American Chemical Society
jp404951e_si_001.pdf (181.99 kB)

Methane C–H Bond Activation by “Naked” Alkali Metal Imidyl and Alkaline Earth Metal Imide Complexes. The Role of Ligand Spin and Nucleophilicity

Download (181.99 kB)
journal contribution
posted on 2013-09-26, 00:00 authored by Bruce M. Prince, Thomas R. Cundari
High accuracy correlation consistent Composite Approach (ccCA) calculations have been used to investigate methane C–H bond activation with alkali metal imidyl and alkaline earth metal imide complexes. Alkali metals (Li, Na) and alkaline earth metals (Be, Mg) are used in this research given their redox innocence, namely, M+ and M2+, respectively. The ccCA calculations for methane activation by imidyl radical NH•– and triplet nitrene NH•• show a thermodynamic (ΔΔH = 13.2 kcal/mol) and kinetic (ΔΔH = 15.9 kcal/mol) preference for the former. Methane activation by LiNH and MgNH proceeds via hydrogen atom abstraction (HAA) and [2 + 2] transition states; only HAA pathways are isolated for NaNH and BeNH. The ccCA computed enthalpies lead to the hypothesis that the nucleophilicity of the nitrogen of the activating ligand (NR) is the key ingredient in activating the strongest sp3 C–H bonds like that of methane.