Department of Polymer Science, University of Akron, Akron, OH, 44325, USA.
Department of Civil Engineering and Geological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA.
Chemistry. 2019 Dec 10;25(69):15741-15745. doi: 10.1002/chem.201903544. Epub 2019 Nov 4.
An interesting phenomenon is reported when uranyl peroxide nanoclusters U (Li K (OH) [UO (O )(OH)] (H O) , m≈20 and n≈310) interact with a small number of cationic surfactant molecules. Cationic surfactant molecules do not distribute evenly around the U clusters during the interaction as expected. Instead, a small fraction of U clusters attract almost all the surfactant molecules, leading to the self-assembly into supramolecular structures by using surfactant-U complexes as building locks, and later further aggregate and precipitate based on hydrophobic interaction, whereas the rest of the clusters remained unbounded soluble macroions in bulk dispersion. This phenomenon nicely demonstrates a unique feature of macroion solutions. Considering that Debye-Hückel approximation is no longer valid in such solutions, the competition between the local electrostatic interaction and hydrophobic interaction becomes important to regulate the solution behaviors of macroions.
当过氧铀纳米团簇 U(LiK(OH)[UO(O)(OH)](H₂O),m≈20 且 n≈310)与少量阳离子表面活性剂分子相互作用时,会出现一个有趣的现象。在相互作用过程中,阳离子表面活性剂分子并没有像预期的那样均匀地分布在 U 团簇周围。相反,一小部分 U 团簇几乎吸引了所有的表面活性剂分子,导致通过使用表面活性剂-U 配合物作为构建锁,自组装成超分子结构,随后进一步基于疏水相互作用聚集和沉淀,而其余的团簇则保持未结合的可溶性大离子在体分散中。这种现象很好地展示了大离子溶液的一个独特特征。考虑到在这种溶液中德拜-休克尔近似不再有效,局部静电相互作用和疏水相互作用之间的竞争对于调节大离子的溶液行为变得很重要。