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Wet-Chemical Synthesis of Chiral Colloids

[Image: see text] We disclose a method for the synthesis of chiral colloids from spontaneously formed hollow sugar-surfactant microtubes with internally confined mobile colloidal spheres. Key feature of our approach is the grafting of colloid surfaces with photoresponsive coumarin moieties, which al...

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Autores principales: Ouhajji, Samia, van Ravensteijn, Bas G. P., Fernández-Rico, Carla, Lacina, Kanvaly S., Philipse, Albert P., Petukhov, Andrei V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307084/
https://www.ncbi.nlm.nih.gov/pubmed/30428258
http://dx.doi.org/10.1021/acsnano.8b05065
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author Ouhajji, Samia
van Ravensteijn, Bas G. P.
Fernández-Rico, Carla
Lacina, Kanvaly S.
Philipse, Albert P.
Petukhov, Andrei V.
author_facet Ouhajji, Samia
van Ravensteijn, Bas G. P.
Fernández-Rico, Carla
Lacina, Kanvaly S.
Philipse, Albert P.
Petukhov, Andrei V.
author_sort Ouhajji, Samia
collection PubMed
description [Image: see text] We disclose a method for the synthesis of chiral colloids from spontaneously formed hollow sugar-surfactant microtubes with internally confined mobile colloidal spheres. Key feature of our approach is the grafting of colloid surfaces with photoresponsive coumarin moieties, which allow for UV-induced, covalent clicking of colloids into permanent chains, with morphologies set by the colloid-to-tube diameter ratio. Subsequent dissolution of tube confinement yields aqueous suspensions that comprise bulk quantities of a variety of linear chains, including single helical chains of polystyrene colloids. These colloidal equivalents of chiral (DNA) molecules are intended for microscopic study of chiral dynamics on a single-particle level.
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spelling pubmed-63070842019-01-02 Wet-Chemical Synthesis of Chiral Colloids Ouhajji, Samia van Ravensteijn, Bas G. P. Fernández-Rico, Carla Lacina, Kanvaly S. Philipse, Albert P. Petukhov, Andrei V. ACS Nano [Image: see text] We disclose a method for the synthesis of chiral colloids from spontaneously formed hollow sugar-surfactant microtubes with internally confined mobile colloidal spheres. Key feature of our approach is the grafting of colloid surfaces with photoresponsive coumarin moieties, which allow for UV-induced, covalent clicking of colloids into permanent chains, with morphologies set by the colloid-to-tube diameter ratio. Subsequent dissolution of tube confinement yields aqueous suspensions that comprise bulk quantities of a variety of linear chains, including single helical chains of polystyrene colloids. These colloidal equivalents of chiral (DNA) molecules are intended for microscopic study of chiral dynamics on a single-particle level. American Chemical Society 2018-11-14 2018-12-26 /pmc/articles/PMC6307084/ /pubmed/30428258 http://dx.doi.org/10.1021/acsnano.8b05065 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Ouhajji, Samia
van Ravensteijn, Bas G. P.
Fernández-Rico, Carla
Lacina, Kanvaly S.
Philipse, Albert P.
Petukhov, Andrei V.
Wet-Chemical Synthesis of Chiral Colloids
title Wet-Chemical Synthesis of Chiral Colloids
title_full Wet-Chemical Synthesis of Chiral Colloids
title_fullStr Wet-Chemical Synthesis of Chiral Colloids
title_full_unstemmed Wet-Chemical Synthesis of Chiral Colloids
title_short Wet-Chemical Synthesis of Chiral Colloids
title_sort wet-chemical synthesis of chiral colloids
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307084/
https://www.ncbi.nlm.nih.gov/pubmed/30428258
http://dx.doi.org/10.1021/acsnano.8b05065
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