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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">Russian Journal of Biological Physics and Chemisrty</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">Russian Journal of Biological Physics and Chemisrty</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>АКТУАЛЬНЫЕ ВОПРОСЫ БИОЛОГИЧЕСКОЙ ФИЗИКИ И ХИМИИ</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="print">2499-9962</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">54093</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>БИООРГАНИЧЕСКАЯ, БИОФИЗИЧЕСКАЯ И МЕДИЦИНСКАЯ ХИМИЯ</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>BIOORGANIC, BIOPHYSICAL AND MEDICINAL CHEMISTRY</subject>
    </subj-group>
    <subj-group>
     <subject>БИООРГАНИЧЕСКАЯ, БИОФИЗИЧЕСКАЯ И МЕДИЦИНСКАЯ ХИМИЯ</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">L-PROLINE BASED ALKYLMETHYLIMIDAZOLIUM IONIC LIQUIDS [Cnmim][Pro]: SYNTHESIS AND SOME PHYSICOCHEMICAL PROPERTIES OF THEIR AQUEOUS SOLUTIONS</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>L-PROLINE BASED ALKYLMETHYLIMIDAZOLIUM IONIC LIQUIDS [Cnmim][Pro]: SYNTHESIS AND SOME PHYSICOCHEMICAL PROPERTIES OF THEIR AQUEOUS SOLUTIONS</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Alopina</surname>
       <given-names>E V</given-names>
      </name>
      <name xml:lang="en">
       <surname>Alopina</surname>
       <given-names>E V</given-names>
      </name>
     </name-alternatives>
     <email>alopina@mail.ru</email>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Dobryakov</surname>
       <given-names>Yu G</given-names>
      </name>
      <name xml:lang="en">
       <surname>Dobryakov</surname>
       <given-names>Yu G</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Safonova</surname>
       <given-names>E A</given-names>
      </name>
      <name xml:lang="en">
       <surname>Safonova</surname>
       <given-names>E A</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-3"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Smirnova</surname>
       <given-names>N A</given-names>
      </name>
      <name xml:lang="en">
       <surname>Smirnova</surname>
       <given-names>N A</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-4"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">St. Petersburg State University</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">St. Petersburg State University</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-2">
    <aff>
     <institution xml:lang="ru">St. Petersburg State University</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">St. Petersburg State University</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-3">
    <aff>
     <institution xml:lang="ru">St. Petersburg State University</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">St. Petersburg State University</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-4">
    <aff>
     <institution xml:lang="ru">St. Petersburg State University</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">St. Petersburg State University</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2016-12-25T20:22:29+03:00">
    <day>25</day>
    <month>12</month>
    <year>2016</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2016-12-25T20:22:29+03:00">
    <day>25</day>
    <month>12</month>
    <year>2016</year>
   </pub-date>
   <volume>1</volume>
   <issue>2</issue>
   <fpage>173</fpage>
   <lpage>175</lpage>
   <history>
    <date date-type="received" iso-8601-date="2016-12-20T20:22:29+03:00">
     <day>20</day>
     <month>12</month>
     <year>2016</year>
    </date>
    <date date-type="accepted" iso-8601-date="2016-12-20T20:22:29+03:00">
     <day>20</day>
     <month>12</month>
     <year>2016</year>
    </date>
   </history>
   <self-uri xlink:href="https://rusjbpc.ru/en/nauka/article/54093/view">https://rusjbpc.ru/en/nauka/article/54093/view</self-uri>
   <abstract xml:lang="ru">
    <p>A modification of synthesis of amino acid ionic liquids (AAILs) based on 1-alkyl-3-methylimidazolium cation and L-prolinate anion [Cnmim][Pro] (n = 4, 8, 12) was developed. The structures of the AAILs based on prolinate were confirmed by 1H NMR and 13C NMR spectroscopies. Densities and refractive indices of aqueous solutions of these AAILs in the concentration range 0-97 wt % (weight percents) were measured at temperature 298.15 K. It has been found that in the field of high AAIL concentrations the dependence of the density value on the AAIL mole fraction for binary water + [Cnmim][Pro] solutions is nonlinear.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>A modification of synthesis of amino acid ionic liquids (AAILs) based on 1-alkyl-3-methylimidazolium cation and L-prolinate anion [Cnmim][Pro] (n = 4, 8, 12) was developed. The structures of the AAILs based on prolinate were confirmed by 1H NMR and 13C NMR spectroscopies. Densities and refractive indices of aqueous solutions of these AAILs in the concentration range 0-97 wt % (weight percents) were measured at temperature 298.15 K. It has been found that in the field of high AAIL concentrations the dependence of the density value on the AAIL mole fraction for binary water + [Cnmim][Pro] solutions is nonlinear.</p>
   </trans-abstract>
   <kwd-group xml:lang="ru">
    <kwd>ionic liquid</kwd>
    <kwd>1-alkyl-3-methylimidazolium cation</kwd>
    <kwd>amino acid ionic liquid</kwd>
    <kwd>L-proline</kwd>
    <kwd>density</kwd>
    <kwd>refractive index</kwd>
   </kwd-group>
   <kwd-group xml:lang="en">
    <kwd>ionic liquid</kwd>
    <kwd>1-alkyl-3-methylimidazolium cation</kwd>
    <kwd>amino acid ionic liquid</kwd>
    <kwd>L-proline</kwd>
    <kwd>density</kwd>
    <kwd>refractive index</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
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