Interaction Between the Rubidium Cation and [2.2.2]Paracyclophane: Experimental and Theoretical Study

Authors

  • Emanuel Makrlík Faculty of Environmental Sciences, Czech University of Life Sciences, Prague, Kamýcká 129, 165 21 Prague 6 - Suchdol, Czech Republic
  • Stanislav Böhm University of Chemistry and Technology, Prague, Technická 5, 166 28 Prague 6, Czech Republic
  • David Sýkora University of Chemistry and Technology, Prague, Technická 5, 166 28 Prague 6, Czech Republic
  • Magdalena Kvíčalová Faculty of Environmental Sciences, Czech University of Life Sciences, Kamýcká 129, 165 21 Prague 6 - Suchdol, Czech Republic
  • Petr Vaňura University of Chemistry and Technology, Prague, Technická 5, 166 28 Prague 6, Czech Republic

DOI:

https://doi.org/10.17344/acsi.2017.3655

Keywords:

[2.2.2]Paracyclophane, Rubidium cation, Cation–π interaction, DFT calculations, Structures

Abstract

By means of electrospray ionization mass spectrometry (ESI-MS), it was evidenced experimentally that the rubidium cation (Rb+) reacts with the electroneutral [2.2.2]paracyclophane ligand (C24H24) to form the cationic complex [Rb(C24H24)]+. Moreover, applying quantum chemical calculations, the most probable conformation of the proven [Rb(C24H24)]+ complex was solved. In the complex [Rb(C24H24)]+ having a symmetry very close to C3, the “central” cation Rb+, fully located in the cavity of the parent [2.2.2]paracyclophane ligand, is coordinated to all three benzene rings of [2.2.2]paracyclophane via cation-π interaction. Finally, the binding energy, E(int), of the considered cation-π complex [Rb(C24H24)]+ was evaluated as –99.3 kJ/mol, confirming the formation of this fascinating complex species as well. This means that the [2.2.2]paracyclophane ligand can be considered as a receptor for the rubidium cation in the gas phase.

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Published

19.06.2018

Issue

Section

Physical chemistry