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作 者:沈桂芝[1,2] 张玉玺[1] 吴飞鹏[1] 王尔鑑[1]
机构地区:[1]中国科学院理化技术研究所,北京100190 [2]中国科学院大学,北京100049
出 处:《影像科学与光化学》2013年第4期286-294,共9页Imaging Science and Photochemistry
摘 要:采用尼罗红(Nile red)染料为探针,利用吸收和发射光谱研究了具有不同烷芳基结构的可聚合阳离子型Hydrotropes(PCHs)的溶液性质,结果表明其在水溶液中易发生自缔合行为并具有两个阈值浓度:分子开始自缔合的临界浓度(CAC)(10-1—10-2 mol/L),开始大幅度提高助溶作用的最小助溶浓度(MHC)(>10-1 mol/L),两阈值浓度均随化合物分子结构中的疏水基团尺寸的增大而减小.两亲化合物聚集体的微环境极性测定的结果显示,其极性比表面活性剂胶束高,并且随着化合物浓度的增大不断下降,表明形成的聚集体结构比较疏松,且其分子堆砌密度随聚集体的增大而逐步升高.此外,通过自由基聚合得到相应的两亲聚合物仍保留Hydrotrope原有的性能,并具有更显著的助溶作用.A series of functional polymerizable cationic hydrotropes(PCHs) with different alkyl aromatic hydrophobic structures were studied. The solubilization properties and assembly behaviors were examined by absorption and emission spectra using Nile Red dye as a multi- functional probe. The result showed that there present two concentration thresholds: the critical association concentration (CAC) (10^-1 -10^-2 tool/L) and the minimal hydrotropie concentration (MHC) (〉 10^-1 mol/L). Both of them decrease obviously with increasing dimension of hydrophobic structure. The microenvironment polarities of aggregates determined have a relatively high value compared with that for surfactant mieelles, and continuously decreased with concentration suggesting formation of loose aggregated structure whose molecular stack density increase gradually with aggregate growth. In addition, hydrotropic polymers of this type obtained by radical polymerization maintained the original hydrotropic properties with more effective solubilization ablitiy.
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