Patchy Micelles Research Articles

Multi-Dimensional Self-Assembly of a Dual-Responsive ABC Miktoarm Star Terpolymer.

This letter reports the first 2D self-assembly of ABC miktoarm star terpolymers based on dual-responsive polycaprolactone-arm-poly(N-isopropylacrylamide)-arm-poly(2-dimethylaminoethyl methacrylate) (μ-CID), which self-assembled into multilayer nanosheets comprising polycaprolactone single crystals in tetrahydrofuran (THF)/methanol mixed solvents. Interestingly, the nanosheets showed pH-responsive morphological transitions in aqueous solutions, yielding multidimensional assemblies, including 2D hexagonal aggregates, patchy nanofibrils, and patchy vesicles, at different pH values. The nanosheets also exhibited thermoresponsive transition to spherical patchy micelles at a temperature above the lower critical solution temperature (LCST) of the poly(N-isopropylacrylamide) block. This study offers a novel system for fundamental study on the self-assembly of miktoarm star terpolymers.

Enabling Heterogeneous Gold Catalysis with Patchy Micelles.

Patch works! Patchy block copolymer micelles with a corona consisting of two chemically different patches have been designed for the selective binding of catalytically active nanoparticles. The fabrication of nonwoven supports by electrospinning was combined with crystallization-driven self-assembly for precise control over micelle formation to prepare a new recyclable catalyst platform.

Supracolloidal chains of patchy micelles of diblock copolymers with in situ synthesized nanoparticles.

Supracolloidal chains of diblock copolymer micelles were functionalized with gold and silver nanoparticles (NPs). Both NPs were independently synthesized in situ in the core of spherical micelles which were then converted to patchy micelles. With these patchy micelles as colloidal monomers, supracolloidal chains were polymerized by combining the patches of neighboring micelles. Since all micelles contained NPs, NPs were incorporated in every repeat unit of chains. In addition, a single gold NP was synthesized in the micellar core in contrast to several silver NPs so that we differentiated the chains with Au NPs from those with Ag NPs by the number of NPs in the repeat unit as well as by plasmonic bands in UV-Vis spectra.

Controlling Multicompartment Morphologies Using Solvent Conditions and Chemical Modification.

The solution self-assembly of amphiphilic diblock copolymers into spheres, cylinders, and vesicles (polymersomes) has been intensely studied over the past two decades, and their morphological behavior is well understood. Linear ABC triblock terpolymers with two insoluble blocks A/B, on the other hand, display a richer and more complex morphological spectrum that has been recently explored by synthetic block length variations. Here, we describe facile postpolymerization routes to tailor ABC triblock terpolymer solution morphologies by altering block solubility (solvent mixtures), blending with homopolymers, and block-selective chemical reactions. The feasibility of these processes is demonstrated on polystyrene-block-polybutadiene-block-poly(methyl methacrylate) (SBM) that assembles to patchy spherical micelles, which can be modified to evolve into double and triple helices or patchy and striped vesicles. These results demonstrate that postpolymerization treatments give access to a broad range of morphologies from single triblock terpolymers without the need for multiple polymer syntheses.

Patchy Wormlike Micelles with Tailored Functionality by Crystallization-Driven Self-Assembly: A Versatile Platform for Mesostructured Hybrid Materials

One-dimensional patchy nanostructures are interesting materials due to their excellent interfacial activity and their potential use as carrier for functional nanoparticles. Up to now only wormlike crystalline-core micelles (wCCMs) with a nonfunctional patchy PS/PMMA corona were accessible using crystallization-driven self-assembly (CDSA) of polystyrene-block-polyethylene-block-poly(methyl methacrylate) (SEM) triblock terpolymers. Here, we present a facile approach toward functional, patchy wCCMs, bearing tertiary amino groups in one of the surface patches. The corona forming PMMA block of a SEM triblock terpolymer was functionalized by amidation with different N,N-dialkylethylenediamines in a polymer analogous fashion. The CDSA of the functionalized triblock terpolymers in THF was found to strongly depend on the polarity/solubility of the amidated PMMA block. The lower the polarity of the amidated PMMA block (increased solubility), the higher is the accessible degree of functionalization upon which define...

Branched and crosslinked supracolloidal chains with diblock copolymer micelles having three well-defined patches.

We report controlled branching and eventual crosslinking in supracolloidal chains by introducing well-defined trifunctional patchy micelles. Uniform micelles having three patches were induced from core-crosslinked micelles of diblock copolymers. Three patches in the micelles served as functional groups for crosslinking as well as branching in supracolloidal polymerization.

ChemInform Abstract: Self‐Assembly of “Patchy” Nanoparticles: A Versatile Approach to Functional Hierarchical Materials

AbstractReview: 108 refs.

Patchy micelles based on coassembly of block copolymer chains and block copolymer brushes on silica particles.

Patchy particles are a type of colloidal particles with one or more well-defined patches on the surfaces. The patchy particles with multiple compositions and functionalities have found wide applications from the fundamental studies to practical uses. In this research patchy micelles with thiol groups in the patches were prepared based on coassembly of free block copolymer chains and block copolymer brushes on silica particles. Thiol-terminated and cyanoisopropyl-capped polystyrene-block-poly(N-isopropylacrylamide) block copolymers (PS-b-PNIPAM-SH and PS-b-PNIPAM-CIP) were synthesized by reversible addition-fragmentation chain transfer polymerization and chemical modifications. Pyridyl disulfide-functionalized silica particles (SiO2-SS-Py) were prepared by four-step surface chemical reactions. PS-b-PNIPAM brushes on silica particles were prepared by thiol-disulfide exchange reaction between PS-b-PNIPAM-SH and SiO2-SS-Py. Surface micelles on silica particles were prepared by coassembly of PS-b-PNIPAM-CIP and block copolymer brushes. Upon cleavage of the surface micelles from silica particles, patchy micelles with thiol groups in the patches were obtained. Dynamic light scattering, transmission electron microscopy, and zeta-potential measurements demonstrate the preparation of patchy micelles. Gold nanoparticles can be anchored onto the patchy micelles through S-Au bonds, and asymmetric hybrid structures are formed. The thiol groups can be oxidized to disulfides, which results in directional assembly of the patchy micelles. The self-assembly behavior of the patchy micelles was studied experimentally and by computer simulation.

Preparation of cylindrical multi-compartment micelles by the hierarchical self-assembly of ABC triblock polymer in solution

Amphiphilic linear ABC triblock copolymer PnBA28-b-PS37-b-P2VP73 was prepared by the RAFT method. Spherical patchy micelles and cylindrical MCMs were formed in different steps of its two-step hierarchical self-assembly in selected solvents.

Highly Symmetric Patchy Multicompartment Nanoparticles from the Self-Assembly of ABC Linear Terpolymers inC-Selective Solvents

Multicompartment micelles, especially those with highly symmetric surfaces such as patchy-like, patchy, and Janus micelles, have tremendous potential as building blocks of hierarchical multifunctional nanomaterials. One of the most versatile and powerful methods to obtain patchy multicompartment micelles is by the solution-state self-assembly of linear triblock copolymers. In this article, we applied the simulated annealing method to study the self-assembly of ABC linear terpolymers in C-selective solvents. Simulations predict a variety of patchy and patchy-like multicompartment micelles with high symmetry and also yield a detailed phase diagram to reveal how to control the patchy multicompartment micelle morphologies precisely. The phase diagram demonstrates that the internal segregated micellar structure depends on the ratio between the volume fractions of the two solvophobic blocks and their incompatibility, whereas the overall micellar shape depends on the copolymer concentration. The relationship between the interfacial energy, stretching energy of chains and the micellar morphology, micellar morphological transition are elucidated by computing the average contact number among the species, the mean square end-to-end distances of the whole terpolymers, the AB blocks in the terpolymers, the AB diblock copolymers, and angle distribution of terpolymers. The anchoring effect of the solvophilic C block on micellar structures is also examined by comparing the morphologies formed from ABC terpolymers and AB diblock copolymers.

Patchy worm-like micelles: solution structure studied by small-angle neutron scattering

Triblock terpolymers exhibit a rich self-organization behavior including the formation of fascinating cylindrical core-shell structures with a phase separated corona. After crystallization-induced self-assembly of polystyrene-block-polyethylene-block-poly(methyl methacrylate) triblock terpolymers (abbreviated as SEMs = Styrene-Ethylene-Methacrylates) from solution, worm-like core-shell micelles with a patchy corona of polystyrene and poly(methyl methacrylate) were observed by transmission electron microscopy. However, the solution structure is still a matter of debate. Here, we present a method to distinguish in situ between a Janus-type (two faced) and a patchy (multiple compartments) configuration of the corona. To discriminate between both models the scattering intensity must be determined mainly by one corona compartment. Contrast variation in small-angle neutron scattering enables us to focus on one compartment of the worm-like micelles. The results validate the existence of the patchy structure also in solution.

Patchy multi-compartment micelles are formed by direct dissolution of an ABC triblock copolymer in water

Patchy multi-compartment micelles are formed on direct dissolution of a primary amine-based triblock copolymer, poly(ethylene oxide)-b-poly(e-caprolactone)-b-poly(2-aminoethyl methacrylate), PEO-b-PCL-b-PAMA, in water, with PCL chains forming the micelle cores and the PEO and PAMA chains forming phase-segregated patchy or hemispherical coronas. By selectively silicifying the PCL cores with tetramethyl orthosilicate (TMOS), the phase-separated character of these micelles is revealed by transmission electron microscopy.