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Effect of Hydrophobicity of Tails and Hydrophilicityof Spacer Group of Cationic Gemini Surfactants on Solvation Dynamicsand Rotational Relaxation of Coumarin 480 in Aqueous Micelles

机译:尾巴的疏水性和亲水性的影响双子表面活性剂间隔基对溶剂化动力学的影响胶束中香豆素480的合成和旋转弛豫

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摘要

Solvation dynamics and rotational relaxation of coumarin 480 in aqueous micelles of cationic gemini surfactants with diethyl ether (EE) spacer group (m–EE–m) and tails with varying tail lengths (m = 12, 14, and 16) have been studied. Studies have been carried out by measuring UV–visible absorption, steady-state fluorescence and fluorescence anisotropy, time-resolved fluorescence and fluorescence anisotropy, 1H NMR spectroscopy, and dynamic light scattering. Effects of hydrocarbon tail length and hydrophilicity of spacer group on solvation dynamics and rotational relaxation processes at inner side of the Stern layer of micelles have been studied. With increasing hydrophobicity of tails of surfactants, water molecules in the Stern layer become progressively more rigid, resulting in a decrease in the rate of solvation process with slow solvation as a major component. With increasing hydrophilicity of the spacer group of gemini surfactant, the extent of free water molecules is decreased, thereby making the duration of the solvation process longer. Solvation times in the micelles of gemini surfactants with hydrophilic spacer are almost 4 times longercompared to those in the micelles of their conventional counterpart.Rotational relaxation time increases with increasing tail length ofsurfactant as a result of increasing microviscosity of micelles withfast relaxation as a major component. With increasing hydrophilicityof the spacer group, the anisotropy decay becomes slower due to theformation of more compact micelles. Rotational relaxation in geminimicelles is also slower compared to that in their conventional counterpart.The anisotropy decay is found to be biexponential with lateral diffusionof the probe along the surface of the micelle as a slow component.Rotational motion of micelle as a whole is a very slow process, andthe motion becomes further slower with increasing size of the micelle.The time constants for wobbling motion and lateral diffusion of theprobe become longer with increasing microviscosity of micelles.
机译:研究了带有乙醚(EE)间隔基团(m–EE–m)和具有不同尾长的尾巴(m = 12、14和16)的阳离子双子表面活性剂的水性胶束中香豆素480的溶解动力学和旋转弛豫。通过测量紫外可见吸收,稳态荧光和荧光各向异性,时间分辨荧光和荧光各向异性, 1 H NMR光谱以及动态光散射进行了研究。研究了烃尾长度和间隔基团的亲水性对胶束斯特恩层内侧溶剂化动力学和旋转弛豫过程的影响。随着表面活性剂尾部的疏水性增加,斯特恩层中的水分子逐渐变得更硬,从而导致以慢速溶剂化为主要成分的溶剂化过程速率降低。随着双子表面活性剂的间隔基的亲水性增加,游离水分子的程度降低,从而使溶剂化过程的持续时间更长。具有亲水性间隔基的双子表面活性剂胶束中的溶剂化时间长将近4倍与传统胶束中的胶束相比。旋转弛豫时间随尾巴长度的增加而增加表面活性剂是由于增加了胶束的微粘度快速放松是主要组成部分。随着亲水性的增加在间隔基团中,由于形成更紧密的胶束。双子星座中的旋转松弛与传统胶束相比,胶束也较慢。发现各向异性衰减与横向扩散是双指数的沿着胶束表面的探针的长度是缓慢的。胶束整体的旋转运动是一个非常缓慢的过程,并且随着胶束尺寸的增加,运动变得更加缓慢。晃动和横向扩散的时间常数随着胶束微粘度的增加,探针变得更长。

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