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借助活性开环聚合反应和紫外光辐照下的分子内交联反应合成新型功能性环状聚(ε-己内酯-co-α-氯代-ε-己内酯)(cP(εCLcoαClεCL)).首先,利用Baeyer-Villiger氧化法将α-氯代环己酮在间氯过氧苯甲酸(mCPBA)的作用下制得功能性单体α-氯代-ε-己内酯(αClεCL).然后,功能性单体αClεCL和ε-己内酯(εCL)在环状引发剂2,2-二丁基-2-锡-1,3-二氧环庚烷(DSDOP)的作用下,进行活性开环聚合反应获得活性环状无规共聚酯(LCP(εCLcoαClεCL))前体,该前体的分子量可以通过改变单体与引发剂的摩尔配比来控制.当单体完全转化后,该活性环状前体再引发反应性单体α-(1-丙烯酰氧乙基)-ε-己内酯(αAEεCL)进行嵌段聚合反应,合成了在活性中心附近带有不饱和双键的功能性环状共聚酯,即活性环状聚(ε-己内酯-co-α-氯代-ε-己内酯)-b-(α-(1-丙烯酰氧乙基)-ε-己内酯).最后该活性环状共聚酯在紫外光辐照下,反应性单体单元中的双键发生分子内交联反应,制得稳定的不含有机锡的新型功能性环状无规共聚酯cP-(εCLcoαClεCL)(M n,NMR=32400).采用SEC,NMR以及DSC等技术对聚合物的结构和性能进行表征,SEC和黏度表征结果显示新型功能性cP(εCLcoαClεCL)与分子量相同的线型共聚酯相比具有较小的动态力学体积,DSC表征结果显示共聚酯环化的结果使其熔点和结晶度下降.该方法的突出特点是能够高效地合成具有高分子量的环状聚合物.
A new type of functional cyclic poly (ε-caprolactone-co-α-chloro-ε-caprolactone) (cP (εCLcoαClεCL) was synthesized by intramolecular crosslinking reaction of living ring-opening polymerization and UV irradiation. ) First, functional α-chloro-ε-caprolactone (αClεCL) was prepared by Baeyer-Villiger oxidation using m-chloroperoxybenzoic acid Then, the functional monomers αClεCL and ε-caprolactone (εCL) under the action of cyclic initiator 2,2-dibutyl-2-tin-1,3-dioxetane (DSDOP) The active ring random copolyester (LCP (εCLcoαClεCL)) precursor is obtained by the living ring-opening polymerization, and the molecular weight of the precursor can be controlled by changing the molar ratio of the monomer and the initiator.When the monomer is fully converted , The active cyclic precursor re-initiates the block polymerization reaction of the reactive monomer α- (1-acryloyloxyethyl) -ε-caprolactone (αAEεCL) to synthesize a block copolymer with unsaturated bis The functional cyclic copolyester of the bond, namely, active cyclic poly (ε-caprolactone-co-α-chloro-ε- caprolactone) -b- (α- (1-acryloyloxyethyl) -ε-caprolactone). Finally, the active cyclic copolyester under UV irradiation, An intramolecular cross-linking reaction of the double bonds in the homopolymerizable monomer units resulted in the formation of a stable, novel organofunctional cyclic random copolyester cP- (εCLcoαClεCL) (M n, NMR = 32400) The structure and properties of the polymers were characterized by SEC, NMR and DSC. The SEC and viscosity characterization results showed that the new functional cP (εCLcoαClεCL) had smaller dynamic mechanical volume than the linear copolyesters with the same molecular weight. The DSC Characterization results show that the cyclization of the copolyester results in a reduction of its melting point and crystallinity, a salient feature of which is its ability to efficiently synthesize cyclic polymers with high molecular weights.