RESUMO
An aliphatic polyester has been prepared from ethylene oxide and maleic anhydride that undergoes reversible transformation between amorphous (Tg =18 °C) and crystalline (Tm =124 °C) states through cis-trans isomerization of the C=C bonds in the polymer backbone without any change in either the molecular weight or dispersity of the polymer. A similar transformation was also observed in chiral unsaturated polyesters formed from enantiopure terminal epoxides, such as epichlorohydrin, phenyl glycidyl ether, and (2,3-epoxypropyl)benzene. These unsaturated polyesters with 100 % E-configuration in the crystalline state were prepared by quantitative isomerization of their Z-configuration analogues in the presence of a catalytic amount of diethylamine, while in the presence of benzophenone, irradiation with 365â nm UV light resulted in the transformation of about 30 % trans-alkene to cis-maleate form, thereby affording amorphous polyesters.
RESUMO
An intensification of the "electrophile-nucleophile" synergistic effect was achieved in a microreactor for the coupling reaction of CO2 and epoxides mediated by the binary Al complex/ternary ammonium salt catalyst system. The microreactor technology is proven to be a powerful tool for the preparation of cyclic carbonates with an improved reaction rate and a wide substrate scope.