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Intra- and intermolecular chain transfer to macromolecules with chain scission. The case of cyclic esters

机译:断链将分子内和分子间链转移至大分子。环酯的情况

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摘要

Chain transfer to macromolecules with chain scission is the most often observed "side" reaction in the polymerization of heterocyclics. In our previous works we analysed quantitatively the intramolecular chain transfer to the own macromolecule (back-biting). This paper gives a general treatment of the kinetics of polymerization with propagation and intermolecular chain transfer to macromolecules, accompanied with chain scission. The numerical solution developed allows determining the k(p)/k(tr) ratio from the dependence of (M) over bar(W)/(M) over bar(n) on monomer conversion. This treatment was applied to the polymerization of L,L-lactide and k(p)/k(tr) ratios were measured for covalent alcoholate active species bearing Al, Fe, Ti, Sm, and La. In this way selectivities of active species (expressed with k(p)/k(tr)) were for the first time measured and finally correlated with the atomic number of the corresponding metal atoms, related to the strength of the bond involved in the monomer addition. [References: 16]
机译:具有断链现象的链转移到大分子是杂环聚合中最常观察到的“副”反应。在我们以前的工作中,我们定量分析了分子内链转移到自己的大分子上(逆向咬合)。本文给出了伴随扩散和分子间链转移到大分子以及断链的聚合动力学的一般处理方法。开发的数值解决方案允许根据(M)高于bar(W)/(M)高于bar(n)对单体转化率的依赖性来确定k(p)/ k(tr)比。将该处理应用于L,L-丙交酯的聚合反应,并测量带有Al,Fe,Ti,Sm和La的共价醇盐活性物质的k(p)/ k(tr)比。这样,活性物质的选择性第一次测量(用k(p)/ k(tr)表示),并最终与相应金属原子的原子数相关,该原子数与单体加成中涉及的键的强度有关。 [参考:16]

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