LAUSR

Abstract Two kinds of pyrogallol-based di-benzoxazines (PG-FA and PG-A) with a free phenolic hydroxyl between two oxazine rings attaching to the same benzene were synthesized. The chemical structures of PG-FA and PG-A were identified by 1H NMR, 13C NMR and FTIR tests. The ring-opening polymerization (ROP) behavior of PG-FA and PG-A was monitored by DSC, TGA, FTIR and in situ FTIR measurements. The pyrogallol-containing benzoxazines showed latent catalytic activity as they reached melting condition. The inter- and intramolecular hydrogen bonds from the phenolic hydroxyl and oxygen or nitrogen were converted into weak OH⋯π intramolecular hydrogen bonding, which easily released the free phenolic hydroxyl. Then, the free hydroxyl could accelerate the breakage of oxazine ring. The para-position of free phenolic hydroxyl in pygarollol-based benzoxazines was preferentially polymerized with the carbocations. The temperature-dependent evolution of the chemical structure of PG-FA and PG-A on ROP was consistent with the change of hydrogen bonds.