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首页> 外文期刊>Macromolecules >Effect of Core Cross-linking on the Physical Properties of Poly(dimethylsiloxane)-Based Diblock Copolymer Worms Prepared in Silicone Oil
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Effect of Core Cross-linking on the Physical Properties of Poly(dimethylsiloxane)-Based Diblock Copolymer Worms Prepared in Silicone Oil

机译:核心交联对硅油制备的聚(二甲基硅氧烷)基二嵌段共聚物蠕虫物理性质的影响

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A trithiocarbonate-capped poly(dimethylsiloxane) (PDMS) precursor is chain-extended via reversible addition-fragmentation chain transfer dispersion polymerization of 2-(dimethylamino)ethyl methacrylate (DMA) in decamethylcyclopentasiloxane (D5) silicone oil at 90 degrees C. For a fixed mean degree of polymerization (DP) of 66 for the PDMS steric stabilizer block, targeting core-forming PDMA block DPs of between 105 and 190 enables the preparation of either well-defined worms or vesicles at a copolymer concentration of 25% w/w. The as-synthesized linear PDMS66-PDMA(100) worms exhibit thermoresponsive behavior in D5, undergoing a worm-to-sphere transition on heating to 100 degrees C. Variable temperature H-1 NMR spectroscopy indicates that this thermal transition is driven by reversible solvent plasticization of the PDMA cores. This change in copolymer morphology is characterized by transmission electron microscopy (TEM) studies, variable temperature dynamic light scattering and small-angle X-ray scattering experiments. Oscillatory rheology studies indicate that degelation occurs at 32 degrees C, but shear-induced polarized light imaging measurements suggest that full conversion of worms into spheres requires significantly higher temperatures (similar to 110 degrees C). 1,2-Bis(2-iodoethoxy)ethane (BIEE) is evaluated as a cross-linker for PDMS66-PDMAx diblock copolymer nano-objects in D5. This bifunctional reagent quaternizes the tertiary amine groups on the DMA residues within the worm cores, introducing cross-links via the Menshutkin reaction. TEM studies confirm that such covalently-stabilized worms no longer undergo a worm-to-sphere transition when heated to 100 degrees C. Kinetic studies performed on PDMS66-PDMA(176) vesicles suggest that cross-linking requires approximately 13 h at 20 degrees C to ensure that these nano-objects remain intact when dispersed in chloroform, which is a good solvent for both blocks. Oscillatory rheology studies of a PDMS66-PDMA(100)
机译:三硫代碳酸酯封端的聚(二甲基硅氧烷)(PDMS)的前体是链延伸通过2-(二甲氨基)乙基甲基丙烯酸酯(DMA)在十甲基环戊硅氧烷(D5)硅油的可逆加成 - 断裂链转移聚合分散在90℃下对于聚合的固定平均程度为PDMS空间稳定剂块66(DP),靶向的105和190之间形成芯 - PDMA块移民使任一明确定义的蠕虫或囊泡的制备在25%的共聚物浓度w / w的。线性PDMS66-PDMA所合成的(100)表现出的蠕虫热响应行为在D5,在加热到100度经历蠕虫到球体转变C.变温度H-1 NMR光谱表明,该热转换是通过可逆溶剂从动该PDMA核塑化。在共聚物形态学的变化是其特征在于通过透射电子显微镜(TEM)研究中,可变温度动态光散射和小角X射线散射实验。振荡流变研究表明,脱胶发生在32℃,但剪切引起的偏振光成像的测量表明,完全转化的蠕虫为球需要显著较高的温度(类似于110摄氏度)。 1,2-双(2-碘乙氧基)乙烷(BIEE)被评价为交联剂用于PDMS66-PDMAX二嵌段共聚物纳米物体在D5。这种双功能试剂quaternizes在蜗杆核心内的DMA的残基,引入经由门秀金反应交联的叔胺基。 TEM研究证实,当加热到100℃的动力学研究上PDMS66-PDMA进行这样的共价稳定的蠕虫不再经历蠕虫到球体转变(176),囊泡表明交联需要在20℃下大约13小时以确保分散在氯仿中,这是两个块的良好溶剂时,这些纳米物体保持完整。一个PDMS66-PDMA的振荡流变研究(100)

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