Self-Assembly of Star Micelle into Vesicle in Solvents of Variable Quality: The Star Micelle Retains Its Core–Shell Nanostructure in the Vesicle
Source abstract
Abstract
Intra- and intermolecular interactions of star polymers in dilute solutions are of fundamental importance for both theoretical interest and hierarchical self-assembly into functional nanostructures. Here, star micelles with a polystyrene corona and a small ionic core bearing platinum(II) complexes have been regarded as a model of star polymers to mimic their intra- and interstar interactions and self-assembled behaviors in solvents of weakening quality. In the chloroform/methanol mixture solvents, the star micelles can self-assemble to form vesicles, in which the star micelles shrink significantly and are homogeneously distributed on the vesicle surface. Unlike the morphological evolution of conventional amphiphiles from micellar to vesicular, during which the amphiphilic molecules are commonly reorganized, the star micelles still retain their core-shell nanostructures in the vesicles and the coronal chains of the star micelle between the ionic cores are fully interpenetrated.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Porphyrin and Phthalocyanine Chemistry · Surfactants and Colloidal Systems · Mesoporous Materials and Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Nonferrous Metals Chemistry and Resources Utilization of Gansu Province, State Key Laboratory of Applied Organic Chemistry, and College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou City, Gansu Province, China
Funding
Ministry of Education of the People's Republic of China · National Natural Science Foundation of China · State Key Laboratory of Supramolecular Structure and Materials, Jilin University
References (27)
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