How Hydrogen Bonds Affect the Growth of Reverse Micelles around Coordinating Metal Ions

被引:61
作者
Qiao, Baofu [1 ]
Demars, Thomas [3 ]
de la Cruz, Monica Olvera [1 ,2 ]
Ellis, Ross J. [3 ]
机构
[1] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[3] Argonne Natl Lab, Argonne Chem Sci & Engn Div, Argonne, IL 60439 USA
关键词
SMALL-ANGLE SCATTERING; EXTRACTION; CHEMISTRY; DYNAMICS;
D O I
10.1021/jz500495p
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
Extensive research on hydrogen bonds (H-bonds) have illustrated their critical role in various biological, chemical and physical processes. Given that existing studies are predominantly performed in aqueous conditions, how H-bonds affect both the structure and function of aggregates in organic phase is poorly understood. Herein, we investigate the role of H-bonds on the hierarchical structure of an aggregating amphiphile-oil solution containing a coordinating metal complex by means of atomistic molecular dynamics simulations and X-ray techniques. For the first time, we show that H-bonds not only stabilize the metal complex in the hydrophobic environment by coordinating between the Eu(NO3)(3) outer-sphere and aggregating amphiphiles, but also affect the growth of such reverse micellar aggregates. The formation of swollen, elongated reverse micelles elevates the extraction of metal ions with increased H-bonds under acidic condition. These new insights into H-bonds are of broad interest to nanosynthesis and biological applications, in addition to metal ion separations.
引用
收藏
页码:1440 / 1444
页数:5
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