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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">From Chemistry Towards Technology Step-By-Step</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">From Chemistry Towards Technology Step-By-Step</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>От химии к технологии шаг за шагом</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="online">2782-1900</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">81498</article-id>
   <article-id pub-id-type="doi">10.52957/2782-1900-2024-4-3-76-80</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>Научные статьи</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>Scientific articles</subject>
    </subj-group>
    <subj-group>
     <subject>Научные статьи</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">Assessment of polyfunctional macrocyclic compounds in solution by cryoscopic method</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Assessment of polyfunctional macrocyclic compounds in solution by cryoscopic method</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Березина</surname>
       <given-names>Надежда Михайловна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Berezina</surname>
       <given-names>Nadezhda Mihaylovna</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Колесов</surname>
       <given-names>Егор Евгеньевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Kolesov</surname>
       <given-names>Egor Evgen'evich</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">Ивановский государственный химико-технологический университет</institution>
    </aff>
    <aff>
     <institution xml:lang="en">Ivanovo State University of Chemistry and Technology</institution>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2023-09-23T00:00:00+03:00">
    <day>23</day>
    <month>09</month>
    <year>2023</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2023-09-23T00:00:00+03:00">
    <day>23</day>
    <month>09</month>
    <year>2023</year>
   </pub-date>
   <volume>4</volume>
   <issue>3</issue>
   <fpage>76</fpage>
   <lpage>80</lpage>
   <history>
    <date date-type="received" iso-8601-date="2023-09-01T00:00:00+03:00">
     <day>01</day>
     <month>09</month>
     <year>2023</year>
    </date>
    <date date-type="accepted" iso-8601-date="2023-09-08T00:00:00+03:00">
     <day>08</day>
     <month>09</month>
     <year>2023</year>
    </date>
   </history>
   <self-uri xlink:href="https://chemintech.ru/en/nauka/article/81498/view">https://chemintech.ru/en/nauka/article/81498/view</self-uri>
   <abstract xml:lang="ru">
    <p>The article considers the synthesis of meso-tetrakis(1'-methyl-pyrid-4-yl)porphyrin tetratosylate and meso-tetrakis(1'-methyl-carboxymethylpyrid-4-yl)porphyrin tetrabromide. The authors qualified the porphyrin ligands in terms of the electron and 1H NMR spectroscopy. The research determines the decrease of freezing point (ΔTfr) of aqueous solutions of porphyrins, as well as a model N-methyl-pyridinium salt (1 methyl-pyridinium iodide). We used the obtained experimental values of ΔT3 to determine the isotonic coefficient. The obtained results indicate the compounds are almost completely dissociated in the indicated concentration range in dilute solutions.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The article considers the synthesis of meso-tetrakis(1'-methyl-pyrid-4-yl)porphyrin tetratosylate and meso-tetrakis(1'-methyl-carboxymethylpyrid-4-yl)porphyrin tetrabromide. The authors qualified the porphyrin ligands in terms of the electron and 1H NMR spectroscopy. The research determines the decrease of freezing point (ΔTfr) of aqueous solutions of porphyrins, as well as a model N-methyl-pyridinium salt (1 methyl-pyridinium iodide). We used the obtained experimental values of ΔT3 to determine the isotonic coefficient. The obtained results indicate the compounds are almost completely dissociated in the indicated concentration range in dilute solutions.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>Water-soluble tetrapyridylporphyrins</kwd>
    <kwd>water</kwd>
    <kwd>isotonic coefficient</kwd>
    <kwd>cryoscopy</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
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 <back>
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