The Fate of a Zwitterion in Water from <i>ab Initio</i> Molecular Dynamics: Monoethanolamine (MEA)-CO₂

Understanding the fundamental reactions accompanying the capture of carbon dioxide in amine solutions is critical for the design of high-performance solvents and requires an accurate modeling of the solute–solvent interaction. As a first step toward this goal, using <i>ab initio</i> molecular dynamics (Car–Parrinello) simulations, we investigate a zwitterionic carbamate, a species long proposed as intermediate in the formation of a stable carbamate, in a dilute aqueous solution. CO₂ release and deprotonation are competitive routes for its dissociation and are both characterized by free-energy barriers of 6–8 kcal/mol. Water molecules play a crucial role in both pathways, resulting in large entropic effects. This is especially true in the case of CO₂ release, which is accompanied by a strong reorganization of the solvent beyond the first coordination shell, leading to the formation of a water cage entrapping the solute (hydrophobic effect). Our results contrast with the assumptions of implicit solvent models