Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/108990
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorDepartment of Food Science and Nutritionen_US
dc.creatorChan, AKHen_US
dc.creatorChau, MHen_US
dc.creatorRen, Yen_US
dc.creatorJiang, JJen_US
dc.creatorWong, MKen_US
dc.creatorLeung, FKCen_US
dc.date.accessioned2024-09-12T03:28:17Z-
dc.date.available2024-09-12T03:28:17Z-
dc.identifier.urihttp://hdl.handle.net/10397/108990-
dc.language.isoenen_US
dc.publisherJohn Wiley & Sonsen_US
dc.rights© 2023 Wiley-VCH GmbHen_US
dc.rightsThis is the peer reviewed version of the following article: Chan, A. K.-H., Chau, M.-H., Ren, Y., Jiang, J.-J., Wong, M.-K., & Leung, F. K.-C. (2024). Controlled Supramolecular Assemblies of Chiral Cyclometalated Gold (III) Amphiphiles in Aqueous Media. ChemPlusChem, 89(2), e202300316, which has been published in final form at https://doi.org/10.1002/cplu.202300316. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en_US
dc.subjectAmphiphilesen_US
dc.subjectChiralityen_US
dc.subjectGolden_US
dc.subjectSelf-assemblyen_US
dc.subjectSupramolecular chemistryen_US
dc.titleControlled supramolecular assemblies of chiral cyclometalated gold (III) amphiphiles in aqueousen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume89en_US
dc.identifier.issue2en_US
dc.identifier.doi10.1002/cplu.202300316en_US
dcterms.abstractGold (III) cyclometalated based amphiphiles in aqueous media have been revealed with excellent supramolecular transformations to external stimuli to open new pathways for soft functional material fabrications. Herein, we report a new chiral cyclometalated gold (III) amphiphile (GA) assembling into lamellar nanostructures in aqueous media confirmed with transmission electron microscopy (TEM). Counterion exchange with D-, L-, or racemic-camphorsulfonates features the significant supramolecular helicity enhancements, enabling transformations of GA from lamellar structure to vesicles and to nanotubes with multi-equivalents of counterion. The limited cytotoxicity of GA in aqueous media exhibits good biocompatibility.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationChemPlusChem, Feb 2024, v. 89, no. 2, e202300316en_US
dcterms.isPartOfChemPlusChemen_US
dcterms.issued2024-02-
dc.identifier.eissn2192-6506en_US
dc.identifier.artne202300316en_US
dc.description.validate202309 bcrcen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera3197-
dc.identifier.SubFormID49771-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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