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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/44009</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/44091" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/44090" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/44089" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/44088" />
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    <dc:date>2026-10-09T13:06:23Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/44091">
    <title>Homolytic displacement at saturated carbon: Part 7&lt;sup&gt;†&lt;/sup&gt;-Synthesis of cyclic, bicyclic and spirocyclic sulphones from the corresponding butenyl cobaloximes with thiophene- 2-sulphonyl chloride</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/44091</link>
    <description>Title: Homolytic displacement at saturated carbon: Part 7&lt;sup&gt;†&lt;/sup&gt;-Synthesis of cyclic, bicyclic and spirocyclic sulphones from the corresponding butenyl cobaloximes with thiophene- 2-sulphonyl chloride
Authors: Gupta, B D; Das, Indira; Dixit, Vandana
Abstract: The reactions of but-3-enyl cobaloximes with thiophene-2-sulphonyl chloride under thermal and photochemical conditions give the corresponding cyclopropylmethyl sulphones. A similar reaction with cyclopent-2-enylmethyl and cyclohex-2-enylmethyl cobaloximes gives a mixture of &lt;em&gt;cis- &lt;/em&gt; and &lt;em&gt;trans- &lt;/em&gt; bicyclic products. Cycloalkane, spirocycloprop-2-yl sulphone is formed exclusively from the reaction of 2-(cycloalk-1-enyl)ethyl cobaloxime. The reactions are interpreted in terms of &lt;em&gt;S&lt;/em&gt;&lt;sub&gt;H&lt;/sub&gt; 2 mechanism.
Page(s): 1019-1022</description>
    <dc:date>1993-12-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/44090">
    <title>Synthesis and curing of bis[4(3'-ethynyl phenyl amino)- 3-nitrophenyl]sulphone</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/44090</link>
    <description>Title: Synthesis and curing of bis[4(3'-ethynyl phenyl amino)- 3-nitrophenyl]sulphone
Authors: Dutta, Pradip K; Maiti, Sukumar
Abstract: A new acetylene terminated nitrophenyl sulphone (ATNPS) has been synthesized by nucleophilic displacement reaction between bis(4-chloro-3-nitrophenyl)sulphone and 3-ethynyl aniline. ATNPS is characterized by elemental analysis, IR and &lt;sup&gt;1&lt;/sup&gt;H-NMR spectroscopies. On heating at ca. 250ᵒC or above ATNPS becomes cross linked due to the presence of the acetylenic end group. The thermal behavior has been studied by DSC and DTA techniques. The kinetic study of the curing has been carried out by both differential and integral methods by use of a computational programming.
Page(s): 1023-1028</description>
    <dc:date>1993-12-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/44089">
    <title>Synthesis of soluble phthalocyanines and study of their aggregation behavior in solution</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/44089</link>
    <description>Title: Synthesis of soluble phthalocyanines and study of their aggregation behavior in solution
Authors: Shankar, Rama; Jha, N K; Vasudevan, P
Abstract: Aryloxy substituted soluble phthalocyanine (pc) and its metal complexes (MPcX&lt;sub&gt;4&lt;/sub&gt;,X=4-ethylphenoxy, M=2H, Cu, Ni, Zn, Fe, Co) have been synthesized and characterized by elemental analysis, &lt;sup&gt;1&lt;/sup&gt;H NMR, UV-visible and IR spectroscopy. Degree of association in toluene solution has been measured by molecular weight determination using vapour pressure osmometry. Association and its relative order have also been established in these complexes by UV-visible spectral studies.
Page(s): 1029-1033</description>
    <dc:date>1993-12-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/44088">
    <title>Synthesis and characterization of hydridocarbonylbis(triphenylphosphine) ruthenium(II) dialkyldithiophosphates</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/44088</link>
    <description>Title: Synthesis and characterization of hydridocarbonylbis(triphenylphosphine) ruthenium(II) dialkyldithiophosphates
Authors: Jain, VimaI K
Abstract: Complexes of the type [RuH{SSP(OR)&lt;sub&gt;2&lt;/sub&gt;}(CO(PPh&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;] (R = Et, Pr&lt;em&gt;&lt;sup&gt;n&lt;/sup&gt;&lt;/em&gt;, Pr&lt;em&gt;&lt;sup&gt;i&lt;/sup&gt;&lt;/em&gt;, Bu&lt;em&gt;&lt;sup&gt;n&lt;/sup&gt;&lt;/em&gt;, Bu&lt;em&gt;&lt;sup&gt;i&lt;/sup&gt;&lt;/em&gt;, Bu&lt;em&gt;&lt;sup&gt;s&lt;/sup&gt;&lt;/em&gt;) have been prepared by the reaction of [RuHCI(CO)(PPh&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;3 &lt;/sub&gt;with ammonium salt of the dialkyldithiophosphoric acid. These complexes have been characterized by elemental analyses and IR and NMR (&lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;31&lt;/sup&gt;P) data. The &lt;sup&gt;1&lt;/sup&gt;H NMR data indicate the phosphine ligands are &lt;em&gt;cis &lt;/em&gt;to hydride.
Page(s): 1034-1036</description>
    <dc:date>1993-12-01T00:00:00Z</dc:date>
  </item>
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