Abstract
A series of main chain degradable polyimides 6 were prepared by the polyaddition of acetalcontaining diamine monomer 4 with various aromatic tetracarboxylic anhydrides 5, followed by chemical imidization without isolating. The structures of polyimides obtained were confirmed by infrared, 1H nuclear magnetic resonance (NMR) and 13C NMR spectroscopy. Their thermal stability, solubility and transparency have also been investigated. Furthermore, the acid-catalyzed degradation reactions of model compound 7 and polyimide 6d have been studied. These results suggest that polyimides 6 can be recognized as photosensitive polyimides.
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.
