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Mechanistic Insights into the Proton Transfer and Substitution Dynamics of N-Atom Center Reactions: A Study of CH 3 O - with NH 2 Cl.
Journal of Physical Chemistry. A 2024 March 20
Bimolecular substitution reactions involving N as the central atom have continuously improved our understanding of substitution dynamics. This work used chemical dynamics simulations to investigate the dynamics of NH2 Cl with N as the central atom and the multiatomic nucleophile CH3 O- and compared these results with the F- + NH2 Cl reaction. The most noteworthy difference is in the competition between proton transfer (PT) and the SN 2 pathways. Our results demonstrate that, for the CH3 O- + NH2 Cl system, the PT pathway is considerably more favorable than the SN 2 pathway. In contrast, no PT pathway was observed for the F- + NH2 Cl system at room temperature. This can be attributed to the exothermic reaction of the PT pathway for the CH3 O- + NH2 Cl reaction and is coupled with a more stable transition state compared to the substitution pathway. Furthermore, the bulky nature of the CH3 O- group impedes its participation in SN 2 reactions, which enhances both the thermodynamic and the dynamic advantages of the PT reaction. Interestingly, the atomic mechanism reveals that the PT pathway is primarily governed by indirect mechanisms, similar to the SN 2 pathway, with trajectories commonly trapped in the entrance channel being a prominent feature. These trajectories are often accompanied by prolonged and frequent proton exchange or proton abstraction processes. This current work provides insights into the dynamics of N-centered PT reactions, which are useful in gaining a comprehensive understanding of the dynamics behavior of similar reactions.
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