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

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dc.contributor.authorLee, Haksu-
dc.contributor.authorKhazi, Mohammed Iqbal-
dc.contributor.authorJang, Daewoong-
dc.contributor.authorKadamannil, Nila Nandha-
dc.contributor.authorJelinek, Raz-
dc.contributor.authorKim, Jong-Man-
dc.date.accessioned2025-04-09T08:00:13Z-
dc.date.available2025-04-09T08:00:13Z-
dc.date.issued2025-03-
dc.identifier.issn0743-7463-
dc.identifier.issn1520-5827-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/207010-
dc.description.abstractForming 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.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleChiral Amine-Induced Assembly of Toroidal Structures with a Carboxylic Acid-Functionalized, Polymerizable Macrocyclic Diacetylene-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acs.langmuir.5c00347-
dc.identifier.scopusid2-s2.0-105001209774-
dc.identifier.wosid001444252200001-
dc.identifier.bibliographicCitationLangmuir, v.41, no.11, pp 7824 - 7834-
dc.citation.titleLangmuir-
dc.citation.volume41-
dc.citation.number11-
dc.citation.startPage7824-
dc.citation.endPage7834-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusTOPOCHEMICAL POLYMERIZATION-
dc.subject.keywordPlusPOLYDIACETYLENE-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusCOPOLYMER-
dc.subject.keywordPlusMICELLES-
dc.subject.keywordPlusNANOTUBE-
dc.subject.keywordPlusGELATION-
dc.subject.keywordPlusSENSOR-
dc.subject.keywordPlusRING-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acs.langmuir.5c00347-
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