Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 128 00 Praha 2, Czech Republic.
Institute of Macromolecular Compounds of the Russian Academy of Sciences, 199004 St. Petersburg, Russia and St. Petersburg National Research University of Information Technologies, Mechanics and Optics, 197101, St. Petersburg, Russia.
Soft Matter. 2016 May 25;12(21):4846-52. doi: 10.1039/c6sm00109b.
Hydrophobic polyelectrolytes exhibit intra-molecular nano-scale self-organization instead of macroscopic phase separation because of the interplay between short-range hydrophobic attraction and long-range electrostatic repulsion. We aim to unravel how the morphology of the intra-molecular nanostructures can be controlled through the topology of the macromolecule on one hand and by adjustable ionization on the other hand. Specifically, we focus on hydrophobic star-branched polyelectrolytes, composed of either strong or weak acidic monomers. While both collapse in a globule when uncharged, and expand to full stretching of arms at high ionization, they exhibit quite different intermediate scenarios. For the strong ones, we observe the formation of bundles of arms as the main structural motif, and for the weak ones the intramolecular micelle-like structure is found at the same overall charge of the macromolecule. Here intramolecular disproportionation leaves some arms in a collapsed virtually neutral core, while others are substantially ionized and stretched in the corona.
疏水型聚电解质由于短程疏水吸引力和长程静电排斥之间的相互作用,表现出分子内纳米级自组织,而不是宏观相分离。我们的目的是揭示如何通过大分子的拓扑结构和可调节的电离来控制分子内纳米结构的形态。具体来说,我们专注于疏水星型支化聚电解质,由强或弱酸性单体组成。虽然在不带电时两者都收缩成一个球,而在高电离时则伸展到完全伸展的臂,但它们表现出非常不同的中间情况。对于强的,我们观察到形成臂束作为主要结构基元,而对于弱的,则在相同的大分子总电荷下发现分子内胶束样结构。在这里,分子内歧化使得一些臂处于几乎中性的塌陷核心中,而其他臂则在冠区中被充分电离和伸展。