首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Microenvironment in the Corona Region of Triblock Copolymer Micelles:Temperature Dependent Solvation and Rotational Relaxation Dynamics of Coumarin Dyes
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Microenvironment in the Corona Region of Triblock Copolymer Micelles:Temperature Dependent Solvation and Rotational Relaxation Dynamics of Coumarin Dyes

机译:三嵌段共聚物胶束电晕区域的微环境:香豆素染料的温度依赖性溶剂化和旋转弛豫动力学

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摘要

Dynamic Stokes' shift and fluorescence anisotropy measurements using coumarin-153 (C153) and coumarin-151 (C151) as the fluorescence probes have been carried out in aqueous poly(ethylene oxide)2o-poly(propylene oxide)_(70)-poly(ethylene oxide)_(20) (P123) and poly(ethylene oxide)_(100)-poly(propylene oxide)_(70)-poly(ethylene oxide)_(100) (F127) block copolymer micelles with an aim to understand the water structures and dynamics in the micellar corona region.It has been established that the probes reside in the micellar corona region.It is indicated that the corona regions of P123 and F127 micelles are relatively less hydrated than the Palisade layers of neutral micelles like Triton-X-100 and Brij-35.From the appraisal of total Stokes' shift values for the probes in the two block copolymer micelles,it is inferred that the F127 micelle is more hydrated than the P123 micelle.It is observed that the dynamic Stokes' shift values for both of the probes remain more or less similar at all the temperatures studied in the P123 micelle.For C153 in F127,however,the observed Stokes' shift is seen to decrease quite sharply with temperature,though it remains quite similar for C151.Moreover,the fraction of the unobserved initial dynamic Stokes' shift is appreciably higher for both the probes in the F127 micelle compared to that in P123.Over the studied temperature range of 293-313 K,the spectral shift correlation function is described adequately by a bi-exponential function.Rotational relaxation times for C153 in both the micelles show a kind of transition at around 303 K.These results have been rationalized assuming collapse of the poly(ethylene oxide) (PEO) blocks and formation of water clusters in the corona region due to dehydration of poly(ethylene oxide) blocks with an increase in temperature.A dissimilar probe location has been inferred for the differences in the results with C153 and C151 probes in F127.Comparison of the microviscosity and the hydration of the block copolymer micelles has also been made with those of the other commonly used neutral micelles,for a better understanding of the results in the block copolymer micelles.
机译:使用香豆素153(C153)和香豆素151(C151)作为荧光探针的动态斯托克斯位移和荧光各向异性测量已在水性聚(环氧乙烷)2o-聚(环氧丙烷)_(70)-聚(环氧乙烷)_(20)(P123)和聚(环氧乙烷)_(100)-聚(环氧丙烷)_(70)-聚(环氧乙烷)_(100)(F127)嵌段共聚物胶束为了了解胶束电晕区域的水结构和动力学,已确定探针位于胶束电晕区域中,这表明P123和F127胶束的电晕区域相对于中性胶束的栅栏层相对较少水合像Triton-X-100和Brij-35。从对两个嵌段共聚物胶束中探针的总斯托克斯位移值的评估中,可以推断出F127胶束比P123胶束的水合程度更高。两种探针的动态斯托克斯位移值在所有情况下都保持或多或少相似。在F123胶束中研究了温度。然而,对于F127中的C153,观察到的斯托克斯位移随温度急剧下降,尽管对于C151仍很相似。此外,未观察到的初始动态斯托克斯位移的比例也相当大。 F127胶束中的两个探针都比P123中的探针更高。在研究的293-313 K的温度范围内,光谱位移相关函数用双指数函数充分描述。在303 K附近显示出一种跃迁。假设聚氧化乙烯(PEO)嵌段的脱水和聚氧化乙烯脱水增加导致的电晕区域中水簇的形成,这些结果是合理的由于F127中的C153和C151探针的结果存在差异,因此推断了一个不同的探针位置。微粘度和嵌段共聚物的水合作用的比较为了更好地理解嵌段共聚物胶束的结果,还与其他常用的中性胶束制备了高聚物胶束。

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