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Chiral Amine-Induced Assembly of Toroidal Structures with a Carboxylic Acid-Functionalized, Polymerizable Macrocyclic Diacetylene

Authors
Lee, HaksuKhazi, Mohammed IqbalJang, DaewoongKadamannil, Nila NandhaJelinek, RazKim, Jong-Man
Issue Date
Mar-2025
Publisher
American Chemical Society
Citation
Langmuir, v.41, no.11, pp 7824 - 7834
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
Langmuir
Volume
41
Number
11
Start Page
7824
End Page
7834
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/207010
DOI
10.1021/acs.langmuir.5c00347
ISSN
0743-7463
1520-5827
Abstract
Forming toroidal structures through self-assembly strategies on a small scale poses significant challenges due to the bending energy barriers involved. Herein, we present the chiral amine-induced fabrication of toroidal structures assembled with a carboxylic acid-functionalized macrocyclic diacetylene (MCDA-COOH/PEA). The formation of microtoroids follows an interesting, heat-induced morphological transition pathway, starting from seeds to the sphere and eventually forming stable microtoroids. The structural arrangements of the microtoroids were analyzed through spectroscopic techniques and X-ray diffraction. These microtoroids further undergo topochemical polymerization upon UV light irradiation, resulting in a blue-phase polymeric PDA structure. This study demonstrates the role of chiral control, intermolecular interactions, and molecular rearrangement via energy minimization in a heat-induced morphological transition pathway. This process induces curvature between adjacent building blocks, promoting the formation of stable toroidal structures with minimized free energy. This study presents a promising self-assembly approach to constructing highly organized functional architectures.
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