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Density functional theory study of π-aromatic interaction of benzene, phenol, catechol, dopamine isolated dimers and adsorbed on graphene surface

  • Elizane  E. de MoraesEmail author
  • Mariana Z. Tonel
  • Solange B. Fagan
  • Marcia C. Barbosa
Original Paper
  • 34 Downloads

Abstract

We analyze the influence of different groups on the intermolecular energy of aromatic homodimers and on the interaction between a single aromatic molecule and a graphene surface. The analysis is performed for benzene, phenol, catechol, and dopamine. For calculating the energies, we employ density functional theory within the local density approximation (LDA-DFT). Our results show that the lowest intermolecular energies between the aromatic molecules are related to the T-shaped configurations. This lower energy results from the quadrupole interaction. In the case of the interaction between the graphene sheet and the aromatic molecules, the lowest energy configuration is the face to face. The adsorption energy of a molecule on a graphene surface involves ππ interactions that explain the face to face arrangement. These results provide insight into the manner by which substituents can be utilized in crystal engineering, supramolecular chemistry, bioinspired materials, formation of various molecular clusters, parameterization of force fields suitable for classical simulations, and design of novel sensing, drug delivery, and filters based on graphene.

Keywords

Graphene Aromatic homodimers Density functional theory Parameterization of force fields suitable for classical simulations 

Notes

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© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Instituto de FísicaUniversidade Federal do Rio Grande do SulPorto AlegreBrazil
  2. 2.Universidade FranciscanaSanta MariaBrazil

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