Enantioselective control of lattice and shape chirality in inorganic nanostructures using chiral biomolecules
Assaf Ben-Moshe,
Sharon Grayer Wolf,
Maya Bar Sadan,
Lothar Houben,
Zhiyuan Fan,
Alexander O. Govorov and
Gil Markovich ()
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Assaf Ben-Moshe: Raymond and Beverly Sackler Faculty of Exact Sciences, School of Chemistry, Tel Aviv University
Sharon Grayer Wolf: Electron Microscopy Unit, Weizmann Institute of Science
Maya Bar Sadan: Ben Gurion University of the Negev
Lothar Houben: Ernst Ruska-Centre for Microscopy and Spectroscopy with Electrons, Forschungszentrum Jülich GmbH
Zhiyuan Fan: Ohio University
Alexander O. Govorov: Ohio University
Gil Markovich: Raymond and Beverly Sackler Faculty of Exact Sciences, School of Chemistry, Tel Aviv University
Nature Communications, 2014, vol. 5, issue 1, 1-9
Abstract:
Abstract A large number of inorganic materials form crystals with chiral symmetry groups. Enantioselectively synthesizing nanostructures of such materials should lead to interesting optical activity effects. Here we report the synthesis of colloidal tellurium and selenium nanostructures using thiolated chiral biomolecules. The synthesis conditions are tuned to obtain tellurium nanostructures with chiral shapes and large optical activity. These nanostructures exhibit visible optical and chiroptical responses that shift with size and are successfully simulated by an electromagnetic model. The model shows that they behave as chiral optical resonators. The chiral tellurium nanostructures are transformed into chiral gold and silver telluride nanostructures with very large chiroptical activity, demonstrating a simple colloidal chemistry path to chiral plasmonic and semiconductor metamaterials. These materials are natural candidates for studies related to interactions of chiral (bio)molecules with chiral inorganic surfaces, with relevance to asymmetric catalysis, chiral crystallization and the evolution of homochirality in biomolecules.
Date: 2014
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms5302
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DOI: 10.1038/ncomms5302
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