A computational investigation of orbital overlap versus energy degeneracy covalency in [UE2]2+ (E = O, S, Se, Te) complexes

Platts, James A. ORCID: https://orcid.org/0000-0002-1008-6595 and Baker, Robert J. 2020. A computational investigation of orbital overlap versus energy degeneracy covalency in [UE2]2+ (E = O, S, Se, Te) complexes. Dalton Transactions 49 (4) 10.1039/C9DT04484A

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Abstract

The extent and nature of covalency in actinide complexes is an important and complex question. There are two main mechanisms of covalency, namely overlap of orbitals or degeneracy of the energies of the ligand and actinide metal, and computational approaches can play a significant part in rationalising the relative importance of each. In this work, we use a suite of computational approaches including Natural Bond Orbitals (NBO), Quantum Theory of Atoms in Molecules (QTAIM) and Interacting Quantum Atoms (IQA) to probe these effects in [EUE]2+ (E = O, S, Se, Te) and [UE2(H2O)5]2+ compounds. All methods indicate increased bond order and reduced charge separation on descending the group. Donation from filled np orbitals on E into formally empty orbitals on U is evident, with 5f and 6d orbitals the most populated. NBO analysis quantifies orbital interactions, finding energy separation is largest for E = O, while for E = Te the atomic orbitals are almost degenerate. However, NBO and IQA data suggests that although overlap is greater for heavier chalcogens, stabilisation due to covalency is greatest for E = O. Thus, for the heavier chalcogens we find that covalency is driven by near-degeneracy of orbitals involved, which does not stabilise the complexes to the same extent as overlap-driven covalency in uranyl. In the hydrated ions the same trends are broadly reproduced, albeit with more stabilisation and a lower HOMO–LUMO gap. The structure and stability of the [OUS]2+ ion is also examined, showing evidence for an inverse trans-influence. Finally bending of the [US2(H2O)5]2+ ion has been examined, suggesting a possible meta-stable cis-form.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Advanced Research Computing @ Cardiff (ARCCA) Chemistry
Publisher:	Royal Society of Chemistry
ISSN:	1477-9226
Date of First Compliant Deposit:	6 January 2020
Date of Acceptance:	16 December 2019
Last Modified:	02 Dec 2024 09:30
URI:	https://orca.cardiff.ac.uk/id/eprint/128238

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