Nitrogen Reduction by Multimetallic trans-Uranium Actinide Complexes: A Theoretical Comparison of Np and Pu to U

Dipak Panthi; Olajumoke Adeyiga; Naveen K Dandu; Samuel O Odoh

doi:10.1021/acs.inorgchem.9b00129

Nitrogen Reduction by Multimetallic trans-Uranium Actinide Complexes: A Theoretical Comparison of Np and Pu to U

Inorg Chem. 2019 May 20;58(10):6731-6741. doi: 10.1021/acs.inorgchem.9b00129. Epub 2019 May 3.

Authors

Dipak Panthi¹, Olajumoke Adeyiga¹, Naveen K Dandu¹, Samuel O Odoh¹

Affiliation

¹ Department of Chemistry , University of Nevada Reno , 1664 North Virginia Street , Reno , Nevada 89557-0216 , United States.

PMID: 31050297
DOI: 10.1021/acs.inorgchem.9b00129

Abstract

There is recent interest in organometallic complexes of the trans-uranium elements. However, preparation and characterization of such complexes are hampered by radioactivity and chemotoxicity issues as well as the air-sensitive and poorly understood behavior of existing compounds. As such, there are no examples of small-molecule activation via redox reactivity of organometallic trans-uranium complexes. This contrasts with the situation for uranium. Indeed, a multimetallic uranium(III) nitride complex was recently synthesized, characterized, and shown to be able to capture and functionalize molecular nitrogen (N₂) through a four-electron reduction process, N₂ → N₂^4-. The bis-uranium nitride, U-N-U core of this complex is held in a potassium siloxide framework. Importantly, the N₂^4- product could be further functionalized to yield ammonia (NH₃) and other desirable species. Using the U-N-U potassium siloxide complex, K₃U-N-U, and its cesium analogue, Cs₃U-N-U, as starting points, we use scalar-relativistic and spin-orbit coupled density functional theory calculations to shed light on the energetics and mechanism for N₂ capture and functionalization. The N₂ → N₂^4- reactivity depends on the redox potentials of the U(III) centers and crucially on the stability of the starting complex with respect to decomposition into the mixed oxidation U(IV)/U(III) K₂U-N-U or Cs₂U-N-U species. For the trans-uranium, Np and Pu analogues of K₃U-N-U, the N₂ → N₂^4- process is endoergic and would not occur. Interestingly, modification of the Np-O and Pu-O bonds between the actinide cores and the coordinated siloxide framework to Np-NH, Pu-NH, Np-CH₂, and Pu-CH₂ bonds drastically improves the reaction free energies. The Np-NH species are stable and can reductively capture and reduce N₂ to N₂^4-. This is supported by analysis of the spin densities, molecular structure, long-range dispersion effects, as well as spin-orbit coupling effects. These findings chart a path for achieving small-molecule activation with organometallic neptunium analogues of existing uranium complexes.