A quantum chemical investigation of energetic, geometric, mechanistic, and kinetic aspects of multiple proton transfer in cyclic H₂O, H₂S, and H₂O‐H₂S clusters

Multiple proton transfers in cyclic homogenous and mixed H 2 O‐H 2 S clusters from trimers to pentamers have been investigated at an affordable and accurate level of theory. Reaction force and Wiberg bond index analyses showed the process to be nearly synchronous in all the homogenous clusters, while asynchronous in the mixed clusters; always initiated by movement of the SH protons to the H‐bonded O atoms. The barriers for proton transfers exhibited a complex pattern, decreasing initially from the homogeneous H 2 O cluster upon replacement of one H 2 O by an H 2 S moiety and subsequently rising monotonically with each subsequent replacement(s) to becoming highest in pure H 2 S clusters. Finally, the impact of the energetic and mechanistic modulations on the proton transfer kinetics has been studied.