Oligophenol-based poly(azomethine-urethane)s (PAMUs) were newly synthesized in two steps. At the first step, the prepolymers including the phenol and oligophenol based-Schiff bases were prepared by a condensation reaction of o-dianisidine with 4-hydroxybenzaldehyde/3-ethoxy-4-hydroxybenzaldehyde, and the polycondensation reactions of the corresponding Schiff bases in an aqueous alkaline media. At the second step, the PAMUs were obtained by copolymerization of the prepolymers with toluene-2,4-diisocyanate (TDI) under an argon atmosphere. The structures of the obtained compounds were confirmed by FTIR, UV-vis, H-1 NMR, and C-13 NMR, and size exclusion chromatography (SEC) techniques. The synthesized compounds were also characterized by TG-DTA and DSC analyses. Thermal decomposition steps at various temperatures were clarified by FTIR analyses of the degraded products. The physical changes to the synthesized PAMUs after exposing them to the thermal degradation steps are displayed.
Oligophenol-based poly(azomethine-urethane)s (PAMUs) were newly synthesized in two steps. At the first step, the prepolymers including the phenol and oligophenol based-Schiff bases were prepared by a condensation reaction of o-dianisidine with 4-hydroxybenzaldehyde/3-ethoxy-4-hydroxybenzaldehyde, and the polycondensation reactions of the corresponding Schiff bases in an aqueous alkaline media. At the second step, the PAMUs were obtained by copolymerization of the prepolymers with toluene-2,4-diisocyanate (TDI) under an argon atmosphere. The structures of the obtained compounds were confirmed by FTIR, UV-vis, 1H NMR, and 13C NMR, and size exclusion chromatography (SEC) techniques. The synthesized compounds were also characterized by TG-DTA and DSC analyses. Thermal decomposition steps at various temperatures were clarified by FTIR analyses of the degraded products. The physical changes to the synthesized PAMUs after exposing them to the thermal degradation steps are displayed.
