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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">catal</journal-id><journal-title-group><journal-title xml:lang="ru">Катализ в промышленности</journal-title><trans-title-group xml:lang="en"><trans-title>Kataliz v promyshlennosti</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1816-0387</issn><issn pub-type="epub">2413-6476</issn><publisher><publisher-name>LLC "KALVIS"</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18412/1816-0387-2024-4-35-59</article-id><article-id custom-type="elpub" pub-id-type="custom">catal-1061</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>КАТАЛИЗ В ХИМИЧЕСКОЙ И НЕФТЕХИМИЧЕСКОЙ ПРОМЫШЛЕННОСТИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CATALYSIS IN CHEMICAL AND PETROCHEMICAL INDUSTRY</subject></subj-group></article-categories><title-group><article-title>Гетерогенное гидрирование и изомеризация карбоциклических соединений норборненового ряда (Обзор)</article-title><trans-title-group xml:lang="en"><trans-title>Heterogeneous hydrogenation and isomerization of carbocyclic compounds of the norbornene series (review)</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>Замалютин</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Zamalyutin</surname><given-names>V. V.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.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>Окунева</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Okuneva</surname><given-names>E. V.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.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>Москвичев</surname><given-names>С. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Moskvichev</surname><given-names>S. S.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.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>Флид</surname><given-names>В. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Flid</surname><given-names>V. R.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Институт тонких химических технологий имени М.В. Ломоносова РТУ МИРЭА, Москва<country>Россия</country></aff><aff xml:lang="en">MIREA – Russian Technological University, Institute of Fine Chemical Technologies named after M.V. Lomonosov, Moscow<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>18</day><month>07</month><year>2024</year></pub-date><volume>24</volume><issue>4</issue><fpage>35</fpage><lpage>59</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; LLC "KALVIS", 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">LLC "KALVIS"</copyright-holder><copyright-holder xml:lang="en">LLC "KALVIS"</copyright-holder><license xlink:href="https://www.catalysis-kalvis.ru/jour/about/submissions#copyrightNotice" xlink:type="simple"><license-p>https://www.catalysis-kalvis.ru/jour/about/submissions#copyrightNotice</license-p></license></permissions><self-uri xlink:href="https://www.catalysis-kalvis.ru/jour/article/view/1061">https://www.catalysis-kalvis.ru/jour/article/view/1061</self-uri><abstract><p>Систематизированы основные закономерности и маршруты протекания жидкофазного гидрирования и изомеризации карбоциклических алкенов и диенов норборненового ряда в присутствии гетерогенных катализаторов, рассмотрены их механизмы. Проведена идентификация продуктов реакций, изучен материальный баланс. Подобраны условия гидрирования и изомеризации соединений, основной целью которых являлось сохранение норборнанового каркаса. Проведена оценка реакционной способности кратных связей в норборненах экспериментальными и квантово-химическими методами. На основе подхода Ленгмюра–Хиншелвуда и в представлении множественной адсорбции субстратов на одном активном центре разработаны адекватные кинетические модели процессов.</p></abstract><trans-abstract xml:lang="en"><p>The main principles and routes of liquid-phase hydrogenation and isomerization of carbocyclic alkenes and dienes of the norbornene series in the presence of heterogeneous catalysts are systematized, and their mechanisms are considered. The reaction products were identified and the material balance was studied. Conditions for the hydrogenation and isomerization of compounds were selected, the main purpose of which was to preserve the norbornane framework. The reactivity of multiple bonds in norbornenes was assessed using experimental and quantum chemical methods. Based on the Langmuir–Hinshelwood approach and the representation of multiple adsorption of substrates on one active site, adequate kinetic models of the processes have been developed.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>дициклопентадиен</kwd><kwd>5-винилнорборнен-2</kwd><kwd>норборнадиен</kwd><kwd>реакции Дильса–Альдера</kwd><kwd>(эндо/экзо)-изомеризация</kwd><kwd>E/Z-изомеризация</kwd><kwd>селективное гидрирование карбоциклических диенов</kwd><kwd>миграция двойной связи</kwd><kwd>палладиевый катализатор</kwd><kwd>активный центр</kwd><kwd>модель Ленгмюра–Хиншелвуда</kwd><kwd>множественная адсорбция</kwd><kwd>кинетическая модель</kwd></kwd-group><kwd-group xml:lang="en"><kwd>dicyclopentadiene</kwd><kwd>5-vinylnorbornene-2</kwd><kwd>norbornadiene</kwd><kwd>Diels-Alder reactions</kwd><kwd>(endo/exo)-isomerization</kwd><kwd>E/Z-isomerization</kwd><kwd>selective hydrogenation of carbocyclic dienes</kwd><kwd>double bond migration</kwd><kwd>palladium catalyst</kwd><kwd>active site</kwd><kwd>Langmuir model Hinshelwood</kwd><kwd>multiple adsorption</kwd><kwd>kinetic model</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">Berenblyum A.S., Podoplelova T.A., Shamsiev R.S., Katsman E.A., Danyushevsky V.Ya., Flid V.R. // Catal. 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