<!DOCTYPE article
PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.4 20190208//EN"
       "JATS-journalpublishing1.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="research-article" dtd-version="1.4" xml:lang="en">
 <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">82938</article-id>
   <article-id pub-id-type="doi">10.52957/27821900_2021_02_160</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">Catalytic oxidation of fluorinated aromatic compounds by hydrogen peroxide in the presence of µ-nitridodimeric iron phthalocyaninate</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Catalytic oxidation of fluorinated aromatic compounds by hydrogen peroxide in the presence of µ-nitridodimeric iron phthalocyaninate</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Кудрик</surname>
       <given-names>Евгений Валентинович</given-names>
      </name>
      <name xml:lang="en">
       <surname>Kudrik</surname>
       <given-names>Evgeniy Valentinovich</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>доктор химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>doctor of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Осокин</surname>
       <given-names>В С</given-names>
      </name>
      <name xml:lang="en">
       <surname>Osokin</surname>
       <given-names>V S</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="2021-06-23T00:00:00+03:00">
    <day>23</day>
    <month>06</month>
    <year>2021</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2021-06-23T00:00:00+03:00">
    <day>23</day>
    <month>06</month>
    <year>2021</year>
   </pub-date>
   <volume>2</volume>
   <issue>2</issue>
   <fpage>160</fpage>
   <lpage>165</lpage>
   <history>
    <date date-type="received" iso-8601-date="2021-04-30T00:00:00+03:00">
     <day>30</day>
     <month>04</month>
     <year>2021</year>
    </date>
    <date date-type="accepted" iso-8601-date="2021-05-19T00:00:00+03:00">
     <day>19</day>
     <month>05</month>
     <year>2021</year>
    </date>
   </history>
   <self-uri xlink:href="https://chemintech.ru/en/nauka/article/82938/view">https://chemintech.ru/en/nauka/article/82938/view</self-uri>
   <abstract xml:lang="ru">
    <p>It has been shown that µ-nitrido(bis) iron phthalocyaninate is an effective catalyst for the oxidation of fluoroaromatic compounds with hydrogen peroxide, including such difficult to oxidized substrates as hexafluorobenzene and pentafluoropyridine. The main fluoride containing product is inorganic fluoride. It has been found that this catalyst, when supported on a graphite, exhibits high stability and can be used after simple regeneration.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>It has been shown that µ-nitrido(bis) iron phthalocyaninate is an effective catalyst for the oxidation of fluoroaromatic compounds with hydrogen peroxide, including such difficult to oxidized substrates as hexafluorobenzene and pentafluoropyridine. The main fluoride containing product is inorganic fluoride. It has been found that this catalyst, when supported on a graphite, exhibits high stability and can be used after simple regeneration.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>oxidation</kwd>
    <kwd>catalytic defluorination</kwd>
    <kwd>iron phthalocyaninate</kwd>
    <kwd>homogeneous and heterogeneous catalysis</kwd>
    <kwd>hydrogen peroxide</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
 <back>
  <ref-list>
   <ref id="B1">
    <label>1.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Baumgartner R., McNeill K. Hydrodefluorination and Hydrogenation of Fluorobenzene under Mild Aqueous Conditions. Environ. Sci. Technol. 2012. V. 46. N 18. P. 10199-10205. DOI: 10.1021/es302188f</mixed-citation>
     <mixed-citation xml:lang="en">Baumgartner R., McNeill K. Hydrodefluorination and Hydrogenation of Fluorobenzene under Mild Aqueous Conditions. Environ. Sci. Technol. 2012. V. 46. N 18. P. 10199-10205. DOI: 10.1021/es302188f</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B2">
    <label>2.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Sorokin A.B. Meunier B., Séris J.-L. Efficient Oxidative Dechlorination and Aromatic Ring Cleavage of Chlorinated Phenols Catalyzed by Iron Sulfophthalocyanine. Science. 1995. V. 268. P. 1163-1166.</mixed-citation>
     <mixed-citation xml:lang="en">Sorokin A.B. Meunier B., Séris J.-L. Efficient Oxidative Dechlorination and Aromatic Ring Cleavage of Chlorinated Phenols Catalyzed by Iron Sulfophthalocyanine. Science. 1995. V. 268. P. 1163-1166.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B3">
    <label>3.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Meunier B., Sorokin A. Oxidation of Pollutants Catalyzed by Metallophthalocyanines. Accounts of Chemical Research. 1997. V. 30. N 11. P. 470-476. DOI: 10.1021/ar960275c</mixed-citation>
     <mixed-citation xml:lang="en">Meunier B., Sorokin A. Oxidation of Pollutants Catalyzed by Metallophthalocyanines. Accounts of Chemical Research. 1997. V. 30. N 11. P. 470-476. DOI: 10.1021/ar960275c</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B4">
    <label>4.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Sorokin A.B. Phthalocyanine Metal Complexes in Catalysis. Chem. Rev. 2013. V. 113. N 10. P. 8152-8191. DOI: 10.1021/cr4000072</mixed-citation>
     <mixed-citation xml:lang="en">Sorokin A.B. Phthalocyanine Metal Complexes in Catalysis. Chem. Rev. 2013. V. 113. N 10. P. 8152-8191. DOI: 10.1021/cr4000072</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B5">
    <label>5.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Sorokin A.B., Kudrik E.V. US Patent № US8884093 B2. 2014.</mixed-citation>
     <mixed-citation xml:lang="en">Sorokin A.B., Kudrik E.V. US Patent № US8884093 B2. 2014.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B6">
    <label>6.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Colomban C., Kudrik E.V., Afanasiev P., Sorokin A.B. Catalytic Defluorination of Perfluorinated Aromatics under Oxidative Conditions Using N-Bridged Diiron Phthalocyanine. J. Am. Chem. Soc. 2014. V. 136. N 32. P. 11321-11330. DOI: 10.1021/ja505437h</mixed-citation>
     <mixed-citation xml:lang="en">Colomban C., Kudrik E.V., Afanasiev P., Sorokin A.B. Catalytic Defluorination of Perfluorinated Aromatics under Oxidative Conditions Using N-Bridged Diiron Phthalocyanine. J. Am. Chem. Soc. 2014. V. 136. N 32. P. 11321-11330. DOI: 10.1021/ja505437h</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B7">
    <label>7.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Goedkent V.L., Ercolani C. Nitrido-bridged iron phthalocyanine dimers: synthesis and characterization. J. Chem. Soc. Chem. Commun. 1984. P. 378-379. DOI: 10.1039/c39840000378</mixed-citation>
     <mixed-citation xml:lang="en">Goedkent V.L., Ercolani C. Nitrido-bridged iron phthalocyanine dimers: synthesis and characterization. J. Chem. Soc. Chem. Commun. 1984. P. 378-379. DOI: 10.1039/c39840000378</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B8">
    <label>8.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Bellack E., Schouboe P.J. Rapid determination of fluoride in water. Use of sodium 2-(p-sulfophenylazo)-1,8-dihydroxynaphthalene-3,6-disulfonate-Zirconium lake. Anal. Chem. 1958. V. 30. N 12. P. 2032-2034.</mixed-citation>
     <mixed-citation xml:lang="en">Bellack E., Schouboe P.J. Rapid determination of fluoride in water. Use of sodium 2-(p-sulfophenylazo)-1,8-dihydroxynaphthalene-3,6-disulfonate-Zirconium lake. Anal. Chem. 1958. V. 30. N 12. P. 2032-2034.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B9">
    <label>9.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Sorokin A.B., Kudrik E.V., Bouchu D. Bio-inspired oxidation of methane in water catalyzed by N-bridged diiron phthalocyanine complex. Chem. Commun. 2008. Iss. 22. P. 2562-2564. DOI: 10.1039/B804405H</mixed-citation>
     <mixed-citation xml:lang="en">Sorokin A.B., Kudrik E.V., Bouchu D. Bio-inspired oxidation of methane in water catalyzed by N-bridged diiron phthalocyanine complex. Chem. Commun. 2008. Iss. 22. P. 2562-2564. DOI: 10.1039/B804405H</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B10">
    <label>10.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Sorokin A.B., Kudrik E.V., Alvarez L.X., Afanasiev P., Millet J.M.M., Bouchu D. Oxidation of methane and ethylene in water at ambient conditions. Catal. Today. 2010. V. 157. N 1-4. P. 149-154. DOI: 10.1016/j.cattod.2010.02.007</mixed-citation>
     <mixed-citation xml:lang="en">Sorokin A.B., Kudrik E.V., Alvarez L.X., Afanasiev P., Millet J.M.M., Bouchu D. Oxidation of methane and ethylene in water at ambient conditions. Catal. Today. 2010. V. 157. N 1-4. P. 149-154. DOI: 10.1016/j.cattod.2010.02.007</mixed-citation>
    </citation-alternatives>
   </ref>
  </ref-list>
 </back>
</article>
