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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">alternative</journal-id><journal-title-group><journal-title xml:lang="ru">Альтернативная энергетика и экология (ISJAEE)</journal-title><trans-title-group xml:lang="en"><trans-title>Alternative Energy and Ecology (ISJAEE)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1608-8298</issn><publisher><publisher-name>Международный издательский дом научной периодики "Спейс</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">alternative-411</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</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CATALYSIS</subject></subj-group></article-categories><title-group><article-title>Квантово-химическое из чение строения и энергии образования стабильных прод ктов взаимодействия молек лярного азота с гидрои дигидрофуллереном С60 и его отрицательными ионами</article-title><trans-title-group xml:lang="en"><trans-title>Quantum-chemical study of the structure and energy of formation of stable products of the interaction of molecular nitrogen with hydro and digidrofullerene C60 and its negative ions</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>Трифонов</surname><given-names>Н. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Trifonov</surname><given-names>N. Yu.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Шестаков</surname><given-names>А. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Shestakov</surname><given-names>A. F.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Институт проблем химической физики РАН<country>Россия</country></aff><aff xml:lang="en">The Institute of Problems of Chemical Physics of the RAS<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>23</day><month>06</month><year>2016</year></pub-date><issue>4</issue><fpage>33</fpage><lpage>39</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Международный издательский дом научной периодики "Спейс, 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Международный издательский дом научной периодики "Спейс</copyright-holder><copyright-holder xml:lang="en">Международный издательский дом научной периодики "Спейс</copyright-holder><license xlink:href="https://www.isjaee.com/jour/about/submissions#copyrightNotice" xlink:type="simple"><license-p>https://www.isjaee.com/jour/about/submissions#copyrightNotice</license-p></license></permissions><self-uri xlink:href="https://www.isjaee.com/jour/article/view/411">https://www.isjaee.com/jour/article/view/411</self-uri><abstract><p>В данной работе были рассмотрены различные варианты механизмов фиксации молекулярного азота в присутствии супрамолекулярного комплекса фуллерена С60 с γ-циклодекстрином в процессе электролиза. Показано, что ни сам фуллерен, ни его низшие гидриды, которые способны образовываться в условиях эксперимента, в различных зарядовых и спиновых состояниях не способны непосредственно присоединять молекулярный азот.</p></abstract><trans-abstract xml:lang="en"><p>Various options of the mechanisms of fixing of molecular nitrogen were examined in the presence of a supramolecular complex of the C60 fullerene with γ-cyclodextrin in the electrolysis process in this paper. It is shown that neither the fullerene nor its lower hydrides that can be formed under the experimental conditions in different charge and spin states are not able to directly connect molecular nitrogen.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>реакционная способность</kwd><kwd>катализ</kwd><kwd>фуллерен С60</kwd><kwd>фиксация азота</kwd><kwd>reactivity</kwd><kwd>catalysis</kwd><kwd>C60 fullerene</kwd><kwd>nitrogen fixation</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">Kim J., Rees D.C. Nitrogenase and biological nitrogen fixation // Biochemistry. 1994. Vol. 33, No. 2. P. 389-397.</mixed-citation><mixed-citation xml:lang="en">Kim J., Rees D.C. Nitrogenase and biological nitrogen fixation // Biochemistry. 1994. Vol. 33, No. 2. 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