Imon Mandal, Itai Zakai, Natalia V. Karimova, Mark A. Johnson and R. Benny Gerber*,
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引用次数: 0
Abstract
Reactions of Cl–, Br–, and I– ions in seawater with incoming molecules from the gas phase are of major atmospheric importance, but their mechanisms are mostly unknown. In this study, using ab initio molecular dynamics (AIMD) simulations, the microscopic mechanism of the halogen exchange reaction in water, HOCl + I– → HOI + Cl–, is unraveled. The main findings are as follows: (1) The reaction proceeds through a halogen-bonded isomer of the complex of HOCl with I–, which is present in water and has a significant lifetime. The hydrogen-bonded isomer of the complex seems to play no role in the reaction. (2) Several water molecules act to catalyze the reaction through a Grotthuss-like mechanism that is totally different from that of halogen exchange in the gas phase. These results may have important implications for the chemistry of seawater, in particular for other reactions involving halogenated species.
Halogen exchange between iodide ions and hypochlorous acid molecules in seawater is catalyzed by the medium through the formation and participation of hydroxyl ions.
期刊介绍:
ACS Central Science publishes significant primary reports on research in chemistry and allied fields where chemical approaches are pivotal. As the first fully open-access journal by the American Chemical Society, it covers compelling and important contributions to the broad chemistry and scientific community. "Central science," a term popularized nearly 40 years ago, emphasizes chemistry's central role in connecting physical and life sciences, and fundamental sciences with applied disciplines like medicine and engineering. The journal focuses on exceptional quality articles, addressing advances in fundamental chemistry and interdisciplinary research.