Hofman Anton H, Pedone Matteo, Kamperman Marleen
Polymer Science, Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands.
ACS Polym Au. 2022 Jun 8;2(3):169-180. doi: 10.1021/acspolymersau.1c00044. Epub 2021 Dec 23.
Because of their permanent charge, strong polyelectrolytes remain challenging to characterize, in particular, when they are combined with hydrophobic features. For this reason, they are typically prepared through a postmodification of a fully hydrophobic precursor. Unfortunately, these routes often result in an incomplete functionalization or otherwise require harsh reaction conditions, thus limiting their applicability. To overcome these problems, in this work a strategy is presented that facilitates the preparation of well-defined strong polyanions by starting from protected 3-sulfopropyl methacrylate monomers. Depending on the chemistry of the protecting group, the hydrophobic precursor could be quantitatively converted into a strong polyanion under nucleophilic, acidic, or basic conditions. As a proof of concept, orthogonally protected diblock copolymers were synthesized, selectively deprotected, and allowed to self-assemble in aqueous solution. Further conversion into a fully water-soluble polyanion was achieved by deprotecting the second block as well.
由于其永久性电荷,强聚电解质的表征仍然具有挑战性,特别是当它们与疏水特性相结合时。因此,它们通常通过对完全疏水的前体进行后修饰来制备。不幸的是,这些方法往往导致功能化不完全,或者需要苛刻的反应条件,从而限制了它们的适用性。为了克服这些问题,在这项工作中提出了一种策略,该策略通过从受保护的甲基丙烯酸3-磺丙酯单体开始,促进了定义明确的强聚阴离子的制备。根据保护基团的化学性质,疏水前体可以在亲核、酸性或碱性条件下定量转化为强聚阴离子。作为概念验证,合成了正交保护的二嵌段共聚物,选择性地脱保护,并使其在水溶液中自组装。通过对第二个嵌段也进行脱保护,进一步实现了向完全水溶性聚阴离子的转化。