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含硒两亲嵌段共聚物的单分子力谱研究:用于解组装聚合物胶束。

Single-molecule force spectroscopy of selenium-containing amphiphilic block copolymer: toward disassembling the polymer micelles.

机构信息

Key Lab of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084, People's Republic of China.

出版信息

Langmuir. 2012 Jun 26;28(25):9601-5. doi: 10.1021/la301703t. Epub 2012 Jun 4.

Abstract

Selenium-containing polymers are a new type of responsive polymer material. Here, a selenium-containing amphiphilic block copolymer (PEG-PUSe-PEG) has been investigated using atomic force microscopy (AFM)-based single-molecule force spectroscopy (SMFS). The deviation between force-extension curves of PEG-PUSe-PEG in water and in DMSO is found to be related to the disassembly of the micellar structures in water. SMFS experiments on PEG-PUSeox-PEG suggest that the change from selenide to oxidized selenone contributes significantly to the change in amphiphilicity, without obviously influencing the single-chain elasticity.

摘要

含硒聚合物是一种新型的响应性聚合物材料。在这里,我们使用原子力显微镜(AFM)基于单分子力谱(SMFS)研究了一种含硒两亲嵌段共聚物(PEG-PUSe-PEG)。发现 PEG-PUSe-PEG 在水中和 DMSO 中的力-延伸曲线之间的偏差与水中胶束结构的解体有关。PEG-PUSeox-PEG 的 SMFS 实验表明,硒化物到氧化硒酮的转变对两亲性的变化有很大贡献,而对单链弹性没有明显影响。

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