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Dimple Colloids with Tunable Cavity Size and Surface Functionalities
[Image: see text] Dimple colloids with well-defined cavities were synthesized by a modified dispersion polymerization. The key step in the procedure is the delayed addition of cross-linkers into the reaction mixture. By systematically studying the effect of the delayed addition time and the concentr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563412/ https://www.ncbi.nlm.nih.gov/pubmed/31231140 http://dx.doi.org/10.1021/acs.macromol.9b00406 |
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author | Guo, Yong van Ravensteijn, Bas G. P. Kegel, Willem K. |
author_facet | Guo, Yong van Ravensteijn, Bas G. P. Kegel, Willem K. |
author_sort | Guo, Yong |
collection | PubMed |
description | [Image: see text] Dimple colloids with well-defined cavities were synthesized by a modified dispersion polymerization. The key step in the procedure is the delayed addition of cross-linkers into the reaction mixture. By systematically studying the effect of the delayed addition time and the concentration of the cross-linker on the resulting particle morphology, we identified the dominating driving force that underlies dimple formation. The delayed addition of cross-linkers results in colloids with a core–shell morphology consisting of a core rich in linear polymers and a cross-linked shell. This morphology was confirmed by selectively etching non-cross-linked material using dimethylformamide. With polymerization proceeding, consumption of monomers present in the swollen particles leads to contraction of the particles, which is larger for the core composed of linear polymers compared to the stiffer cross-linked shell. To accommodate this decrease in volume, the outer cross-linked shell has to buckle, resulting in a well-defined dimple. Furthermore, we extended the procedure to incorporate functional monomers, yielding chemically modifiable dimple particles. Subsequently, we showed that by leveraging the core–shell structure, these dimple particles can be used to prepare dumbbell-shaped colloids with one hollow and one solid lobe. These partially hollow anisotropic particles assemble into strings with well-defined orientations in an alternating current electric field. |
format | Online Article Text |
id | pubmed-6563412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-65634122019-06-20 Dimple Colloids with Tunable Cavity Size and Surface Functionalities Guo, Yong van Ravensteijn, Bas G. P. Kegel, Willem K. Macromolecules [Image: see text] Dimple colloids with well-defined cavities were synthesized by a modified dispersion polymerization. The key step in the procedure is the delayed addition of cross-linkers into the reaction mixture. By systematically studying the effect of the delayed addition time and the concentration of the cross-linker on the resulting particle morphology, we identified the dominating driving force that underlies dimple formation. The delayed addition of cross-linkers results in colloids with a core–shell morphology consisting of a core rich in linear polymers and a cross-linked shell. This morphology was confirmed by selectively etching non-cross-linked material using dimethylformamide. With polymerization proceeding, consumption of monomers present in the swollen particles leads to contraction of the particles, which is larger for the core composed of linear polymers compared to the stiffer cross-linked shell. To accommodate this decrease in volume, the outer cross-linked shell has to buckle, resulting in a well-defined dimple. Furthermore, we extended the procedure to incorporate functional monomers, yielding chemically modifiable dimple particles. Subsequently, we showed that by leveraging the core–shell structure, these dimple particles can be used to prepare dumbbell-shaped colloids with one hollow and one solid lobe. These partially hollow anisotropic particles assemble into strings with well-defined orientations in an alternating current electric field. American Chemical Society 2019-05-17 2019-06-11 /pmc/articles/PMC6563412/ /pubmed/31231140 http://dx.doi.org/10.1021/acs.macromol.9b00406 Text en Copyright © 2019 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 | Guo, Yong van Ravensteijn, Bas G. P. Kegel, Willem K. Dimple Colloids with Tunable Cavity Size and Surface Functionalities |
title | Dimple Colloids with Tunable Cavity Size and Surface Functionalities |
title_full | Dimple Colloids with Tunable Cavity Size and Surface Functionalities |
title_fullStr | Dimple Colloids with Tunable Cavity Size and Surface Functionalities |
title_full_unstemmed | Dimple Colloids with Tunable Cavity Size and Surface Functionalities |
title_short | Dimple Colloids with Tunable Cavity Size and Surface Functionalities |
title_sort | dimple colloids with tunable cavity size and surface functionalities |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563412/ https://www.ncbi.nlm.nih.gov/pubmed/31231140 http://dx.doi.org/10.1021/acs.macromol.9b00406 |
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