<?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/123456789/65751</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 20:35:26 GMT</pubDate>
    <dc:date>2026-10-10T20:35:26Z</dc:date>
    <item>
      <title>Studying synthesis of a new polymer sorbent based on o-phenylenediamine and epichlorohydrin and its sorption properties</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/65763</link>
      <description>Title: Studying synthesis of a new polymer sorbent based on o-phenylenediamine and epichlorohydrin and its sorption properties
Authors: A, Ahatov A; Kh, Turaev Kh; R, Tillaev Kh.; A, Kasimov Sh; K, Nomozov A
Abstract: This article is devoted to the synthesis and sorption properties of a new polymer sorbent (FD-EXG) based on&#xD;
o-phenylenediamine and epichlorohydrin, which separates metal ions from solutions with high precision. In the process of&#xD;
synthesis, the starting materials: o-phenylenediamine and epichlorohydrin are taken in a 1:2 mol ratio. Ethylenediamine is&#xD;
used as a polymerizing and binding agent. The composition, physicochemical and sorption-desorption properties of the&#xD;
obtained polymer sorbent have been studied. In the IR spectrum analysis of the sorbent, we can see the presence of n(OH)&#xD;
functional groups in the 3371 cm–1 and 3313 cm–1 and n(NH) ion exchange functional groups in the 1558 cm–1 region.&#xD;
Based on X-ray phase analysis methods, the degree of crystallization of the obtained sorbent and its compound with metal&#xD;
cation (Ni(II)) has been determined. Also, the morphology and thermal properties of the obtained sorbent have been studied&#xD;
using SEM analysis and TGA and DTA analysis methods. The surface area and the pore size of the polymer sorbent have&#xD;
been determined, and its morphology has been determined to be macroporous. It has been proven that the synthesized&#xD;
polymer sorbent can be reused many times during the sorption process. It is proved that the obtained polymer sorbent can&#xD;
efficiently remove Ni(II), Co(II), Cu(II), Zn(II) and Cd(II) ions from aqueous solutions. The static exchange capacity (SEC)&#xD;
of the obtained polymer sorbent has been determined to be SECNi=9.67, SECCo=8.33, SECCu=7.01, SECZn=6.67 and&#xD;
SECCd=5.01. It has been proven that the static exchange capacity is
Page(s): 353-360</description>
      <pubDate>Tue, 01 Apr 2025 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/65763</guid>
      <dc:date>2025-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>A new approach for the synthesis of strobilurin fungicide analogues: Synthesis, characterization, antifungal study and molecular docking investigation</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/65762</link>
      <description>Title: A new approach for the synthesis of strobilurin fungicide analogues: Synthesis, characterization, antifungal study and molecular docking investigation
Authors: Hebbar, Nagashree U; Shanbhag, Arpita A; Shastri, Lokesh A; Shinde, Smita; Jambale, Umashri; T, Shivasharana C; Shastri, Sudhesh L; N, Vijaykumar K
Abstract: In an effort to protect plants from fungal diseases and to enhance the stability of the strobilurin fungicides, we report&#xD;
herein, an efficient and simple approach for the synthesis of strobilurin fungicide analogues. The synthesised compounds&#xD;
were characterised by IR, NMR and LC-MS spectroscopic techniques. The antifungal efficacies of the synthesised&#xD;
compounds were tested against plant pathogens namely Curvularialunata, Rhizoctonia solani and Sclerotium rolfsii by&#xD;
using poison food/pour plate and spore germination methods. Azoxystrobin and Tebuconazole are used as standards in the&#xD;
analysis. Further, the synthesized compounds were subjected to in silico studies to know the bonding interactions with&#xD;
bovine cytochrome Bc1 and CYP51 protein of cytochrome 450.
Page(s): 361-372</description>
      <pubDate>Tue, 01 Apr 2025 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/65762</guid>
      <dc:date>2025-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis, characterization of N-(1-(4-nitrophenyl)ethylidene)- 1H-benzo[d]imidazol-2-amine and amino acid alanine and it’s metal complexes</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/65761</link>
      <description>Title: Synthesis, characterization of N-(1-(4-nitrophenyl)ethylidene)- 1H-benzo[d]imidazol-2-amine and amino acid alanine and it’s metal complexes
Authors: Shamili, Sriramoju
Abstract: Transition metal ion complexes that include a variety of ligands have distinct biological effects. Schiff bases that&#xD;
comprise amino acids and azomethine may be used as building blocks for ternary complexes. In an effort to produce a novel&#xD;
metal(II) complexes, the conventional reflux method has been used to the interaction of two ligands, N-(1-(4-&#xD;
nitrophenyl)ethylidene)-1H-benzo[d]imidazol-2-amine as L1, and an amino acid alanine as L2, with freshly produced&#xD;
cuprous chloride solution in a 1:1:1 molar ratio. The synthesized ligand and metal(II) complexes are characterized using&#xD;
elemental analysis, molecular weight, magnetic moment, thermal analysis, and spectroscopic techniques. Bacillus subtilis,&#xD;
Escherichia coli, and Candida albicans have been used as test organisms to evaluate the compounds’ antibacterial activities.&#xD;
These metal(II) complexes have been observed to have powerful antibacterial and antifungal activities.
Page(s): 373-377</description>
      <pubDate>Tue, 01 Apr 2025 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/65761</guid>
      <dc:date>2025-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>An environmentally benign protocol for the synthesis of quinoxaline derivatives under ultrasound irradiation</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/65760</link>
      <description>Title: An environmentally benign protocol for the synthesis of quinoxaline derivatives under ultrasound irradiation
Authors: Rishi, Harsha; Sain, Anushka; Kanwar, Neeraj; Bhargava, Sangeeta
Abstract: In continuation of our efforts to develop green synthetic routes for the formation of biologically active quinoxalines, we&#xD;
report oxidative cyclization of o-phenylenediamine and α-bromo ketones. The efficacy of this reaction is illustrated by the&#xD;
compatibility with chloro, bromo, nitro, methoxy, furyl, etc. groups. All the new compounds have been characterized by IR,&#xD;
NMR and elemental analysis. The foremost feature of this methodology is environmentally benign reaction, simple work-up,&#xD;
mild reaction conditions and less reaction time.
Page(s): 378-382</description>
      <pubDate>Tue, 01 Apr 2025 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/65760</guid>
      <dc:date>2025-04-01T00:00:00Z</dc:date>
    </item>
  </channel>
</rss>

