ArticleJournal of the American Chemical Society2025
Chiral Aromatic Micelles as Chiroptical Host Tools for Large Metallodyes in Water.
Article in Journal of the American Chemical Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed.
- Aqueous Accumulation and Co-Accumulation of Multiple Cationic Porphyrins within a Polyaromatic Capsule.JACS Au · 2026Article
- Chiral Micellar Assemblies for Circularly Polarized Luminescence Amplification, Dye Encapsulation, and Multilevel Information Encryption.Angewandte Chemie (International ed. in English) · 2026Article
- Challenging the dry core paradigm: hydrated reactivity emerges within micellar cores.Chemical science · 2026Article
- Cavity Constriction and Chiralization of Polyaromatic Subnanotubes via Post-assembly Ligand/Metal Modification.Journal of the American Chemical Society · 2026Article
- Self-Assembly of Unconventional Triphenylene-Based Frustrated Amphiphile in Solution.Langmuir : the ACS journal of surfaces and colloids · 2026Article
- Hybridized Host Functions in Polyaromatic Tube-in-Capsule Composites.Angewandte Chemie (International ed. in English) · 2026Article
- Design and Structural Transformations of Zinc(II) Knotted Cage Frameworks.Angewandte Chemie (International ed. in English) · 2025Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In contrast to abundant aliphatic chiral cavities in nature, synthetic chiral cavities formed by self-assembly of aromatic subunits are quite rare, particularly providing an ability in induced chirality. Here, we report new chiral aromatic micelles capable of inducing the optical chirality of large metallodyes upon encapsulation. The aromatic micelle, with a core diameter of ∼3 nm, forms from axially chiral amphiphiles featuring a bent mesityl-substituted BINOL framework. Unlike alkyl and aromatic micelles reported previously, the obtained micelle emits strong fluorescence (Φ
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.