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dc.contributor.authorVan Gordon, Kyle
dc.contributor.authorBaúlde, Sandra
dc.contributor.authorMychinko, Mikhail
dc.contributor.authorHeyvaert, Wouter
dc.contributor.authorObelleiro-Liz, Manuel
dc.contributor.authorCriado, Alejandro
dc.contributor.authorBals, Sara
dc.contributor.authorLiz-Marzán, Luis
dc.contributor.authorMosquera Mosquera, Jesús
dc.date.accessioned2024-08-08T11:29:55Z
dc.date.available2024-08-08T11:29:55Z
dc.date.issued2023-10-25
dc.identifier.citationKyle Van Gordon, Sandra Baúlde, Mikhail Mychinko, Wouter Heyvaert, Manuel Obelleiro-Liz, Alejandro Criado, Sara Bals, Luis M. Liz-Marzán, and Jesús Mosquera Nano Letters 2023 23 (21), 9880-9886. DOI: 10.1021/acs.nanolett.3c02800es_ES
dc.identifier.issn1530-6984
dc.identifier.issn1530-6992 (eISSN)
dc.identifier.urihttp://hdl.handle.net/2183/38491
dc.description.abstract[Abstract]: The bottom-up production of chiral gold nanomaterials holds great potential for the advancement of biosensing and nano-optics, among other applications. Reproducible preparations of colloidal nanomaterials with chiral morphology have been reported, using cosurfactants or chiral inducers such as thiolated amino acids. However, the underlying growth mechanisms for these nanomaterials remain insufficiently understood. We introduce herein a purposely devised chiral inducer, a cysteine modified with a hydrophobic chain, as a versatile chiral inducer. The amphiphilic and chiral features of this molecule provide control over the chiral morphology and the chiroptical signature of the obtained nanoparticles by simply varying the concentration of chiral inducer. These results are supported by circular dichroism and electromagnetic modeling as well as electron tomography to analyze structural evolution at the facet scale. Our observations suggest complex roles for the factors involved in chiral synthesis: the chemical nature of the chiral inducers and the influence of cosurfactants.es_ES
dc.description.sponsorshipJ.M. Taboada and F. Obelleiro are thanked for support with electromagnetic simulations. The authors acknowledge financial support by the European Research Council (ERC CoG No. 815128 REALNANO to S. Bals; ERC AdG No. 787510, 4DbioSERS to L.M.L.-M.) and from MCIN/AEI/10.13039/501100011033 and “ESF Investing in your future” (Grant PID2020-117779RB-I00 to L.M.L.-M., Grant RYC2020-030183-I to A.C., and Grants RYC2019-027842-I, PID2020-117885GA-I00 to J.M.).es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/815128es_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/787510es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-117779RB-I00/ES/es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RYC2020-030183-I/ES/es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RYC2019-027842-I/ES/es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-117885GA-I00/ES/es_ES
dc.relation.urihttps://doi.org/10.1021/acs.nanolett.3c02800es_ES
dc.rights© 2023 The Authors. Published by American Chemical Society. This article is licensed under CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/)es_ES
dc.subjectChiral nanoparticleses_ES
dc.subjectGold nanoparticleses_ES
dc.subjectCircular dichroismes_ES
dc.subjectPlasmonic chiralityes_ES
dc.subjectElectron tomographyes_ES
dc.titleTuning the Growth of Chiral Gold Nanoparticles Through Rational Design of a Chiral Molecular Induceres_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleNano Letterses_ES
UDC.volume23es_ES
UDC.issue21es_ES
UDC.startPage9880es_ES
UDC.endPage9886es_ES
dc.identifier.doihttps://doi.org/10.1021/acs.nanolett.3c02800


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