摘要
A series of cis-5-norbornene-endo-2,3-dicarboxylic anhydride （NDCA, M1） derivatives （M2-M4） with different types of nonpolar substituted groups were synthesized and characterized by 1H/13C-NMR and mass spectrometry （MS）. Ring- opening metathesis polymerization （ROMP） of these monomers using the Grubbs third generation catalyst （G3） generated high molecular weight polymers with much improved solubility compared with the NDCA＇s homopolymer. It was found that the solubility of these polymers increased with increased substituent＇s steric hindrance. The living polymerization of NDCA derivative containing the bulkiest substituent （M4） catalyzed by G3 in tetrahydrofuran was confirmed by the kinetic studies with low polydispersity indices （PDI） （〈 1.30）. By using sequential ROMP, well-defined diblock copolymers containing anhydride groups were synthesized.
A series of cis-5-norbornene-endo-2,3-dicarboxylic anhydride （NDCA, M1） derivatives （M2-M4） with different types of nonpolar substituted groups were synthesized and characterized by 1H/13C-NMR and mass spectrometry （MS）. Ring- opening metathesis polymerization （ROMP） of these monomers using the Grubbs third generation catalyst （G3） generated high molecular weight polymers with much improved solubility compared with the NDCA＇s homopolymer. It was found that the solubility of these polymers increased with increased substituent＇s steric hindrance. The living polymerization of NDCA derivative containing the bulkiest substituent （M4） catalyzed by G3 in tetrahydrofuran was confirmed by the kinetic studies with low polydispersity indices （PDI） （〈 1.30）. By using sequential ROMP, well-defined diblock copolymers containing anhydride groups were synthesized.
基金
financially supported by the National Natural Science Foundation of China(Nos.21234006 and 21574098)
