Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical & Materials Engineering, Jiangnan University , Wuxi 214122, P. R. China.
Langmuir. 2018 Feb 13;34(6):2302-2311. doi: 10.1021/acs.langmuir.7b03837. Epub 2018 Jan 31.
Multiresponsive wormlike micelles (WLMs) remain a significant challenge in the construction of smart soft materials based on surfactants. Herein, we report the preparation of a viscoelastic wormlike micellar solution based on a new redox-responsive surfactant, sodium dodecylselanylpropyl sulfate (SDSePS), and commercially available benzyl tertiary amine (BTA) in the presence of CO. In this system, SDSePS can be reversibly switched on (selenide) and off (selenoxide) by a redox reaction, akin to that previously reported for benzylselanyl or phenylselanyl surfactants. By alternately adding HO and NH·HO, WLMs can be reversibly broken and formed because of the transformation of the hydrophilic headgroup of SDSePS, originating from the reversible formation of selenoxide. Moreover, WLMs can also be switched on and off by cyclically bubbling CO and N because of the variation of the binding interaction between SDSePS and BTA, resulting from the reversible protonation of BTA. This interesting and unique multiresponsive behavior makes the current WLMs a potential candidate for smart control of the "sol-gel" transition or substantial thickening of solutions.
基于表面活性剂的智能软物质的构建中,多响应蠕虫状胶束(WLMs)仍然是一个重大挑战。在此,我们报告了一种基于新型氧化还原响应性表面活性剂十二烷基硒基丙磺酸钠(SDSePS)和商业上可获得的苄基叔胺(BTA)在 CO 存在下制备粘弹性蠕虫状胶束溶液。在该体系中,SDSePS 可以通过氧化还原反应可逆地开启(硒化物)和关闭(硒氧化物),类似于先前报道的苄基硒基或苯基硒基表面活性剂。通过交替添加 HO 和 NH·HO,由于 SDSePS 的亲水基团的转化,WLMs 可以可逆地断裂和形成,这源于硒氧化物的可逆形成。此外,由于 SDSePS 和 BTA 之间的结合相互作用的变化,WLMs 也可以通过循环鼓入 CO 和 N 来开启和关闭,这是由于 BTA 的可逆质子化。这种有趣且独特的多响应行为使得当前的 WLMs 成为智能控制“溶胶-凝胶”转变或溶液显著增稠的潜在候选者。