Lyu Wei, Alotaibi Maha, Bell O Alexander, Watanabe Kazuyoshi, Harniman Robert, Mills Benjamin M, Seddon Annela M, Rogers Sarah E, King Stephen M, Yan Wei, Faul Charl F J
School of Chemistry , University of Bristol , Bristol , BS8 1TS , UK . Email:
Department of Environmental Science and Engineering , Xi'an Jiaotong University , 710049 , Xi'an , P. R. China.
Chem Sci. 2018 Apr 2;9(19):4392-4401. doi: 10.1039/c8sc00068a. eCollection 2018 May 21.
We present a newly developed approach to non-covalently address the packing parameter of an electroactive amphiphile. The pH-responsive reversible switching of a tetra(aniline)-based cationic amphiphile, -pentyl trimethylammonium bromide (), between self-assembled vesicles and nanowires by acid/base chemistry in aqueous solution is used to exemplify this approach. Trifluoroacetic acid () was selected as a prototypical acid to form emeraldine salt (ES) state () vesicles for this new class of small-molecule supramolecular amphiphiles. UV-vis-NIR spectroscopy, transmission electron microscopy (TEM), tapping-mode atomic force microscopy (AFM), and fluorescence spectroscopy were used to investigate the reversible structural transformation from vesicles to nanowires. We show that utilising different protonic acid-dopants for can regulate the packing parameter, and thus the final self-assembled structures, in a predictable fashion. We envisage potential application of this concept as smart and switchable delivery systems.
我们提出了一种新开发的方法,用于非共价调节电活性两亲物的堆积参数。以四(苯胺)基阳离子两亲物——五烷基三甲基溴化铵( )为例,通过水溶液中的酸碱化学作用,其在自组装囊泡和纳米线之间进行pH响应的可逆切换,以此来说明该方法。对于这类新型小分子超分子两亲物,选择三氟乙酸( )作为典型酸来形成翡翠盐(ES)态( )囊泡。利用紫外-可见-近红外光谱、透射电子显微镜(TEM)、轻敲模式原子力显微镜(AFM)和荧光光谱来研究从囊泡到纳米线的可逆结构转变。我们表明,利用不同的质子酸掺杂剂对 进行处理,可以以可预测的方式调节堆积参数,进而调节最终的自组装结构。我们设想这一概念在智能和可切换递送系统方面具有潜在应用。