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Solvent Tunable Self-Assembly of Amphiphilic Rod-Coil Block Copolymers with Chiral, Helical Polycarbodiimide Segments: Polymeric Nanostructures with Variable Shapes and Sizes

机译:具有手性,螺旋聚碳二亚胺链段的两亲杆-油嵌段共聚物的溶剂可调自组装:具有可变形状和大小的聚合物纳米结构

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The nanoscale self-assembly of four amphiphilic rod-coil di- and triblock copolymers with chiral, rodlike poly(N-1-phenethyl-N'-methylcarbodiimide) (PPMC) segments and random coil, hydrophilic PEG blocks has been investigated using dynamic light scattering (DLS) and tapping-mode atomic force microscopy (AFM). This self-assembly proved to be highly tunable simply upon altering the concentration and chemical structure of the hydrophilic selective solvent and/or blending the copolymers with polycarbodiimide homopolymer. When spin-coated from dilute (c = 0.5 mg/mL) THF/H2O solutions, these interesting polymers adopted either simple spherical micelles or spherical polymersomes depending on the relative amount of H2O used for dissolution. Switching selective solvent from H2O to MeOH induced changes in aggregation behavior, as evidenced by DLS and AFM, with interesting nanoworm and nanomaggot micelle assemblies observed when spin-coated from dilute THF/MeOH solutions. Blending high-MW PPMC homopolymer with the block copolymers and spin-coating from dilute THF/25 vol % MeOH solutions resulted in the formation of long, interconnected nanofibers with several different observed tangling pathways including parallel packing, perpendicular wrapping, and helical twisting of nanofibers. Additionally, a large number of toroid nanostructures were also identified by AFM when spin-coated from these conditions. Finally, spin-coating copolymer/homopolymer blends from THF/25 vol % EtOH induced the nanoscale formation of long, bundled superhelical nanofibers with defined helical structures depending on the homopolymer copolymer chiral pairing (i.e., (R)-(R) pairing formed P superhelical nanofibers and M superhelix for (S)-(S) pairing). The highly tunable nature of these polymeric nanostructures offers new opportunities for the formation of nanoparticles with variable shapes and sizes simply upon altering the solvent combinations opening up new applications as biological mimics and drug delivery agents.
机译:使用动态光研究了具有手性,棒状聚(N-1-苯乙基-N'-甲基碳二亚胺)(PPMC)链段和无规卷曲,亲水性PEG嵌段的两种两亲杆-螺旋二嵌段和三嵌段共聚物的纳米级自组装散射(DLS)和敲击模式原子力显微镜(AFM)。仅在改变亲水性选择性溶剂的浓度和化学结构和/或将共聚物与聚碳二亚胺均聚物共混时,这种自组装就被证明是高度可调的。从稀的(c = 0.5 mg / mL)THF / H2O溶液旋涂时,这些有趣的聚合物根据溶解的H2O的相对量采用简单的球形胶束或球形聚合物小体。如DLS和AFM所证明的,将选择性溶剂从H2O转换为MeOH会引起聚集行为的变化,当从稀THF / MeOH溶液中旋涂时,观察到有趣的纳米蠕虫和纳米mag胶束组件。将高分子量PPMC均聚物与嵌段共聚物混合,然后从稀THF / 25%(体积)的MeOH溶液中旋涂,形成长的,相互连接的纳米纤维,并具有几种观察到的缠结路径,包括平行堆积,垂直包裹和纳米纤维的螺旋扭曲。 。另外,当从这些条件旋涂时,AFM还鉴定出大量环形纳米结构。最后,由THF / 25%(体积)EtOH旋涂的共聚物/均聚物共混物诱导纳米级形成长束的超螺旋纳米纤维,该纤维具有定义的螺旋结构,取决于均聚物共聚物的手性配对(即(R)-(R)对形成的P (S)-(S)配对的超螺旋纳米纤维和M超螺旋)。这些聚合物纳米结构的高度可调节的性质为改变形状和尺寸的纳米颗粒的形成提供了新的机会,只需改变溶剂组合,就可以开辟出新的应用,如生物模拟物和药物递送剂。

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