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非离子型 Brij 表面活性剂的微极性、胶束前和胶束聚集的荧光探针研究。

Fluorescent probe studies of micropolarity, premicellar and micellar aggregation of non-ionic Brij surfactants.

机构信息

Department of Chemistry, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India.

出版信息

J Colloid Interface Sci. 2010 Apr 1;344(1):97-104. doi: 10.1016/j.jcis.2009.12.021. Epub 2009 Dec 16.

DOI:10.1016/j.jcis.2009.12.021
PMID:20089255
Abstract

The dipolar nature of trans-2-[4-(dimethylamino)styryl]benzothiazole (DMASBT) in its twisted intramolecular charge transfer (TICT) excited state makes it useful as a surface probe for phenomena such as premicellar and micellar aggregation of non-ionic Brij surfactants. The process of micellization of Brij 35, Brij 58, Brij 78, and Brij 98 through the formation of smaller premicellar aggregates results in a progressive change in the nature of the DMASBT molecule and its location in the aggregates, reflecting the changes in its photophysical properties, which have been studied using steady-state fluorescence, fluorescence anisotropy, and time-correlated single-photon counting measurements. The microenvironment polarity around the DMASBT probe in the micellar phase is greater than that in corresponding premicellar phases. The orders of premicellar as well as micellar concentrations are Brij 35 > Brij 58 > Brij 98 > Brij 78. The lower fluorescence anisotropies observed in the case of Brij 78 aggregates compared to those in other Brijs studied could be due to the accessibility of a nonrigid environment as a result of a folded conformation of a part of the nonpolar long chain of surfactant molecules near the core of aggregates. Three different locations of DMASBT were noted for Brijs 35, Brij 78, and Brij 98, whereas for Brij 58 only two locations are observed. The micropolarity of the environment around DMASBT in aggregation states has been determined.

摘要

反式-2-[4-(二甲氨基)苯乙烯基]苯并噻唑(DMASBT)在扭曲的分子内电荷转移(TICT)激发态下的偶极性质使其成为非离子型 Brij 表面活性剂的胶束前聚集体和胶束聚集等现象的有用表面探针。Brij 35、Brij 58、Brij 78 和 Brij 98 通过形成较小的胶束前聚集体而发生胶束化的过程导致 DMASBT 分子的性质及其在聚集体中的位置发生变化,反映了其光物理性质的变化,这些变化已经通过稳态荧光、荧光各向异性和时间相关单光子计数测量进行了研究。DMASBT 探针在胶束相中的微环境极性大于相应的胶束前相。胶束前以及胶束浓度的顺序为 Brij 35>Brij 58>Brij 98>Brij 78。与研究的其他 Brijs 相比,Brij 78 聚集体中观察到的荧光各向异性较低,这可能是由于非极性长链表面活性剂分子的一部分在聚集体核心附近的折叠构象导致了非刚性环境的可及性。对于 Brijs 35、Brij 78 和 Brij 98,观察到 DMASBT 的三个不同位置,而对于 Brij 58,只观察到两个位置。已经确定了在聚集态下 DMASBT 周围环境的微极性。

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