<?xml version="1.0" encoding="UTF-8"?>
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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31715" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/31715</id>
  <updated>2026-10-10T09:32:58Z</updated>
  <dc:date>2026-10-10T09:32:58Z</dc:date>
  <entry>
    <title>Synthesis and dyeing characteristics of 2-arylazo-3-dicyanomethyleneindan-1-one</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/32441" />
    <author>
      <name>Rangnekar, D W</name>
    </author>
    <author>
      <name>Kamat, P Y</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/32441</id>
    <updated>2016-07-20T05:27:56Z</updated>
    <published>1993-03-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and dyeing characteristics of 2-arylazo-3-dicyanomethyleneindan-1-one
Authors: Rangnekar, D W; Kamat, P Y
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" color:black;mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:="" ar-sa"=""&gt;3-Dicyanomethyleneindan-1-one (&lt;b&gt;II&lt;/b&gt;), prepared by the condensation&#xD;
of indan-1,3-dione (&lt;b&gt;I&lt;/b&gt;) with malononitrile, was coupled with three&#xD;
representative 4-substituted phenyldiazonium salts &lt;span style="font-size:11.0pt;line-height:115%;font-family:" calibri","sans-serif";="" mso-ascii-theme-font:minor-latin;mso-fareast-font-family:"times="" new="" roman";="" mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:minor-latin;="" mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;color:#0c0c0c;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;(&lt;b&gt;&lt;span style="font-size:11.0pt;line-height:115%;font-family:" calibri","sans-serif";="" mso-ascii-theme-font:minor-latin;mso-fareast-font-family:"times="" new="" roman";="" mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:minor-latin;="" mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;color:black;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;III&lt;/span&gt;&lt;/b&gt;&lt;span style="font-size:11.0pt;line-height:115%;font-family:" calibri","sans-serif";="" mso-ascii-theme-font:minor-latin;mso-fareast-font-family:"times="" new="" roman";="" mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:minor-latin;="" mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;color:#0c0c0c;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;) &lt;span style="font-size:11.0pt;line-height:115%;font-family:" calibri","sans-serif";="" mso-ascii-theme-font:minor-latin;mso-fareast-font-family:"times="" new="" roman";="" mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:minor-latin;="" mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;color:black;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;to&#xD;
give 2-arylazo-3-dicyanomethyleneindan-1-ones (&lt;b&gt;lVa-c&lt;/b&gt;). These compounds&#xD;
when applied on polyester fibres gave bright yellow to orange shades with&#xD;
excellent pick-up&lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" color:#0c0c0c;mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:="" ar-sa"=""&gt;, &lt;span style="font-size:11.0pt;line-height:115%;font-family:&#xD;
" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" color:black;mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:="" ar-sa"=""&gt;moderate light fa&lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" color:#0c0c0c;mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:="" ar-sa"=""&gt;s&lt;span style="font-size:11.0pt;line-height:115%;font-family:" calibri","sans-serif";="" mso-ascii-theme-font:minor-latin;mso-fareast-font-family:"times="" new="" roman";="" mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:minor-latin;="" mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;color:black;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;tness&#xD;
and very good sublimation fastness.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 54-56</summary>
    <dc:date>1993-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:11.0pt;line-height:115%; font-family:"Calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family: "Times New Roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font: minor-latin;mso-bidi-font-family:Calibri;mso-bidi-theme-font:minor-latin; mso-ansi-language:EN-US;mso-fareast-language:EN-US;mso-bidi-language:AR-SA"&gt;Synthesis of ethyl &lt;i&gt;α&lt;/i&gt;-substituted-&lt;i&gt;β&lt;/i&gt;-(2-methoxyquinoxalin-6-amino) acrylates and 3-methoxypyrido [3,2-f]quinoxalin-10(7&lt;i&gt;H&lt;/i&gt;)-ones and their application on polyster fibres&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/32440" />
    <author>
      <name>Rangnekar, D W</name>
    </author>
    <author>
      <name>Tagdiwala, P V</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/32440</id>
    <updated>2016-07-20T05:25:32Z</updated>
    <published>1993-03-01T00:00:00Z</published>
    <summary type="text">Title: &lt;span style="font-size:11.0pt;line-height:115%; font-family:"Calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family: "Times New Roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font: minor-latin;mso-bidi-font-family:Calibri;mso-bidi-theme-font:minor-latin; mso-ansi-language:EN-US;mso-fareast-language:EN-US;mso-bidi-language:AR-SA"&gt;Synthesis of ethyl &lt;i&gt;α&lt;/i&gt;-substituted-&lt;i&gt;β&lt;/i&gt;-(2-methoxyquinoxalin-6-amino) acrylates and 3-methoxypyrido [3,2-f]quinoxalin-10(7&lt;i&gt;H&lt;/i&gt;)-ones and their application on polyster fibres&lt;/span&gt;
Authors: Rangnekar, D W; Tagdiwala, P V
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;6-Amino-2-methoxyquinoxaline&#xD;
(&lt;b&gt;I&lt;/b&gt;) obtained from quinoxal-2-one by nitration, chlorination,&#xD;
methoxylation and reduction was condensed with conjugated enol ethers such as&#xD;
diethyl ethoxymethylenemalonic ester (&lt;b&gt;IIa&lt;/b&gt;) and ethyl&#xD;
ethoxymethylene(cyano)acetate (&lt;b&gt;IIb&lt;/b&gt;) to give ethyl &lt;i&gt;α&lt;/i&gt;-substituted-&lt;i&gt;β&lt;/i&gt;-(2-methoxy-quinoxalin-6amino)&#xD;
acrylates (&lt;b&gt;III&lt;/b&gt;). The cyclization of III in refluxing dowtherm resulted&#xD;
in the formation of 3-methoxy-9-substituted pyrido(3,2-&lt;i&gt;f&lt;/i&gt;)quinoxalin-10(7&lt;i&gt;H&lt;/i&gt;)-ones&#xD;
(&lt;b&gt;IV&lt;/b&gt;). The fluorescent properties of &lt;b&gt;III&lt;/b&gt; and &lt;b&gt;IV&lt;/b&gt; were&#xD;
studied. When applied on polyester fibres these compounds resulted in poor to&#xD;
moderate whitening effects.&lt;/span&gt;
Page(s): 51-53</summary>
    <dc:date>1993-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Rot- and mildew-proofing of jute fabric with quaternary ammonium compounds</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/32439" />
    <author>
      <name>Majumdar, S</name>
    </author>
    <author>
      <name>Chatterjee, S</name>
    </author>
    <author>
      <name>Dey, S</name>
    </author>
    <author>
      <name>Ghosh, B L</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/32439</id>
    <updated>2016-07-20T05:23:30Z</updated>
    <published>1993-03-01T00:00:00Z</published>
    <summary type="text">Title: Rot- and mildew-proofing of jute fabric with quaternary ammonium compounds
Authors: Majumdar, S; Chatterjee, S; Dey, S; Ghosh, B L
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;Benzalkonium&#xD;
chloride (BKC)and cetyltrimethylammonium bromide (CTAB), the two bactericidal&#xD;
cationic surfactants of the quaternary ammonium group, have been found to&#xD;
impart high rot and mildew resistance to bleached jute without affecting its&#xD;
aesthetic appeal. Unlike cotton, BKC- or CTAB-treated jute retains considerable&#xD;
microbial resistance on leaching. This difference with cotton is due to the&#xD;
higher absorption capacity of jute which is further enhanced on bleaching.&lt;/span&gt;
Page(s): 48-50</summary>
    <dc:date>1993-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Electrically conducting natural fibres</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/32438" />
    <author>
      <name>Bhadani, S N</name>
    </author>
    <author>
      <name>Gupta, S K Sen</name>
    </author>
    <author>
      <name>Gupta, M K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/32438</id>
    <updated>2016-07-20T05:20:54Z</updated>
    <published>1993-03-01T00:00:00Z</published>
    <summary type="text">Title: Electrically conducting natural fibres
Authors: Bhadani, S N; Gupta, S K Sen; Gupta, M K
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;A&#xD;
study on the electrochemical grafting of polypyrrole and polythiophene onto&#xD;
cotton, silk and wool fibres has been made. These fibres become moderately&#xD;
conducting after their electrical treatment in the polymerizing solution of&#xD;
pyrrole/thiophene in 1,2-dichloroethane containing tetrabutylammonium&#xD;
hexachloroantimonate as supporting electrolyte.&lt;/span&gt;
Page(s): 46-47</summary>
    <dc:date>1993-03-01T00:00:00Z</dc:date>
  </entry>
</feed>

