language:en-us;="" mso-bidi-language:hi"="" lang="EN-GB"&gt;The synthesis and characterization of&#xD;
tetraaquabis(4-methoxyphenylacetato-O')magnesium(II) dihydrate (&lt;b style="mso-bidi-font-weight:normal"&gt;1&lt;/b&gt;) and catena-&lt;span style="font-size:11.0pt;font-family:" times="" new="" roman","serif";mso-fareast-font-family:="" "times="" roman";mso-bidi-font-family:mangal;letter-spacing:-.1pt;mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:hi"="" lang="EN-GB"&gt;poly[[(diaqua)manganese(II)]bis(μ&lt;sub&gt;2&lt;/sub&gt;-4-methoxyphenylacetato-O,O')]&lt;span style="font-size:11.0pt;font-family:" times="" new="" roman","serif";="" 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; (&lt;b style="mso-bidi-font-weight:normal"&gt;2&lt;/b&gt;) based on 4-methoxyphenylacetic acid&#xD;
(4-mpaH) ligand is reported. In &lt;b style="mso-bidi-font-weight:normal"&gt;1&lt;/b&gt;,&#xD;
the unique 4-mpa functions as a monodentate ligand for Mg(II) situated on an&#xD;
inversion centre, resulting in a monomeric Mg(II) complex. The Mn(II) in &lt;b style="mso-bidi-font-weight:normal"&gt;2&lt;/b&gt; is also located on an inversion&#xD;
centre and the μ&lt;sub&gt;2&lt;/sub&gt;-bridging bidentate coordination mode of the unique&#xD;
4-mpa ligand results in the formation of a &#xD;
two-dimensional manganese coordination polymer.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 170-176</description>
    <dc:date>2016-02-15T17:43:12Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/33770">
    <title>Micellar parameters and thermodynamics of interaction of fluoroquinolone drugs with cetyldimethylethylammonium bromide</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33770</link>
    <description>Title: Micellar parameters and thermodynamics of interaction of fluoroquinolone drugs with cetyldimethylethylammonium bromide
Authors: Ahsan, Sk. Md. Ali; Hossain, Mohammed Delwar; Hoque, Md. Anamul; Khan, Mohammed Abdullah
Abstract: &lt;span style="font-size:11.0pt;font-family:&#xD;
" times="" new="" roman","serif";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;Interaction of fluoroquinolone antibiotic drugs, viz., ciprofloxacin&#xD;
hydrochloride, levofloxacin hemihydrate and lomefloxacin hydrochloride, with&#xD;
the cationic surfactant cetyldimethylethylammonium bromide (CDMEAB) has been&#xD;
studied by conductance measurements in water and in the presence of salts such&#xD;
as NaCl, Na&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; and Na&lt;sub&gt;3&lt;/sub&gt;PO&lt;sub&gt;4&lt;/sub&gt;·12H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;&#xD;
&lt;/sub&gt;over the temperature range of 298.15–318.15 K. Two critical micelle&#xD;
concentrations (&lt;i style="mso-bidi-font-style:normal"&gt;c&lt;/i&gt;*) are obtained for&#xD;
drug-CDMEAB systems in all the cases. The change of &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;c&lt;/i&gt;* values of CDMEAB due to the addition of the drugs is indicative&#xD;
of the interaction between drugs and CDMEAB. Favourable micellization of&#xD;
drug-CDMEAB systems&lt;span style="mso-bidi-font-weight:bold"&gt; is observed in the&#xD;
presence of salts. The ∆&lt;i&gt;G&lt;/i&gt;&lt;sup&gt;0&lt;/sup&gt;&lt;sub&gt;m&lt;/sub&gt; values were&#xD;
negative in all the cases. The values of &lt;i&gt;∆H&lt;/i&gt;&lt;sup&gt;0&lt;/sup&gt;&lt;sub&gt;m&lt;/sub&gt; and &lt;i&gt;∆S&lt;/i&gt;&lt;sup&gt;0&lt;/sup&gt;&lt;sub&gt;m&lt;/sub&gt;&#xD;
reveal that the binding interactions between drug and CDMEAB in water are both&#xD;
electrostatic and hydrophobic in nature. The existence of linear correlation&#xD;
between &lt;i&gt;∆H&lt;/i&gt;&lt;sup&gt;0&lt;/sup&gt;&lt;sub&gt;m&lt;/sub&gt; and &lt;i&gt;∆S&lt;/i&gt;&lt;sup&gt;0&lt;/sup&gt;&lt;sub&gt;m&lt;/sub&gt;&#xD;
values is observed in all cases.&lt;/span&gt;&lt;/span&gt;
Page(s): 160-169</description>
    <dc:date>2016-02-15T17:41:10Z</dc:date>
  </item>
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