Abstract
the photodissociation of oxalyl chloride anti 2,3-butanedione at 193nm and 248nm have been studied by time-resolved ftir emission spectroscopy, the ir fluorescence emission was observed and the rotational and vibrational populations ai the co product were obtained. it is suggested that the photolysis mechanism is two rco radicals formed via a fission of c-c bond, followed by a decomposition of the rco intermediate to vibrationally excited co(v) and r radical.
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 callDisclaimer: 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.
