Polyacrylonitrile (PAN) with high molecular weight and low dispersity is successfully synthesized by visible‐light‐induced metal‐free radical polymerization at room temperature. This polymerization technique uses organic dye Eosin Y as photocatalyst and benzenediazonium tetrafluoroborates as initiator. Gel permeation chromatography‐multiangle laser light scattering shows the absolute molar weight of the PAN more than 1.50 × 105 g mol−1 with a polydispersity index < 1.3 while MALDI‐TOF MS and 19F NMR spectroscopy indicate the F‐chain‐end process. The first‐order kinetic behavior, molecular weight distributions shifting, and “ON/OFF” experiment results suggest this reaction may follow the atom‐transfer‐like radical polymerization mechanism. In addition, this new approach allows for the efficient synthesis of well‐defined random copolymers.
Alternating copolymers of an oligopeptide (N3‐GVGV‐N3, where G: glycine; V: valine) and an oligothiophene (5,5′‐bis(ethynyl)‐3,3'‐dioctyltetrathiophene) are prepared by click chemistry. The experimental results discover that these copolymers exhibit strong molecular‐weight‐dependent self‐assembly behaviors. The copolymer P1 with the lowest weight‐average molecular weight ( = 7400 g mol?1), assembles into well‐ordered fibrous nanostructures. P3 ( = 16 980 g mol?1) assembles into nanoballs. P2, which has the medium between P1 and P3, ( = 14 800 g mol?1), exhibits more‐complicated self‐assembly behaviors, more like a transition state between the other two. All of the results suggest the self‐assembly ability of these oligopeptide segments might be the major reason for the nano‐structure evolution.
Monomer conversion versus time profiles for the radical polymerization of ionized acrylic acid (AA), 0.6 to 0.8 mol L?1 in aqueous solution, are measured at 50 °C via inline near‐infrared spectroscopy mostly on fully ionized AA, i.e., of alkali acrylates. Ionization reduces polymerization rate with the size of this effect being dependent on the type and on the concentration of the alkali counter cation, which is varied from lithium to rubidium. Polymerization rate becomes very small upon shielding the cation by complexation, whereas an enhancement of cation concentration, by addition of alkali chloride, may enhance polymerization rate such as to even reach the high rates observed with the radical polymerization of nonionized AA.
Two thioxanthone based acrylated one‐component visible light photoinitiators, 2‐(methyl(4‐((methyl(9‐oxo‐9H‐thioxanthen‐2‐yl)amino)methyl)benzyl)amino)ethyl acrylate (TX‐EA) and ((4‐((methyl(9‐oxo‐9H‐thioxanthen‐2‐yl)amino)methyl)benzyl)azanediyl)bis(ethane‐2,1‐diyl)diacrylate (TX‐BDA), are designed and synthesized. The results of photopolymerization and migration study demonstrate that TX‐EA and TX‐BDA are more effective one‐component visible light photoinitiators for free radical polymerization with excellent migration stability than 4‐((methyl(9‐oxo‐9H‐thioxanthen‐2‐yl)amino)methyl)phenyl acrylate. The mass fraction of the extracted TX‐BDA in a cured 1,6‐hexanediol diacrylate polymer film is as low as 0.55% and the residual amount is estimated to be only 90 ppm. TX‐BDA would have great potential to be used in visible light curing systems, particularly in the food packing or biomedical fields. Results demonstrate that the synergistic effect of hydrogen donors and polymerizable groups in photoinitiator plays an important role in realizing high performance and low migration in photopolymerization system.
Functional nanowires with photochromic spiropyran (SP) species are prepared by reversible addition–fragmentation transfer (RAFT) dispersion polymerization of styrene using poly(4‐vinylpyridine‐co‐spiropyranyl methacrylate) as a macro‐RAFT agent, and then electrospinning technology is used to fabricate fibers from the functional nanowires. The photoisomerization of SP in the nanowires and fibers is studied, and reversible photochromism for both nanowires and fibers is observed. Since the merocyanine (ME form) of the SP emits fluorescence and the SP form is non‐fluorescent, the fluorescence of the nanowires and the fibers can be switched on and off upon alternating UV and visible‐light irradiation.
Stationary and time‐resolved electron spin resonance spectroscopy measurements are employed to investigate the kinetics of the surface‐initiated reversible addition fragmentation chain transfer (RAFT) polymerization of n‐butyl acrylate from silica nanoparticles using both R‐ and Z‐group‐attached trithiocarbonates as RAFT agents. The obtained kinetic parameters reveal that the addition rate coefficient in the main equilibrium of RAFT graft polymerizations is significantly smaller than the one for comparable RAFT polymerizations in solution phase, as translational diffusion of surface‐attached molecules is limited. In comparison to the R‐group approach, the equilibrium constants of the Z‐group approach are about one to two orders of magnitude smaller due to a stronger shielding of the RAFT moieties.
Novel nitrogen‐doped graphene nanoribbons (GNR‐Ns) are synthesized by the coupling reaction between a pyrazine (or benzene) derivative and naphthalene followed by cyclodehydrogenation. The amount of nitrogen doping in the GNR‐Ns is controlled by changing the monomer feed ratio of pyrazine to benzene for polymerization. The electron mobility of the GNR‐Ns increases while the hole mobility decreases, as the amount of nitrogen doping in the GNR increases, indicating that the charge‐transport behavior of GNRs is changed from ambipolar to an n‐type semiconductor. The threshold voltage of the GNR‐Ns also shifts from 20 to ?6 V as the amount of nitrogen doping increases.
Triple hydrophilic asymmetric poly(2‐hydroxyethyl acrylate)‐b‐poly(ethylene oxide)‐b‐poly(2‐hydroxyethyl acrylate) (PHEA‐b‐PEO‐b‐PHEA) triblock copolymers are obtained by copper(0) catalyzed reversible deactivation radical polymerization (RDRP). Copper wire catalyzed polymerization of HEA from large PEO (Mn = 35 000 g mol?1) macroinitiator in dimethylsulfoxide or in water fails to reach high monomer conversion in a controlled manner contrary to what is previously published with a shorter PEO macroinitiator. Catalysis by nascent Cu(0) particles generated by disproportionating CuBr in water allows rapid polymerization and high monomer conversion with a rather good control of both dispersity and HEA block length. Model disproportionation experiment shows that HEA influences the disproportionation/comproportionation equilibrium. Larger quantities of HEA lead to higher apparent rate constants and less disproportionation of CuBr which is in agreement with the supplemental activator and reducing agent atom transfer radical polymerization (SARA ATRP) mechanism and not with the single electron transfer–living radical polymerization (SET‐LRP) mechanism.
This paper designs and synthesizes a novel amphiphilic fluorinated block copolymer, composed of oligo ethylene glycol methyl ether methacrylate, 2‐(N ,N‐dimethylamino)ethyl methacrylate, and developing 2‐((2‐methacryloyloxy ethyl) disulfanyl) ethyl 3,5‐bis(trifluoromethyl) benzoate, by reversible addition–fragmentation chain transfer polymerization. This amphiphilic block copolymer can self‐assemble with hydrophobic lanthanide‐based upconversion nanoparticles to form hybrid colloidal nanoclusters. The obtained nanoclusters exhibit not only good water‐dispersibility, high biocompatibility, and strong stability in biological milieu, but excellent pH/redox‐dual‐responsive release in vitro behavior for doxorubicin (DOX). And the DOX‐loaded nanoclusters have much better therapeutic effect than free DOX and can be uptaken by MCF‐7 cells with evident upconversion luminescence signal for intracellular imaging.
The radical copolymerization of N‐substituted maleimides containing polymethylene and poly(ethylene oxide) side chains as the N‐substituent groups with isobutene, styrene, and α‐methylstyrene as the electron‐donating monomers is carried out in order to investigate the structure and thermal properties of the resulting comb‐like copolymers. The obtained copolymers show excellent thermal stability and their glass transition temperatures vary depending on the chain length of the introduced N‐substituents. The main‐ and side‐chain motions of the copolymers are investigated by dynamic mechanical analysis at various frequencies over the temperature range of ?150 to 100 °C.
Synthesis of complex macromolecular architectures exhibiting no chain ends such as flower‐like polymers is still of interest in the aim of investigating their physicochemical properties. For this purpose, poly(3,4‐dimethyl maleic imidoethyl acrylate)‐block‐polybutadiene‐block‐poly(3,4‐dimethyl maleic imidoethyl acrylate) triblock copolymer is synthesized in a convergent manner using a combination of living polymerization (anionic polymerization), reversible deactivation radical polymerization, and click chemistry. This copolymer is self‐assembled in a selective solvent (heptane/THF mixture) of the polybutadiene block leading to the formation of flower‐like micelles in thermodynamic equilibrium in dilute solution. These resulting transient architectures are fixed by covalently crosslinking the micelles core by inducing [2+2] cyclodimerization of the 3,4‐dimethyl maleic imidoethyl groups borne by the short solvophobic blocks under UV irradiation. Single flowers are isolated from residual non‐crosslinked chains by semipreparative size exclusion chromatography (SEC) and characterized by 1H NMR, SEC, dynamic light scattering (DLS), and transmission electron microscopy (TEM).
Iron‐mediated atom‐transfer radical polymerization (ATRP) of methyl methacrylate (MMA) in N‐methylpyrrolidin‐2‐one (NMP) solution is investigated via online VIS/NIR spectroscopy up to 2500 bar. The activation–deactivation equilibrium constant, KATRP, decreases towards higher NMP content due to the formation of catalytically less active FeII/NMP species. The reaction volume increases from 1 to 15 cm3 mol?1 in passing from 16 to 92 mol% NMP. The same effects are observed for monomer‐free model systems with poly(MMA)–Br as the initiator. Investigations into iron‐catalyzed ATRP of MMA in less polar solvents or even without an additional solvent (i.e., for bulk ATRP) yield KATRP values, which are by two to three orders of magnitude higher than in the presence of NMP.
Two natural polymers, namely, cellulose and pullulan, are selectively oxidized employing the well‐established (2,2,6,6‐tetramethylpiperidine‐1‐yl)‐oxyl radical protocol in order to introduce in their structural unit negatively charged carboxylic groups. These newly introduced moieties further serve as efficient matrix for the in situ iron oxide nanoparticles fabrication. The morphology, structure, stability, and magnetic properties of the as‐prepared carboxylated polysaccharides embedded ultrasmall iron oxide nanoparticles are analyzed using various techniques, such as Fourier transform infrared spectroscopy, dynamic light scattering, zeta potential, transmission electron microscopy, energy dispersive X‐ray spectroscopy, thermogravimetric analyses, and vibrating sample magnetometer. The results show that the two used polysaccharides are excellent materials to produce highly uniform shaped nanoparticles with an average size of about 3 nm. Moreover, the nanoparticles have excellent water dispersibility and stability. The prepared magnetic samples show antibacterial effect against Gram‐positive bacteria and also exhibit characteristics as contrasting agent for noninvasive cellular and molecular imaging.
Novel self‐healing silicone rubbers are prepared by a two‐step procedure: aminopropyl methyl phenyl polysiloxanes is first reacted with salicylaldehyde and then with copper acetate. The reversible nature of the metal–ligand coordination interaction between polysiloxanes with pendent Schiff‐base groups and Cu2+ has endowed silicone rubbers with superior self‐healing properties. As compared with other self‐healing silicone rubbers based on hydrogen bonds or Diels–Alder reaction, this cross‐linked system shows high healing power. The materials are cut into two parts and put together in a mold for 1 h at 30 °C, observing a macroscopic healing and a strength recovery up to 87.0%.
Synthesis of multiarm star polymers via “core first” method but possibly through two different chain growth fashions has been described. Two distinct styrenyl‐TEMPO‐based G3 and G4 dendritic unimolecular initiators have been used for this method. Polymerization of styrene using these core‐cum‐initiators at 125 °C varying the monomer to initiator ratio and polymerization time yields multiarm star polymers with molecular weight (Mw) in the range of 1.71 × 105 to 4.75 × 105 g mol?1 and polydispersity in the range of 1.34–1.46. Hydrolysis leading to degradation of inner polyurethane core yields highly narrow dispersed—PDI 1.00 to 1.04—polystyrene chains, and the SEC‐MALLS data of these chains confirm the accurate control on predetermination in the number of arms up to 48 of star polymers. The specific refractive index increment (dn/dc) of the polymers is found to be decreased with decreasing weight fraction of core. The transmission electron microscope (TEM) and atomic force microscopy (AFM) images and hydrodynamic radius of chosen polymers confirm the two different chain growth fashions leading to the formation of star polymers as discrete nanoparticle in the case of initiator in which TEMPO is anchored and formation of peripherally low entangled short chains in the case of initiators in which TEMPO is end‐capped.
This study reports the synthesis and characterization of poly(3‐hexylthiophene) (P3HT) from a direct heteroarylation polymerization of two isomeric monomers, 2‐bromo‐3‐hexylthiophene (monomer 1 ) and 2‐bromo‐4‐hexylthiophene (monomer 2 ). Using the Herrmann–Beller catalyst along with P(o‐NMe2Ph)3, the resulting polymers are obtained in excellent yields and exhibit a good number‐average molecular weight (Mn of 33 and 16 kDa, respectively). Detailed 1H NMR analyses reveal less than 1% of homocouplings and no evidence of β‐branching. Dehalogenation is identified as the main chain termination step and preferentially occurs on monomer 2 . The melting temperature (237 °C) and hole mobility (up to 0.19 cm2 V?1.s?1) of the nearly defect‐free P3HT obtained from this simple polymerization of monomer 1 are comparable, if not superior, to those obtained with commercially available GRIM and Rieke samples.
Reverse iodine transfer polymerization (RITP) of 1,1,2,2‐tetrahydroperfluorodecyl acrylate (FDA) is successfully performed in supercritical carbon dioxide (scCO2) at 70 °C under a CO2 pressure of 300 bar. PolyFDA (PFDA) of increasing molecular weights (from 10 000 to 100 000 g mol?1) is synthesized with good agreement between theoretical, 1H NMR spectroscopy and and size exclusion chromatography/refractive index/right‐angle laser‐light scattering/differential viscometer (SEC/RI/RALLS/DV)‐estimated molecular weights (). Furthermore, the increase of goes with a decrease of the dispersity of the polymers (? from 2.06 to 1.33), which is consistent with a controlled radical polymerization (CRP). Lastly, the structure of final PFDA and therefore the RITP process are confirmed by matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS) analyses.
Three perylene‐containing conjugated microporous polymers (PrCMPs) are synthesized via Suzuki–Miyaura cross‐coupling reaction from perylene with four polymerizable functional groups and a range of different substituted benzene derivatives. The pore property and bandgap of the resulting PrCMPs can be tuned by changing the comonomer of benzene with different substituted groups and positions. The photocatalytic performances of the polymers are highly dependent on the surface area, geometry, and bandgap of the PrCMPs. It was found that the 1,2,4,5‐linked polymer of PrCMP‐3 shows the highest hydrogen evolution rate (HER) of 12.1 µmol h−1 under UV–vis light irradiation among the three polymers because of its high surface area, broad light absorption, and suitable bandgap. PrCMP‐3 also exhibits good photocatalytic stability for prolonged hydrogen production reaction. This result demonstrates that the crucial role of the linkage geometry offers a general principle for the rational design of conjugated microporous polymer photocatalysts.
The Janus polymerization combines cationic and anionic polymerizations into growing chains with two different chain ends. This provides a novel pathway to produce topologically interesting polymers. Here this polymerization is applied to allow the synthesis of branched polytetrahydrofuran (bPTHF) and poly(tetrahydrofuran‐co‐ε‐caprolactone) (bPTC). Rare earth triflates [RE(OTf)3] (RE = Lu, Sc, and Y) are used as catalyst, and small amounts (0.10–0.15 mol%) of ethylene glycol diglycidyl ether act as both initiator and comonomer due to the different reactivities of the two epoxide groups. The poly(ε‐caprolactone) block in bPTC provides crystalline domains and potential degradation under acidic conditions. The products of bPTHF show unusual tensile properties with a high strain at break of 1070% differing greatly from linear PTHF. Due to the large number of terminal hydroxyl groups and their strong hydrogen bonding, bPTHF has self‐healing properties with potentially promising applications.
The development of bioinspired, novel, high‐performance, “artificial muscle” materials is a topic of high current interest. Flexibility for folding and actuation are key parameters in the development of such artificial muscles, especially for self‐assembly and origami engineering. A current challenge is to develop a multifunctional material that combines the biological functions of actuation, sensing, and healing. In this work, for the first time experimental and modeling results of the actuation capability of a multifunctional magnet–polymer (Magpol) composite material that is already capable of damage sensing and self‐healing are reported. Actuation by constrained buckling of Magpol in an external magnetic field shows two buckling modes. The stress and strain are studied and optimized for various actuator geometries. Work density of up to 16 J kg?1 is obtained, comparable to electroactive polymers. Magpol is successfully able to lift more than four times its own weight at relatively low applied magnetic field. Good agreement is observed between the experimental and modeling results. An Ashby design chart is employed to compare its performance to other actuators. This work provides insight into the development of next generation flexible, active multifunctional materials.
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