Reversible Addition-fragmentation Chain Transfer Research Articles

Silica Nanoparticles Tailored with a Molecularly Imprinted Copolymer Layer as a Highly Selective Biorecognition Element.

Molecularly imprinted silica nanoparticles (SP-MIP) are synthesized for the real-time optical detection of low-molecular-weight compounds. Azo-initiator-modified silica beads are functionalized through reversible addition-fragmentation chain transfer (RAFT) polymerization, which leads to efficient control of the grafted layer. The copolymerization of methacrylic acid (MAA) and ethylene glycol dimethacrylate (EDMA) on azo initiator-coated silica particles (≈100nm) using chain transfer agent (2-phenylprop-2-yl-dithiobenzoate) is carried out in the presence of a target analyte molecule (l-Boc-phenylalanine anilide, l-BFA). The chemical and morphological properties of SP-MIP are characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, Brunauer-Emmett-Teller surface analysis, and thermogravimetric analysis. Finally, SP-MIP is located on the gold surface to be used as a biorecognition layer on the surface plasmon resonance spectrometer (SPR). The sensitivity, response time, and selectivity of SP-MIP are investigated by three similar analogous molecules (l-Boc-Tryptophan, l-Boc-Tyrosine, and l-Boc-Phenylalanine) and the imprinted particle surface showed excellent relative selectivity toward l-Boc-Phenylalanine (l-BFA) (k=61), while the sensitivity is recorded as limit of detection=1.72×10-4m.

Easily water soluble cellulose-based fluorescent probes for the detection of 4-nitrophenol

Cellulose, an abundantly available natural polymer, is generally insoluble in water or common organic solvents. In this study, fluorescent probes based on cellulose were fabricated, rendering them soluble in H2O and capable of selectively recognizing 4-nitrophenol (4-NP). Firstly, the modified cellulose with -Cl was prepared by the substitution reaction of –OH and SOCl2 on cellulose. Secondly, the reversible addition-fragmentation chain transfer (RAFT) reagent FNT with –NO2 and –CHO was obtained by reacting p-nitrophenylthiophenol with p-chloromethyl benzaldehyde. It was then reacted with 2,4-dimethylpyrrole to obtain a fluoroboronodipyrrole fluorescent RAFT reagent BNT with –NO2, followed by the reduction of –NO2 to –NH2 to obtain ABT. RAFT polymerization was conducted using reagent ABT with sodium vinyl sulfonate (SVS), sodium p-styrene sulfonate (SSS), sodium allyl sulfonate (SAS) in DMF. In the polymerization process, azobisisobutyronitrile (AIBN) was used as the initiator, yielded polymers with superior water solubility. Finally, three cellulose based fluorescent probes were prepared by substitutional reaction between -Cl on cellulose and –NH2 on the as-prepared polymers. The solubility of the probes was much higher than that of the original cellulose, and it can be served as macromolecular probes for the detection of 4-NP, and applied in environmental systems.

Combining linear and cyclic sulfones as a strategy for elaborating more efficient high-dielectric polymer materials: A second case of dipolar glass copolymers

Motivated by the excellent features exhibited by sulfone functional groups in the development of high-dielectric polymer materials, this work assesses the combination of linear and cyclic sulfone structures through copolymerization to prepare novel polymer materials exhibiting high dielectric constants (ԑr'), low dissipative behavior, and improved thermal properties. Five new polymethacrylate-based copolymers with varying compositions were synthesized through reversible addition-fragmentation chain transfer (RAFT) polymerization. The correct structure and macromolecular nature of the devised materials were confirmed by infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (1H/13C NMR), and gel permeation chromatography (GPC), while their thermal properties were evaluated using thermogravimetry analysis (TGA) and differential scanning calorimetry (DSC). All specimens exhibited adequate thermal properties for most capacitor applications in terms of onset degradation (Ti) and glass transition (Tg) temperatures. All materials degraded well above 250 °C, with increased Ti and Tg values depending on the final composition of the cyclic sulfone monomer in the material. The incorporation of cyclic sulfones not only increased the thermal robustness of the specimens but also raised their Tg values to as high as 189 °C, notably expanding the range of temperatures where these systems can operate without dissipative phenomena. More importantly, broadband dielectric spectroscopy (BDS) revealed that all samples exhibited dielectric properties notably superior to those of conventional polymer materials, with high ԑr' values between 6.0 and 8.9 (at 25 °C and 1 Hz) and low loss factors (Tan(δ) < 0.018). Overall, the present work successfully demonstrates the advantages of including cyclic structures with high dipole moments in polymeric backbones, offering a new strategy to enhance the thermal and dielectric properties of high-dielectric polymer materials.

RAFT Dispersion PISA with Poly(methyl methacrylate) as Stabilizer Block in Alcohol/Water: Unconventional PISA Morphology Transitions.

Reversible addition-fragmentation chain transfer (RAFT) dispersion polymerization-induced self-assembly (PISA) was conducted in the presence of poly(methyl methacrylate) (PMMA) stabilizer in ethanol/water mixture (80/20 by volume). Two different systems were explored by utilizing (i) 2-ethylhexyl methacrylate (EHMA) and (ii) n-butyl methacrylate (BMA). The morphology transitions of these systems were investigated by varying the polymerization conditions, i.e., the presence of the solvophilic comonomer MMA, the solids content, and the target degree of polymerization (DP). As observed in conventional PISA, the presence of solvophilic comonomer, increase in solids content and target DP promoted the formation of high-order morphology. However, unusual morphology transitions were observed whereby the morphology transformed from high-order morphologies to a mixture of spherical nanoparticles, worms, and vesicles and finally to vesicles with increasing target DP. This unusual evolution may be attributed to the limited solubility of PMMA in the ethanol/water solvent mixture, whereby PMMA is soluble at the polymerization temperature but insoluble at lower temperatures.

Galactose Glycopolymer-Grafted Silica Nanoparticles: Synthesis and Binding Studies with Lectin.

Weak binding of carbohydrates with protein receptors possesses serious drawbacks in the advancement of therapeutics; however, the development of strategies for multipoint interactions between carbohydrates and protein can overcome these challenges. One such method is developed in this work where glycopolymer-grafted silica nanoparticles with a large number of carbohydrate units are prepared for the interactions with multiple binding sites of the protein. First, a glycomonomer, β-d-galactose-hydroxyethyl methacrylate (β-GEMA), was synthesized in a two-step process by coupling β-d-galactose pentaacetate and hydroxyethyl methacrylate (HEMA), followed by deacetylation for the preparation of poly(β-GEMA) glycopolymers (GPs). Further, the poly(β-GEMA) chains were grafted onto the silica nanoparticle (SiNP) surface by utilizing the "grafting-from" strategy of surface-initiated reversible addition-fragmentation chain transfer (RAFT) polymerization to prepare p(β-GEMA)-grafted SiNPs (GNPs). Five different chain lengths ranging from 10 to 40 kDa of the GPs and the GNPs were prepared, and various characterization techniques confirmed the formation of GPs and grafting of the GPs on the SiNP surface. The particle size of GNPs and the number of GPs grafted on the SiNP surface showed a strong dependence on the chain length of the GPs. Further, the GNPs were subjected to a binding study with β-galactose-specific protein peanut agglutinin (PNA). A much stronger binding in the case of GNPs was observed with an association constant ∼320 times and ∼53 times than that of the monomeric methyl-β-d-galactopyranoside and the GPs, respectively. Additionally, the binding of the PNA with GNPs and GPs was also studied with varying chain lengths to understand the effects of the chain length on the binding affinity. A clear increase in binding constants was observed in the case of GNPs with increasing chain length of grafted GPs, attributed to the enhanced enthalpic and entropic contributions. This work holds its uniqueness in these improved interactions between carbohydrates and proteins, which can be used for carbohydrate-based targeted therapeutics.

Tuning the Mechanical Properties of 3D-Printed Objects by Mixing Chain Transfer Agents in Norrish Type I Photoinitiated RAFT Polymerization.

Photoinduced 3D printing via photocontrolled reversible-deactivation radical polymerization (photoRDRP) techniques has emerged as a robust technique for creating polymeric materials. However, methods for precisely adjusting the mechanical properties of these materials remain limited. In this study, we present a facile approach for adjusting the mechanical properties of 3D-printed objects by adjusting the polymer dispersity within a Norrish type I photoinitiated reversible addition-fragmentation chain transfer (NTI-RAFT) polymerization-based 3D printing process. We investigated the effects of varying the concentrations and molar ratios of trithiocarbonate (BTPA) and xanthate (EXEP) on the mechanical properties of the printed materials. Our findings demonstrate that increased concentrations of RAFT agents or higher proportions of the more active BTPA lead to a decrease in Young's modulus and glass transition temperatures, along with an increase in elongation at break, which can be attributed to the enhanced homogeneity of the polymer network. Using a commercial LCD printer, the NTI-RAFT-based 3D printing system effectively produced materials with tailored mechanical properties, highlighting its potential for practical applications.

A highly efficient oxygen tolerant visible-light mediated RAFT polymerization

Recently, oxygen-tolerant reversible addition-fragmentation chain transfer (RAFT) polymerization has attracted increasing attention in polymer chemistry. Inspired by the monomers containing glycol ethers group have high polymerization rates and even achieved a desirable oxygen tolerance. Herein, we proposed a simple, effective, low-cost, and eco-friendly strategy to accomplish the oxygen-tolerant visible-light activated RAFT polymerization of acrylates and acrylamides in a mixed solution of glycol ether and water at ambient temperature. This photo-mediated RAFT polymerization does not require additives, prior deoxygenation, or inert gas protection. The acrylates and acrylamides with high conversion under irradiation for 2 h, and the resulting polymers were narrow unimodal and narrow molecular weight distributions (PDI<1.3). In addition, the “living” and well-controlled behaviors of this oxygen-tolerant photo-mediated RAFT polymerization were demonstrated through water content in solvents, headspace, initial concentration of monomers, various monomers, chain lengths, light ON/OFF experiment, and high-end group fidelity of block copolymers. This RAFT polymerization also opens up a wide avenue for the industrial production of functional polymeric materials via an in situ chain extension strategy. These results indicate that the mixed solution of glycol ethers and water are effective green media for promoting photo-mediated RAFT polymerization without additives or tedious degassing processes.

Ultraviolet-induced controlled radical polymerization using titanium dioxide nanoparticles via the reversible addition–fragmentation chain transfer process

Abstract Herein, we report the ultraviolet (UV)-induced controlled radical polymerization facilitated by titanium dioxide nanoparticles and trithiocarbonate derivatives, serving as photocatalysts and chain transfer agents, respectively. The polymerization proceeded through a reversible addition–fragmentation chain transfer (RAFT) process. The resulting polymers exhibited well-controlled molecular weights and relatively low polydispersity. Additionally, the chain extension reaction via UV-induced RAFT polymerization using titanium dioxide nanoparticles yielded higher molecular weight polymer products.

Synthesis of multi-stimuli-responsive flocculants using reversible addition-fragmentation chain transfer polymerization: Investigating the performance and mechanism of kaolin coagulation

Coumarin-containing amphiphilic block copolymers with different compositions, as a new class of pH- and photo-responsive flocculants, were synthesized through reversible addition-fragmentation chain transfer polymerization of dimethyl aminoethyl methacrylate (DMAEMA), methyl methacrylate, and 7-acryloyloxy 4-methylcoumarin. Proton nuclear magnetic resonance spectroscopy was used to study the structure and composition of the copolymers. Zeta potential results show that the copolymers are applicable as amphoteric flocculants. The optimal flocculant concentration was calculated using the Jar analysis for kaolin flocculation, and the results show that the flocculation dependence on the flocculent concentration decreases with increasing its molecular weight. The dominance of charge neutralization in the flocculants with lower molecular weights and the dominance of adsorption bridging and hydrophobic association in the flocculants with higher molecular weights were indicated. These results are in agreement with the rheological data. To investigate the governing mechanism more precisely, the flocculation rate was calculated using turbidity measurements at different pH values over time. The highest final flocculation rate (99.25 %) corresponds to pH 4.5, which caused by the protonation of the amine groups of the DMAEMA repeating units. The dependence of settling rate on pH indicates the pH-dependent performance of the flocculants. Finally, fluorescence microscopy image of the flocculants shows its proper functioning of in the vicinity of kaolin, which has a promising industrial application.

Visible light-driven photoreforming of polystyrene segmented glycopolymer architectures for enhanced hydrogen generation

In this report, a series of polystyrene segmented new glycopolymer architectures are synthesized, which are utilized in the photoreforming process to achieve a remarkable rate of hydrogen production. The primary building blocks of mono-, bi-, and tetra-functional photo-iniferter were employed in the RAFT polymerization process to design a series of block copolymer architectures using styrene and acetylated glucose methacrylate monomers. Acetylated polymer architectures exhibited higher thermal stability compared to deacetylated polymers. Deacetylated polymers showed lower Tg values than the acetylated polymers. In addition, a wide range of Tg values (55–96 °C) and variations in the Tm values of the acetylated polymers indicate the dependence on the nature of the pendant unit and macromolecular architecture. The deacetylated macromolecule, 1A-PS-b-PGMD diblock copolymer exhibits a hydrogen generation rate of ∼753 μmol/g/h with an AQY of ∼1.84% compared to that of the polystyrene segment alone (53 μmol/g/h, AQY of ∼0.02%). Within the range of possible synthesized glycopolymer architectures, linear and glucose-based triblock glycopolymers show promising activity. The kinetics of the water-splitting reaction are influenced by adjustments to both the solution's pH and the hydrophilicity of the glycomacromolecular chains.

Efficient Synthesis of μ-A(BC)C Miktoarm Star Polymer Assemblies via Aqueous Photoinitiated Polymerization-Induced Self-Assembly.

In this study, green light-activated photoiniferter reversible addition-fragmentation chain transfer (RAFT) polymerization of glycerol methacrylate was performed using an ω,ω-heterodifunctional macro-RAFT agent. Because of the different RAFT controllability of two RAFT groups toward methacrylic monomers, only one RAFT group was activated under green light irradiation, leading to the formation of a diblock copolymer macro-RAFT agent with one RAFT group located at the chain end and the other RAFT group located between two blocks. The obtained diblock copolymer macro-RAFT agent was then used to mediate aqueous photoinitiated RAFT dispersion polymerization of diacetone acrylamide (DAAM), which formed μ-A(BC)C miktoarm star polymer assemblies with a diverse set of morphologies. Comparing with the ABC triblock copolymer, it was found that the architecture of the μ-A(BC)C miktoarm star polymer facilitated the formation of higher-order morphologies. Kinetic studies indicated that the aqueous photoinitiated RAFT dispersion polymerization exhibited ultrafast polymerization behavior, with quantitative monomer conversion being achieved within 5 min. Size exclusion chromatography analysis confirmed that good RAFT control was maintained during the polymerization. A morphological phase diagram for μ-A(BC)C miktoarm star polymer assemblies was constructed by varying the monomer concentration and the [DAAM]/[Macro-RAFT] ratio. We expect that this study not only develops an approach for the preparation of miktoarm star polymer assemblies but also provides mechanistic insights into the polymerization-induced self-assembly of nonlinear polymers.

Crystallization-Driven Controlled 2D Self-Assemblies via Aqueous RAFT Emulsion Polymerization.

Aqueous emulsion polymerization is a robust technique for preparing nanoparticles of block copolymers; however, it typically yields spherical nanoassemblies. The scale preparation of nanoassemblies with nonspherical high-order morphologies is a challenge, particularly 2D core-shell nanosheets. In this study, the polymerization-induced self-assembly (PISA) and crystallization-driven self-assembly (CDSA) are combined to demonstrate the preparation of 2D nanosheets and their aggregates via aqueous reversible addition-fragmentation chain transfer (RAFT) emulsion polymerization. First, the crucial crystallizable component for CDSA, hydroxyethyl methacrylate polycaprolactone (HPCL) macromonomer is synthesized by ring opening polymerization (ROP). Subsequently, the RAFT emulsion polymerization of HPCL is conducted to generate crystallizable nanomicelles by a grafting-through approach. This PISA process simultaneously prepared spherical latices and bottlebrush block copolymers comprising poly(N',N'-dimethylacrylamide)-block-poly(hydroxyethyl methacrylate polycaprolactone) (PDMA-b-PHPCL). The latexes are now served as seeds for inducing the formation of 2D hexagonal nanosheets, bundle-shaped and flower-like aggregation via the CDSA of PHPCL segments and unreacted HPCL during cooling. Electron microscope analysis trace the morphology evolution of these 2D nanoparticles and reveal that an appropriate crystallized component of PHPCL blocks play a pivotal role in forming a hierarchical structure. This work demonstrates significant potential for large-scale production of 2D nanoassemblies through RAFT emulsion polymerization.

Non-Biochemical Gradient Sequence-Controlled Polymers with Tuned Kinetics and Self-Assembled Morphologies.

Two key challenges in the multidisciplinary field of sequence-controlled polymers are their efficient synthesis and the establishment of correlation with polymer properties. In this context, in this paper, gradient architecture in the hydrophobic tail of an amphiphile is implemented and synthesized for a fixed hydrophilic unit (polyethylene glycol, PEG), by means of two monomers (2-hydroxypropyl methacrylate, HPMA, and diacetone acrylamide, DAAM) of contrasting reactivities. The resulting non-biochemical gradient sequence-controlled polymers are generated from a one-pot, homogeneous mixture through a PET-RAFT-PISA (photoinduced electron/energy transfer-reversible addition-fragmentation chain transfer-polymerization-induced self-assembly) method. In addition, the initial concentration ratio of the monomers in the gradient is varied as an input for a set of fixed experimental parameters and conditions, and its correlation with kinetics, gradient and self-assembled morphologies is established, as the output of the process. These results are extensively corroborated via nuclear magnetic resonance (NMR) spectroscopy analysis, together with transmission electron microscopy (TEM) images, dynamic light scattering (DLS), and gel permeation chromatography (GPC) experiments. These results have implications for chemical computation carried out by PISA, programmable self-assembly, information storage, biomimetics, origins of life and synthetic protocell studies.

RAFT copolymerization of methyl methacrylate and di(ethylene glycol) methyl ether methacrylate in a hexylpyridinium ionic liquid

AbstractSmart polymers undergo significant physical or chemical changes in response to stimuli like temperature and pH. Achieving a narrow molecular weight distribution is crucial for their sensitivity. Reversible addition–fragmentation chain transfer (RAFT) in ionic liquids is an effective method for synthesizing such polymers due to its favorable kinetics and environmental benefits. Most studies use imidazolium ionic liquids, while pyridinium ionic liquids are less common despite their easy synthesis. This study reports the first successful RAFT copolymerization of di(ethylene glycol) methyl ether methacrylate (DEGMEMA) and methyl methacrylate in N‐hexylpyridinium hexafluorophosphate ([HPY][PF6]). Both linear and hyperbranched copolymers (Mn &gt; 25,000) with narrow molecular weight distribution were synthesized, showing observable temperature responses and biocompatibility. The linear copolymers had a desirable dispersity (Ð) of less than 1.10, while the hyperbranched copolymer had a Ð of 2.034. The lower critical solution temperatures (LCSTs) of the copolymers were close to or below the LCST of PDEGMEMA (26°C). This study indicates that pyridinium ionic liquids can be explored as a suitable solvent for synthesizing methacrylate‐based smart polymers.

Tuning the Mechanical Properties of 3D-printed Objects by Mixing Chain Transfer Agents in Radical Promoted Cationic RAFT Polymerization.

The utilization of (cationic) reversible addition-fragmentation chain transfer (RAFT) polymerization in photoinduced three-dimensional (3D) printing has emerged as a robust technique for fabricating a variety of stimuli-responsive materials. However, methods for precisely adjusting the mechanical properties of these materials remain limited, thereby constraining their broader applicability. In this study, a facile way is introduced to modulate the mechanical properties of 3D printed objects by mixing two chain transfer agents (CTAs) within a radical-promoted cationic RAFT (RPC-RAFT) polymerization-based 3D printing process. Through systematic investigations employing tensile testing and dynamic mechanical analysis (DMA), the influence of CTA concentration and molar ratio between two CTAs on the mechanical behavior of the printed objects are explored. These findings demonstrate that higher concentrations of CTAs or a greater molar ratio of the more active CTA within the mixed CTAs result in decreased Young's modulus and glass transition temperatures of the printed objects. Moreover, the tensile failure strain increased with the increasing CTA content, i.e., the samples became more ductile. This methodology broadens the toolbox available for tailoring the mechanical properties of 3D printed materials.

Changing the Linking Functionality in a Triblock Co-Polymer for Electrolyzer or Fuel Cell Membrane or Ionomer for Chemical Stability Improvements and Potentially Other Consequences.

We have developed a versatile scalable triblock polymer system for anion exchange membrane (AEM) based electrochemical energy conversion devices. This system is uniquely suited to solving both the membrane and ionomer challenges for the commercialization of AEM water electrolysis or fuel cells. Using our advanced fundamental understanding of AEMs based on our work which began in 2010, we can design systems from first principles to match the needs of the device. A triblock ABA polymer is readily fabricated that has both chemical and mechanical stability. The synthesis of these systems is robust, high yield and amenable to high volume production. It utilizes a novel dual chain transfer agent to mediate the chain-transfer ring-opening metathesis polymerization (ROMP) of cyclooctene (COE) or the polymerization of isoprene (IP) to give the hydrophobic B block of the polymer. This is followed by the reversible addition-fragmentation chain transfer radial polymerization of chloromethylstyrene (CMS). The polyCMS (pCMS) blocks are then quaternized with an amine to give the cationic hydrophilic A block. Before quaternization the B block is hydrogenated to give either semi-crystalline polyethylene (pE) or amorphous polymethylbutylene (pMB) from pCOE and pIP respectively. The obvious achilles heal in this system from a chemical durability standpoint is the linking ether functionality between the hydrophobic and hydrophilic blocks. The material we have synthesized to date have exceptional chemical and mechanical stability. It performs very well in ex-situ testing with KOH solutions and in device testing we have demonstrated >500 h at 50°C in water electrolysis in 5 cm2 cells in 1M carbonate electrolyte at 0.5 A cm-2. We attribute the chemical stability to the fact that we post quaternize the membrane to give methylpipiridinium cations and we assume that this reaction does not fully penetrate down the hydrophilic chain. This leaves a hydrophobic un-quaternized region close to the hydrophobic block that does not allow access to the ether linkage by the hydrated hydroxide anion. Recently a new approach to the telehelic mid block pCOE has been reported that has no ether linkages and allows the hydrophobic outer blocks to be linked by a methylene linker. This gives use an opportunity to directly contrast the chemical stability of two identical triblock co-polymers one with an ether linkage and one with a methylene linkage between blocks. In this presentation we will show the results from ex-situ chemical stability test one at low temperatures and higher hydroxide concentration and one at higher temperature and lower hydroxide concentration. There are many examples in polymer electrolyte chemistry where a simple change leads to unintended consequences. The geometry of the ether linkage versus the methylene linkage will change the way that the polymer chains will organize and entangle in ways that are not currently predictable. To probe the mechanical, chemical and morphological difference between these two polymers we will fully characterize and contrast both polymers physical chemical properties including water uptake, ionic conductivity, DSC, TGA, tensile strength and morphology through SAXS, WAXS and HRTEM. Data for the two polymer membranes will also be contrasted and compared in small laboratory 5 cm2 single cells for both electrolysis in dilute carbonate and H2/O2 fuel cells using conventional catalysts.

Jeffamine-based diblock copolymer nanoparticles via reverse sequence polymerization-induced self-assembly in aqueous media

Jeffamines® are commercially available amine-capped poly (alkylene oxides) that have been used for various applications. In this study, a weakly hydrophobic monoamine-capped propylene oxide-rich Jeffamine® (M2005) is derivatized to introduce a trithiocarbonate end-group via amidation. This precursor is then dissolved using N,N′-dimethylacrylamide (DMAC), 2-(N-acryloyloxy)ethyl pyrrolidone (NAEP) or N-acryloylmorpholine (NAM) as a co-solvent to produce a concentrated aqueous reaction mixture containing 20 % w/w water. Subsequently, reversible addition-fragmentation chain transfer (RAFT) polymerization is used to prepare Jeffamine®-core diblock copolymer nanoparticles by reverse sequence polymerization-induced self-assembly (PISA). At intermediate conversion, additional degassed water is added and each polymerization continues to almost full conversion (>99 %) within 4 h at 60 °C, resulting in a 10–20 % w/w aqueous dispersion of sterically-stabilized Jeffamine®-core nanoparticles. Efficient chain extension of the Jeffamine® precursor is achieved in most cases and relatively narrow molecular weight distributions are obtained (Mw/Mn < 1.30) as judged by GPC analysis. Transmission electron microscopy studies confirm a polydisperse spherical morphology and dynamic light scattering studies report hydrodynamic diameters ranging from 145 to 312 nm. Finally, aqueous electrophoresis studies indicate essentially neutral nanoparticles over a wide range of solution pH, as expected for the three types of non-ionic steric stabilizer chains selected for this study.

Antibacterial Nanoplatelets via Crystallization-Driven Self-Assembly of Poly(l-lactide)-Based Block Copolymers.

Membrane-active antimicrobial materials are promising substances to fight antimicrobial resistance. Herein, crystallization-driven self-assembly (CDSA) is employed for the preparation of nanoparticles with different morphologies, and their bioactivity is explored. Block copolymers (BCPs) featuring a crystallizable and antimicrobial block were synthesized using a combination of ring-opening and photoiniferter RAFT polymerizations. Subsequently formed nanostructures formed by CDSA could not be deprotected without degradation of the structures. CDSA of deprotected BCPs yielded 2D diamond-shaped nanoplatelets in MeOH, while spherical nanostructures were observed for assembly in water. Platelets exhibited improved antibacterial capabilities against two Gram-negative bacteria (Escherichia coli and Pseudomonas aeruginosa) compared to their spherical counterparts. The absence of hemolytic activity leads to the excellent selectivity of platelets. A mechanism based on membrane permeabilization was confirmed via dye-leakage assays. This study emphasized the impact of the shape of nanostructures on their interaction with bacterial cells and how a controlled assembly can improve bioactivity.

A Minimalist Method for Fully Oxygen-Tolerant RAFT Polymerization through Sulfur-Centered Trithiocarbonate Radical Initiation.

In recent years, the fully oxygen-tolerant reversible deactivation radical polymerization (RDRP) has become a highly researched area. In this contribution, a new and minimalist method is successfully employed to accomplish fully oxygen-tolerant reversible addition-fragmentation chain transfer (RAFT) polymerization using bis(trithiocarbonate) disulfides (BisTTC) as an iniferter agent, where the released sulfur-centered trithiocarbonate (TTC) radical can initiate monomer. Furthermore, polymerization kinetics revealed the typical "living" features of this polymerization system. More importantly, by high-throughput screening, it is found that dodecyl-substituted TTC is responsible for the fully oxygen-tolerant RAFT polymerization though trithiocarbonate radical initiation and R radical deoxygenation. It is believed that trithiocarbonate radical initiation strategy provides a powerful and minimalist tool for fully oxygen-tolerant RDRPs.

Esterified styrene-maleic acid copolymer modified silica as mixed-mode polymer-brush stationary phases for chromatographic separation

Styrene-maleic acid (SMA) copolymer has received much attention for its excellent solubilization characteristics. In this work, SMA copolymer brush-based chromatographic stationary phases were exploited and developed for the first time. First, SMA copolymer brush was in situ grown on the surface of spherical silica via living/controlled reversible addition-fragmentation chain transfer (RAFT) polymerization method. Subsequently, as a proof-of-concept demonstration, the copolymer was esterified by diethylene glycol mono-2-ethylhexyl ether (DGME) and 2-(2-ethylhexyloxy) ethanol (EHOE), respectively. The obtained Sil-SMA-DGME and Sil-SMA-EHOE copolymer-brush chromatographic stationary phases were characterized by transmission electron microscopy, Fourier transform infrared spectrometer, X-ray photoelectron spectroscopy, and thermogravimetric analysis, respectively. The chromatographic retention mechanism indicated that both the two packed columns exhibited hydrophilic/reverse mixed-mode retention modes. The maximum column efficiency was up to 71,000 N/m. The chromatographic separation performance evaluation indicated that the novel kind of stationary phases had excellent separation capabilities for hydrophilic, hydrophobic compounds and phospholipid standards. In addition, by combination with mass spectrometry identification, the Sil-SMA-DGME column was further exploited for separation and identification of phospholipids in human lung cancer cells. Totally, 9 classes including 186 phospholipid species were successfully identified. The results demonstrated the promising application prospects of the novel kind of SMA copolymer-brush chromatographic stationary phases.