Abstract
The photochemical behaviour of benzophenoneimine and fluorenoneimine in several solvents on irradiation in the 200 – 300 (400) nm range was studied. Reduction to hydrocarbons diphenylmethane and fluorene was consistently observed, although to varying extents, with corresponding oxidation of the reactive solvents to dimers. Variable amounts of nitrogenous compounds were observed in addition to radical coupling and dimerization products. A certain amount of polymeric material accompanied all the photolyses. The product study was also extended to the photolysis in methanol of the benzophenoneimine and fluorenoneimine hydrochlorides.
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 callMore From: Journal of Photochemistry & Photobiology, A: Chemistry
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.
