<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0">
  <channel>
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/54680</link>
    <description />
    <pubDate>Sun, 11 Oct 2026 11:53:28 GMT</pubDate>
    <dc:date>2026-10-11T11:53:28Z</dc:date>
    <item>
      <title>Molybdenum compounds bearing pymS (pyrimidine-2-thiolato) and tertiary phosphine ligands</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/54691</link>
      <description>Title: Molybdenum compounds bearing pymS (pyrimidine-2-thiolato) and tertiary phosphine ligands
Authors: Roknuzzaman; Khan, Mahadhi H.; Abedin, S. M. Tareque; Kabir, Shariff E.
Abstract: In this paper we have reported mono- and dinuclear molybdenum compounds containing doubly bridging pymS (pyrimidine-2-thiolato) and P(Fu)&lt;sub&gt;3 &lt;/sub&gt;{(Fu = (2-furyl)phosphine)} or P(OMe)&lt;sub&gt;3 &lt;/sub&gt;(trimethyl phosphite). One-pot reaction between [Mo(CO)&lt;sub&gt;3&lt;/sub&gt;(NCMe)&lt;sub&gt;3&lt;/sub&gt;] and pymSH (pyrimidine-2-thiol) in the presence of P(Fu)&lt;sub&gt;3&lt;/sub&gt; in THF at 50 °C gives the previously reported eight coordinate compound [Mo(к&lt;sup&gt;2&lt;/sup&gt;-pymS)&lt;sub&gt;4&lt;/sub&gt;] (&lt;strong&gt;1&lt;/strong&gt;) in 17% yield and two new compounds [Mo(CO)&lt;sub&gt;4&lt;/sub&gt;(P(Fu)&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;] (&lt;strong&gt;2&lt;/strong&gt;) and [Mo&lt;sub&gt;2&lt;/sub&gt;(CO)&lt;sub&gt;4&lt;/sub&gt;(μ-к&lt;sup&gt;2&lt;/sup&gt;-pymS)&lt;sub&gt;2&lt;/sub&gt;(P(Fu)&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;] (&lt;strong&gt;3&lt;/strong&gt;) in 51 and 15% yields, respectively. A similar reaction involving P(OMe)&lt;sub&gt;3 &lt;/sub&gt;furnishes two mononuclear compounds [Mo(CO)&lt;sub&gt;2&lt;/sub&gt;(κ&lt;sup&gt;2&lt;/sup&gt;-pyS)&lt;sub&gt;2&lt;/sub&gt;(P(OMe)&lt;sub&gt;3&lt;/sub&gt;)] (&lt;strong&gt;4&lt;/strong&gt;) and [Mo(CO)&lt;sub&gt;4&lt;/sub&gt;(P(OMe)&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;] (&lt;strong&gt;5&lt;/strong&gt;) in 20 and 35% yields, respectively. Compounds &lt;strong&gt;2&lt;/strong&gt; and &lt;strong&gt;4&lt;/strong&gt; are characterized by single-crystal X-ray diffraction analysis in addition to IR, &lt;sup&gt;1&lt;/sup&gt;H NMR and &lt;sup&gt;31&lt;/sup&gt;P{&lt;sup&gt;1&lt;/sup&gt;H} NMR spectroscopic methods.
Page(s): 741-746</description>
      <pubDate>Mon, 01 Jun 2020 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/54691</guid>
      <dc:date>2020-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis of Na+/Ca2+ ions modified TiO2 xerogels through co precipitation method</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/54690</link>
      <description>Title: Synthesis of Na+/Ca2+ ions modified TiO2 xerogels through co precipitation method
Authors: Prathyusha, K.R; Sreenivasan, Koliyat Parayil
Abstract: We report a facile method for the synthesis of Na&lt;sup&gt;+&lt;/sup&gt;/Ca&lt;sup&gt;2+&lt;/sup&gt; ions modified TiO&lt;sub&gt;2 &lt;/sub&gt;xerogels by coprecipitation followed by calcination process. The resultant materials are well characterized by powder X-ray diffraction, Raman spectroscopy, ultraviolet-visible diffuse reflectance spectroscopy and high resolution transmission electron microscopy. Presence of sodium and calcium ions can influence the crystallinity of rutile TiO&lt;sub&gt;2&lt;/sub&gt;. The photocatalytic performances of bare rutile TiO&lt;sub&gt;2&lt;/sub&gt; along with modified materials such as Na-TiO&lt;sub&gt;2&lt;/sub&gt;, Ca-TiO&lt;sub&gt;2&lt;/sub&gt;, Na-Ca-TiO&lt;sub&gt;2 &lt;/sub&gt;materials are evaluated by calculating the amount of hydrogen evolved during the photocatalytic decomposition of water under light irradiation.This study will be effective informulating the effect of alkali/alkaline earth metal ions on the photocatalytic activity of rutile TiO&lt;sub&gt;2&lt;/sub&gt;.
Page(s): 747-751</description>
      <pubDate>Mon, 01 Jun 2020 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/54690</guid>
      <dc:date>2020-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Microwave assisted template synthesis of metal based EGFR, TRK inhibitors, molecular docking and in vitro biological studies</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/54689</link>
      <description>Title: Microwave assisted template synthesis of metal based EGFR, TRK inhibitors, molecular docking and in vitro biological studies
Authors: Jain, Preeti; Singh, Vandna; Tripathi, Vishwas
Abstract: Metal based biologically active compounds have been synthesized by microwave assisted template condensation method and characterized by spectro-analytical techniques like molar conductance, UV-visible, infrared and mass spectroscopy and thermogravimetric analysis. The metal is arranged in octahedral geometry surrounded by tetradentate ligand framework. The binding affinity of all the metal complexes has been evaluated theoretically by molecular docking studies against epidermal growth factor receptor (EGFR) and tyrosine kinase (TRK) receptor molecules which are further verified by in vitro anticancer activity. Complex [Cr(C&lt;sub&gt;16&lt;/sub&gt;H&lt;sub&gt;11&lt;/sub&gt;N&lt;sub&gt;4&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;)(NO&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;]NO&lt;sub&gt;3 &lt;/sub&gt;have showed potent &lt;em&gt;in vitro&lt;/em&gt; cytotoxicity (IC&lt;sub&gt;50&lt;/sub&gt; value 39.5μM) against SCC4 cancer cell line. Antioxidant study has also performed by DPPH assay and significant results are found.[Fe(C&lt;sub&gt;16&lt;/sub&gt;H&lt;sub&gt;11&lt;/sub&gt;N&lt;sub&gt;4&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;)(OAc)&lt;sub&gt;2&lt;/sub&gt;]OAc and [Cr(C&lt;sub&gt;16&lt;/sub&gt;H&lt;sub&gt;11&lt;/sub&gt;N&lt;sub&gt;4&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;) (OAc)&lt;sub&gt;2&lt;/sub&gt;]OAc are most effective antioxidants with 78.7% and 76.8% free radical scavenging activity, respectively.
Page(s): 752-759</description>
      <pubDate>Mon, 01 Jun 2020 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/54689</guid>
      <dc:date>2020-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Thermodynamic and kinetic studies on novel Platinum(II) Complex containing bidentate N,N-donor ligands in ethanol-water medium</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/54688</link>
      <description>Title: Thermodynamic and kinetic studies on novel Platinum(II) Complex containing bidentate N,N-donor ligands in ethanol-water medium
Authors: Nandi, Debabrata; Karmakar, Parnajyoti; Dey, Anwesha; Sarkar, Roshni (Sain); Ghosh, Alak K.
Abstract: Kinetic and mechanistic investigations have been made on the displacement of the two aqua molecules from the complex &lt;strong&gt;1 &lt;/strong&gt;i.e., [Pt(2,2′-bipyridine)(H&lt;sub&gt;2&lt;/sub&gt;O)&lt;sub&gt;2&lt;/sub&gt;]&lt;sup&gt;2+ &lt;/sup&gt;represented as {Pt(bpy)} (bpy = 2,2′-bipyridine) at pH 4.0. All the substitution reactions have been monitored at 264, 284 &amp; 317 nm, where the spectral difference between the reactant and product is maximum. Two consecutive reaction steps have been observed for the substitution of aqua molecules with some bidentate N,N-donor ligands namely, dimethylglyoxime (L&lt;sub&gt;1&lt;/sub&gt;H), 1, 2-cyclohexanedionedioxime (L&lt;sub&gt;2&lt;/sub&gt;H) and α-furildioxime (L&lt;sub&gt;3&lt;/sub&gt;H) in ethanol-water medium using variable-temperature and stopped-flow spectrophotometry. Among the two steps, the former is ligand dependent and the later is ligand independent, where chelation is observed. All rate and activation parameters are consistent with associative substitution mechanisms. The thermodynamic parameters have been also calculated, which gives a negative DG&lt;sup&gt;0&lt;/sup&gt; value at all temperatures studied, supporting the spontaneous formation of an outer sphere association complex. The products of the reaction have been characterized with the help of IR and ESI-MS spectroscopic analysis.
Page(s): 760-767</description>
      <pubDate>Mon, 01 Jun 2020 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/54688</guid>
      <dc:date>2020-06-01T00:00:00Z</dc:date>
    </item>
  </channel>
</rss>

