Abstract
AbstractPhotosensitized reactions of tetrahydrofuran (THF) and dichloromethane (DCM) solutions of polyene sequences introduced into poly(vinyl chloride) molecules by chemical degradation have been investigated. The distribution of polyenes produced following further thermal degradation in DCM were shifted toward longer sequences than were observed for the same reaction in THF. Benzophenone‐sensitized bleaching of the polyene absorption in aerated THF solutions was characterized by induction periods, but the presence of oxygen had little effect on the same reaction in DCM. The bleaching process seems to involve reaction of the polyenes with the tetrahydrofuranyl radical formed by abstraction of the α‐hydrogen from THF by triplet benzophenone. No induction periods were observed for benzoin‐sensitized reactions, but the rate of reaction was faster in DCM than in THF. The differences are discussed in terms of the difference in reactivity of the alkyl and alkoxy radicals.
Published Version
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.
