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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">666947</article-id><article-id pub-id-type="doi">10.31857/S0044460X23060033</article-id><article-id pub-id-type="edn">FKASGI</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">Intramolecular noncovalent interactions in bis-imidazolium dications with short aliphatic spacers</article-title><trans-title-group xml:lang="ru"><trans-title>Внутримолекулярные нековалентные взаимодействия в дикатионах бисимидазолия с короткими алифатическими мостиками</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zarechnaya</surname><given-names>O. M</given-names></name><name xml:lang="ru"><surname>Заречная</surname><given-names>О. М</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Mikhailov</surname><given-names>V. A</given-names></name><name xml:lang="ru"><surname>Михайлов</surname><given-names>В. А</given-names></name></name-alternatives><email>v_mikhailov@yahoo.com</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">L. M. Litvinenko Institute of Physical Organic and Coal Chemistry</institution></aff><aff><institution xml:lang="ru">Институт физико-органической химии и углехимии имени Л. М. Литвиненко</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>840</fpage><lpage>857</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/666947">https://transsyst.ru/0044-460X/article/view/666947</self-uri><abstract xml:lang="en"><p>Stretched all-trans conformations were found preferable in computed structures of bis-imidazolium dications with short aliphatic (С<sub>1</sub>-С<sub>4</sub>) and hydroxyl substituted -СН<sub>2</sub>-СНОН-СН<sub>2</sub>- spacers. Maxima of molecular electrostatic potential were established near С<sup>2</sup>Н imidazolium and spacer hydrogens, for α,ω-alkenyl spacers, and close to hydroxyl hydrogen for hydroxypropane spacer. Sufficiently higher rotational barrier around С<sup>1</sup>-C<sup>2 </sup>bond in -СН<sub>2</sub>-СНОН-СН<sub>2</sub>- spacer compared with polymethylene is supported with intramolecular hydrogen bonds С-Н···О-Н between imidazolium hydrogens and hydroxyl oxygen.</p></abstract><trans-abstract xml:lang="ru"><p>Конформационный анализ бисимидазолиевых дикатионов с короткими алифатическими (С<sub>1</sub>-С<sub>4</sub>)и гидроксилзамещенным (-СН<sub>2</sub>-СНОН-СН<sub>2</sub>-) мостиками выявил предпочтительность структур с максимально вытянутой трансоидной конфигурацией алкильных фрагментов. Молекулярный электростатический потенциал в дикатионах распределен неравномерно, с максимумами в области С<sup>2</sup>Н имидазола и мостиковых атомов водорода для α,ω-алкенильных, и в области гидроксильного атома водорода для гидроксипропанового мостиков. Внутримолекулярные водородные связи С-Н···ОН вносят свой вклад в существенно больший (по сравнению с полиметиленовыми) барьер вращения по связи С<sup>1</sup>-С<sup>2 </sup>в дикатионах с гидроксипропановым мостиком.</p></trans-abstract><kwd-group xml:lang="en"><kwd>bis-imidazolium salts</kwd><kwd>molecular electrostatic potential</kwd><kwd>Intramolecular hydrogen bonds</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>бисимидазолиевые соли</kwd><kwd>молекулярный электростатический потенциал</kwd><kwd>внутримолекулярные водородные связи</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Albrecht M., Miecznikowski J.R., Samuel A., Faller J.W., Crabtree R.H. // Organometallics 2002. Vol. 21 P. 3596. doi 10.1021/om020338x</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Okuyama K., Sugiyama J., Nagahata R., Asai M., Ueda M., Takeuchi K. // J. Mol. Catal. (A). 2003. Vol. 203. N 1-2. 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