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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/39847</link>
    <description />
    <pubDate>Thu, 08 Oct 2026 17:59:40 GMT</pubDate>
    <dc:date>2026-10-08T17:59:40Z</dc:date>
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      <title>Magnetic field effect on polymers and polymerization</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/40261</link>
      <description>Title: Magnetic field effect on polymers and polymerization
Authors: Maiti, Sukumar; Bag, Dibyendu S
Abstract: The influence of magnetic field on polymerization reaction, polymer structure and properties has been discussed in the light of the radical pair theory and the cage effect to explain the kinetics of polymerization and crosslinking reactions. The rate of polymerization and crosslinking increases due to the singlet (&lt;img src='http://www.niscair.res.in/jinfo/leftrightarrow.gif' border=0&gt;) triplet intersystem crossing mechanism. While the molecular weight increases, the molecular weight distribution decreases under magnetic field. The polymer microstructure viz., tacticity, copolymer composition and monomer sequence in the copolymer chain are also affected by the magnetic field. Polymerization of liquid crystal monomers under magnetic field results in highly oriented liquid crystal polymers. As a result, the polymer properties like crystallinity, chain flexibility, solubility, thermal behaviour are also changed. Conducting polyacetylene and magnetic polymers prepared under magnetic field also exhibit higher conductivity and magnetic properties respectively. Studies on biopolymers, solid state and plasma polymerization under magnetic field have also been reported.
Page(s): 673-687</description>
      <pubDate>Fri, 01 Sep 1995 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/40261</guid>
      <dc:date>1995-09-01T00:00:00Z</dc:date>
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    <item>
      <title>Some properties of Calvin's model of spontaneous chiral amplification</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/40257</link>
      <description>Title: Some properties of Calvin's model of spontaneous chiral amplification
Authors: Gutman, Ivan
Abstract: The kinetic scheme for spontaneous chiral amplification, put forward by Calvin, is examined and some of its general properties are established. Analytical solutions of Cailvin's model are found in two important limiting cases, namely, when the system is open and the concentration of the substrate is constant, and when the system is closed.
Page(s): 688-691</description>
      <pubDate>Fri, 01 Sep 1995 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/40257</guid>
      <dc:date>1995-09-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Electron addition to triethylphosphite induced by ionising radiation: An ESR study</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/40255</link>
      <description>Title: Electron addition to triethylphosphite induced by ionising radiation: An ESR study
Authors: Rai, U S
Abstract: With a view to obtain [°P(OEt)&lt;sub&gt;3&lt;/sub&gt;]&lt;sup&gt;-&lt;/sup&gt; radical anions and to establish their preferred structure, solutions of triethylphosphite in different solvents have been exposed to &lt;sup&gt;60&lt;/sup&gt;CO &lt;img src='/image/spc_char/gamma2.gif' border=0&gt;-rays at 77K and studied by ESR spectroscopy. Two phosphorus centred radicals suggested are parent radical anion and .P(OEt)&lt;sub&gt;2&lt;/sub&gt; formed by dissociative electron capture. In methyltetrahydrofuran an electron adduct with A = 264G and small value of A is assigned to the primary radical anion having a planar T structure with SOMO on 3&lt;i&gt;p &lt;/i&gt; of phosphorus, normal to the radical plane. In a methanolic solution, the same radical anion with extensive protonation having a phosphoranyl type radical with large &lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;31&lt;/sup&gt;P hyperfine splitting is formed. The well defined triplets due to &lt;sup&gt;2&lt;/sup&gt;H adduct, obtained in CD&lt;sub&gt;3&lt;/sub&gt;OD glasses, confirm this assignment. Other phosphorus centred radicals are MeO-P(OEt)&lt;sub&gt;3 &lt;/sub&gt;and the cation dimer (E&lt;i&gt;t&lt;/i&gt;O)&lt;sub&gt;3&lt;/sub&gt;P—P(OEt)&lt;img src='http://www.niscair.res.in/jinfo/plusthree.gif' border=0&gt;.
Page(s): 692-695</description>
      <pubDate>Fri, 01 Sep 1995 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/40255</guid>
      <dc:date>1995-09-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Studies on photoelectroactive (CdHg)Se films</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/40253</link>
      <description>Title: Studies on photoelectroactive (CdHg)Se films
Authors: Singh, Kehar; Tanveer, Md. Rashid
Abstract: (CdHg)Se films prepared by electrochemical deposition have been subjected to thermal treatment and tested for their photoresponsiveness. These studies in conjunction with capacitance measurements show that all (CdHg)Se films are endowed with n-type semiconductivity in contradiction to p-type semi-conductivity behaviour exhibited by some of the untreated preparations. Electrochemical impedance studies have also been carried out for the examination of corrosion characteristics of (CdHg)Se films.
Page(s): 696-699</description>
      <pubDate>Fri, 01 Sep 1995 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/40253</guid>
      <dc:date>1995-09-01T00:00:00Z</dc:date>
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