Electronic Structure and Spectroscopic Properties of Group-7 Tri-Oxo-Halides MO₃X (M = Mn-Bh, X = F-Ts)

The 24 trioxide halide molecules MO₃X of the manganese group (M = Mn-Bh; X = F-Ts), which are iso-valence-electronic with the famous MnO₄ ion, have been quantum-chemically investigated by quasi-relativistic density-functional and ab initio correlated approaches. Geometric and electronic structures, valence and oxidation numbers, vibrational and electronic spectral properties, energetic stabilities of the monomers in the gas phase, and the decay mode of MnO₃F have been investigated. The light Mn-3d species are most strongly electron-correlated, indicating that the concept of a closed-shell Lewis-type single-configurational structure [Mn⁺⁷(d⁰) O^-2(p⁶)₃ F^-(p⁶)] reaches its limits. The concept of real-valued spin orbitals φ(r)·α and φ(r)·β breaks down for the heavy Bh-6d, At-6p and Ts-7p elements because of the dominating spin-orbit coupling. The vigorous decomposition of MnO₃F at ambient conditions starts by the autocatalyzed release of n O₂ and the formation of MnO₃F clusters, triggered by the electron-depleted "oxylic" character of the oxide ligands in MnO₃X.