Polymer nanoparticles with low curvature, especially two-dimensional (2D) soft materials, are rich in functions and outstanding properties and have received extensive attention. Crystallization-driven self-assembly (CDSA) of linear semicrystalline block copolymers is currently a common method of constructing 2D platelets of uniform size. Although accompanied by high controllability, this CDSA method usually and inevitably requires a longer aging time and lower assembly concentration, limiting the large-scale preparation of nanoaggregates. In this study, a series of all-bottlebrush-type block copolymers, poly(octadecyl acrylate)--poly(oligoethylene glycol methyl ether methacrylate)s are prepared by living polymerization. Driven by the synergistic crystallization of crystalline side chains and the rapid microphase separation of bottlebrush topology, these polymers can assemble into uniform 2D circular platelet micelles in a few minutes, without being affected by a high assembly concentration. In this process, epitaxial growth of the bottlebrush molecules proceeds with rigid cylindrical molecular conformation at the micelle crystallization sites and eventually provides a sandwich-type micelle according to a head-to-head stacking mode. This is explained as a "crystallization-assisted rapid microphase separation" mechanism. The micelle structures are affected by the assembly solvent and temperature, the size of which shows a linear dependence on the assembly temperature below the melting point of the crystalline block, which can be used to precisely control the morphology of these 2D platelets. This study establishes an efficient and rapid method to prepare 2D polymer nanosoft materials, which are promising candidates for further development, preparation, and application of various nanomaterials.
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http://dx.doi.org/10.1021/jacs.4c16546 | DOI Listing |
J Am Chem Soc
January 2025
Tianjin Key Laboratory of Brine Chemical Engineering and Resource Eco-utilization, College of Chemical Engineering and Materials Science, Tianjin University of Science & Technology, Tianjin 300457, P. R. China.
Polymer nanoparticles with low curvature, especially two-dimensional (2D) soft materials, are rich in functions and outstanding properties and have received extensive attention. Crystallization-driven self-assembly (CDSA) of linear semicrystalline block copolymers is currently a common method of constructing 2D platelets of uniform size. Although accompanied by high controllability, this CDSA method usually and inevitably requires a longer aging time and lower assembly concentration, limiting the large-scale preparation of nanoaggregates.
View Article and Find Full Text PDFMacromol Rapid Commun
December 2024
Key Laboratory of Special Functional and Smart Polymer Materials of Ministry of Industry and Information Technology, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an, 710072, China.
Creating elastomers with high strength, toughness, and rapid self-healing remains a key challenge. These seemingly contradictory properties require innovative design strategies. Herein, a novel approach is proposed by simultaneously incorporating a unique triple hydrogen bond unit, benzene-1,3,5-tricarboxamide (BTA), and imidazole-Zn dynamic coordination into the elastomer.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
TUM School of Natural Sciences, Department of Physics, Chair for Functional Materials, Technical University of Munich, James-Franck-Street 1, 85748 Garching, Germany.
Ternary hybrid thin films composed of a diblock copolymer templating two types of nanoparticles (NPs) expand the functionality of binary systems, which renders them interesting for magnetic sensing or magnetic data storage applications. Herein, one-pot slot-die printed hybrid polystyrene--poly(methyl methacrylate) (PS--PMMA) thin films are prepared with iron oxide (magnetite, FeO, = 20 nm) and nickel NPs (Ni, = 46 nm) in one step by the advanced slot-die coating technique, which facilitates upscaling of fabrication. The evolution of the hybrid film morphology is probed with in situ grazing-incidence small-angle X-ray scattering and compared to that of a PS--PMMA thin film without NPs.
View Article and Find Full Text PDFMacromol Rapid Commun
October 2024
Helmholtz-Zentrum Hereon, Institute of Membrane Research, Max-Planck-Straße 1, 21502, Geesthacht, Germany.
In this study, reversible addition-fragmentation chain- transfer (RAFT) polymerization combined with the polymerization-induced self-assembly (PISA) technique is used to synthesize polyisoprene (PI)-based block and random copolymers with polystyrene (PS), aiming for high molecular weight and monomer conversion. The focus is to optimize the polymerization conditions to overcome the existing challenge of cross-linking and Diels-Alder reactions during the polymerization of isoprene, which typically constrain the reaction conversion and molecular weight of the final polymers. Using a poly(methacrylic acid) (PMAA) macroRAFT agent synthesized in ethanol at 80 °C, random and block copolymers of PS-PI with a target molecular weight of 50 000 g mole and a high monomer conversion of ≈80% are achieved under optimized conditions in water-emulsion at 35 °C.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
Institute of Polymer Science and Engineering, National Taiwan University, No. 1, Sec. 4 Roosevelt Road, Taipei 106319, Taiwan.
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