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Hierarchical chiral supramolecular assemblies with strong and invertible chiroptical properties

Title
Hierarchical chiral supramolecular assemblies with strong and invertible chiroptical properties
Authors
Kim M.; Zhang M.; Zhu Y.; Yan Y.; Pu X.; Choi W.; Chung S.; Cho K.; Kim J.; Tsukruk V.V.
Ewha Authors
김동하
SCOPUS Author ID
김동하scopus
Issue Date
2025
Journal Title
Science
ISSN
0036-8075JCR Link
Citation
Science vol. 389, no. 6761
Keywords
N,n Dimethylformamide; Hitachi S3400; Hitachi Su8230; Invenio Ftir Spectrometer; Jasco Fp-8500 Spectrophotometers; Jem-2100plus; Jsm- 7610f; Shimadzu Uv-2450; Spin- 1200d X- Ray Diffractometer; Nanocrystal; Chemical Bonding; Chemical Property; Crystal Structure; Hydrogen; Aggregation-induced Emission; Anisotropy; Article; Atomic Force Microscopy; Biology; Chemistry; Chiral Supramolecular Assemblies; Chiroptical Properties; Circular Dichroism; Circularly Polarized Luminescence; Data Clustering; Density Functional Theory; Dispersity; Encryption; Energy Dispersive X Ray Spectroscopy; Fourier Transform Infrared Spectroscopy; Gel Permeation Chromatography; Hydrodynamics; Hydrogen Bond; Hydrolysis; Imaging; Luminescence; Medical Procedures; Molecular Dynamics; Photon Correlation Spectroscopy; Physics; Polymerization; Precipitation; Quantum Yield; Scanning Electron Microscopy; Simulation; Temperature; Thermodynamics; Transmission Electron Microscopy; X Ray Diffraction; Chirality; Color; Controlled Study; Kinetics; Micelle; Pharmaceutics
Publisher
American Association for the Advancement of Science
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
supramolecular assemblies hold great promise for advanced chiral materials because of their structural diversity and dynamic features, but their low chiroptical activity limits practical applications. We report hierarchical supramolecular assemblies with giant chiroptical activity and mechanical attributes achieved through coassembly of achiral amphiphilic unimolecular micelles and chiral additives. Chiral fibrillar assemblies emerge from the nanostructured environment imposed by the micelles, driven by progressive chirality transfer through multiple hydrogen bonds between components. Integrating multifarious achiral luminescent molecules and nanocrystals into these assemblies leads to full-color circularly polarized luminescence–active materials with dissymmetry factors of ~10−1. A concentration-dependent chirality inversion is accessed through tailoring the coassembly kinetics. this strategy enables efficient red CPL, crucial for quantum and optical technologies. © 2025 Elsevier B.V., All rights reserved.
DOI
10.1126/science.adu0296
ISBN
9781844654512

9781844652044
Appears in Collections:
자연과학대학 > 화학·나노과학전공 > Journal papers
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