化学
胶束
动态光散射
氢键
小泡
酰胺
肺表面活性物质
摩尔浓度
分子
羧酸盐
离子
结晶学
霍夫迈斯特系列
分子动力学
无机化学
有机化学
高分子化学
化学工程
膜
水溶液
计算化学
纳米颗粒
生物化学
工程类
作者
Lijie Sun,Jiani Gong,Bo Xu,Yuzhao Wang,Xiaoxuan Ding,Yongliang Zhang,Changyao Liu,Li Zhao,Baocai Xu
出处
期刊:Langmuir
[American Chemical Society]
日期:2022-04-27
卷期号:38 (20): 6295-6304
被引量:14
标识
DOI:10.1021/acs.langmuir.1c03415
摘要
Ion-specific effects widely exist in biological and chemical systems and cannot be explained by classical theories. The complexity of ion-specific effects in protein systems at the molecular level necessitates the use of mimetic models involving smaller molecules, such as amino acids, oligopeptides, and other organic molecules bearing amide bonds. Therefore, it is of theoretical value to determine the effect of additional salts on the aggregation transitions of acyl amino acid surfactants. Herein, the effects of specific tetraalkylammonium ions (TAA+) on sodium lauroyl glycinate (SLG) aggregation were studied by dynamic light scattering (DLS) and transmission electron microscopy. Although previous studies have shown that the kosmotropic TAA+ ions tend to induce micellar growth or micelle-to-vesicle transitions of some anionic surfactants, TAA+ addition in the present study induced partial vesicle-to-micelle transitions in SLG solutions. The chemical trapping (CT) method was employed to estimate changes in the interfacial molarities of water, amide bonds, and carboxylate groups during such transitions. The vesicle-to-micelle transitions were accompanied by a marked rise in interfacial water molarity and a decline in interfacial amide bonds molarity, suggesting that the hydrated TAA+ entered the interfacial region and disrupted hydrogen bonding, thus preventing the SLG monomers from packing tightly. Molecular dynamic simulation was also performed to demonstrate the salt-induced cleavage of amide–amide bonds between SLG headgroups. Furthermore, both CT and DLS results show that the ability of tetraalkylammonium cations to induce such transitions increased with increasing size and hydrophobicity of the cation, which follows the Hofmeister series. The current study offers critical molecular-level evidence for understanding the specific effects of tetraalkylammonium ions on the aggregation transitions of an acyl amino acid surfactant.
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