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Template-free fabrication of non-spherical polymeric nanoparticles is desirable for various applications, but has had limited success owing to thermodynamic favorability of sphere formation. Herein we present a simple way to prepare cubic nanoparticles of block copolymers by self-assembly from aqueous solutions at room temperature. Nanocubes with edges of 40-200 nm are formed spontaneously on different surfaces upon water evaporation from micellar solutions of triblock copolymers containing a central poly(ethylene oxide) block and terminal trimethylene carbonate/dithiolane blocks. These polymers self-assemble into 28±5 nm micelles in water. Upon drying, micelle aggregation and a kinetically controlled crystallization of central blocks evidently induce solid cubic particle formation. An approach for preserving the structures of these cubes in water by thiol- or photo-induced crosslinking was developed. The ability to solubilize a model hydrophobic drug, curcumin, was also explored.
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http://dx.doi.org/10.1002/anie.201709564 | DOI Listing |
ACS Macro Lett
September 2025
Department of Chemistry, Yonsei University, Seoul 03722, Republic of Korea.
Alkyne groups provide exceptional versatility for functionalization in macromolecular systems. However, the controlled anionic ring-opening polymerization (AROP) of epoxide monomers bearing terminal alkynes remains challenging due to the lability of alkynes under strongly basic conditions. Herein, we present a controlled AROP of glycidyl propargyl ether enabled by Lewis pair organocatalysis, employing a phosphazene base and triethylborane.
View Article and Find Full Text PDFRegen Ther
December 2025
Univ Toulouse, Inserm, ToNIC, Toulouse, France.
Background: Brain regeneration after injury is a challenge being tackled by numerous therapeutic strategies in pre-clinical development. There is growing interest in scaffolds implanted in brain lesions. Developments in 3D printing offer the possibility of designing complex structures of varying compositions adapted to tissue anatomy.
View Article and Find Full Text PDFJ Chem Theory Comput
September 2025
National Laboratory of Solid State Microstructure, Department of Physics, Nanjing University, Nanjing 210093, China.
Single-chain nanoparticles (SCNPs) represent a class of folded macromolecules that mimic biologically derived structures through the covalent cross-linking of polymer backbones. This study explores the interactions between SCNPs and lipid bilayers, focusing on the modulation of the membrane permeability and lipid dynamics. By employing coarse-grained Monte Carlo simulations, we investigate the behavior of diblock, triblock, and random copolymers of varying hydrophobicities and cross-linking densities in contact with lipid membranes.
View Article and Find Full Text PDFJ Phys Chem A
August 2025
Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Polymer-networked nanoparticles are a promising alternative to silicon semiconductors for the realization of neuromorphic computing platforms. Variations in the interaction between gold nanoparticles (AuNPs) and polyelectrolyte linkers lead to the controlled formation of engineered nanoparticle network (ENPN) structures exhibiting a broad range of topologies and dynamics. Using dissipative particle dynamics (DPD) simulations, we designed triblock copolymers with polyelectrolyte ends that can selectively attach to each of two AuNPs and bridged them together through a middle polymer segment (or block).
View Article and Find Full Text PDFQuasi-two-dimensional (quasi-2D) perovskites hold promise for flexible optoelectronics but suffer from mechanical brittleness. Here, we enhance their flexibility by incorporating a styrene-ethylene-butylene-styrene (SEBS) triblock copolymer during antisolvent-assisted crystallization. The resulting composite films exhibit ~100× lower Young's modulus and wrinkled morphologies that boost light absorption.
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