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Intermolecular π–π Stacking Interactions Made Visible

[Image: see text] Mixing the liquids hexafluorobenzene (1) and 1,3,5-trimethylbenzene (mesitylene, 2) results in a crystalline solid with a melting point of 34 °C. The solid consists of alternating π–π stacked pillars of both aromatics. This simple experiment can be used to visually demonstrate the...

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Autores principales: Timmer, Brian Jacobus Jozefus, Mooibroek, Tiddo Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and Division of Chemical Education, Inc. 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876799/
https://www.ncbi.nlm.nih.gov/pubmed/33583952
http://dx.doi.org/10.1021/acs.jchemed.0c01252
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author Timmer, Brian Jacobus Jozefus
Mooibroek, Tiddo Jonathan
author_facet Timmer, Brian Jacobus Jozefus
Mooibroek, Tiddo Jonathan
author_sort Timmer, Brian Jacobus Jozefus
collection PubMed
description [Image: see text] Mixing the liquids hexafluorobenzene (1) and 1,3,5-trimethylbenzene (mesitylene, 2) results in a crystalline solid with a melting point of 34 °C. The solid consists of alternating π–π stacked pillars of both aromatics. This simple experiment can be used to visually demonstrate the existence and the effect of noncovalent intermolecular π–π stacking interactions. Both benzene derivatives are relatively benign and widely available, and the experiment can be performed within minutes for less than $15 when done on a 22 mL scale (total volume). The demonstration is very robust, as 1:2 mixtures in volume ratios between 2/3 and 3/2 all give a visually similar result (molar ratios of 1.8–0.8). Substituting 2 with the liquid aromatics o-xylene, p-xylene, and aniline also resulted in the formation of a crystalline solid, while using many other liquid aromatics did not.
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spelling pubmed-78767992021-02-12 Intermolecular π–π Stacking Interactions Made Visible Timmer, Brian Jacobus Jozefus Mooibroek, Tiddo Jonathan J Chem Educ [Image: see text] Mixing the liquids hexafluorobenzene (1) and 1,3,5-trimethylbenzene (mesitylene, 2) results in a crystalline solid with a melting point of 34 °C. The solid consists of alternating π–π stacked pillars of both aromatics. This simple experiment can be used to visually demonstrate the existence and the effect of noncovalent intermolecular π–π stacking interactions. Both benzene derivatives are relatively benign and widely available, and the experiment can be performed within minutes for less than $15 when done on a 22 mL scale (total volume). The demonstration is very robust, as 1:2 mixtures in volume ratios between 2/3 and 3/2 all give a visually similar result (molar ratios of 1.8–0.8). Substituting 2 with the liquid aromatics o-xylene, p-xylene, and aniline also resulted in the formation of a crystalline solid, while using many other liquid aromatics did not. American Chemical Society and Division of Chemical Education, Inc. 2020-12-04 2021-02-09 /pmc/articles/PMC7876799/ /pubmed/33583952 http://dx.doi.org/10.1021/acs.jchemed.0c01252 Text en © 2020 American Chemical Society and Division of Chemical Education, Inc. This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Timmer, Brian Jacobus Jozefus
Mooibroek, Tiddo Jonathan
Intermolecular π–π Stacking Interactions Made Visible
title Intermolecular π–π Stacking Interactions Made Visible
title_full Intermolecular π–π Stacking Interactions Made Visible
title_fullStr Intermolecular π–π Stacking Interactions Made Visible
title_full_unstemmed Intermolecular π–π Stacking Interactions Made Visible
title_short Intermolecular π–π Stacking Interactions Made Visible
title_sort intermolecular π–π stacking interactions made visible
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876799/
https://www.ncbi.nlm.nih.gov/pubmed/33583952
http://dx.doi.org/10.1021/acs.jchemed.0c01252
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