Does Reduction-Induced Isomerization of a Uranium(III) Aryl Complex Proceed via C-H Oxidative Addition and Reductive Elimination across the Uranium(II/IV) Redox Couple?

Abstract

Reaction of the uranium(III) bis(amidinate) aryl complex {TerphC(NiPr)2}2U(Terph) (2, where Terph = 4,4″-di-tert-butyl-m-terphenyl-2′-yl) with a strong reductant enabled isolation of isomeric uranium(III) bis(amidinate) aryl product {TerphC(NiPr)2}2U(Terph*) (3, where Terph∗ = 4,4″-di-tert-butyl-m-terphenyl-4′-yl). In terms of connectivity, 3 differs from 2 only in the positions of the U-C and C-H bonds on the central aryl ring of the m-terphenyl-based ligand. A deuterium labeling study ruled out mechanisms for this isomerization involving intermolecular abstraction or deprotonation of the ligand C-H bonds activated during the reaction. Due to the complexity of this rapid, heterogeneous reaction, experimental studies could not further distinguish between two different intramolecular C-H activation mechanisms. However, high-level computational studies were consistent with a mechanism that included two sets of unimolecular, mononuclear C-H oxidative addition and reductive elimination steps involving uranium(II/IV).