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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Sodium Bromide Induced Micelle to Vesicle Transitions of Newly Synthesized Anionic Surface Active Ionic Liquids Based on Dodecylbenzenesulfonate
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Sodium Bromide Induced Micelle to Vesicle Transitions of Newly Synthesized Anionic Surface Active Ionic Liquids Based on Dodecylbenzenesulfonate

机译:基于十二烷基苯磺酸盐的新合成阴离子表面活性离子液体的溴化钠诱导胶束向囊泡的转变

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Dodecylbenezenesulfonate-based anionic surface active ionic liquids (DBS-ILs) paired with onium cations, n-butyltrimethylammonium ([N-1114]), 1-butyl-3-methylimidazolium ([C(4)mim]), and N-butylpyridinium ([C4Py]) have been synthesized. DBS-ILs were found to be highly surface active having critical micelle concentration (CMC) lower than that of their conventional analogue sodium dodecylbenezenesulfonate ([Na][DBS]). The CMC values of DBS-ILs were determined from surface tension (ST) and isothermal titration calorimetry (ITC). DBS-ILs formed micelles predominantly in the aqueous medium, and unlike [Na]DBS, the micelles of DBS-ILs could be transformed into vesicles with the addition of sodium bromide (NaBr). Micelle to vesicle transitions (MVTs) were evidenced from dynamic light scattering (DLS), turbidity, proton nuclear magnetic resonance (H-1 NMR), and cryo-TEM techniques. Thermodynamics of aggregation was investigated from ITC which indicated that the aggregation process is primarily driven by the entropy factor. The formation of a vesicle upon addition of NaBr has been accounted to the increased electrostatic interactions between the less hydrated sulfonate headgroup and the more populated bigger sized counterions along with the favored cation-pi or pi-pi interactions between them as evidenced from 2D-NOESY NMR experiments. The stimuli-responsive morphological transitions in the self-assembly of the reported anionic surface active ionic liquids (SAILs) will be useful for encapsulation and delivery of active (bio)molecules in the targeted biomedical applications.
机译:基于十二烷基苯磺酸盐的阴离子表面活性离子液体(DBS-ILs)与鎓阳离子,正丁基三甲基铵([N-1114]),1-丁基-3-甲基咪唑鎓([C(4)mim])和N-丁基吡啶鎓配对([C4Py])已合成。发现DBS-IL具有高表面活性,其临界胶束浓度(CMC)低于其常规类似物十二烷基苯磺酸钠([Na] [DBS])。 DBS-IL的CMC值由表面张力(ST)和等温滴定量热(ITC)确定。 DBS-ILs主要在水性介质中形成胶束,并且与[Na] DBS不同,DBS-ILs的胶束可以通过添加溴化钠(NaBr)而转化为囊泡。从动态光散射(DLS),浊度,质子核磁共振(H-1 NMR)和冷冻TEM技术可以证明胶束到囊泡的转变(MVT)。 ITC对聚集的热力学进行了研究,结果表明聚集过程主要由熵因子驱动。从2D-NOESY可以看出,添加NaBr后形成囊泡的原因是水合度较低的磺酸根与较大的较大抗衡离子之间的静电相互作用增强,以及它们之间的阳离子-pi或pi-pi相互作用更有利。 NMR实验。报道的阴离子表面活性离子液体(SAIL)自组装中的刺激响应形态学转变将用于目标生物医学应用中活性(生物)分子的包封和递送。

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