Abstract
AbstractThe preparation and polymerization of representative 1‐(perfluoroacyl)aziridines were examined. Polymerization of the aziridines was induced by heat, by certain inorganic nucleophiles such as cyanide, fluoride, and chloride, and by organic bases. Certain other inorganic nucleophilic reagents such as KI and KBr effected the rearrangement of the 1‐(perfluoroacyl)aziridines to the isomeric 2‐perfluoroalkyl‐2‐oxazolines. A possible reaction mechanism involving anionic polymerization in competition with oxazoline formation was discussed.
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.
