文摘
A series of sulfur-containing hyperbranched polymeric photoinitiators end-capped with benzophenone (BP) and tertiary amine moieties (B/A-HPIs) were synthesized via the simultaneous double thiol-ene click reactions of thiolated hyperbranched polymer with both dimethylaminoethyl acrylate and 3-(4-benzoylphenoxy)propyl acrylate. The molecular structures were characterized by 1H NMR and FT-IR spectroscopy. From the UV¨Cvis spectra, B/A-HPIs showed the stronger n-¦Ð* absorption at ?40 nm with a higher molar extinction coefficients of 371 L mol? cm? than 148 L mol? cm? of BP, and an obvious red shift of ¦Ð¨C¦Ð* absorption from ?50 nm of BP to ?80 nm. According to the photo-DSC study, the photopolymerization rate of 1,6-hexanediol diacrylate initiated by 5 wt % B/A-HPI was twice higher than that by BP. The DMTA results showed the good miscibility of B/A-HPIs with acrylate resins and high crosslinking density of cured films.