Bonding in a crystalline tri-thorium cluster. Not σ-aromatic but still unique

Very recently, Boronski et al. reported the first thorium-thorium bond in a crystalline cluster prepared under normal experimental conditions. By using a range of experimental techniques and computational models, the authors found that the isolated actinide cluster contains at its heart two paired electrons delocalized over the tri-thorium ring. The recorded Raman spectrum allegedly confirmed the existence of a σ-aromatic three-center two-electron bond. In the following we demonstrate that the experimentally observed broad inelastic scattering bands between 60 and 135 cm${}^{-1}$, originally assigned by the authors to thorium-thorium vibrations, represent the combination of Th-Cl stretching and Th-Cl-Th bending modes, and they establish the existence of an unprecedented multicenter charge-shift bonding (ThCl${}_2$)${}_3$ rather than the σ-aromatic bonding Th${}_3$. In the light of the presented findings, the latter remains experimentally unproven and computationally questionable. (© 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH)