作者: Yingna Zhang , Hui Tang , Peiyi Wu
DOI: 10.1039/C7CP05846B
关键词:
摘要: The effect of multiple interactions including anion-macromolecule interaction, water-mediated ion-macromolecule interaction and hydrophobic on the phase transition behaviors random copolymers P(OEGMA-co-BVIm[X]) comprising oligo(ethylene glycol)methacrylate (OEGMA) imidazolium-based ionic liquids is investigated in present study. Temperature-variable 1H NMR FT-IR investigations demonstrated that hydration CH2 side chains P(OEGMA-co-BVIm[SCN]) was enhanced due to anion-dipole between a chaotropic anion SCN- groups, dehydration C[double bond, length as m-dash]O groups served driving force transition. In particular, formation m-dash]OD2O-PIL hydrogen bonds preferred during process considering IL-D2O associations groups. This acted "linkage" among polymers, resulting gradual stable small size micelles. As for P(OEGMA-co-BVIm[NTf2]), water molecules were sequentially squeezed out polymer upon heating self-aggregation carried through OEGMA with IL segments wrapped aggregates.