Publications by authors named "Emrick T"

Article Synopsis
  • The paper discusses the preparation of mesoscale polymer filaments to explore their properties, which exist between molecular and bulk scales.
  • It describes a method involving flow coating and evaporative deposition to create charged polymer filaments, specifically using thiol-ene reactions.
  • The research finds that these filaments change shape in different aqueous environments, revealing important information about the structure of soft materials at multiple length scales.
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While free radical polymerization methods are employed frequently to prepare sub-micron polymer particles, we hypothesized that surfactant-free emulsion polymerization (SFEP) methodology may prove beneficial for obtaining functional polymer particles by solution polymerization methods that preclude the need for conventional surfactants. To test the effectiveness of SFEP for the preparation of functional colloids, solution polymerization of several monomers, including propargyl acrylate (PA), styrene (Sty) and tert-butyl acrylate (t-BA), was performed over a range of monomer ratios and reaction scales. Electron microscopy and infrared spectroscopy were employed to evaluate the outcome of SFEP for particle size, shape, surface anisotropy, and chemical composition.

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Disulfide-containing polyolefins were synthesized by ring-opening metathesis polymerization (ROMP) of the 6-membered disulfide-containing cyclic olefin, 3,6-dihydro-1,2-dithiine, which was prepared by ring-closing metathesis of diallyl disulfide. This approach facilitated the production of disulfide-containing unsaturated polyolefins as copolymers with disulfide monomer units embedded within a poly(cyclooctene) or poly(norbornene) framework. The incorporation of disulfides into the polymer backbone imparts redox responsiveness and enables polymer degradation chemical reduction or thiol-disulfide exchange.

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Understanding the electronic properties resulting from soft-hard material interfacial contact has elevated the utility of functional polymers in advanced materials and nanoscale structures, such as in work function engineering of two-dimensional (2D) materials to produce new types of high-performance devices. In this paper, we describe the electronic impact of functional polymers, containing both zwitterionic and fluorocarbon components in their side chains, on the work function of monolayer graphene through the preparation of negative-tone photoresists, which we term "fluorozwitterists." The zwitterionic and fluorinated groups each represent dipole-containing moieties capable of producing distinct surface energies as thin films.

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We report the use of fluorinated polymer zwitterions to build hybrid systems for efficient CO electroreduction. The unique combination of hydrophilic phosphorylcholine and hydrophobic fluorinated moieties in these polymers creates a fractal structure with mixed branched cylinders on the surface of gold nanoparticles (AuNPs). In the presence of these polymers, the CO faradaic efficiency improves by 50-80% in the range of -0.

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Synthetic replication of the precise mesoscale control found in natural systems poses substantial experimental challenges due to the need for manipulation across multiple length scales (from nano- to millimeter). We address this challenge by using a 'flow coating' method to fabricate polymer ribbons with precisely tunable dimensions and mechanical properties. Overcoming barriers that previously limited the achievable range of properties with this method, we eliminate the need for substrate patterning and post-processing etching to facilitate the production of high aspect ratio, filament-like ribbons across a range of polymers-from glassy polystyrene to elastomeric poly(butadiene), as well as poly(butadiene--styrene).

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We describe the preparation of a new set of fluorinated sulfobetaine (FSB) zwitterionic polymers in which fluorocarbon moieties are attached directly to the zwitterionic components. An efficient two-step modification to the conventional sulfobetaine methacrylate monomer synthesis gave access to a series of polymer zwitterions containing varying extents of fluorocarbon character. FSB methacrylates proved amenable to homo- and copolymerizations using reversible addition-fragmentation chain transfer (RAFT) conditions, affording polymers with molecular weights ranging from 5 to 20 kDa and with low molecular weight distributions.

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Amphiphilic bottlebrush block copolymers (BBCPs), having a hydrophilic bottlebrush polymer (BP) linked covalently to a hydrophobic BP, were found to segregate to liquid-liquid interfaces to minimize the free energy of the system. The key parameter influencing the outcome of the experiments is the ratio between the degree of polymerization of the backbone () and that of the side-chain brushes (). Specifically, a spherical, star-like configuration results when < , while a cylindrical, bottlebrush-like shape is preferred when > .

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We formed core-shell-like polyelectrolyte complexes (PECs) from an anionic bottlebrush polymer with poly (acrylic acid) side chains with a cationic linear poly (allylamine hydrochloride). By varying the pH, the number of side chains of the polyanionic BB polymers (N), the charge density of the polyelectrolytes, and the salt concentration, the phase separation behavior and salt resistance of the complexes could be tuned by the conformation of the BBs. By combining the linear/bottlebrush polyelectrolyte complexation with all-liquid 3D printing, flow-through tubular constructs were produced that showed selective transport across the PEC membrane comprising the walls of the tubules.

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Conventional ligands for CsPbBr perovskite nanocrystals (NCs), composed of polar, coordinating head groups (e.g., ammonium or zwitterionic) and aliphatic tails, are instrumental in stabilizing the NCs against sintering and aggregation.

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Bottlebrush random copolymers (BRCPs), consisting of a random distribution of two homopolymer chains along a backbone, can segregate to the interface between two immiscible homopolymers. BRCPs undergo a reconfiguration, where each block segregates to one of the homopolymer phases, adopting a Janus-type structure, reducing the interfacial tension and promoting adhesion between the two homopolymers, thereby serving as a Janus bottlebrush copolymer (JBCP) compatibilizer. We synthesized a series of JBCPs by copolymerizing deuterated or hydrogenated polystyrene (DPS/PS) and poly(-butyl acrylate) (PtBA) macromonomers using ruthenium benzylidene-initiated ring-opening metathesis polymerization (ROMP).

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The compositional scope of polymer zwitterions has grown significantly in recent years and now offers designer synthetic materials that are broadly applicable across numerous areas, including supracolloidal structures, electronic materials interfaces, and macromolecular therapeutics. Among recent developments in polymer zwitterion syntheses are those that allow insertion of reactive functionality directly into the zwitterionic moiety, yielding new monomer and polymer structures that hold potential for maximizing the impact of zwitterions on the macromolecular materials chemistry field. This manuscript describes the preparation of zwitterionic choline phosphate (CP) methacrylates containing either aromatic or aliphatic thiols embedded directly into the zwitterionic moiety.

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The in-plane packing of gold (Au), polystyrene (PS), and silica (SiO) spherical nanoparticle (NP) mixtures at a water-oil interface is investigated in situ by UV-vis reflection spectroscopy. All NPs are functionalized with carboxylic acid such that they strongly interact with amine-functionalized ligands dissolved in an immiscible oil phase at the fluid interface. This interaction markedly increases the binding energy of these nanoparticle surfactants (NPSs).

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Article Synopsis
  • Bottlebrush polymer surfactants (BPSs) are formed through interactions between bottlebrush polymers with poly(acrylic acid) side chains and amine-functionalized ligands at fluid-fluid interfaces, significantly impacting assembly and stability.
  • The degree of polymerization of the backbone and side chains influences initial assembly speed, interface packing efficiency, and stress relaxation behavior, with specific ratios affecting the shape and effective surface coverage of the polymers.
  • This study demonstrates how changing the molecular architecture of BPSs affects their macroscopic properties, ultimately leading to improved stabilization of all-liquid printed structures.
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In this manuscript, we report the synthesis of zwitterionic copolymers and their ability to form antifouling coatings on porous hydroxyapatite as a mimic of dental coatings. Specifically, we systematically investigated how altering the composition of copolymers of catechol methacrylate (Cat-MA or ) and methacryloyloxyethyl phosphorylcholine (-MPC) with varying catechol-to-zwitterion ratios impacted their adhesive and antifouling properties, allowing for the rational design of functional coatings. Characterization by ellipsometry, contact angle goniometry, and X-ray photoelectron spectroscopy revealed the presence of hydrophilic copolymer coatings of ∼10 nm thickness.

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Hydrogels are water-swollen, typically soft networks useful as biomaterials and in other fields of biotechnology. Hydrogel networks capable of sensing and responding to external perturbations, such as light, temperature, pH, or force, are useful across a wide range of applications requiring on-demand cross-linking or dynamic changes. Thus far, although mechanophores have been described as strain-sensitive reactive groups, embedding this type of force-responsiveness into hydrogels is unproven.

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Filamentous bundles are ubiquitous in Nature, achieving highly adaptive functions and structural integrity from assembly of diverse mesoscale supramolecular elements. Engineering routes to synthetic, topologically integrated analogs demands precisely coordinated control of multiple filaments' shapes and positions, a major challenge when performed without complex machinery or labor-intensive processing. Here, we demonstrate a photocreasing design that encodes local curvature and twist into mesoscale polymer filaments, enabling their programmed transformation into target 3-dimensional geometries.

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A one-step dispersion copolymerization technique is demonstrated to fabricate biphasic particles as an approach to streamline the production of particles with complex morphology. The model system studies a monomer feed of hydrophobic styrene and hydrophilic, zwitterionic sulfobetaine methacrylate (SBMA) in a water/isopropanol cosolvent mixture. The resulting particles have a core-shell morphology that can be transformed, simply by washing the particles with water, into particles with a single surface opening connected to an interior cavity.

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Stabilization of fluid droplets, classically as oil-in-water or water-in-oil emulsions, is typically conducted using molecular surfactants or small particulates that localize at oil-water interfaces. In this paper, we describe a method whereby thin polymer films are converted photolithographically to ribbon-like mesoscale objects, which, in turn, adsorb to fluid interfaces where they extend as appendages, or arms, from the droplet surface. These "mesoscale polymer surfactants", or MPSs, were prepared from thin polymer films containing reactive functional moieties, including coumarin for photo-cross-linking, triphenylsulfonium for photoacid generation, and -butyl ester for solubility switching.

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Membrane fouling remains a key challenge for membrane separations. Hydrophilic membrane surface modification can mitigate irreversible foulant deposition, thereby improving fouling resistance. We report new hydrophilic membrane coatings based on 1,4-benzoquinone and various commercially available polyetheramines.

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Gene delivery as a therapeutic tool continues to advance toward impacting human health, with several gene therapy products receiving FDA approval over the past 5 years. Despite this important progress, the safety and efficacy of gene therapy methodology requires further improvement to ensure that nucleic acid therapeutics reach the desired targets while minimizing adverse effects. Synthetic polymers offer several enticing features as nucleic acid delivery vectors due to their versatile functionalities and architectures and the ability of synthetic chemists to rapidly build large libraries of polymeric candidates equipped for DNA/RNA complexation and transport.

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Post-synthesis anion exchange of all-inorganic cesium lead halide perovskite nanocrystals (CsPbX NCs, where X=Cl, Br, and/or I) provides a rapid and simple means of tuning their band gap and photoluminescence emission wavelengths. Here we report color-shifting of CsPbX nanocrystals induced by a macromolecular source of halide ions, specifically using polystyrene with ammonium halides as pendent groups. This strategy for introducing new halides to the perovskite nanocrystals gave access to perovskite-polymer hybrid materials as solutions, thin films, or free-flowing powders.

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We report fabrication of highly flexible micron-sized helices from nanometer-thick ribbons. Building upon the helical coiling of such ultrathin ribbons mediated by surface tension, we demonstrate that the enhanced creep properties of highly confined materials can be leveraged to shape helices into the desired geometry with full control of the final shape. The helical radius, total length, and pitch angle are all freely and independently tunable within a wide range: radius within ∼1-100 μm, length within ∼100-3000 μm, and pitch angle within ∼0-70°.

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Organic solar cells (OSCs) and perovskite solar cells (PVSCs) are promising candidates for next-generation thin film photovoltaic technologies. The integration of OSCs with PVSCs in tandem devices is now attracting significant attention due to their similar fabrication procedures and the potential to afford a higher device performance. Here, a thickness-insensitive and solvent-resistant interconnecting layer is developed to efficiently connect perovskite and organic subcells with low contact resistance.

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Rheumatoid arthritis (RA) is a chronic autoimmune disease which is characterized primarily by synovial hyperplasia and accumulation of several types of immune infiltrates that promote progressive destruction of the articular structure. Glucocorticoids are often prescribed to treat RA because of their strong anti-inflammatory and immunosuppressive effects. However, their application must be limited to the short-term due to a risk of adverse events.

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