Autor: |
Kurka DW; Organic Chemistry Institute and Center for Soft Nanoscience, Westfälische Wilhelms-Universität Münster, Corrensstraße 40, 48149 Münster, Germany., Niehues M; Organic Chemistry Institute and Center for Soft Nanoscience, Westfälische Wilhelms-Universität Münster, Corrensstraße 40, 48149 Münster, Germany., Ravoo BJ; Organic Chemistry Institute and Center for Soft Nanoscience, Westfälische Wilhelms-Universität Münster, Corrensstraße 40, 48149 Münster, Germany. |
Jazyk: |
angličtina |
Zdroj: |
Langmuir : the ACS journal of surfaces and colloids [Langmuir] 2020 Apr 14; Vol. 36 (14), pp. 3924-3931. Date of Electronic Publication: 2020 Mar 30. |
DOI: |
10.1021/acs.langmuir.9b03891 |
Abstrakt: |
The preparation of colloidal molecules (CMs), that is, clusters of colloids with a defined aggregation number and configuration, is of continued and significant interest in colloid chemistry and materials science and numerous interactions have been utilized to drive their (self-)assembly. However, only very few reports are available on the assembly of CMs based on host-guest chemistry. In this paper, we investigate the assembly of like-charged silica particles into well-defined, core-satellite AB n -type CMs in water, mediated by host-guest interactions and geometric constraints. Exploiting the inherent dynamics of noncovalent attraction and making use of a soft polymer shell to enhance multivalent host-guest interactions, we successfully synthesized AB 3 , AB 4 , and AB 6 CMs by selecting the appropriate size ratio of satellite to core particles. |
Databáze: |
MEDLINE |
Externí odkaz: |
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