
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/">
  <dc:identifier>https://phaidrabg.bg.ac.rs/o:28851</dc:identifier>
  <dc:identifier>doi:10.1177/1468678319825724 </dc:identifier>
  <dc:identifier>ISSN: 1468-6783</dc:identifier>
  <dc:rights>All rights reserved</dc:rights>
  <dc:title xml:lang="eng">Study on the reactions between dichlorido[2,2´:6´,2´´-terpyridine] zinc(II) and biologically relevant nucleophiles in aqueous solution</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:subject xml:lang="eng">Keywords: Zinc(II), kinetics, biologically relevant nucleophiles, terpyridine</dc:subject>
  <dc:date>2019</dc:date>
  <dc:language>eng</dc:language>
  <dc:description xml:lang="eng">Abstract:
Substitution reactions of square-pyramidal [ZnCl2(terpy)] complex (terpy = 2,2´:6´,2´´-terpyridine) with biologically relevant nucleophiles such as imidazole, glutathione, 1,2,4-triazole,
and pyrazine were investigated at pH 7.0 as a function of nucleophile concentration. The
reactions were followed under pseudo first-order conditions by UV-Vis spectrophotometry. The
substitution reactions comprised two steps of consecutive displacement of chlorido ligands.
Different reaction pathways for the first reaction step of nucleophilic substitution were defined.
The order of reactivity of the investigated nucleophiles for the first reaction was
Imidazole &gt; glutathione  &gt; pyrazine &gt; 1,2,4-triazole, while for the second reaction step it was
pyrazine  &gt;  1,2,4-triazole  &gt;  imidazole  &gt;  glutathione.
</dc:description>
  <dc:source>Progress in Reaction Kinetics and Mechanism 44(2)</dc:source>
  <dc:creator id="https://orcid.org/0000-0002-8212-4378">Selimović, Enisa</dc:creator>
  <dc:creator id="https://orcid.org/0000-0003-3010-6503">Soldatović, Tanja</dc:creator>
  <dc:format>application/pdf</dc:format>
  <dc:format>491828 bytes</dc:format>
</oai_dc:dc>
