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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">vestich</journal-id><journal-title-group><journal-title xml:lang="ru">Известия Национальной академии наук Беларуси. Серия химических наук</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of the National Academy of Sciences of Belarus, Chemical Series</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1561-8331</issn><issn pub-type="epub">2524-2342</issn><publisher><publisher-name>The Republican Unitary Enterprise Publishing House "Belaruskaya Navuka"</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.29235/1561-8331-2019-55-2-196-204</article-id><article-id custom-type="elpub" pub-id-type="custom">vestich-391</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>ХИМИЯ ВЫСОКОМОЛЕКУЛЯРНЫХ СОЕДИНЕНИЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>POLYMER CHEMISTRY</subject></subj-group></article-categories><title-group><article-title>Палладий-полимерный нанокомпозит: эффективный катализатор зеленых процессов кросссочетания по Сузуки–Мияуре и восстановления нитробензола по Мотт-Шотки</article-title><trans-title-group xml:lang="en"><trans-title>PalladiumPolymer Nanocomposite: An Efficient Catalyst for Green Suzuki–Miyaura Cross-Coupling and Mott-Schottky Nitrobenzene Reduction Processes</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>Зураев</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Zuraev</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Зураев Александр Викторович – аспирант кафедры неорганической химии, Белорусский государственный университет</p><p>пр. Независимости, 4, 220030, Минск;</p><p> мл. науч. сотрудник, Научно-исследовательский институт физико-химических проблем Белорусского государственного университета</p><p>ул. Ленинградская, 14, 220030, Минск</p></bio><bio xml:lang="en"><p>Alexandr V. Zuraev – Postgraduate student, Belarusian State University</p><p>4, Nezavisimosti Ave., 220030, Minsk;</p><p>Junior researcher, Research Institute for Physical Chemical Problems of the Belarusian State University</p><p>14, Leningradskaya Str., 220030, Minsk</p></bio><email xlink:type="simple">alex.zuraev@gmail.com</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>Григориев</surname><given-names>Ю. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Grigoriev</surname><given-names>Y. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Григориев Юрий Викторович – канд. хим. наук, зав. лаб.</p><p>ул. Ленинградская, 14, 220030, Минск</p></bio><bio xml:lang="en"><p>Yurii V. Grigoriev – Ph. D. (Chemistry), Head of the laboratory</p><p>14, Leningradskaya Str., 220030, Minsk</p></bio><email xlink:type="simple">azole@bsu.by</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Вербило</surname><given-names>К. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Verbilo</surname><given-names>C. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Вербило Кирилл Маратович – студент</p><p>пр. Независимости, 4, 220030, Минск</p></bio><bio xml:lang="en"><p>Ciryl M. Verbilo – student</p><p>4, Nezavisimosti Ave., 220030, Minsk</p></bio><email xlink:type="simple">cyrilvermar@gmail.com</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ивашкевич</surname><given-names>Л. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivashkevich</surname><given-names>L. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ивашкевич Людмила Сергеевна – канд. хим. наук, доцент, зав. лаб.</p><p>ул. Ленинградская, 14, 220030, Минск</p></bio><bio xml:lang="en"><p>Ludmila S. Ivashkevich – Ph. D. (Chemistry), Associate Professor, Head of Laboratory</p><p>14, Leningradskaya Str., 220030, Minsk</p></bio><email xlink:type="simple">iva@bsu.by</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ляхов</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Lyakhov</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ляхов Александр Семенович – канд. хим. наук, доцент, вед. науч. сотрудник</p><p>ул. Ленинградская, 14, 220030, Минск</p></bio><bio xml:lang="en"><p>Alexandr S. Lyakhov – Ph. D. (Chemistry), the Professor, assistant, Leading research</p><p>14, Leningradskaya Str., 220030, Minsk</p></bio><email xlink:type="simple">lyakhov@bsu.by</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ивашкевич</surname><given-names>О. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivashkevich</surname><given-names>O. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ивашкевич Олег Анатольевич – академик, д-р хим. наук, профессор, первый проректор</p><p>пр. Независимости, 4, 220030, Минск</p></bio><bio xml:lang="en"><p>Oleg A. Ivashkecich – Academician, D. Sc. (Chemistry), Professor, the First Prorector</p><p>4, Nezavisimosti Ave., 220030, Minsk</p></bio><email xlink:type="simple">IvashkevichO@bsu.by</email><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт физико-химических проблем Белорусского государственного университета;&#13;
Белорусский государственный университет</institution></aff><aff xml:lang="en"><institution>Research Institute for Physical Chemical Problems of Belarusian State University;&#13;
Belarusian State University</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Научно-исследовательский институт физико-химических проблем Белорусского государственного университета</institution></aff><aff xml:lang="en"><institution>Research Institute for Physical Chemical Problems of Belarusian State University</institution></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Белорусский государственный университет</institution></aff><aff xml:lang="en"><institution>Belarusian State University</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>29</day><month>06</month><year>2019</year></pub-date><volume>55</volume><issue>2</issue><fpage>196</fpage><lpage>204</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Зураев А.В., Григориев Ю.В., Вербило К.М., Ивашкевич Л.С., Ляхов А.С., Ивашкевич О.А., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Зураев А.В., Григориев Ю.В., Вербило К.М., Ивашкевич Л.С., Ляхов А.С., Ивашкевич О.А.</copyright-holder><copyright-holder xml:lang="en">Zuraev A.V., Grigoriev Y.V., Verbilo C.M., Ivashkevich L.S., Lyakhov A.S., Ivashkevich O.A.</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://vestichem.belnauka.by/jour/article/view/391">https://vestichem.belnauka.by/jour/article/view/391</self-uri><abstract><p>Посредством термолиза поли-5-винилтетразолата палладия(II) был получен новый катализатор для зеленых процессов кросс-сочетания Сузуки–Мияуры и восстановления нитробензола по Мотт-Шотки. Гетерогенный катализатор содержит наночастицы Pd, стабилизированные полимерной матрицей. Данный катализатор является легко восстанавливаемым и пригодным для повторного использования, а также катализирует реакции, проводимые в водной среде при комнатной температуре в аэробных условиях.</p></abstract><trans-abstract xml:lang="en"><p>A new catalyst for green Suzuki–Miyaura cross-coupling and Mott-Schottky nitrobenzene reduction processes was prepared by thermolysis of palladium (II) poly-5-vinyltetrazolate. Heterogeneous catalyst includes Pd-nanoparticles supported on polymeric matrix. It presents recoverable and recyclable catalyst and the catalyzed reactions proceed in aqueous media at room temperature in aerobic conditions.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>поли-5-винилтетразолат палладия(II)</kwd><kwd>наночастицы палладия</kwd><kwd>кросс-сочетание Сузуки– Мияуры</kwd><kwd>восстановление нитробензола по Мотт-Шотки</kwd><kwd>1</kwd><kwd>1′-бифенил</kwd></kwd-group><kwd-group xml:lang="en"><kwd>palladium(II) poly-5-vinyltetrazolate</kwd><kwd>palladium nanoparticles</kwd><kwd>Suzuki–Miyaura cross-coupling</kwd><kwd>MottSchottky nitroarene reduction</kwd><kwd>1</kwd><kwd>1’-biphenyl</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">Choi S. K. Mechanistic basis of light induced cytotoxicity of photoactive nanomaterials. NanoImpact, 2016, vol. 3–4, pp. 81–89. https://doi.org/10.1016/j.impact.2016.09.001</mixed-citation><mixed-citation xml:lang="en">Choi S. K. Mechanistic basis of light induced cytotoxicity of photoactive nanomaterials. NanoImpact, 2016, vol. 3–4, pp. 81–89. https://doi.org/10.1016/j.impact.2016.09.001</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Yola M. L., Eren T., Atar N. A novel effcient photocatalyst based on TiO2 nanoparticles involved boron enrichment waste for photocatalytic degradation of atrazine. Chem. Eng. J., 2014, vol. 250, pp. 288–294. https://doi.org/10.1016/j.cej.2014.03.116</mixed-citation><mixed-citation xml:lang="en">Yola M. L., Eren T., Atar N. A novel effcient photocatalyst based on TiO2 nanoparticles involved boron enrichment waste for photocatalytic degradation of atrazine. Chem. Eng. J., 2014, vol. 250, pp. 288–294. https://doi.org/10.1016/j.cej.2014.03.116</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Yola M. L., Eren T., Atar N. A sensitive molecular imprinted electrochemical sensor based on gold nanoparticles decorated graphene oxide: Application to selective determination of tyrosine in milk. Sens. Actuators B Chem., 2015, vol. 210, pp. 149–157. https://doi.org/10.1016/j.snb.2014.12.098</mixed-citation><mixed-citation xml:lang="en">Yola M. L., Eren T., Atar N. A sensitive molecular imprinted electrochemical sensor based on gold nanoparticles decorated graphene oxide: Application to selective determination of tyrosine in milk. Sens. Actuators B Chem., 2015, vol. 210, pp. 149–157. https://doi.org/10.1016/j.snb.2014.12.098</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Beytur M., Kardas F., Akyildirim O., Ozkan A., Bankoglu B., Yuksek H., Yola M. L., Atar N. A highly selective and sensitive voltammetric sensor with molecularly imprinted polymer based silver@gold nanoparticles/ionic liquid modifed glassy carbon electrode for determination of ceftizoxime. J. Mol. Liq., 2018, vol. 251, pp. 212–217. https://doi.org/10.1016/j.molliq.2017.12.060</mixed-citation><mixed-citation xml:lang="en">Beytur M., Kardas F., Akyildirim O., Ozkan A., Bankoglu B., Yuksek H., Yola M. L., Atar N. A highly selective and sensitive voltammetric sensor with molecularly imprinted polymer based silver@gold nanoparticles/ionic liquid modifed glassy carbon electrode for determination of ceftizoxime. J. Mol. Liq., 2018, vol. 251, pp. 212–217. https://doi.org/10.1016/j.molliq.2017.12.060</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Barbaro P., Liguori F. Ion Exchange Resins: Catalyst Recovery and Recycle. Chem. Rev., 2009, vol. 109, no. 2, pp. 515–529. https://doi.org/10.1021/cr800404j</mixed-citation><mixed-citation xml:lang="en">Barbaro P., Liguori F. Ion Exchange Resins: Catalyst Recovery and Recycle. Chem. Rev., 2009, vol. 109, no. 2, pp. 515–529. https://doi.org/10.1021/cr800404j</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Kazmaier U., Pohlman M. Cross-Coupling Reactions via π-Allyl Metal Intermediates / U. Kazmaier, M. Pohlman // MetalCatalyzed Cross-Coupling Reactions / Wiley-VCH ; A. de Meijere, F. Diederich (Eds.). – Weinheim, 2004. – P. 531–583.</mixed-citation><mixed-citation xml:lang="en">Kazmaier U., Pohlman M. Cross-Coupling Reactions via π-Allyl Metal Intermediates / U. Kazmaier, M. Pohlman // MetalCatalyzed Cross-Coupling Reactions / Wiley-VCH ; A. de Meijere, F. Diederich (Eds.). – Weinheim, 2004. – P. 531–583.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Chartoire A., Nolan S.P. Advances in C–C and C–X Coupling Using Palladium-N-Heterocyclic Carbene (Pd-NHC) Complexes / A. Chartoire, S.P. Nolan // New Trends in Cross-Coupling: Theory and Applications / Royal Society of Chemistry ; J. Spivey [et al.] (Eds.). – Cambridge, 2014. – P. 139–219.</mixed-citation><mixed-citation xml:lang="en">Chartoire A., Nolan S.P. Advances in C–C and C–X Coupling Using Palladium-N-Heterocyclic Carbene (Pd-NHC) Complexes / A. Chartoire, S.P. Nolan // New Trends in Cross-Coupling: Theory and Applications / Royal Society of Chemistry ; J. Spivey [et al.] (Eds.). – Cambridge, 2014. – P. 139–219.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Jekab A., Dalicsek Z., Holczbauer T., Hamza A., Papai I., Finta Z., Timari G., Soos T. Superstable Palladium(0) Complex as an Air- and Thermostable Catalyst for Suzuki Coupling Reactions. Eur. J. Org. Chem., 2015. vol. 2015, no. 1, pp. 60–66. https://doi.org/10.1002/ejoc.201403214</mixed-citation><mixed-citation xml:lang="en">Jekab A., Dalicsek Z., Holczbauer T., Hamza A., Papai I., Finta Z., Timari G., Soos T. Superstable Palladium(0) Complex as an Air- and Thermostable Catalyst for Suzuki Coupling Reactions. Eur. J. Org. Chem., 2015. vol. 2015, no. 1, pp. 60–66. https://doi.org/10.1002/ejoc.201403214</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Cantillo D., Kappe C. O. Immobilized Transition Metals as Catalysts for Cross-Couplings in Continuous Flow-A Critical Assessment of the Reaction Mechanism and Metal Leaching. ChemCatChem., 2014, vol. 6, no. 12, pp. 3286–3305. https://doi.org/10.1002/cctc.201402483</mixed-citation><mixed-citation xml:lang="en">Cantillo D., Kappe C. O. Immobilized Transition Metals as Catalysts for Cross-Couplings in Continuous Flow-A Critical Assessment of the Reaction Mechanism and Metal Leaching. ChemCatChem., 2014, vol. 6, no. 12, pp. 3286–3305. https://doi.org/10.1002/cctc.201402483</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Becht J. M., le Drian C. Biaryl Synthesis via Decarboxylative Pd-Catalyzed Reactions of Arenecarboxylic Acids and Diaryliodonium Triﬂates. Org. Lett., 2008, vol. 10, no. 14, pp. 3161–3164. https://doi.org/10.1021/ol8011293</mixed-citation><mixed-citation xml:lang="en">Becht J. M., le Drian C. Biaryl Synthesis via Decarboxylative Pd-Catalyzed Reactions of Arenecarboxylic Acids and Diaryliodonium Triﬂates. Org. Lett., 2008, vol. 10, no. 14, pp. 3161–3164. https://doi.org/10.1021/ol8011293</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Farrusseng D., Tuel A. Perspectives on zeolite-encapsulated metal nanoparticles and their applications in catalysis. New J. Chem., 2016, vol. 40, no. 5, pp. 3933–3949. https://doi.org/10.1039/C5NJ02608C</mixed-citation><mixed-citation xml:lang="en">Farrusseng D., Tuel A. Perspectives on zeolite-encapsulated metal nanoparticles and their applications in catalysis. New J. Chem., 2016, vol. 40, no. 5, pp. 3933–3949. https://doi.org/10.1039/C5NJ02608C</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Kalidindi S. B., Nayak S., Briggs M. E., Jansat S., Katsoulidis A. P., Miller G. J., Warren J. E., Antypov D., Cora F., Slater B., Prestly M. R., Marti-Gastaldo C., Rosseinsky M. J. Chemical and Structural Stability of Zirconium-based Metal–Organic Frameworks with Large Three-Dimensional Pores by Linker Engineering. Angew. Chem. Int. Ed. Engl., 2015, vol. 54, no. 1, pp. 221–226. https://doi.org/10.1002/anie.201406501</mixed-citation><mixed-citation xml:lang="en">Kalidindi S. B., Nayak S., Briggs M. E., Jansat S., Katsoulidis A. P., Miller G. J., Warren J. E., Antypov D., Cora F., Slater B., Prestly M. R., Marti-Gastaldo C., Rosseinsky M. J. Chemical and Structural Stability of Zirconium-based Metal–Organic Frameworks with Large Three-Dimensional Pores by Linker Engineering. Angew. Chem. Int. Ed. Engl., 2015, vol. 54, no. 1, pp. 221–226. https://doi.org/10.1002/anie.201406501</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Gaponik P. N., Ivashkevich O. A., Karavai V. P., Lesnikovich A. I., Chernavina N. I., Sukhanov G. T., Gareev G. A. Polymers and copolymers based on vinyl tetrazoles, 1*. Synthesis of poly(5-vinyl tetrazole) by polymer-analogous conversion of polyacrylonitrile. Angew. Makromol. Chem., 1994, vol. 219, no. 1, pp. 77–88. https://doi.org/10.1002/apmc.1994.052190107</mixed-citation><mixed-citation xml:lang="en">Gaponik P. N., Ivashkevich O. A., Karavai V. P., Lesnikovich A. I., Chernavina N. I., Sukhanov G. T., Gareev G. A. Polymers and copolymers based on vinyl tetrazoles, 1*. Synthesis of poly(5-vinyl tetrazole) by polymer-analogous conversion of polyacrylonitrile. Angew. Makromol. Chem., 1994, vol. 219, no. 1, pp. 77–88. https://doi.org/10.1002/apmc.1994.052190107</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Zuraev A. V., Grigoriev Y. V., Ivashkevich L. S., Lyakhov A. S., Ivashkevich O. A. Copper-Polymer Nanocomposite Catalyst for Synthesis of 1,4-Diphenylbutadiyne-1,3. Z. Anorg. Allg. Chem., 2017, vol. 643, no. 19, pp. 1215–1219. https://doi.org/10.1002/zaac.201700213</mixed-citation><mixed-citation xml:lang="en">Zuraev A. V., Grigoriev Y. V., Ivashkevich L. S., Lyakhov A. S., Ivashkevich O. A. Copper-Polymer Nanocomposite Catalyst for Synthesis of 1,4-Diphenylbutadiyne-1,3. Z. Anorg. Allg. Chem., 2017, vol. 643, no. 19, pp. 1215–1219. https://doi.org/10.1002/zaac.201700213</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Zuraev A. V., Grigoriev Y. V., Budevich V. A., Ivashkevich O. A. Copper-polymer nanocomposite: An effcient catalyst for green Huisgen click synthesis. Tetrahedron Lett., 2018, vol. 59, no. 16, pp. 1583–1586. https://doi.org/10.1016/j.tetlet.2018.03.028</mixed-citation><mixed-citation xml:lang="en">Zuraev A. V., Grigoriev Y. V., Budevich V. A., Ivashkevich O. A. Copper-polymer nanocomposite: An effcient catalyst for green Huisgen click synthesis. Tetrahedron Lett., 2018, vol. 59, no. 16, pp. 1583–1586. https://doi.org/10.1016/j.tetlet.2018.03.028</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Levchik S. V., Bolvanovich E. E., Lesnikovich A. I., Ivashkevich O. A., Gaponik P. N., Vyazovakin S. V. Thermal decomposition of tetrazole-containing polymers. I. Poly-5-vinyltetrazole thermolysis. Thermochim. Acta., 1990, vol. 168, pp. 211–221. https://doi.org/10.1016/0040-6031(90)80640-K</mixed-citation><mixed-citation xml:lang="en">Levchik S. V., Bolvanovich E. E., Lesnikovich A. I., Ivashkevich O. A., Gaponik P. N., Vyazovakin S. V. Thermal decomposition of tetrazole-containing polymers. I. Poly-5-vinyltetrazole thermolysis. Thermochim. Acta., 1990, vol. 168, pp. 211–221. https://doi.org/10.1016/0040-6031(90)80640-K</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>
