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Control of M_n, M_w/M_n End-Groups, and Kinetics in Living Polymerization of Cyclic Esters

机译:控制酯类聚合的M_N,M_W / M_N末端组和动力学

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Factors affecting molar mass, molar mass distribution, end-groups, and kinetics control in polymerization of ε-caprolactone (CL) and L,L-dilactide (LA) initiated by covalent alkylmetal alkoxides, metal alkoxides, and metal carboxylates are discussed. First, an importance of the reliable molar mass measurements of the resulting polyesters is stressed. Then, it is shown that R_2AlOR', A1(OR)_3, Sn(OR)_2, and Sn[(O)OCR')]_2/ROH initiators provide living polymerization of cyclic esters, in spite of the extensive aggregation phenomena. In LA polymerization Sn(II)-alkoxides appeared to be particularly effective, allowing M_n control in the range from 10~2 up to 10~6. Conditions enabling side chain transfer reactions to be eliminated are also discussed.
机译:讨论了通过共价烷基醇盐,金属醇盐,金属醇盐和金属羧酸盐引发的ε-己内酯(Cl)和L,L-替代(La)聚合的摩尔质量,摩尔质量分布,端基和动力学对照的因素。首先,强调所得聚酯可靠摩尔质量测量的重要性。然后,示出了R_2ALOR',A1(或)_3,Sn(或)_2和Sn [(O)OCR')] _ 2 / RoH引发剂提供环状酯的活性聚合,尽管存在广泛的聚集现象。在La聚合Sn(II)中 - 烷氧基似乎是特别有效的,使M_N控制在10〜2至10〜6的范围内。还讨论了能够消除侧链转移反应的条件。

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