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Self-Assembly and Disassembly of Vesicles as Controlled by Anion-pi Interactions

机译:阴离子-pi相互作用控制的囊泡的自组装和拆卸

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摘要

Anion-pi interactions have been widely studied as new noncovalent driving forces in supramolecular chemistry. However, self-assembly induced by anion-pi interactions is still largely unexplored. Herein we report the formation of supramolecular amphiphiles through anion-pi interactions, and the subsequent formation of self-assembled vesicles in water. With the pi receptor 1 as the host and anionic amphiphiles, such as sodium dodecylsulfate (SDS), sodium laurate (SLA), and sodium methyl dodecylphosphonate (SDP), as guests, the sequential formation of host-guest supramolecular amphiphiles and self-assembled vesicles was demonstrated by SEM, TEM, DLS, and XRD techniques. The intrinsic anion-pi interactions between 1 and the anionic amphiphiles were confirmed by crystal diffraction, HRMS analysis, and DFT calculations. Furthermore, the controlled disassembly of the vesicles was promoted by competing anions, such as NO3-, Cl-, and Br-, or by changing the pH value of the medium.
机译:阴离子-π相互作用已作为超分子化学中新的非共价驱动力得到了广泛研究。然而,由阴离子-π相互作用引起的自组装仍在很大程度上未被探索。在本文中,我们报告了通过阴离子-pi相互作用形成超分子两亲物,以及随后在水中形成自组装囊泡的现象。以pi受体1为宿主,以阴离子两亲物(如十二烷基硫酸钠(SDS),月桂酸钠(SLA)和十二烷基膦酸钠(SDP))为客人,客体客体超分子两亲物的顺序形成和自组装囊泡通过SEM,TEM,DLS和XRD技术证实。通过晶体衍射,HRMS分析和DFT计算确认了1与阴离子两亲物之间的固有阴离子-π相互作用。此外,通过竞争性阴离子(例如NO3-,Cl-和Br-)或通过改变培养基的pH值,可促进小泡的受控分解。

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