Long-Range Hofmeister Effects of Anionic and Cationic Amphiphiles

被引:22
作者
Enami, Shinichi [1 ,2 ,3 ]
Colussi, Agustin J. [4 ]
机构
[1] Kyoto Univ, Hakubi Ctr Adv Res, Kyoto 6068302, Japan
[2] Kyoto Univ, Res Inst Sustainable Humanosphere, Uji, Kyoto 6110011, Japan
[3] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
[4] CALTECH, Ronald & Maxine Linde Ctr Global Environm Sci, Pasadena, CA 91125 USA
基金
美国国家科学基金会; 日本科学技术振兴机构;
关键词
ATMOSPHERICALLY RELEVANT IONS; WATER; SURFACE; ADSORPTION; AIR/WATER; INTERFACE; SPECTROSCOPY; REACTIVITY; TERPENES; DYNAMICS;
D O I
10.1021/jp401285f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Specific ion effects at aqueous interfaces play key roles in many important phenomena. We recently reported that ions interact specifically over unexpectedly long distances on the surface of sub-micromolar electrolyte solutions (Enami et al. J. Chem. Phys. 2012, 136, 154707). Whether the anionic and cationic headgroups of the organic amphiphiles present at most water/hydrophobe interfaces act similarly or display new behaviors, however, is not known. Here we report the results of experiments in which we apply online electrospray ionization mass spectrometry (ESI-MS) to investigate how carboxylate, RCOO- (R = CH3, C5H11, C7H15), and alkylammonium, R'(CH3)(3)N+ (R' = CH3, C14H29), ions affect the ratio chi = I-/Br- at the aerial interface of 1 mu M (NaI + NaBr) aqueous solutions. We found that chi is systematically but selectively depressed by these ionic amphiphiles and minimally affected by the neutral surfactant 1-octanol. The depressing effects induced by cationic headgroups are stronger than those caused by anionic surfactants and always increase with the length of the alkyl chains.
引用
收藏
页码:6276 / 6281
页数:6
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