超分子化学
卟啉
范德瓦尔斯力
聚合物
高分子
超分子聚合物
结晶学
乙醚
化学
超分子组装
材料科学
高分子化学
晶体结构
分子
光化学
有机化学
生物化学
作者
Ryoga Hori,Koichi Higashimine,Osamu Notoya,Ken‐ichi Shinohara
出处
期刊:Langmuir
[American Chemical Society]
日期:2024-02-26
卷期号:40 (10): 5535-5544
标识
DOI:10.1021/acs.langmuir.4c00164
摘要
We report the synthesis and microscopic investigations of two chiral helical porphyrin supramolecular polymers with different coordinating metals that are expected to be capable of serving as synthetic macromolecular motors driven by thermal fluctuations. Furthermore, based on their microscopic images, we propose a stepwise process for the formation of higher-order structures. These porphyrins formed completely different association states, and this was reflected in the marked differences in the shapes of the supramolecular polymers. The Cu-TChOAlaCPP supramolecular polymers formed H-aggregate rods in diisopropyl ether, then grew into superhelices and then into ribbons. On the other hand, Zn-TChOAlaCPP supramolecular polymers formed aggregates based on van der Waals interactions in diethyl ether, then grew into fibers and then grew into multiple-helices and ribbons. In addition, we imaged the interaction between long and short chains of the Cu-TChOAlaCPP supramolecular polymer by fast-scanning atomic force microscopy, and we indicated the availability as a macromolecular motor driven by thermal fluctuations.
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