Stacking Interactions: A Supramolecular Approach to Upgrade Weak Halogen Bond Donors / S. V. Baykov, D. M. Ivanov, S. O. Kasatkina [et al.]

Уровень набора: Chemistry - A European JournalАльтернативный автор-лицо: Baykov, S. V., chemist, Researcher at Tomsk Polytechnic University, Candidate of Chemical Sciences, 1987-, Sergey Valentinovich;Ivanov, D. M., Chemist, Senior researcher of Tomsk Polytechnic University, Candidate of chemical sciences, 1992-, Daniil Mikhaylovich;Kasatkina, S. O., Svetlana Olegovna;Galmes, B., Bartomeu;Frontera, A., Antonio;Resnati, D. P., Chemist, The Head of the Laboratory of Tomsk Polytechnic University, PhD, 1955-, Dzhuzeppe Paolo;Kukushkin, A. Yu., Vadim YurjevichКоллективный автор (вторичный): Национальный исследовательский Томский политехнический университет, Исследовательская школа химических и биомедицинских технологий (ИШХБМТ), (2017- )Язык: английский.Резюме или реферат: The co-crystallization of tetracyanobenzene (TCB) with haloarenes ArX provided six new co-crystals TCB ⋅ ArX (ArX=PhCl, PhBr, 4-MeC6H4Cl, 4-MeC6H4Br, 4-MeOC6H4Cl, 1,2-Br2C6H4) which were studied by X-ray diffraction. In these systems, the strong collective effect of π⋅⋅⋅π stacking interactions and lone pair-(X)⋅⋅⋅π-hole-(C) bondings between TCB and ArX promote the strength of X⋅⋅⋅Ncyano halogen bonding (HaB). Theoretical studies showed that the stacking interactions affect the σ-hole depth of the haloarenes, thus significantly boosting their ability to function as HaB donors. According to the molecular electrostatic potential calculations, the σ- hole-(Cl) value (1.5 kcal/mol) in the haloarene 4-MeOC6H4Cl (featuring an electron-rich arene moiety and exhibiting very poor σ-hole-(Cl) ability) increases significantly in the stacked trimer (TCB)2 ⋅ 4-MeOC6H4Cl (12.5 kcal/mol). Theoretical DFT calculations demonstrate the dramatic increase of X⋅⋅⋅Ncyano HaB strength for stacked trimers in comparison with parent unstacked haloarenes..Примечания о наличии в документе библиографии/указателя: [References: 88 tit.].Аудитория: .Тематика: труды учёных ТПУ | электронный ресурс | crystal engineering | DFT calculations | halogen bonding | noncovalent interactions | staking | кристаллотехника | галогенные связи | нековалентные взаимодействия Ресурсы он-лайн:Щелкните здесь для доступа в онлайн
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[References: 88 tit.]

The co-crystallization of tetracyanobenzene (TCB) with haloarenes ArX provided six new co-crystals TCB ⋅ ArX (ArX=PhCl, PhBr, 4-MeC6H4Cl, 4-MeC6H4Br, 4-MeOC6H4Cl, 1,2-Br2C6H4) which were studied by X-ray diffraction. In these systems, the strong collective effect of π⋅⋅⋅π stacking interactions and lone pair-(X)⋅⋅⋅π-hole-(C) bondings between TCB and ArX promote the strength of X⋅⋅⋅Ncyano halogen bonding (HaB). Theoretical studies showed that the stacking interactions affect the σ-hole depth of the haloarenes, thus significantly boosting their ability to function as HaB donors. According to the molecular electrostatic potential calculations, the σ- hole-(Cl) value (1.5 kcal/mol) in the haloarene 4-MeOC6H4Cl (featuring an electron-rich arene moiety and exhibiting very poor σ-hole-(Cl) ability) increases significantly in the stacked trimer (TCB)2 ⋅ 4-MeOC6H4Cl (12.5 kcal/mol). Theoretical DFT calculations demonstrate the dramatic increase of X⋅⋅⋅Ncyano HaB strength for stacked trimers in comparison with parent unstacked haloarenes.

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