Mechanistic Insights into Chloric Acid Production by Hydrolysis of Chlorine Trioxide at an Air–Water Interface

• Published in: Journal of the American Chemical Society Vol. 146; no. 30; pp. 21052 - 21060
• Main Authors: Fang, Ye-Guang, Wei, Laiyang, Francisco, Joseph S., Zhu, Chongqin, Fang, Wei-Hai
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 31.07.2024
• Subjects: Arctic region; chlorine; Gibbs free energy; hydrolysis; liquid-air interface; molecular dynamics; oxidation; ozone depletion; perchloric acid; quantum mechanics; solvation; Arctic region
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.4c06269

Chlorine oxides play crucial roles in ozone depletion, and the final oxidation steps of chlorine oxide potentially result in the formation of chloric acid (HClO3) or perchloric acid (HClO4). Herein, the solvation and reactive uptake of three stable isomers of chlorine trioxide (Cl2O3), namely, ClOCl­(O)­O, ClClO3, and ClOOOCl, at the air–water interface were investigated using classical and hybrid quantum mechanics/molecular mechanics (QM/MM) molecular dynamics (MD) coupled with advanced free energy methods. Two distinct mechanisms were revealed for the hydrolysis of ClOCl­(O)O and ClClO3: molecular and ionic mechanisms. A comparison of the computed free-energy profiles for the gaseous and air–water interfacial systems indicated that the air–water interface could markedly lower the free-energy barrier for ClO 3 − or HClO3 formation while stabilizing the product state. In particular, the hydrolysis of ClClO3 at the air–water interface was barrierless. In contrast, our calculations showed that the hydrolysis of ClOOOCl was very slow, indicating that ClOOOCl was inert to water at the air–water interface. This study provides theoretical evidence for the hypothesis that HClO3 is a sink for chlorine oxides and for the widespread distributions of HClO3 recently observed in the Arctic region.