Issue 45, 2015

Multi-center covalency: revisiting the nature of anion–π interactions

Abstract

Exploring the nature of anion–π bonding by means of the Quantum Theory of Atoms in Molecules (QTAIM) and an energy decomposition scheme on the basis of Interacting Quantum Atoms (IQA) theory led us to conclude that these non-classical interactions benefit from “multi-center covalency” far more than from the electrostatics. Comparing anion–π systems to closely related covalent anion–σ complexes reveals that the anion–π systems benefit from an extensive degree of electron sharing between the anions and all atoms of the π-rings. Besides, decomposition of the binding energy into classical (electrostatics) and non-classical (exchange–correlation) components demonstrates that in contrast to previous reports, the anion–π complexes are local minima, if and only if the non-classical contribution to binding energy surpasses that of the electrostatics. This suggests that the stable anion–π complexes with the anions atop the π-rings might be prepared with π-systems that benefit more from the exchange–correlation term, such as extended π-systems, but not with strong electrostatic π-receptors. This conclusion is in line with the tendency of strong π-acids to form the σ-complexes with more covalent character instead of the π-complexes.

Graphical abstract: Multi-center covalency: revisiting the nature of anion–π interactions

Supplementary files

Article information

Article type
Paper
Submitted
26 Sep 2015
Accepted
26 Oct 2015
First published
26 Oct 2015

Phys. Chem. Chem. Phys., 2015,17, 30670-30679

Author version available

Multi-center covalency: revisiting the nature of anion–π interactions

C. Foroutan-Nejad, Z. Badri and R. Marek, Phys. Chem. Chem. Phys., 2015, 17, 30670 DOI: 10.1039/C5CP05777A

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