Kumbhakar Manoj, Goel Teena, Nath Sukhendu, Mukherjee Tulsi, Pal Haridas
Radiation & Photochemistry Division, Bhabha Atomic Research Center, Mumbai 400 085, India.
J Phys Chem B. 2006 Dec 28;110(51):25646-55. doi: 10.1021/jp063839v.
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)20-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.
使用香豆素 - 153(C153)和香豆素 - 151(C151)作为荧光探针进行了动态斯托克斯位移和荧光各向异性测量,测量在水性聚(环氧乙烷)20 - 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)嵌段共聚物胶束中进行,目的是了解胶束冠层区域的水结构和动力学。已经确定探针位于胶束冠层区域。结果表明,与Triton - X - 100和Brij - 35等中性胶束的栅栏层相比,P123和F127胶束的冠层区域水化程度相对较低。通过评估两种嵌段共聚物胶束中探针的总斯托克斯位移值,可以推断出F127胶束比P123胶束水化程度更高。观察到在P123胶束中研究的所有温度下,两种探针的动态斯托克斯位移值或多或少保持相似。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来说它保持相当相似。此外,与P123相比,F127胶束中两种探针未观察到的初始动态斯托克斯位移分数明显更高。在293 - 313 K的研究温度范围内,光谱位移相关函数可以用双指数函数充分描述。两种胶束中C153的旋转弛豫时间在约303 K处显示出一种转变。假设随着温度升高,聚(环氧乙烷)(PEO)嵌段发生塌缩并在冠层区域形成水簇,这些结果得到了合理的解释。对于F127中C153和C151探针结果的差异,推断出探针位置不同。还将嵌段共聚物胶束的微观粘度和水化程度与其他常用中性胶束进行了比较,以便更好地理解嵌段共聚物胶束中的结果。