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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2018
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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. |
format | Online Article Text |
id | pubmed-6307084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
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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