Abstract
Photodissociation provides an ideal proving ground for an in‐depth understanding of the microscopic mechanism and dynamics of bond breaking processes at a state‐to‐state level. After a brief outline of the requisite theory, we review the latest developments on the state‐to‐state photodissociation dynamics of the water molecule via the lowest two excited states, focusing on the absorption spectrum and product state distributions. A detailed discussion is given on the competition between different adiabatic and nonadiabatic pathways of the dissociation. Quantum mechanical studies of this prototypical system on accurate coupled potential energy surfaces not only offer an interpretation of the existing experimental results but also provide a clear and comprehensive dynamical picture of water photodissociation. WIREs Comput Mol Sci 2018, 8:e1350. doi: 10.1002/wcms.1350This article is categorized under: Theoretical and Physical Chemistry > Reaction Dynamics and Kinetics
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
