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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">vuzbiochemi</journal-id><journal-title-group><journal-title xml:lang="ru">Известия вузов. Прикладная химия и биотехнология</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of Universities. Applied Chemistry and Biotechnology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2227-2925</issn><issn pub-type="epub">2500-1558</issn><publisher><publisher-name>ИРНИТУ</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21285/2227-2925-2018-8-4-192-196</article-id><article-id custom-type="elpub" pub-id-type="custom">vuzbiochemi-165</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BRIEF COMMUNICATION</subject></subj-group></article-categories><title-group><article-title>НОВЫЕ ТЕРМОСТОЙКИЕ ФУНКЦИОНАЛЬНЫЕ СОПОЛИМЕРЫ</article-title><trans-title-group xml:lang="en"><trans-title>NEW HEAT-RESISTANT FUNCTIONAL COPOLYMERS</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Прозорова</surname><given-names>Г. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Prozorova</surname><given-names>G. F.</given-names></name></name-alternatives><email xlink:type="simple">prozorova@irioch.irk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ермакова</surname><given-names>Т. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Ermakova</surname><given-names>T. G.</given-names></name></name-alternatives><email xlink:type="simple">ermakova@irioch.irk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кузнецова</surname><given-names>Н. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuznetsova</surname><given-names>N. P.</given-names></name></name-alternatives><email xlink:type="simple">nkuznetsova@irioch.irk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коржова</surname><given-names>С. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Korzhova</surname><given-names>S. A.</given-names></name></name-alternatives><email xlink:type="simple">korzhova@irioch.irk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Емельянов</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Emel’Yanov</surname><given-names>A. I.</given-names></name></name-alternatives><email xlink:type="simple">emelyanov@irioch.irk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Иркутский институт химии им. А.Е. Фаворского СО РАН</institution><country>Россия</country></aff><aff xml:lang="en"><institution>A.E. Favorsky Irkutsk Institute of Chemistry SB RAS</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>23</day><month>09</month><year>2019</year></pub-date><volume>8</volume><issue>4</issue><fpage>192</fpage><lpage>196</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Прозорова Г.Ф., Ермакова Т.Г., Кузнецова Н.П., Коржова С.А., Емельянов А.И., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Прозорова Г.Ф., Ермакова Т.Г., Кузнецова Н.П., Коржова С.А., Емельянов А.И.</copyright-holder><copyright-holder xml:lang="en">Prozorova G.F., Ermakova T.G., Kuznetsova N.P., Korzhova S.A., Emel’Yanov A.I.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://vuzbiochemi.elpub.ru/jour/article/view/165">https://vuzbiochemi.elpub.ru/jour/article/view/165</self-uri><abstract><p>Взаимодействием винилацетата с 1-винил-1,2,4-триазолом в условиях свободнорадикального инициирования синтезированы функциональные сополимеры, содержащие в своей структуре гидрофильные триазольные и гидрофобные ацетатные фрагменты. Варьированием соотношения мономеров в исходной реакционной смеси получены сополимеры разного состава, хорошо растворимые в воде и органических растворителях. Оценены реакционные активности мономеров, установлено, что 1-винил-1,2,4-триазол проявляет большую реакционную способность по сравнению с винилацетатом. Сополимеры проявляют свойства высокоомных органических полупроводников, характеризуются удельной электрической проводимостью порядка 10-14-10-15 См/см; обладают высокой стойкостью к термоокислительной деструкции: начало термического разложения происходит при температурах 300-330 °С. Структура, состав и физико-химические свойства сополимеров охарактеризованы методами элементного анализа, ИК и ЯМР1H спектроскопии, турбидиметрического титрования, термогравиметрического анализа.</p></abstract><trans-abstract xml:lang="en"><p>The interaction of vinyl acetate with 1-vinyl-1,2,4-triazole under conditions of free radical initiation of functional copolymers, containing hydrophilic triazole and hydrophobic acetate fragments in their structure, are synthesised. In order to obtain copolymers of different composition that are well-soluble in water and organic solvents, the ratio of monomers in the initial reaction mixture was varied. By evaluating the reactivity of monomers, it was established that 1-vinyl-1,2,4-triazole exhibits greater reactivity compared to vinyl acetate. Copolymers exhibiting the properties of high-resistance organic semiconductors, characterised by a specific electrical conductivity of the order 10-14-10-15 S/cm, have high resistance to thermal-oxidative degradation: the beginning of thermal decomposition occurs at temperatures of 300-330 °C. The structure, composition and physicochemical properties of the copolymers were characterised by elemental analysis methods, IR and NMR1H spectroscopy, turbidimetric titration, as well as thermogravimetric analysis.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>сополимеры</kwd><kwd>винилацетат</kwd><kwd>радикальная сополимеризация</kwd></kwd-group><kwd-group xml:lang="en"><kwd>1-винил-1</kwd><kwd>2</kwd><kwd>4-триазол</kwd><kwd>copolymers</kwd><kwd>1-vinyl-1</kwd><kwd>2</kwd><kwd>4-triazole</kwd><kwd>vinyl acetate</kwd><kwd>radical copolymerisation</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Розенберг М.Э. Полимеры на основе винилацетата. Л.: Химия, 1983. 176 с.</mixed-citation><mixed-citation xml:lang="en">Розенберг М.Э. Полимеры на основе винилацетата. Л.: Химия, 1983. 176 с.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Saunders K.J. Poly(Vinyl Acetate) and Related Polymers // Organic Polymer Chemisry. 1988. P. 113-124.</mixed-citation><mixed-citation xml:lang="en">Saunders K.J. Poly(Vinyl Acetate) and Related Polymers // Organic Polymer Chemisry. 1988. P. 113-124.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Santhosh Kumar K.S., Gnanou Y., Champouret Y., Daran J.-C., Poli R. Radical Polymerization of Vinyl Acetate with Bis(tetramethylheptadionato)cobalt // Chem. Eur. J. 2009. Vol. 15. P. 4874-4885.</mixed-citation><mixed-citation xml:lang="en">Santhosh Kumar K.S., Gnanou Y., Champouret Y., Daran J.-C., Poli R. Radical Polymerization of Vinyl Acetate with Bis(tetramethylheptadionato)cobalt // Chem. Eur. J. 2009. Vol. 15. P. 4874-4885.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Banerjee S., Domenichelli I., Ameduri B. Nitro-xide-Mediated Alternating Copolymerization of Vinyl Acetate with tert-Butyl-2-trifluoromethacrylate Using a SG1-Based Alkoxyamine // ACS Macro Lett. 2016. Vol. 5. P. 1232-1236.</mixed-citation><mixed-citation xml:lang="en">Banerjee S., Domenichelli I., Ameduri B. Nitro-xide-Mediated Alternating Copolymerization of Vinyl Acetate with tert-Butyl-2-trifluoromethacrylate Using a SG1-Based Alkoxyamine // ACS Macro Lett. 2016. Vol. 5. P. 1232-1236.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Ермакова Т.Г., Шаулина Л.П., Кузнецова Н.П., Волкова Л.И., Поздняков А.С., Прозорова Г.Ф. Сорбция соединений благородных металлов сетчатым сополимером 1-винил-1,2,4-триазола с акриловой кислотой // Журнал прикладной химии. 2012. Т. 85. N 1. С. 38-43.</mixed-citation><mixed-citation xml:lang="en">Ермакова Т.Г., Шаулина Л.П., Кузнецова Н.П., Волкова Л.И., Поздняков А.С., Прозорова Г.Ф. Сорбция соединений благородных металлов сетчатым сополимером 1-винил-1,2,4-триазола с акриловой кислотой // Журнал прикладной химии. 2012. Т. 85. N 1. С. 38-43.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Прозорова Г.Ф., Поздняков А.С., Емельянов А.И., Коржова С.А., Ермакова Т.Г., Трофимов Б.А. Водорастворимые нанокомпозиты серебра с сополимером 1-винил-1,2,4-триазола // Доклады Академии наук. Химия. 2013. Т. 449. № 2. С. 172-173. DOI: 10.7868/80869565213080136</mixed-citation><mixed-citation xml:lang="en">Прозорова Г.Ф., Поздняков А.С., Емельянов А.И., Коржова С.А., Ермакова Т.Г., Трофимов Б.А. Водорастворимые нанокомпозиты серебра с сополимером 1-винил-1,2,4-триазола // Доклады Академии наук. Химия. 2013. Т. 449. № 2. С. 172-173. DOI: 10.7868/80869565213080136</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Pozdnyakov A.S., Emel'yanov A.I., Kuznetsova N.P., Ermakova T.G., Fadeeva T.V., Sosedova L.M., Prozorova G.F. Nontoxic hydrophilic polymeric nanocomposites containing silver nanoparticles with strong antimicrobial activity // International Journal of Nanomedicine. 2016. Vol. 11. P. 1295-1304. DOI: org/10.2147/IJN.S98995</mixed-citation><mixed-citation xml:lang="en">Pozdnyakov A.S., Emel'yanov A.I., Kuznetsova N.P., Ermakova T.G., Fadeeva T.V., Sosedova L.M., Prozorova G.F. Nontoxic hydrophilic polymeric nanocomposites containing silver nanoparticles with strong antimicrobial activity // International Journal of Nanomedicine. 2016. Vol. 11. P. 1295-1304. DOI: org/10.2147/IJN.S98995</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Pozdnyakov A.S., Emel'yanov A.I., Kuznetsova N.P., Ermakova T.G., Bolgova Yu.I., Trofimova O.M., Albanov A.I., Borodina T.N., Smirnov V.I., Prozorova G.F. A Polymer Nanocomposite with CuNP Stabilized by 1-Vinyl-1,2,4-triazole and Acrylonitrile Copolymer // Synlett. 2016. Vol. 27. P. 900-904. DOI: 10.1055/s-0035-1561292; Art ID: st-2015-d0751-l.</mixed-citation><mixed-citation xml:lang="en">Pozdnyakov A.S., Emel'yanov A.I., Kuznetsova N.P., Ermakova T.G., Bolgova Yu.I., Trofimova O.M., Albanov A.I., Borodina T.N., Smirnov V.I., Prozorova G.F. A Polymer Nanocomposite with CuNP Stabilized by 1-Vinyl-1,2,4-triazole and Acrylonitrile Copolymer // Synlett. 2016. Vol. 27. P. 900-904. DOI: 10.1055/s-0035-1561292; Art ID: st-2015-d0751-l.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Ермакова Т.Г., Татарова Л.А., Кузнецова Н.П. Винилирование 1,2,4-триазола // Журнал общей химии. 1997. Т. 67. Вып. 5. С. 859-861.</mixed-citation><mixed-citation xml:lang="en">Ермакова Т.Г., Татарова Л.А., Кузнецова Н.П. Винилирование 1,2,4-триазола // Журнал общей химии. 1997. Т. 67. Вып. 5. С. 859-861.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Kelen T., Tudos F. Analysis of the Linear Methods for Determining Copolymerization Reactivity Ratios // J. Macromol. Sci.-Chem. 1975. Vol. 9. P. 1-27.</mixed-citation><mixed-citation xml:lang="en">Kelen T., Tudos F. Analysis of the Linear Methods for Determining Copolymerization Reactivity Ratios // J. Macromol. Sci.-Chem. 1975. Vol. 9. P. 1-27.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
