Computational Investigation of the Bonding in [(η5–Cp′)3(η1–Cp′)M]1– (M = Pu, U, Ce)

• Published in: Organometallics 2021-06, Vol.40 (11), p.1577-1587
• Main Authors: Celis-Barros, Cristian, Albrecht-Schönzart, Thomas, Windorff, Cory J
• Format: Article
• Language: English
• Subjects: Chemistry
• ISSN: 0276-7333; 1520-6041
• DOI: 10.1021/acs.organomet.0c00803

Despite the similar ionic radii for Ce3+, U3+, and Pu3+, [(η5–Cp′)3(η1–Cp′)­Ce]1– (Cp′ = C5H4SiMe3, 1-Ce) displays a significantly longer η1–Cp′ distance in the solid state compared to the U3+ and Pu3+ analogues. To better understand this observation, a theoretical investigation was undertaken to examine the differences in bonding between the actinides 1-Pu and 1-U and how they compare with 1-Ce. The results show that although the bonding is largely ionic and dominated by ligand (2p)–metal (6d/5d) interactions, the polarization of 5f orbitals plays a significant role for 1-Pu and 1-U compared to the 4f-orbitals of 1-Ce. The lack of Ce­(4f) interactions is compensated for by increased participation of the Ce­(5d) orbitals relative to the actinide 6d orbitals, particularly for the σ-bound η1–Cp′ ligand. The use of multiple theoretical approaches including topological, localization, and energy decomposition approaches shows that 1-Pu and 1-U are very similar in covalent character compared to 1-Ce, though the composition and energy of the different interactions suggest that 1-U presents the strongest overall interactions.