Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560012, India.
Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore 632 014, Tamil Nadu, India.
Langmuir. 2021 Oct 26;37(42):12457-12465. doi: 10.1021/acs.langmuir.1c02156. Epub 2021 Oct 13.
Periodically grafted amphiphilic copolymers (PGACs) were earlier shown by us to adopt a zigzag folded conformation in the solid state, which enabled the backbone and pendant segments to segregate and occupy alternate layers in a lamellar structure. The conformational transition from a random coil to a zigzag folded chain in solution is an interesting problem, which is largely unexplored. To examine this, an orthogonally clickable parent polyester was sequentially clicked with two types of poly(ethylene glycol) (PEG) segments: one is a simple PEG and the other is a PEG that carries a dipolar chromophore. These two hydrophilic PEG segments, installed in a periodic and alternating fashion along the hydrocarbon-rich (HC) polyester backbone, ensure that the folded chains are formed upon folding and carry chromophoric dipoles oriented along the same direction, thereby generating a large net dipole. The folding-induced alignment of chromophores in solution was followed using second harmonic light scattering (SHLS), wherein the intensity of the frequency-doubled scattered light () is measured. Folding was induced by adding a polar solvent, like methanol, to a chloroform solution of the polymer; methanol desolvates the HC backbone but solubilizes the pendant PEG segments, thus inducing folding. The second harmonic intensity () increased initially with methanol concentration and then saturated; in contrast, remained invariant with the solvent composition in the case of an analogous model chromophore. Furthermore, in a model PGAC carrying chromophore-bearing PEG segments on every repeat unit, decreased with increasing methanol composition, revealing the formation of a centrosymmetric folded chain, wherein the chromophoric dipoles on either side cancel each other. Thus, this study clearly reveals that the zigzag chain folding of PGACs can be induced by a segment-selective solvent, resulting in the rather elusive directional ordering of chromophoric dipoles in solution.
周期性接枝两亲共聚物(PGAC)早前已被我们证明在固态下采取之字形折叠构象,这使得主链和侧链段在层状结构中分离并占据交替层。在溶液中从无规线团到之字形折叠链的构象转变是一个有趣的问题,目前尚未得到充分探索。为了研究这个问题,我们使用正交 click 反应,将一种双亲聚酯依次与两种类型的聚乙二醇(PEG)片段进行 click 反应:一种是简单的 PEG,另一种是带有偶极生色团的 PEG。这两种亲水性 PEG 片段沿富含碳氢化合物(HC)的聚酯主链周期性和交替排列,确保折叠链在折叠时形成,并携带沿相同方向取向的偶极生色团,从而产生大的净偶极矩。通过使用二次谐波光散射(SHLS)来跟踪溶液中折叠诱导的生色团取向,其中测量倍频散射光()的强度。通过向聚合物的氯仿溶液中添加极性溶剂(如甲醇)来诱导折叠;甲醇去溶剂化 HC 主链但溶解侧链 PEG 片段,从而诱导折叠。随着甲醇浓度的增加,折叠诱导的二次谐波强度()最初增加,然后达到饱和;相比之下,在类似的模型生色团的情况下,随着溶剂组成的变化,仍保持不变。此外,在每个重复单元上带有生色团的 PEG 片段的模型 PGAC 中,随着甲醇组成的增加, 降低,揭示了形成对称折叠链的情况,其中两侧的偶极生色团相互抵消。因此,这项研究清楚地表明,PGAC 的之字形链折叠可以通过选择性溶剂来诱导,从而导致溶液中偶极生色团的难以捉摸的定向有序。