Abstract
A μ-η(1):η(1)-N(2)-bridged Mo dimer, {(η(5)-C(5)Me(5))[N(Et)C(Ph)N(Et)]Mo}(2)(μ-N(2)), cleaves dinitrogen thermally resulting in a crystallographically characterized bis-μ-N-bridged dimer, {(η(5)-C(5)Me(5))[N(Et)C(Ph)N(Et)]Mo}(2)(μ-N)(2). A structurally related Mo dimer with a bulkier amidinate ligand, ([N((i)Pr)C(Me)N((i)Pr)]), is only capable of photochemical dinitrogen activation. These opposing reactivities were rationalized as steric switching between the thermally and photochemically active species. A computational analysis of the geometric and electronic structures of intermediates along the isomerization pathway from Mo(2)(μ-η(1):η(1)-N(2)) to Mo(2)(μ-η(2):η(1)-N(2)) and Mo(2)(μ-η(2):η(2)-N(2)), and finally Mo(2)(μ-N)(2), is presented here. The extent to which dispersion affects the thermodynamics of the isomers is evaluated, and it is found that dispersion interactions play a significant role in stabilizing the product and making the reaction exergonic. The concept of steric switching is further explored with theoretical models with sterically even less demanding ligands, indicating that systematic ligand modifications could be used to rationally design the N(2) activation energy landscape. An analysis of electronic excitations in the computed UV-vis spectra of the two complexes shows that a particular type of asymmetric excitations is only present in the photoactive complex.