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Synthesis and electrokinetics of cationic spherical nanoparticles in salt-free non-polar media

机译:无盐非极性介质中阳离子球形纳米粒子的合成和动力学

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摘要

Cationic diblock copolymer nanoparticles have been prepared in n-dodecane via polymerization-induced self-assembly (PISA). A previously reported poly(stearyl methacrylate)–poly(benzyl methacrylate) (PSMA–PBzMA) PISA formulation (Chem. Sci. 2016, >7, 5078–5090) was modified by statistically copolymerizing an oil-soluble cationic methacrylic monomer, (2-(methacryloyloxy)ethyl)trimethylammonium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, with either SMA or BzMA, to produce either charged shell or charged core nanoparticles. The electrokinetics were studied as a function of many variables (function of volume function, particle size, solvent viscosity, and number of ions per chain). These data are consistent with electrophoresis controlled by counterion condensation, which is typically observed in salt-free media. However, there are several interesting and unexpected features of interest. In particular, charged shell nanoparticles have a lower electrophoretic mobility than the equivalent charged core nanoparticles, and the magnitude of the electrophoretic mobility increases as the fraction of cationic stabilizer chains in the shell layer is reduced. These results show that cationic PSMA–PBzMA spheres provide an interesting new example of electrophoretic nanoparticles in non-polar solvents. Moreover, they should provide an ideal model system to evaluate new electrokinetic theories.
机译:阳离子二嵌段共聚物纳米粒子已通过聚合诱导自组装(PISA)在正十二烷中制备。通过统计共聚合油溶性化合物,修改了先前报道的聚甲基丙烯酸硬脂酯-甲基丙烯酸苄酯(PSMA-PBzMA)PISA配方(Chem。Sci。2016,> 7 ,5078-5090)阳离子甲基丙烯酸单体,具有(SMA)或BzMA的四[3,5-双(三氟甲基)苯基]硼酸(2-(甲基丙烯酰氧基)乙基)三甲基铵,可制得带电的壳或带电的核纳米粒子。研究了作为许多变量的函数(体积函数,粒度,溶剂粘度和每条链上的离子数的函数)的函数的电动学。这些数据与反离子缩合控制的电泳一致,这通常在无盐介质中观察到。但是,有几个有趣而出乎意料的特性。特别地,带电的壳纳米颗粒具有比等效的带电核纳米颗粒更低的电泳迁移率,并且随着壳层中阳离子稳定剂链的分数减少,电泳迁移率的大小增加。这些结果表明,阳离子PSMA–PBzMA球为非极性溶剂中的电泳纳米颗粒提供了一个有趣的新实例。此外,他们应该提供一个理想的模型系统来评估新的电动理论。

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