Perevyazko Igor, Mikusheva Nina, Lezov Alexey, Gubarev Alexander, Enke Marcel, Winter Andreas, Schubert Ulrich S, Tsvetkov Nikolay
Department of Molecular Biophysics and Polymer Physics, St. Petersburg University, Universitetskaya Nab. 7/9, 199034 Saint-Petersburg, Russia.
Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldt Str. 10, 07743 Jena, Germany.
Polymers (Basel). 2022 Feb 26;14(5):944. doi: 10.3390/polym14050944.
The contribution deals with the synthesis of the poly(methacrylate)-based copolymers, which contain ferrocene and/or terpyridine moieties in the side chains, and the subsequent analysis of their self-assembly behavior upon supramolecular/coordination interactions with Eu3+ and Pd2+ ions in dilute solutions. Both metal ions provoke intra and inter molecular complexation that results in the formation of large supra-macromolecular assembles of different conformation/shapes. By applying complementary analytical approaches (i.e., sedimentation-diffusion analysis in the analytical ultracentrifuge, dynamic light scattering, viscosity and density measurements, morphology studies by electron microscopy), a map of possible conformational states/shapes was drawn and the corresponding fundamental hydrodynamic and macromolecular characteristics of metallo-supramolecular assemblies at various ligand-to-ion molar concentration ratios (M/L) in extremely dilute polymer solutions (c[η]≈0.006) were determined. It was shown that intramolecular complexation is already detected at (L≈0.1), while at M/L>0.5 solution/suspension precipitates. Extreme aggregation/agglomeration behavior of such dilute polymer solutions at relatively “high” metal ion content is explained from the perspective of polymer-solvent and charge interactions that will accompany the intramolecular complexation due to the coordination interactions.
该论文涉及含二茂铁和/或三联吡啶侧基的聚甲基丙烯酸酯基共聚物的合成,以及随后对其在稀溶液中与Eu3+和Pd2+离子发生超分子/配位相互作用时自组装行为的分析。两种金属离子都会引发分子内和分子间的络合作用,从而形成不同构象/形状的大型超分子聚集体。通过应用互补的分析方法(即分析超速离心机中的沉降-扩散分析、动态光散射、粘度和密度测量、电子显微镜形态学研究),绘制了可能的构象状态/形状图,并确定了在极稀聚合物溶液(c[η]≈0.006)中不同配体与离子摩尔浓度比(M/L)下金属超分子聚集体相应的基本流体动力学和大分子特征。结果表明,在(L≈0.1)时已检测到分子内络合作用,而在M/L>0.5时溶液/悬浮液会沉淀。从聚合物-溶剂和电荷相互作用的角度解释了在相对“高”金属离子含量下这种稀聚合物溶液的极端聚集/团聚行为,这种相互作用会伴随由于配位相互作用导致的分子内络合作用。