Abstract

In liquids and electrolyte solutions, elementary radical reactions may be investigated on the time scale of molecular motions by femtosecond visible-IR absorption spectroscopy. Some studies devoted to the microscopic understanding of sub-picosecond prehydration electron transfer between an aqueous halide ion (Cl-) and ionic acceptors (Cd++, H+) are presented. Within an electron hydration regime, the one-electron reduction of a metallic ion or a hydrated proton (hydronium or dihydronium ion) is totally achieved in less than 2 × 10-12 s at 294 K. The consequences of an early partition between reactive and nonreactive IR electronic pathways on the electron hydration process are discussed.

Full Text
Paper version not known

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

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.