Abstract

AbstractThe UV photodissociation of ethyl nitrite at excitation wavelenghts of 350, 248 and 193 nm was studied by photofragment translational spectroscopy in a pulsed molecular beam. At all three wavelengths the first dissociation step yields nitric oxide and ethoxy radicals, accompanied by a considerable release of translational energy. At 350 nm the ethoxy radicals are formed with internal energy low enough to be stable under collisionless conditions. At 248 and 193 nm significant fractions of the ethoxy radicals emerge with sufficient internal energy to decay spontaneously into formaldehyde and methyl radicals. At 248 nm a kinematic analysis of the photofragment arrival time distributions is consistent with a sequential dissociation mechanism.

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.