Glycol Methyl Ether Acrylate Research Articles

On Lubrication States after a Running-In Process in Aqueous Lubrication

Recently, many studies have reported the ultralow friction coefficient of sliding friction between rigid solid surfaces in aqueous lubrication. A running-in process that goes through high-friction and friction-decreasing regions to a stable ultralow friction region is often required. However, the role of the friction-decreasing region is often ascribed to tribofilm formation in which complexity hindered the quantitative description of the running-in process and the prediction of its subsequent lubrication state. In this work, the frictional energy (Ef) dissipated in the running-in process of a poly(oligo(ethylene glycol) methyl ether acrylate) aqueous lubrication was related to the wear of solid surfaces under different conditions and lubrication states. Experimental results indicated that the high-friction region was in a boundary lubrication state, contributed to most of the wear, and significantly reduced the contact pressure, whereas the friction-decreasing region was in a mixed lubrication state, contributed only to the slight and slow removal of materials, and slightly reduced the contact pressure. Therefore, by establishing relationships among the wear scar diameter, Ef, and the Stribeck curve of the tribological system, the subsequent lubrication state after a running-in process under various working loads and sliding speeds could be quantitatively predicted. The running-in experiments with different aqueous lubrication systems showed good agreement with the prediction of this method. This investigation provides an effective method for the wear and lubrication state prediction after a running-in process, further proving the importance of the Stribeck curve for a lubrication system. This study may also have important implications for the strategy design of the running-in process in various industrial applications.

Synthesis and self‐assembly of thermoresponsive poly(N‐isopropylacrylamide)‐b‐poly(oligo ethylene glycol methyl ether acrylate) double hydrophilic block copolymers

ABSTRACTWe report on the synthesis of novel poly(N‐isopropylacrylamide)‐b‐poly(oligo ethylene glycol methyl ether acrylate) (PNIPAM‐b‐POEGA) thermoresponsive block copolymers using reversible addition–fragmentation chain transfer polymerization methodologies. The synthesized block copolymers are characterized by gel permeation chromatography, nuclear magnetic resonance, Fourier transform infrared (FTIR) techniques in terms of molecular weight and composition. Their thermoresponsive self‐assembly in aqueous media is investigated using dynamic and static light scattering. The PNIPAM‐b‐POEGA thermoresponsive block copolymers formed aggregates in water by increasing the temperature above the lower critical solution temperature value of PNIPAM block. Solution pH seems to affect the self‐assembly behavior in some cases due to the presence of COOH end groups. Therefore, the copolymers were utilized as “smart” nanocarries for the hydrophobic drug indomethacin, implementing a novel encapsulation protocol taking advantage of the thermoresponsive character of the PNIPAM block. The empty and loaded self‐assembled nanocarriers systems were studied by light scattering techniques, ultraviolet–visible, and FTIR spectroscopy, which gave information on the size and structure of the nanocarriers, the drug loading content and the interactions between the drug and the components of the block copolymers. Drug loaded nanostructures show stability at room temperature, due to active drug/block copolymer interactions. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1467–1477

Dual-responsive copolymer hydrogel as broad-spectrum adsorbents for metal ions

A copolymeric hydrogel (PEGMA) with poly(ethylene glycol) methyl ether acrylate (PEGA), 2-methoxyethyl acrylate (MEA) and acrylic acid (AA) was synthesized in this study. The obtained PEGMA hydrogel exhibited sensitive response to pH and temperature and showed excellent adsorption properties for many metal ions, such as Fe(Ⅲ), Pb(Ⅱ), Zn(II), Ni(II), Mn(II) and Co(II), etc. Fe(Ⅲ) and Pb(Ⅱ) were selected to study thermodynamics and kinetics. The adsorption process followed pseudo-second-order kinetics equation. The adsorption isotherms could be described by Freundlich isotherm models. The maximum adsorption amount was calculated to be 195.43 (Fe3+) and 176.06 (Pb2+) mg/g. Besides, using the thermal and pH responsiveness, the PEGMA hydrogels can quickly release the adsorbed molecules with control. The heavy metal ions loaded PEGMA hydrogels could also be easily regenerated by diluted hydrochloric acid and still keep a major adsorption capacity. After five cycles, the adsorption ability remained more than 90% of the original PEGMA. Thus, the PEGMA hydrogels may be new high-performance and environment friendly material for metal pollution treatment with promising developmental potential.

Effect of Selected Comonomers on the Transition Temperature of Thermosensitive NIPA Derivatives Synthesized with an Anionic Initiator.

The present study evaluates the effect of the cationic initiator on the hydrodynamic diameter of copolymers of N-isopropylacrylamide nanogels synthesized via a surfactant-free precipitation polymerization at 70 °C in the presence of the cationic initiator 2,2'-azobis[2- methylpropionamidine] dihydrochloride. Three types of polymeric nanoparticles were synthesized using N, N'-methylenebisacrylamide as a crosslinker. The first batch was used as a reference. The second type of particles included a poly(ethylene glycol) methyl ether-acrylate monomer, while the third type used an N-tert-butylacrylamide comonomer. The hydrodynamic diameters of the synthesized particles were between 160 and 970 nm at 18 °C. The chemical composition and morphology of the synthesized co-polymeric nanoparticles were confirmed using infrared spectroscopy, nuclear magnetic resonance and scanning electron microscopy. The zeta potentials measured via dynamic light scattering were 20.0, 17.0, -0.1 mV for the three types, respectively. The volume phase transition temperature was between 22 and 41 °C. The polydispersity index of particles synthesized with N-tert-butylacrylamide varied depending on the measurement temperature.

In-situ photochemical synthesis of Au nanoparticles in polymer matrix with one-component thioxanthone disulfide for detection of benzene, toluene and xylene vapours

Thioxanthonation of diphenyl units of diphenyl disulfide was achieved successfully. The photoreduction and photostabilization ability of 2, 2′-disulfanediylbis (9H-thioxanthen-9-one) was used for in-situ preparation of Au nanoparticles either in solution or in poly(ethylene glycol) methyl ether acrylate / poly(ethylene glycol) diacrylate polymer matrix. SPR(Surface Plasmon Resonance) absorption band of formed Au NPs were recorded at 550 nm by UV–vis spectroscopy. Indeed, formation of elliptical shaped nanoparticles (4–8 μm) as well as spherical ones (11–14 nm) in nanocomposite films were obtained depending on UV irradiation time. DLS (Dynamic Light Scattering) measurements also changed from 440 nm to about 200 nm as a function of irradiation time. The potential of Au NPs/ polymer nanocomposite film as a sensing element for benzene, toluene, xylene (BTX) sensing was studied at different temperatures. An overall evaluation of the experimental results showed that Au NPs/ polymer nanocomposite film has good potential as a sensing element for the detection of BTX vapours.

Brush-shaped RAFT polymer micelles as nanocarriers for a ruthenium (II) complex photodynamic anticancer drug

Amphiphilic polymers containing brush-shaped poly(polyethylene glycol methyl ether acrylate) (PEGA) as a hydrophilic segment may form a stable hydrophilic shell for a polymeric micelle due to a strong interaction among the brush shaped molecules. In this paper, polymeric micelles with brush-shaped poly(PEGA) as hydrophilic shell were designed and formulated as nanocarriers for a new ruthenium (II) complex anticancer drug to address its poor water solubility. Well defined brush-shaped poly(PEGA)-containing amphiphilic block polymers were synthesised by reversible addition-fragmentation chain transfer (RAFT) polymerisation. The as-prepared amphiphilic polymers formed stable polymeric micelle nanocarriers for the hydrophobic ruthenium (II) complex, resulting in greatly increased solubility of the drug by inhibiting its aggregation in aqueous environment. Cytotoxicity studies demonstrated that the use of polymeric micelle nanocarriers increased the drug’s toxicity to human liver cancer cells (SK-HEP-1) by 3 fold under dark and 12 fold under light conditions. However, both bare drug and encapsulated drug showed no toxicity to the normal cells, demonstrating the drug’s potential targeting capacity to cancer cells.

Enzyme-initiated free radical polymerizations of vinyl monomers using horseradish peroxidase.

In this chapter, we highlight the use of horseradish peroxidase (HRP) as a catalyst to initiate free radical polymerizations of vinyl monomers under benign reaction conditions. A variety of vinyl monomers, including 4-acryloylmorpholine (AM), 2-hydroxyethyl methacrylate (HEMA), and poly(ethylene glycol) methyl ether acrylate (PEGA) were polymerized. The enzyme converts exogenous hydrogen peroxide into a usable radical source, which when coupled with a β-diketone, yields a radical that initiates chain growth in the presence of monomers. The resulting polymers were characterized using nuclear magnetic resonance (NMR) spectroscopy and gel permeation chromatography (GPC). By using enzymatic free radical polymerizations, polymers can be generated in a sustainable, environmentally-friendly, and scalable fashion.

Self-Assembling Protein-Polymer Bioconjugates for Surfaces with Antifouling Features and Low Nonspecific Binding.

A new method is demonstrated for preparing antifouling and low nonspecific adsorption surfaces on poorly reactive hydrophobic substrates, without the need for energy-intensive or environmentally aggressive pretreatments. The surface-active protein hydrophobin was covalently modified with a controlled radical polymerization initiator and allowed to self-assemble as a monolayer on hydrophobic surfaces, followed by the preparation of antifouling surfaces by Cu(0)-mediated living radical polymerization of poly(ethylene glycol) methyl ether acrylate (PEGA) performed in situ. By taking advantage of hydrophobins to achieve at the same time the immobilization of protein A, this approach allowed to prepare surfaces for IgG1 binding featuring greatly reduced nonspecific adsorption. The success of the surface modification strategy was investigated by contact angle, XPS, and AFM characterization, while the antifouling performance and the reduction of nonspecific binding were confirmed by QCM-D measurements.

Sono-RAFT Polymerization-Induced Self-Assembly in Aqueous Dispersion: Synthesis of LCST-type Thermosensitive Nanogels

The first sonochemically induced reversible addition–fragmentation chain transfer by the polymerization-induced self-assembly process (Sono-RAFT-PISA) has been investigated. High-frequency ultrasound (490 kHz, 40 W) was applied for the controlled polymerization of N-isopropylacrylamide (NIPAM) in aqueous dispersion via the Sono-RAFT-PISA technique using poly(poly(ethylene glycol) methyl ether acrylate) (PPEGA) as both macromolecular chain transfer agent and surfactant (macro-transurf). The synthesis of PPEGA-b-PNIPAM copolymers in aqueous media at 20 °C (DPn,NIPAM = 204) was found to reach total NIPAM conversion in a short time (60 min.) with narrow molecular weight distribution (Đ < 1.26). Furthermore, PNIPAM-based spherical nanogels (Dh ≤ 69 nm, pdi ≤ 0.26) were successfully synthesized by Sono-RAFT-PISA (aqueous dispersion, 45 °C), qualifying as a highly “green” method due to the complete monomer conversion, absence of organic initiator, of residues, and to the unique use of water as initiator and solv...

Exploiting Macromolecular Design To Optimize the Antibacterial Activity of Alkylated Cationic Oligomers.

There is growing interest in synthetic polymers which co-opt the structural features of naturally occurring antimicrobial peptides. However, our understanding of how macromolecular architecture affects antibacterial activity remains limited. To address this, we investigated whether varying architectures of a series of block and statistical co-oligomers influenced antibacterial and hemolytic activity. Cu(0)-mediated polymerization was used to synthesize oligomers constituting 2-(Boc-amino)ethyl acrylate units and either diethylene glycol ethyl ether acrylate (DEGEEA) or poly(ethylene glycol) methyl ether acrylate units with varying macromolecular architecture; subsequent deprotection produced primary amine functional oligomers. Further guanylation provided an additional series of antimicrobial candidates. Both chemical composition and macromolecular architecture were shown to affect antimicrobial activity. A broad spectrum antibacterial oligomer (containing guanidine moieties and DEGEEA units) was identified that possessed promising activity (MIC = 2 μg mL-1) toward both Gram-negative and Gram-positive bacteria. Bacterial membrane permeabilization was identified as an important contributor to the mechanism of action.

Performance of cross-linked polymers based gel electrolyte in the fabrication of quasi-solid state dye-sensitized solar cells

ABSTRACTCross-linked polymer (CLP) composed of poly(ethylene glycol) methyl ether acrylate and poly(ethylene glycol) diacrylate has been used in synthesizing gel electrolyte. A set of electrolyte samples was synthesized using gel casting method by varying the weight percentage ratio of cross-linked polymers from 2–14 % in an incremental order (2 %) with respect to poly (ethylene oxide) (PEO) and evaluated its performance by employing in the fabrication of dye-sensitized solar cells. The synthesized polymer was subjected to different analytical techniques such as NMR, TGA, DSC, GPC, and FTIR to confirm the materials. The molecular weight of the CLP has been measured using GPC and the obtained value is found to be 3.655 KDa with polydispersity of 1.94. The CLP-PEO gel electrolyte with 10 % weight ratio has obtained the highest ionic conductivity of 3.07 × 10−6 S/cm−1 at room temperature and best photo-conversion efficiency of 5.1 % was achieved for the same.

Synthesis of Well-Defined Pyrrolidone-Based Homopolymers and Stimulus-Responsive Diblock Copolymers via RAFT Aqueous Solution Polymerization of 2-(N-Acryloyloxy)ethylpyrrolidone.

Poly(N-vinylpyrrolidone) (PNVP) is a well-known, highly polar, nonionic water-soluble polymer. However, N-vinylpyrrolidone (NVP) usually exhibits strongly non-ideal behavior when copolymerized with methacrylic or styrenic monomers. Moreover, NVP is not particularly well-controlled under living radical polymerization conditions. For these reasons, alternative pyrrolidone-based monomers have been investigated. For example, the reversible addition–fragmentation chain transfer (RAFT) polymerization of 2-(N-methacryloyloxy)ethylpyrrolidone (NMEP) has been recently investigated using various polymerization formulations. However, PNMEP homopolymers are significantly less hydrophilic than PNVP and exhibit inverse temperature solubility in aqueous solution. In the present work, we studied the RAFT aqueous solution polymerization of 2-(N-acryloyloxy)ethylpyrrolidone (NAEP) using either AIBN at 70 °C or a low-temperature redox initiator at 30 °C. PNAEP homopolymers are obtained in high yield (>99%) with good control (Mw/Mn < 1.20) for target degrees of polymerization (DP) of up to 400 using the latter initiator, which produced relatively fast rates of polymerization. However, targeting DPs above 400 led to lower NAEP conversions and broader molecular weight distributions. 2-Hydroxyethyl acrylate (HEA) and oligo(ethylene glycol) methyl ether acrylate (OEGA) were chain-extended using a PNAEPx macro-CTA via RAFT aqueous solution polymerization, yielding double-hydrophilic acrylic diblock copolymers with high conversions (>99%) and good control (Mw/Mn < 1.31). In addition, a PNAEP95 macro-CTA was chain-extended via RAFT aqueous solution polymerization of N-isopropylacrylamide (NIPAM) at 22 °C. Dynamic light scattering (DLS) analysis indicated that heating above the lower critical solution temperature of PNIPAM led to so-called “anomalous micellization” at 35 °C and the formation of near-monodisperse spherical micelles at 40 °C. Finally, 2-(diethylamino)ethyl methacrylate (DEA) was polymerized using an N-morpholine-functionalized trithiocarbonate-based RAFT chain transfer agent and subsequently chain-extended using NAEP to form a novel pH-responsive diblock copolymer. Above the pKa of PDEA (∼7.3), DLS and 1H NMR studies indicated the formation of well-defined PDEA-core spherical micelles.

RAFT Polymerization of an Intrinsically Stretchable Water-Soluble Block Copolymer Scaffold for PEDOT.

Despite the common association of π-conjugated polymers with flexible and stretchable electronics, these materials can be rigid and brittle unless they are designed otherwise. For example, low modulus, high extensibility, and high toughness are treated as prerequisites for integration with soft and biological structures. One of the most successful and commercially available organic electronic materials is the conductive and brittle polyelectrolyte complex poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS). To make this material stretchable, additives such as ionic liquids must be used. These additives may render the composite incompatible with biological tissue. In this work, we describe the synthesis of an intrinsically stretchable variant of the conductive polymer PEDOT:PSS that is free of additives. The approach involves the synthesis of a block copolymer comprising soft segments of poly(polyethylene glycol methyl ether acrylate) (PPEGMEA) and hard segments of poly(styrene sulfonate) (PSS) using a reversible addition-fragmentation chain transfer (RAFT) polymerization. Subsequently, we used the newly synthesized ionic elastomer PSS-b-PPEGMEA as a matrix for the oxidative polymerization of EDOT. The resulting polyelectrolyte elastomer, PEDOT:PSS-b-PPEGMEA, can withstand elongations up to 128% and has a toughness up to 10.1 MJ m-3. While the polyelectrolyte elastomer is not as conductive as the commercial material, the toughness and extensibility are each more than an order of magnitude higher. Moreover, the electrical conductivity of the polyelectrolyte elastomer exhibits minimal decrease with strain within the elastic regime. We then compared the block copolymer to physical blends of PEDOT:PSS and PPEGMEA. The blend material had a much lower failure strain of only 38% and a maximum toughness of 4.9 MJ m-3. This approach thus emphasizes the importance of the covalent linking of the PSS and PPEGMEA blocks. Furthermore, we demonstrate that the conductivity of scratched films can be restored upon exposure to water.

Ion Transport in Solvent-Free, Crosslinked, Single-Ion Conducting Polymer Electrolytes for Post-Lithium Ion Batteries

Solvent-free, single-ion conducting electrolytes are sought after for use in electrochemical energy storage devices. Here, we investigate the ionic conductivity and how this property is influenced by segmental mobility and conducting ion number in crosslinked single-ion conducting polyether-based electrolytes with varying tethered anion and counter-cation types. Crosslinked electrolytes are prepared by the polymerization of poly(ethylene glycol) diacrylate (PEGDA), poly(ethylene glycol) methyl ether acrylate, and ionic monomers. The ionic conductivity of the electrolytes is measured and interpreted in the context of differential scanning calorimetry and Raman spectroscopy measurements. A lithiated crosslinked electrolyte prepared with PEG31DA and (4-styrenesulfonyl)(trifluoromethanesulfonyl)imide (STFSI) monomers is found to have a lithium ion conductivity of 3.2 × 10−6 and 1.8 × 10−5 S/cm at 55 and 100 °C, respectively. The percentage of unpaired anions for this electrolyte was estimated at about 23% via Raman spectroscopy. Despite the large variances in metal cation–STFSI binding energies as predicted via density functional theory (DFT) and large variations in ionic conductivity, STFSI-based crosslinked electrolytes with the same charge density and varying cations (Li, Na, K, Mg, and Ca) were estimated to all have unpaired anion populations in the range of 19 to 29%.

Transesterification of triolein with ethanol using lipase-entrapped NIPA-co-PEGMEA gel beads

Monodisperse, millimeter-sized, lipase-entrapped NIPA-co-PEGMEA (N-isopropylacrylamide-co-poly(ethylene glycol) methyl ether acrylate) gel beads were prepared by sedimentation polymerization. The feasibility of the lipase-entrapped gel for use in biodiesel fuel (BDF) production was evaluated by studying its catalytic performance in transesterification of triolein with ethanol as the model. The reaction rate was expressed by the ping-pong bi-bi mechanism with ethanol inhibition; the parameters for the immobilized lipase were as follows; the maximum reaction rate, Vmax, was 0.405 mol/(min kg − Lipase PS); the Michaelis constants for triolein and ethanol, Km,T and Km,EtOH, were 481 and 1770 mol/m3, respectively; the ethanol inhibition constant, Ki, was 394 mol/m3. The NIPA-co-PEGMEA gel support improved the stability of the immobilized lipase. We developed a water-washing process wherein the by-product glycerol, which is absorbed and accumulated in the NIPA-co-PEGMEA gel, is removed, so that the lipase-entrapped gel could be reused for multiple cycles (10 cycles were confirmed). The glycerol absorbability of the NIPA-co-PEGMEA gel makes it promising for use in facile BDF production, as it allows for the simultaneous enzymatic reaction and glycerol removal.

Green nanofillers: Plant virus reinforcement in hydrophilic polymer nanocomposites

Aqueous polymeric systems are critical components for a bevy of uses, most notably in biomedical sciences. However, these materials typically have inherently weak mechanical properties. A critical area of research in recent years is the development of new biocompatible nanofillers to reinforce these polymeric matrices and enhance mechanical properties. In particular, high aspect ratio nanotubes provide the greatest mechanical reinforcement when blended into composite materials. Unfortunately, there are few options for water dispersible nanofillers that would be appropriate for water-soluble polymers. In this study, a plant virus protein nanotube, tobacco mosaic green mild virus (TMGMV), was used to strengthen two hydrophilic composites. In the first example, a cross-linked poly(poly(ethylene glycol) methyl ether acrylate) hydrogel (PPEGMEA) was synthesized with varying amounts of TMGMV. TMGMV was an effective reinforcing agent at low concentrations, increasing the storage and compressive modulus when compared to neat PPEGMEA hydrogels. To further validate the broad applicability of TMGMV reinforcement, polyvinyl alcohol (PVA)/TMGMV composite films were studied. TMGMV was found to have a similar reinforcing effect on these film systems. Rod-shaped viruses may represent a broad based reinforcing agent for aqueous systems in the future.

Ion-responsive fluorescence resonance energy transfer between grafted polyacrylic acid arms of star block copolymers

Interactions between polyacrylic acid (PAA) arms of star block copolymers through metal ions were investigated by fluorescence resonance energy transfer (FRET). Dendritic polyester (DPE) core was grafted with block copolymer arms of oligo (ethylene glycol) methyl ether acrylate (OEGA) and PAA. Fluorescein o-methacrylate (FMA) or methacryloxyethyl thiocarbamoyl rhodamine B (MTR) was introduced via copolymerization to the terminated PAA blocks. The unique copolymer structure enabled FRET between PAA chains without causing precipitation, which inevitably occurs for linear PAA. Addition of metal ions such as Zn2+, Ca2+, or Na+ induced FRET, the order of which was Zn2+>Ca2+≫Na+. FRET intensity was also correlated with concentration of each ion. Furthermore, in situ FRET measurement during the hydrogel formation of the star block copolymers was performed by mixing the star block copolymers and Zn2+.

Communication—Synthesis of Fluorine-Free Highly Ion Conductive Polymer Electrolyte Having Lithium Bissulfonimide Unit

A highly ion conductive polymer was designed based on lithium N-methanesulfonylvinylsulfoneimide (LiMSVSI), a new vinyl monomer consisting of the smallest skeleton except the lithium bisulfonimide moieties. Its copolymer with poly(ethylene glycol) methyl ether acrylate exhibited good ionic conductivity in the range of 10−4–10−5 S/cm.

Effect of Side-Chain Branching on Enhancement of Ionic Conductivity and Capacity Retention of a Solid Copolymer Electrolyte Membrane

Low current drain driven by the low ionic conductivity of a solid polymer electrolyte is one of the major obstacles of solid-state battery. In an effort to improve the ionic conductivity of a solid polymer electrolyte membrane (PEM), polyethylene glycol diacrylate (PEGDA) and monofunctional polyethylene glycol methyl ether acrylate (PEGMEA) were copolymerized via photopolymerization to afford a PEGDA network with dangling PEGMEA side chains. By attaching PEGMEA side branches to the PEGDA network backbone, the glass transition temperature (Tg) was found to decrease, which may be controlled by relative amounts of PEGMEA and PEGDA. Concurrently, the ionic conductivity of a co-PEM consisting of lithium bis(trifluoromethane)sulfonylimide (LiTFSI) salt and a succinonitrile plasticizer in the PEGMEA-co-PEGDA copolymer network was enhanced with increasing PEGMEA side branching. The relationship between the network Tg and ionic conductivity of the branched co-PEM was analyzed in the context of the Vogel-Tammann-Fulcher equation. The plasticized branched co-PEM network exhibited room-temperature ionic conductivity at a superionic conductor level of 10-3 S/cm. Of particular importance is the fact that excellent capacity retention at a high current rate (2 C) in charge/discharge cyclings of Li4Ti5O12/co-PEM/Li and LiFePO4/co-PEM/Li half-cells was achieved. This improved charge retention may be attributed to lower frictional surfaces of the electrodes afforded by side brushes, which probably alleviates formation of irreversible reaction byproducts at the electrode/electrolyte interface.

Organic Nanoprobes for Fluorescence and 19F Magnetic Resonance Dual‐Modality Imaging

Multimodal imaging techniques have been demonstrated to be greatly advantageous in achieving accurate diagnosis and gained increasing attention in recent decades. Herein, we present a new strategy to integrate the complementary modalities of 19F magnetic resonance imaging (19F MRI) and fluorescence imaging (FI) into a polymer nanoprobe composed of hydrophobic fluorescent organic core and hydrophilic fluorinated polymer shell. The alkyne‐terminated fluorinated copolymer (Pn) of 2,2,2‐trifluoroethyl acrylate (TFEA) and poly(ethylene glycol) methyl ether acrylate (PEGA) was first prepared via atom transfer radical polymerization (ATRP). The PEGA plays an important role in both improving 19F signal and modulating the hydrophilicity of Pn. The alkynyl tail in Pn is readily conjugated with azide modified tetra‐phenylethylene (TPE) through click chemistry to form azo polymer (TPE‐azo‐Pn). The core‐shell nanoprobes (TPE‐P3N) with an average particle size of 57.2 ± 8.8 nm are obtained via self‐assembly with ultrasonication in aqueous solution. These nanoprobes demonstrate high water stability, good biocompatibility, strong fluorescence and good 19F MRI performance, which present great potentials for simultaneous fluorescence imaging and 19F–MR imaging.