首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Study on premicellar and micellar aggregates of gemini surfactants with hydroxyl substituted spacers in aqueous solution using a probe showing TICT fluorescence properties
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Study on premicellar and micellar aggregates of gemini surfactants with hydroxyl substituted spacers in aqueous solution using a probe showing TICT fluorescence properties

机译:使用显示TICT荧光特性的探针研究水溶液中带有羟基取代间隔基的双子表面活性剂的双胶束和胶束聚集体

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The aggregation properties of two gemini surfactants, 12-3(OH)-12,2Br~- and 12-4(OH)2-12,2Br~- with hydroxyl substituted spacer group have been studied. The changes in photophysical properties of a single probe, trans-2-[4-(dimethylamino)styryl]benzothiazole (DMASBT) showing dipolar nature in its twisted intramolecular charge transfer (TICT) excited state have been exploited rather than using multiple probes to describe various properties of micellar aggregates. Formation of a number of premicellar aggregates has been demonstrated in addition to the description of the micropolarity and the micro-viscosity of environment using steady-state fluorescence spectroscopy and fluorescence anisotropy of DMASBT. Conductometric measurements have been carried out to determine degree of micellar ionization (α) and to verify critical micelle concentration (CMC) values estimated by fluorescence method. Hydroxyl substituted spacer group induces the formation of premicellar aggregates. The micropolarity of environment around probe molecules increases on going from premicellar to micellar aggregates. The growth of micellar aggregates has been demonstrated by a continuous increase in the microviscosity of environment. The micropolarity of micellar environment of 12-4(OH)2-12 is found to be less than that of 12-3(OH)-12. The microviscosity of premicellar and micellar aggregates of 12-4(OH)2-12 are higher than that of 12-3(OH)-12. CMC increases, whereas a decreases with increasing spacer chain length as well as number of hydroxyl substitution of a spacer group.
机译:研究了两种双羟基表面活性剂,具有羟基取代的间隔基的12-3(OH)-12,2Br〜-和12-4(OH)2-12,2Br〜-的聚集特性。已开发出单个探针,反式-2- [4-(二甲基氨基)苯乙烯基]苯并噻唑(DMASBT)在其扭曲的分子内电荷转移(TICT)激发态下显示偶极性质的光物理性质变化,而不是使用多个探针来描述胶束聚集体的各种特性。除了使用稳态荧光光谱和DMASBT的荧光各向异性来描述环境的微极性和微粘度外,还证明了许多早胶束聚集体的形成。已经进行了电导测量,以确定胶束电离度(α)并验证通过荧光法估算的临界胶束浓度(CMC)值。羟基取代的间隔基团诱导形成胶束前聚集体。从前胶束聚集体到胶束聚集体,探针分子周围环境的微极性增加。胶束聚集体的生长已通过环境微粘度的持续增加得到证明。发现胶束环境12-4(OH)2-12的微极性小于12-3(OH)-12。 12-4(OH)2-12的胶束前和胶束聚集体的微粘度高于12-3(OH)-12。 CMC增加,而随着间隔链长度的增加以及间隔基团羟基取代数的增加而降低。

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