• Shi, Ming W.
• Mebs, Stefan
• Beckmann, Jens
• Chen, Yu Sheng
• Luger, Peter
• Grabowsky, Simon
• Hesse, Malte
• Malaspina, Lorraine A.
• Wiecko, Michal
• Pal, Rumpa
• Krzeszczakowska, Joanna M.

Abstract

<p>In the family of metallocenes, MgCp∗₂ (Cp∗ = pentamethylcyclopentadienyl) exhibits a regular linear sandwich structure, whereas CaCp∗₂ is bent in both the gas phase and solid state. Bending is typically observed for metal ions which possess a lone pair. Here, we investigate which electronic differences cause the bending in complexes lacking lone pairs at the metal atoms. The bent gas-phase geometry of CaCp∗₂ suggests that the bending must have an intramolecular origin. Geometry optimizations with and without dispersion effects/d-type polarization functions on MCp₂ and MCp∗₂ gas-phase complexes (M = Ca, Mg) establish that attractive methyl⋯methyl London dispersion interactions play a decisive role in the bending in CaCp∗₂. A sufficient polarizability of the metal to produce a shallow bending potential energy curve is a prerequisite but is not the reason for the bending. Concomitant ligand-induced charge concentrations and localizations at the metal atoms are studied in further detail, for which real-space bonding and orbital-based descriptors are used. Low-temperature crystal structures of MgCp∗₂ and CaCp∗₂ were determined which facilitated the identification and characterization of intermolecular pseudo-pregostic interactions, C-H⋯Ca, in the CaCp∗₂ crystal structure.</p>

Topics

• impedance spectroscopy
• dispersion
• gas phase