Issue 17, 2016

The making of ring currents

Abstract

Benzene, planar cyclooctatetraene, and borazine have been taken into account as archetypal aromatic, anti-aromatic, and non-aromatic systems. Then, the making of the π-electron diatropic ring current of benzene, huge paratropic ring current of planar cyclooctatetraene, and weak diatropic ring current of borazine, has been monitored by means of DFT calculations of current density maps and bond current strengths along a concerted, highly symmetric reaction pathway for the trimerization and tetramerization of acetylene to benzene and planar cyclooctatetraene and the trimerization of the simplest iminoborane (BH2N) to borazine. Besides, a simple model is presented that permits to infer the presence of a ring current only on account of the sum of homotropic local vortices. The model works satisfactorily for borazine and surely as well for benzene with a substantial difference. On the one hand, for borazine, the evolution of the current density along the formation reaction can be recast summing three virtually unchanged diatropic current loops with respect to parent iminoborane molecules. On the other hand, the benzene ring current is an emerging property that can be re-elaborated as the sum of three diatropic current loops of increased diatropicity with respect to parent acetylene molecules, i.e., the radius of the maximum current increases form 0.76 to 0.97 Å and the current strength increases from 3.6 to 6.7 nA T−1. In these terms, the difference between the aromatic benzene and non-aromatic borazine can be understood as the attitude of the acetylene molecules to form always wider and stronger current loops as they get closer, a behavior not shared by the iminoborane molecules. For planar cyclooctatetraene, the paratropic circulation arising from the HOMO–LUMO transition makes the model inapplicable, since the initial hypothesis of homotropic circulations over the reaction coordinate is violated. In a sense, the fact that the model works only for a bit of the planar cyclooctatetraene formation reaction is itself distinctive of the anti-aromatic magnetic response.

Graphical abstract: The making of ring currents

Supplementary files

Article information

Article type
Paper
Submitted
24 11 2015
Accepted
05 1 2016
First published
11 1 2016

Phys. Chem. Chem. Phys., 2016,18, 11800-11812

Author version available

The making of ring currents

G. Monaco and R. Zanasi, Phys. Chem. Chem. Phys., 2016, 18, 11800 DOI: 10.1039/C5CP07250F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements