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Glass Transition Behavior of Dendritic Polymers Containing Mobile Aliphatic Polyether Cores and Glassy Peripheral Polystyrenes

机译:含移动性脂肪族聚醚核和玻璃态周边聚苯乙烯的树枝状聚合物的玻璃化行为

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We investigated the glass transition temperatures (Tg) of dendrons consisting of conformationally mobile aliphatic polyether dendritic cores plus glassy peripheral polystyrenes (PSs), and linear PSs in the molecular weight range of 1000-8500 g/mol. We compared their Tg behavior depending on their polymeric architecture. The linear PSs show a typical growth of Tg up to 92.5 oC as the molecular weight increases to 8300 g/mol, while the dendrons display nearly constant Tg values of 58-61 oC, despite the increase of molecular weight with each generation. The striking contrast of Tg behavior would be mainly attributed to the fact that the dendrons keep the ratio of Ne/M (Ne: number of peripheral chain ends, M: molecular weight) over all the generations. Additionally, for the influence of dendritic spacers on glass transition temperature we prepared dimeric PSs with different linkage groups such as aliphatic ether, ester and amide bonds. We found that the dimer with the ether spacer exhibited the lowest glass transition at 55.4 ∩, while the amide linked dimer showed the highest glass transition temperature at 74.2 ∩. This indicates that the peripheral PS chains are effectively decoupled by the conformationally flexible ether spacer. The results from this study demonstrated that polymeric architecture and dendritic core structures play a crucial role in the determination of glass transition behavior, providing a strategy for the systematic engineering of polymer chain mobility.
机译:我们研究了树枝状分子的玻璃化转变温度(T g ),该树枝状分子由构象可移动的脂肪族聚醚树枝状核加上玻璃状外围聚苯乙烯(PSs)和线性PS组成,分子量范围为1000-8500 g / mol 。我们根据其聚合物结构比较了它们的T g 行为。随着分子量增加至8300 g / mol,线性PS表现出T g 的典型增长,直至92.5 oC,而树突的T g 值几乎保持恒定,为58 -61 oC,尽管每一代分子量都增加。 T g 行为的明显对比主要归因于树突在所有世代中都保持Ne / M之比(Ne:外围链端数,M:分子量)。此外,对于树枝状间隔基对玻璃化转变温度的影响,我们制备了具有不同连接基团(例如脂族醚,酯和酰胺键)的二聚PS。我们发现,带有醚间隔基的二聚体在55.4 exhibit处显示出最低的玻璃化转变温度,而酰胺键连接的二聚体在74.2 showed处显示出最高的玻璃化转变温度。这表明外围的PS链被构象上灵活的醚间隔基有效地解偶联。这项研究的结果表明,聚合物结构和树枝状核结构在确定玻璃化转变行为中起着至关重要的作用,为聚合物链迁移性的系统工程化提供了策略。

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