Silicon dumbbells constitute identifiable anionic molecular species in Zintl phases and so-called covalent metals holding units with homopolar bonding inside a metallic framework. Based on electron-precise Ca5Si3 and metallic CaSi3, the chemical bonding in Si2 units is investigated by computational quantum chemical methods considering the dual nature of the wave function. This concerted wave-vector and real space study substantiates that the Si2 dumbbells in Ca5Si3 can be referred to as molecular building units Si26– with additional metallic and ionic contributions in the solid. In the covalent metal CaSi3, however, the bonding within the dumbbells falls short of fulfilling the octet rule. As a result, antibonding states of the Si2 building units are depopulated and attend metallic interactions, simultaneously giving rise to stronger covalent Si–Si bonds.
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Finzel et al. (2024) studied this question.
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