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Polyferrocene-Based Cubosomes : Conversion to Magnetic Mesoporous Microparticles, Supramolecular Modification, and Oxidation Response

DOI zum Zitieren der Version auf EPub Bayreuth: https://doi.org/10.15495/EPub_UBT_00009070
URN to cite this document: urn:nbn:de:bvb:703-epub-9070-3

Title data

Wong, Chin Ken ; Azhdari, Suna ; Foith, Marvin ; Chen, Chen ; Gröschel, André H.:
Polyferrocene-Based Cubosomes : Conversion to Magnetic Mesoporous Microparticles, Supramolecular Modification, and Oxidation Response.
In: Advanced Functional Materials. Vol. 36 (2026) Issue 19 . - e22652.
ISSN 1616-3028
DOI der Verlagsversion: https://doi.org/10.1002/adfm.202522652

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Project information

Project title:
Project's official title
Project's id
Polymer Cubosome: Synthese, Selbstassemblierung und Umwandlung zu Elektro- and Photokatalysatoren
526222003
Open Access Publizieren
No information

Project financing: Deutsche Forschungsgemeinschaft

Abstract

Polymer cubosomes (PCs) are an emerging class of mesoporous microparticles that are produced through solution self-assembly of highly asymmetric block copolymers (BCPs). They proved useful for encapsulation or templating replicas for catalysis and energy storage. Although PCs made from BCPs with intrinsic functions such as response to stimuli, degradation, or coordination canopen their use for more diverse applications, reports on PCs with innate functions are still rare. Herein, PCs based on organometallic BCPs bearing pendant ferrocene moieties is reported. The poly(ethylene oxide)-block-poly(2-(methacryoyloxy)ethyl ferrocene carboxylate) BCPs (PEO44-b-PFcEMAx) with highly asymmetric weight fraction is synthesized in favor of the hydrophobic block (x = 76–245). Of these, PEO44-b-PFcEMA96 assembled into PCs with an average particle diameter of 1.82 ± 0.48 µm, a double diamond lattice, and a pore diameter of ≈30–40 nm. The functionality of these PCs are showcased by i) templating metal oxide replica with concurrent decoration of magnetic iron oxide upon calcination, ii) supramolecular modification of the PC wall via host-guest chemistry, and iii) degradation of the PC structure on demand through oxidation. Exploring these and other block chemistries enriches thetoolbox for PC applications and fosters theunderstanding about PCs by identifying differences or communalities in formation mechanisms and particle structure.

Further data

Item Type: Article in a journal
DDC Subjects: 500 Science
Institutions of the University: Faculties
Faculties > Faculty of Biology, Chemistry and Earth Sciences
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Polymer Materials for Electrochemical Storage
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Polymer Materials for Electrochemical Storage > Chair Polymer Materials for Electrochemical Storage - Univ.-Prof. Dr. André Gröschel
Research Institutions
Research Institutions > Central research institutes
Research Institutions > Central research institutes > Bayreuth Institute of Macromolecular Research - BIMF
Research Institutions > Central research institutes > Bayerisches Zentrum für Batterietechnik - BayBatt
Research Institutions > Affiliated Institutes
Research Institutions > Affiliated Institutes > Bavarian Polymer Institute (BPI)
Language: English
Originates at UBT: Yes
URN: urn:nbn:de:bvb:703-epub-9070-3
Date Deposited: 02 Apr 2026 12:03
Last Modified: 02 Apr 2026 12:03
URI: https://epub.uni-bayreuth.de/id/eprint/9070

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