Chiral Amine-Induced Assembly of Toroidal Structures with a Carboxylic Acid-Functionalized, Polymerizable Macrocyclic Diacetylene
- Authors
- Lee, Haksu; Khazi, Mohammed Iqbal; Jang, Daewoong; Kadamannil, Nila Nandha; Jelinek, Raz; Kim, 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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