Synthesis and polymerization reactions of cyclic imino ethers. 5: naphthalene unit-containing poly(ether amide)s

Poly(ether amide)s containing naphthalene unit were prepared either by the polyaddition reaction of aromatic bis(2-oxazoline)s with the different dihydroxynaphthalenes or by the homopolyaddition of a monomer containing an oxazoline, a hydroxy, and naphthalene moieties. First, polymerization method represents AA?+?BB mode where 1,4-phenylene-2,2'-bis(2-oxazoline) (A) and 1,3-phenylene-2,2'-bis(2-oxazoline) (B) were used as AA monomers and four different dihydroxynaphthalenes 14 were used as BB monomers. In the second case, 2-(6-hydroxynaphthalene-2-yl)-2-oxazoline (5) was used as AB-type monomer in thermally induced polymerizations. The time dependences of polyadditions in bulk as well as in the solution were examined. The reduction of molar mass was observed after the initial fast increase of molar mass. This can be explained by the presence of side and degradation reactions. In both cases, polyadditions resulted in the linear poly(ether amide)s, which were characterized by 1H and 13C NMR spectroscopy. Thermal properties of the prepared polymers were studied by differential scanning calorimetry (DSC) measurements. Comparison of the temperatures of glass transition for polymers prepared in AA?+?BB mode shows the strong dependence of thermal properties on the structure of the polymers. The values were in the range of 136171 degrees C. The glass-transition temperature (Tg) of poly[2-(6-hydroxynaphthalene-2-yl)-2-oxazoline] prepared by AB-type polyaddition is 183 degrees C, which corresponds to the higher contents of hard aromatic segments in the latter type of polymers compared to the polymers prepared in the AA?+?BB-type polyadditions. The described polymers represent novel naphthalene unit-containing poly(ether amide)s for different applications in material science. Copyright (c) 2011 John Wiley & Sons, Ltd.