Coumarin- and Carboxyl-Functionalized Supramolecular Polybenzoxazines Form Miscible Blends with Polyvinylpyrrolidone

In this study, we synthesized a novel multifunctional benzoxazine monomer (Coumarin-COOH BZ), possessing both coumarin and COOH groups, through the reaction of 4-methyl-7-hydroxycoumarin, 4-aminobenzoic acid, and paraformaldehyde in 1,4-dioxane, with the structure confirmed using ¹H and ¹³C nuclear magnetic resonance and Fourier transform infrared (FTIR) spectroscopy. Differential scanning calorimetry (DSC), FTIR spectroscopy, and thermogravimetric analysis were then employed to monitor the thermal curing behavior of Coumarin-COOH BZ and its blends with poly(N-vinyl-2-pyrrolidone) (PVP), both before and after photodimerization of the coumarin moieties. DSC revealed a single glass transition temperature for each Coumarin-COOH BZ/PVP blend composition; a large positive deviation based on the Kwei equation suggested that strong hydrogen bonding existed between the Coumarin-COOH BZ and PVP segments, confirmed through FTIR spectroscopic analyses. The thermal properties improved (i.e., increased glass transition and thermal degradation temperatures) as a result of the increased crosslinking density after photodimerization under UV exposure.