Summary: Magnetic nanoparticles have been prepared by a co‐precipitation method and modified with methacryloxypropyltrimethoxysilane. Magnetic molecularly imprinted polymer particles have been prepared by suspension polymerization in silicone oil. The particles possess a high affinity to the template molecules and are rapidly separated under a magnetic field.
Summary: Self‐oscillating polymers and nano‐gel particles consisting of N‐isopropylacrylamide and the ruthenium catalyst of the Belousov‐Zhabotinsky reaction have been prepared. In order to clarify the crosslinking effect on the self‐oscillating behavior, the phase transition behaviors were investigated by measuring the transmittance and the fluorescence intensity of the polymer solution and the gel bead suspension. Cooperative effects due to crosslinking will play an important role for the design of nanoactuators.
Chemical structure of poly(NIPAAm‐co‐Ru(bpy)3). 相似文献
We report syntheses of phenylene‐, biphenylene‐, and terphenylene‐layered polymers with a xanthene scaffold by the modified Suzuki‐Miyaura coupling reaction. Their optical properties were studied in detail. The polymer end‐capped by nitrobenzene units, which act as fluorescence quenchers, exhibited the photo‐excited energy transfer from the layered oligophenylenes to the terminal units.
This review article describes the preparation of polymer brushes by nitroxide‐mediated radical polymerization using either the ‘grafting to’ or the ‘grafting from’ approach. The use of TEMPO as a classical initiator is intensively described. More sophisticated nitroxides are also included in the discussion. Brush formation on flat surfaces such as wafers and also on particles is reported. Finally, some applications of polymer brushes are presented.
Equilibrium P–V–T properties of randomly crosslinked amorphous polymer networks are modeled via molecular dynamics simulation for connectivity ratios between 1.0 and 1.5. The relation between connectivity ratio and network shrinkage is studied over a wide range of temperatures and pressures. The simulation results are compared to a mean‐field Flory–Huggins lattice model.
Supramolecular complexes of a poly(tert‐butoxystyrene)‐block‐polystyrene‐block‐poly(4‐vinylpyridine) triblock copolymers and less than stoichiometric amounts of pentadecylphenol (PDP) are shown to self‐assemble into a core–shell gyroid morphology with the core channels formed by the hydrogen‐bonded P4VP(PDP)complexes. After structure formation, PDP was removed using a simple washing procedure, resulting in well‐ordered nanoporous films that were used as templates for nickel plating.
Perfectly alternating copolymers can be synthesised by reacting diacrylates with terminal dienes using alternating diene metathesis polycondensation (ALTMET). This novel method is very versatile and allows preparation of diverse structures of polymers, including main‐chain liquid crystalline polymers.
Main‐chain liquid crystalline polymer obtained by ALTMET. 相似文献
The nucleophilic living ring‐opening polymerization of N‐substituted glycine N‐carboxyanhydrides using solid‐phase synthesis resins is reported. By variation of experimental parameters, products with near Poisson distributions are obtained. As opposed to reversible deactivation radical polymerization, the living polymerization is demonstrated to be viable to high monomer conversion and through multiple monomer addition steps. Successful preparation of a multiblock copolypeptoid is proof for a highly living and robust character of the solid‐phase peptoid polymerization.
A new methodology for creating patterned fluorescence images was developed based on acrylate polymers that have pendant triphenylmethane derivatives as precursor fluorophores. Photoinduced oxidation of the substituted nonfluorescent triphenylmethane substituents on the polymers results in the generation of fluorescent cationic species. Patterned fluorescence images were obtained when the polymer film was subjected to photomasked UV‐irradiation. The rate of formation and quality of the patterned images were found to be dependent on the nature of substituents on the methane carbon of the triphenylmethane group. Inefficient image formation takes place with the polymer derived from the H‐substituted derivative owing to the inefficient oxidation of the triphenylmethane group. In contrast, photomasked UV‐irradiation of a thin polymer film derived from the CN‐substituted triphenylmethane derivative leads to fast (1 s irradiation, 12 mW · cm−2) and finely resolved patterned fluorescence images.
A polymer system based on polydiacetylene (PDA) supramolecules that emits red, green, and blue fluorescence has been constructed. The three‐color emitting system is comprised of red‐fluorescent PDA vesicles in which green‐fluorescent fluorescein molecules are encapsulated. Finally, the blue‐fluorescence component is introduced by reacting terminal amine groups on the PDA vesicle surfaces with fluorescamine. Thin PDA‐polymer‐containing poly(vinyl alcohol) films formed by using this strategy display red, green, and blue fluorescence upon excitation with light at specific wavelengths.
Summary: We describe an interesting approach to the fabrication of wettability gradients from hydrophobicity to superhydrophobicity in low‐density polyethylene (LDPE) films by first forming high porosity surfaces and placing the specimens onto linear temperature gradients. While the polymer chosen for the study is non‐polar, its microporous layer provides sufficient superhydrophobicity. Lateral gradient heating of the layer results in partial melting of the polymer and correspondingly decreases porosity thus decreasing hydrophobicity.
The influence of Hofmeister salts was investigated on the cloud point of three poly(2‐oxazoline)s, namely poly(2‐ethyl‐2‐oxazoline) [PEtOx], poly(2‐n‐propyl‐2‐oxazoline) [PnPropOx], and poly(2‐isopropyl‐2‐oxazoline) [PiPropOx]. In addition, a comb polymer based on oligo‐2‐ethyl‐2‐oxazoline side chains and a methacrylate backbone (POEtOxMA) was included in this investigation. It was found that the ionic response of the poly(2‐oxazoline)s strongly depends on their hydrophilicity. The comb polymer POEtOxMA revealed a strikingly similar response to the salts as linear PEtOx even though the cloud points of the polymers in water differ. This indicates that the architecture does not significantly influence the effect of the Hofmeister ions, even though there is a difference in the absolute cloud point.
Summary: Reversible pH‐induced swelling of (PAH/PSS) polyelectrolyte microcapsules is accompanied by increased porosity, making them permeable to poly(acrylic acid) (PAA) at pH values higher than 11.2. This pH‐switchable permeability was used to encapsulate the polyanion in alkaline conditions. Relationship between starting PAA concentration in solution and amount finally being encapsulated has been established and can be used further as calibration curve. A desired amount of encapsulated polymer in the picogram range per capsule can be achieved. The loaded capsules were then used as microreactors by forming a complex between the PAA and Ca2+ ions.
General scheme for pH‐induced encapsulation of (PAA) in alkali condition by switching their permeability. 相似文献
Liquid crystal polymer nanofibers with a diameter ranging from 0.13 to 4.71 µm were prepared by electrospinning from a main‐chain liquid crystalline polyester, BB‐5(3‐Me). WAXD measurements showed that the formation and orientation of the ordered structure in the electrospun fibers were controlled by the fiber diameter formed during electrospinning. For BB‐5(3‐Me), the SmA structure with two layer spacings was formed in the fiber during the electrospinning. Under optimal spinning conditions, the SmA structure is highly oriented in the fiber. In addition, annealing transformed the metastable SmA structure in the BB‐5(3‐Me) fiber into stable SmCA one.
One‐dimensional methyl orange fibrils can be easily prepared. They are stable in acidic aqueous solutions and soluble in neutral water. When used to synthesize conducting polymer microtubules, the fibrils act as “hard templates” formally but as “soft templates” effectively. Microtubular structures of polypyrrole, polyaniline, and poly(3,4‐ethylenedioxythiophene) have been achieved successfully via such water‐soluble versatile templates.
The preparation, characterization and properties of novel millable polyurethane/organoclay nanocomposites are reported. Clay treated with methyl tallow bis(2‐hydroxyethyl) quaternary ammonium chloride was used as an organoclay for nanocomposite preparation. X‐ray diffraction indicated the intercalation of polymer chains inside the interlayer spacings of the clay. Dynamic mechanical analysis showed a significant increase in storage modulus, and tensile strength increases with increased organoclay loading.
X‐ray diffraction patterns of millable polyurethane/organoclay nanocomposites. 相似文献
Water‐soluble single‐ and multi‐walled carbon nanotubes (CNTs) were prepared by grafting polyacrylamide chains from the graphitic surface via ceric ion‐induced redox radical polymerization. The reducing functionalities were covalently attached to the tubes by peroxide‐assisted radical reaction. The results showed that polymer chains were grafted onto CNTs by the redox process. The redox radical polymerization initiated by carbon nanotube‐bearing functionalities not only provides a powerful strategy for modifying the carbon nanostructures but also gives us the knowledge of their sidewall chemistry.
Organic polymers that contain ligated metals offer a variety of unique properties which include luminescence, electro‐ and photochemistry, catalysis, charge, magnetism, and thermochromism. These organic–inorganic hybrid materials have the potential to offer novel active matrixes for advanced devices. Continued progress in synthetic chemistry and molecular characterization will enable such advanced materials. Here the focus is restricted to side‐chain metal complexes with emissive properties that highlight the use of lanthanide ions as opposed to the often‐studied transition metal complexes.
