Nguyen R, Jouault N, Zanirati S, Rawiso M, Allouche L, Fuks G, Buhler E, Giuseppone N
Institut Charles Sadron, CNRS, University of Strasbourg, 23 rue du Loess, BP 84047, 67034 Strasbourg Cedex 2, France.
Soft Matter. 2014 Jun 14;10(22):3926-37. doi: 10.1039/c4sm00072b. Epub 2014 Apr 4.
Dynamic covalent surfactants have been obtained by the reversible condensation of a hydrophobic aldehyde (ended by an ionic tip) with various neutral polyethylene glycol based hydrophilic amines. In water, the duality between the two hydrophilic domains (charged and neutral) leads to their segregation when the surfactants are self-assembled within micelles. Depending on the number of polyethylene glycol units, a core-shell inversion leading to a switching orientation of the ionic tips from the inside to the outside of the micelles has been demonstrated by a combination of scattering techniques. In competition experiments, when several amines of different pKas and hydrophilic polyethylene glycol chains are competing for the same aldehyde, it becomes possible to trigger this core-shell inversion by pH modulation and associated dynamic constitutional reorganization.
通过疏水性醛(以离子端基结尾)与各种基于中性聚乙二醇的亲水性胺的可逆缩合反应,制备了动态共价表面活性剂。在水中,当表面活性剂在胶束内自组装时,两个亲水性区域(带电和中性)之间的二元性导致它们分离。通过散射技术的组合证明,根据聚乙二醇单元的数量,会发生核壳反转,导致离子端基从胶束内部向外部的取向切换。在竞争实验中,当几种具有不同pKa值的胺和亲水性聚乙二醇链竞争同一个醛时,通过pH调节和相关的动态结构重组,可以触发这种核壳反转。