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首页> 外文期刊>Journal of Colloid and Interface Science >Tuning thermoresponsive behavior of diblock copolymers and their gold core hybrids: Part 1. Importance of placement of amphiphilic end groups on the diblock copolymers
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Tuning thermoresponsive behavior of diblock copolymers and their gold core hybrids: Part 1. Importance of placement of amphiphilic end groups on the diblock copolymers

机译:调节二嵌段共聚物及其金核杂化物的热响应行为:第1部分。两亲端基在二嵌段共聚物上的位置重要性

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We report the effects of use and placement of amphiphilic end groups as a valuable tool to achieve significant changes in the thermoresponsive properties of diblock copolymers without the need to resort to compositional changes. We prepared diblock copolymers of di(ethylene glycol) methyl ether methacrylate and oligo(ethylene glycol) methyl ether acrylate with phenyl dithioester and carboxylic acid chain ends and compared the effects of placement of these amphiphilic chain ends on the cloud points of the copolymers. All the copolymers were high molecular weight (greater than 20. kDa) with a polydispersity between 1.1 and 1.2, and the cloud points were measured by UV-vis spectrophotometry and reported as the temperature at 50% normalized transmission. The thermoresponse showed a significant dependency on end group placement, reaching as much as a 28. °C difference in measured cloud point simply by exchanging end group placement rather than compositional changes. The effect is attributed to changes in the solvation and mobility from chain end placement affecting the degree of association of the chains. The underlying effect is due to the hydrophilic/hydrophobic balance in combination with the use of amphiphilic chain end placement that can be applied to copolymers with different blocks at the chain ends. This work shows that substantial changes in thermo-response properties can be achieved by re-arranging monomer components rather than changing monomer composition. This may have value in biomedical materials where the range of acceptable monomers is limited.
机译:我们报告了使用和放置两亲端基的效果,这是一种有价值的工具,可实现对二嵌段共聚物热响应性能的重大改变,而无需诉诸成分变化。我们制备了甲基丙烯酸二(乙二醇)甲基醚和丙烯酸丙烯酸低聚(乙二醇)甲基醚的二嵌段共聚物,并带有苯基二硫酯和羧酸链端,并比较了两亲性链端的位置对共聚物浊点的影响。所有共聚物均为高分子量(大于20 kDa),多分散度在1.1至1.2之间,浊点通过UV-vis分光光度法测量,并以50%归一化透射率记录为温度。热响应显示出对末端基团位置的显着依赖性,仅通过交换末端基团位置而不是组成变化,测得的浊点差高达28°C。该作用归因于来自链末端位置的溶剂化和迁移率的变化影响链的缔合程度。潜在的效果是由于亲水性/疏水性平衡以及与两亲性链端位置的结合使用,该两亲性链端位置可应用于链端具有不同嵌段的共聚物。这项工作表明,通过重新排列单体组分而不是改变单体组成,可以实现热响应性能的实质性变化。这在可接受的单体范围受到限制的生物医学材料中可能具有价值。

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