MC6Li6 (M = Li, Na and K): A New Series of Aromatic Superalkalis

TL;DR

This study introduces a new series of aromatic superalkalis, MC6Li6 (M = Li, Na, K), characterized by stability, aromaticity, and low ionization energies, expanding the understanding and potential applications of organic superalkalis.

Contribution

The paper reports the discovery of a new series of aromatic superalkalis, MC6Li6, with detailed stability, aromaticity, and electronic properties analyzed via density functional theory.

Findings

All complexes are planar and stable against dissociation.

Aromaticity increases from M=Li to K, unlike their cations.

Ionization energies suggest they are a new series of aromatic superalkalis.

Abstract

Organic superalkalis are carbon-based species possessing lower ionization energy than alkali atom. In the quest for new organic superalkalis, we study the MC6Li6 (M = Li, Na, and K) complexes and their cations by decorating hexalithiobenzene with an alkali atom using density functional theory. All MC6Li6 complexes are planar and stable against dissociation into M + C6Li6 fragments, irrespective of their charge. These complexes are stabilized by charge transfer from M to C6Li6, although the back-donation of charges tends to destabilize neutral species. Furthermore, their degree of aromaticity increases monotonically from M = Li to K, unlike MC6Li6+ cations, which are not aromatic as suggested by their NICS values. The adiabatic ionization energies of MC6Li6 (3.08-3.22 eV) and vertical electron affinities of MC6Li6+ (3.04-3.15 eV) suggest that MC6Li6 species form a new series of aromatic superalkalis. The variation of the ionization energy of MC6Li6 is found to be in accordance with the NICS values of MC6Li6+. The superalkali nature of MC6Li6 and its relation with NICS values are explained on the basis of the positive charge delocalization. We believe that these species will not only enrich the aromatic superalkalis but also their possible applications will be explored.