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<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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of General Chemistry</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of General Chemistry</journal-title><trans-title-group xml:lang="ru"><trans-title>Журнал общей химии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0044-460X</issn><issn publication-format="electronic">3034-5596</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">666969</article-id><article-id pub-id-type="doi">10.31857/S0044460X23060136</article-id><article-id pub-id-type="edn">FMNSOW</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Effect of the nature of nitrogen-containing bases on their catalytic activity in the reaction of zinc compleх formation with tetra(4-<italic>tert</italic>-butyl-5-phenylsulfanyl)phtalocyanine in benzene</article-title><trans-title-group xml:lang="ru"><trans-title>Влияние природы азотсодержащих оснований на их каталитическую активность в реакции образования комплекса цинка с тетра(4-<italic>трет</italic>-бутил-5-фенилсульфанил)фталоцианином в бензоле</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Petrov</surname><given-names>O. A</given-names></name><name xml:lang="ru"><surname>Петров</surname><given-names>О. А</given-names></name></name-alternatives><email>poa@isuct.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Mayzlish</surname><given-names>V. E</given-names></name><name xml:lang="ru"><surname>Майзлиш</surname><given-names>В. Е</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Ivanovo State University of Chemistry and Technology</institution></aff><aff><institution xml:lang="ru">Ивановский государственный химико-технологический университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-06-15" publication-format="electronic"><day>15</day><month>06</month><year>2023</year></pub-date><volume>93</volume><issue>6</issue><issue-title xml:lang="en">NO6 (2023)</issue-title><issue-title xml:lang="ru">№6 (2023)</issue-title><fpage>944</fpage><lpage>950</lpage><history><date date-type="received" iso-8601-date="2025-02-26"><day>26</day><month>02</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2023, Russian Academy of Sciences</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, Российская академия наук</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="en">Russian Academy of Sciences</copyright-holder><copyright-holder xml:lang="ru">Российская академия наук</copyright-holder></permissions><self-uri xlink:href="https://transsyst.ru/0044-460X/article/view/666969">https://transsyst.ru/0044-460X/article/view/666969</self-uri><abstract xml:lang="en"><p>The catalytic action of the cyclic and acyclic organic nitrogen bases on the complex formation between zinc and tetra(4- tert -buthyl-5-phenylsulfanyl)phtalocyanine in benzene was studied. The acid-base interaction was shown to precede the complexation and to play a key role in it. The scheme of complex formation of zinc with tetra(4- tert -buthyl-5-phenylsulfanyl)phtalocyanine in the system containing also organic nitrogen base and benzene was given. The relationship between catalytic activity of the base and its ability to accept proton as well as structure was described.</p></abstract><trans-abstract xml:lang="ru"><p>Изучено влияние циклических и ациклических азотсодержащих органических оснований на образование комплекса цинка с тетра(4- трет -бутил-5-фенилсульфанил)фталоцианином в бензоле. Показано, что кислотно-основное взаимодействие предшествует комплексообразованию и играет в нем ключевую роль. Приведена схема образования комплекса цинка с тетра(4- трет -бутил-5-фенилсульфанил)фталоцианином в системе азотсодержащее основание-бензол. Установлена взаимосвязь между каталитической активностью основания и его протоноакцепторной способностью, а также строением.</p></trans-abstract><kwd-group xml:lang="en"><kwd>tetra(4-tert-buthyl-5-phenylsulfanyl)phthalocyanine</kwd><kwd>zinc acetate</kwd><kwd>base</kwd><kwd>acid-base interaction</kwd><kwd>catalysis</kwd><kwd>complex formation</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>тетра(4-трет-бутил-5-фенилсульфанил)фталоцианин</kwd><kwd>ацетат цинка</kwd><kwd>основания</kwd><kwd>кислотно-основное взаимодействие</kwd><kwd>катализ</kwd><kwd>комплексообразование</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Novakova V., Donzello M.P. Ercolani C., Zimcik P., Stuzhin P.A. // Coord. Chem. Rev. 2018. Vol. 361. P. 1. doi 10.1016/j. ccr.2018.01.05.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Gounden D.I., Van Zul W.E., Nombona N. // Coord. Chem. Rev. 2020. Vol. 420. P. 213359. doi 10.1016/j. ccr. 213359</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Ibrahim-Ouali M., Dumur M. // Molecules. 2019. Vol. 24. P. 1412. doi 10.3390/ molecules24071412</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Кольман Я., Рем К.-Г. Наглядная биохимия. М.: Бином, 2011. 469 с.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Петров О.А. // Изв. АН. Сер. хим. 2022. Т. 71. С. 613</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Petrov O.A. // Russ. Chem. Bull. 2022. Vol. 71. P. 613. doi 10.1007/S11172-022-34-59-5</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Петров О.А. // ЖФХ. 2021. Т. 95. № 4. C. 549</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Petrov O.A. // Russ. J. Phys. Chem. (A). 2021. Vol. 95. N 4. P. 696. doi 10.318.57/s004445372104021х.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Петров О.А., Осипова Г.В., Майзлиш В.Е., Аганичева К.А., М.М. Чуркина М.М. // ЖОрХ. 2021. Т. 57. № 9. С.1281</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Petrov O.A., Osipova G.V., Mayzlish V.E., Aganicheva K.A., Churkina M.M. // Russ. J. Org. Chem. 2021. Vol. 57. P. 1428. doi 10.1134/S1070363218040187</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>The Handbook of Chemistry and Physics / Ed. W.M. Haynes. Boca-Raton; London; New York: Taylor and Francis, 2013. 2668 p.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Anet F.A.L., Yavari I. // J. Am. Chem. Soc. 1977. Vol. 99. P. 2794. doi org/10.1021/ja00450a 064</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Blackburne I.D., Katrizky A.R., Takeuchi Y. // Acc. Chem. Res. 1975. Vol. 8. P. 300.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Майзлиш В.Е., Тихомирова Т.В., Знойко С.А., Александрийский В.В., Вашурин А.С., Шапошников Г.П. // ЖОХ. 2018. Т. 88. С. 655</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Mayzlish V.E., Tikhomirova T.E., Znoiko S.A., Aleksandriiskii A.A., Vashurin A.S., Shaposhnikov G.P. // Russ. J. Gen. Chem. 2018. Vol. 88. P. 736. doi 101134/S1070363218040187</mixed-citation></ref></ref-list></back></article>
