Zhou Yifan, Wei Jingfan, Li Xiangqian, Wąsik Patryk, Liu Hao, Liu Tianbo
School of Polymer Science and Polymer Engineering, The University of Akron, Akron, Ohio 44325, United States.
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low-Dimension Materials, Donghua University, Shanghai 201620, China.
ACS Appl Mater Interfaces. 2024 Sep 25;16(38):51512-51520. doi: 10.1021/acsami.4c10543. Epub 2024 Sep 13.
We report complex macrophase and microphase transitions of rigid amphiphiles with spherical Keggin molecular clusters as the solvophilic block and rod-like rigid oligofluorene (OF) as the solvophobic block in mixed solvents of water and polar organic solvent. By properly adjusting the solvent polarity, the amphiphiles are found to respond accordingly by self-assembling into multilayered incomplete onion-like structures (10-25 vol % THF), single-layered vesicular structures (60 vol % THF), and an unexpected macrophase separation in the middle (40-50 vol % THF), which is due to the anomalous trends in Keggin solubility as a result of the nature of TBA counterions. The rigidity of the OF block prevents the amphiphile from assembling by following the rule of packing parameters; instead, interdigitation among different rods leads to the formation of the solvophobic domain to achieve self-assembly. The incomplete onion structures are controlled by the interdigitation of rigid rods for the number of layers and the electrostatic interaction among Keggin head groups for the interlayer distance. When the degree of interdigitation becomes lower, the self-assembly process shows a trend that can be explained by the traditional rule of packing parameter. This study demonstrates the formation of different self-assembled structures by rigid amphiphiles and their transitions induced by solvent composition. The self-assembly (microphase separation) of rigid amphiphiles in a dilute solution could indeed represent a broad area containing complicated, uncharted rules.
我们报道了刚性两亲分子的复杂宏观相和微观相转变,该两亲分子以球形Keggin分子簇作为亲溶剂嵌段,以棒状刚性低聚芴(OF)作为疏溶剂嵌段,存在于水和极性有机溶剂的混合溶剂中。通过适当调节溶剂极性,发现两亲分子会相应地做出响应,通过自组装形成多层不完全洋葱状结构(10 - 25体积%四氢呋喃)、单层囊泡结构(60体积%四氢呋喃),以及中间出现的意想不到的宏观相分离(40 - 50体积%四氢呋喃),这是由于TBA抗衡离子的性质导致Keggin溶解度出现异常趋势。OF嵌段的刚性阻止了两亲分子按照堆积参数规则进行组装;相反,不同棒状分子之间的相互交错导致了疏溶剂域的形成以实现自组装。不完全洋葱结构由刚性棒状分子的相互交错控制层数,由Keggin头基之间的静电相互作用控制层间距。当相互交错程度变低时,自组装过程呈现出一种可以用传统堆积参数规则解释的趋势。本研究展示了刚性两亲分子形成不同的自组装结构及其由溶剂组成诱导的转变。刚性两亲分子在稀溶液中的自组装(微相分离)确实可能代表一个包含复杂、未知规则的广阔领域。