Institute for Global Prominent Research (IGPR), Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba, 263-8522, Japan.
Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba, 263-8522, Japan.
Angew Chem Int Ed Engl. 2021 Dec 20;60(52):26986-26993. doi: 10.1002/anie.202110224. Epub 2021 Nov 22.
Synthesis of one-dimensional nanofibers with distinct topological (higher-order structural) domains in the same main chain is one of the challenging topics in modern supramolecular polymer chemistry. Non-uniform structural transformation of supramolecular polymer chains by external stimuli may enable preparation of such nanofibers. To demonstrate feasibility of this post-polymerization strategy, we prepared a photoresponsive helically folded supramolecular polymers from a barbiturate monomer containing an azobenzene-embedded rigid π-conjugated scaffold. In contrast to previous helically folded supramolecular polymers composed of a more flexible azobenzene monomer, UV-light induced unfolding of the newly prepared helically folded supramolecular polymers occurred nonuniformly, affording topological block copolymers consisting of folded and unfolded domains. The formation of such blocky copolymers indicates that the photoinduced unfolding of the helically folded structures initiates from relatively flexible parts such as termini or defects. Spontaneous refolding of the unfolded domains was observed after visible-light irradiation followed by aging to restore fully folded structures.
在同一条主链上合成具有不同拓扑(高阶结构)结构域的一维纳米纤维是现代超分子聚合物化学的挑战性课题之一。通过外部刺激对超分子聚合物链进行非均匀的结构转变可能会制备出这种纳米纤维。为了证明这种聚合后策略的可行性,我们从含有偶氮苯嵌入刚性π共轭支架的巴比妥酸单体制备了光响应性螺旋折叠超分子聚合物。与以前由更灵活的偶氮苯单体组成的螺旋折叠超分子聚合物相比,新制备的螺旋折叠超分子聚合物的 UV 光诱导解折叠是非均匀的,得到了由折叠和未折叠域组成的拓扑嵌段共聚物。这种块状共聚物的形成表明,螺旋折叠结构的光诱导解折叠是从相对灵活的部分(如末端或缺陷)开始的。在可见光照射后,观察到未折叠域的自发折叠,然后老化以恢复完全折叠的结构。