Facultad de Química, Química Orgánica e Inorgánica (IUQOEM), Universidad de Oviedo, Julián Clavería s/n, 33006, Oviedo, Spain.
Angew Chem Int Ed Engl. 2016 Aug 16;55(34):10102-7. doi: 10.1002/anie.201605317. Epub 2016 Jul 26.
We herein report the formation of two complex nanostructures, toroidal micelles and bicontinuous nanospheres, by the self-assembly of the single structurally simple crystalline-b-coil diblock copolymer poly[bis(trifluoroethoxy)phosphazene]-b-poly(styrene), PTFEP-b-PS, in one solvent (THF) and without additives. The nature of these nanostructures in solution was confirmed by DLS and cryo-TEM experiments. The two morphologies are related by means of a new type of reversible morphological evolution, bicontinuous-to-toroidal, triggered by changes in the polymer concentration. WAXS experiments showed that the degree of crystallinity of the PTFEP chains located at the core of the toroids was higher than that in the bicontinuous nanospheres, thus indicating that the final morphology of the aggregates is mostly determined by the ordering of the PTFEP core-forming blocks.
我们在此报告了由单一结构简单的结晶-b-共聚物聚[双(三氟乙氧基)膦腈]-b-聚苯乙烯(PTFEP-b-PS)在一种溶剂(THF)中自组装形成两种复杂的纳米结构,即环形胶束和双连续纳米球,且无需添加任何助剂。通过 DLS 和 cryo-TEM 实验证实了溶液中这些纳米结构的性质。这两种形态通过一种新的可逆形态演变,即双连续到环形,通过聚合物浓度的变化触发,从而相关联。WAXS 实验表明,位于环形胶束核心的 PTFEP 链的结晶度高于双连续纳米球中的结晶度,这表明聚集物的最终形态主要由 PTFEP 核形成嵌段的有序性决定。