A preliminary study on polyhydrazides incorporating furan moieties

Solution and interfacial polycondensation of difuranic dihydrazides with aromatic or aliphatic dicarboxylic acid dichlorides led to the corresponding polyhydrazides which were characterized in terms of structure and average chain length. Their conversion to the corresponding polyoxadiazoles was also examined. Model compounds were prepared to facilitate the synthesis and the characterization of the polymers.     

Furan-based Polysemiacylcarbazides by Polyaddition of Bis(furanic hydrazide)s with Diisocyanates

A solution polyaddition procedure was applied to prepare furanic polyacylsemicarbazides based on 2,2′-isopropylidene-bis(5-(2-furoyl) hydrazide) and aliphatic or aromatic diisocyanates. Model compounds were prepared to facilitate the synthesis and the characterization of the polymers. A systematic study of reaction parameters (the nature of the organic phase, the temperature, the reaction time, and the concentration of monomers) was carried out. High MW polymers were obtained after 12 h reaction at 20°C with 0.2 M monomer solutions in dimethylacetamide. In fact, the polyacylsemicarbazides obtained had inherent viscosities ranging from 0.63 to 0.85 dL/g. There showed good solubility in aprotic polar solvents. The ¹H and ¹³C-NMR spectra were consistent with the expected structures. These furan-based polyacylsemicarbazides are thermally stable up to 290°C, but exhibit a complex thermal behavior. This was explained by the cyclohydration of acylsemicarbazide groups into NH-substituted oxadiazoles, resulting in rigid and high melting polymers, less stable, however, than conventional aromatic polyoxadiazoles.