Chlorine‐functionalized TEMPO‐capped polystyrenes were investigated using the matrix‐assisted laser desorption/ionization time‐of‐flight (MALDI‐TOF) technique. Amine‐ and acrylate‐functionalized agents and bifunctional TEMPO‐capped polystyrene were also analyzed to demonstrate the applicability of this method. Using this technique allowed to analyze the conversion of the chlorine function to an acrylate function, which was previously difficult to detect with other methods.
MALDI‐TOF mass spectrum of a polystyrene described in this article, as obtained with DHB as the matrix. 相似文献
Summary: The synthesis of aqueous dispersions of hybrid acrylic copolymer particles with either a monofunctional or a multifunctional polyhedral oligomeric silsesquioxane methacrylate comonomer has been performed by free radical heterophase polymerization. The miniemulsion process gives stable latexes, whereas the less controlled emulsion route results in colloidal instability of the products. The thermal and mechanical properties of the nanocomposite latex films have been preliminarily investigated.
The nanocomposite latex particles based on hybrid copolyacrylates with highly dispersed POSS cages. 相似文献
Direct atom transfer radical polymerization (ATRP) of iso‐butyl methacrylate in microemulsion has been performed successfully for the first time. ATRP was performed at 40 °C with different emulsifier systems: i) the cationic emulsifier n‐tetradecyltrimethylammonium bromide (TTAB); and ii) mixed emulsifier systems based on TTAB and the non‐ionic emulsifiers Emulgen 911 or Emulgen 931. All polymerizations proceeded in a controlled/living fashion, and the microemulsions were transparent with particle diameters less than 15 nm. The emulsifier system TTAB/Emulgen 911 exhibited better control than TTAB only. This is proposed to be caused by complex formation between Emulgen 911 in the organic phase and CuBr2 (the deactivator), thus reducing the extent of exit of CuBr2 to the aqueous phase. The more hydrophilic Emulgen 931 did not lead to improved control.
A novel phenylacetylene ( 1 ) having two hydroxyl groups and a chiral pinanyl group together with the other three related phenylacetylenes has been synthesized and (co)polymerized by using an achiral catalytic system. Among the four monomers, only 1 is suitable to the asymmetric‐induced polymerization ( AIP ). Chiral amplification phenomenon is only observed in the copolymerization of 1 with an achiral phenylacetylene having two hydroxyl groups ( 3 ). The tight helical cis‐cisoidal main chain formed by making intramolecular hydrogen bonds between the hydroxyl groups in the copoly( 1 / 3 ) enhances the efficiency of chiral induction and as a result chiral amplification phenomenon is observed during the copolymerization.
A two‐armed polymer with a crown ether core self‐assembles to produce macroporous films with pores perpendicularly reaching through the film down to the substrate. A possible assembling mechanism is discussed. The pore size can be conveniently adjusted by changing the solution concentration. These through‐hole macroporous films provide a template for fabricating an array of Cu nanoparticle aggregates.
Summary: A series of novel mesogen‐jacketed liquid crystal miktoarm star rod‐coil block copolymers were synthesized via atom transfer radical polymerization (ATRP). Their architectures {coil conformation of styrene segment and rigid rod conformation of {2,5‐bis[(4‐methoxyphenyl)oxycarbonyl]styrene} (MPCS) segment} were confirmed by GPC, 1H NMR, and MALDI‐TOF studies. The liquid crystalline behaviors of the synthesized copolymers are evidenced from POM observation. The liquid crystalline phase depends on the molecular weights of the rigid rod arm of miktoarm star copolymers.
A novel amphiphilic diblock copolymer composed of a hydrophilic poly(ethylene oxide) and a hydrophobic polymethacrylate with photochromic azopyridine moieties in the side groups was synthesized by atom transfer radical polymerization. The copolymeric vesicles showed photoinduced circular process including fusion, damage and defect formation, disruption, disintegration and rearrangement in H2O/THF during the irradiation of UV light. The process of photoresponsive cycle can be inhibited at any moment by visible light.
Computer simulations reveal the unique conformation of or erythro diisotactic polynorbornene, a polymer with numerous important applications in microelectronics. While previous simulations suggested that this polymer adopts a helix‐kink morphology, the results presented herein indicate that the reversal of the helix symmetry is the origin of such kinks which cause a transition from a rigid‐rod conformation to a random coil with increasing molecular weight. An RIS model was developed that accurately predicts the unique conformation of this polymer. This model predicts a rigid‐rod helical conformation that eventually transitions to a random coil at a degree of polymerization of approximately 500.
We report a facile method to accomplish the crosslinking reaction of PVA with SWNTs, MWNTs, and C‐60 using MW irradiation. Nanocomposites of PVA crosslinked with SWNT, MWNT and C‐60 were prepared expeditiously by reacting the respective carbon nanotubes with 3 wt.‐% PVA under MW irradiation, maintaining a temperature of 100 °C, representing a radical improvement over literature methods to prepare such crosslinked PVA composites. This general preparative procedure is versatile and provides a simple route to manufacture useful SWNT, MWNT and C‐60 nanocomposites.
Summary: A novel polymerization procedure to synthesize latex stabilized by alkali‐soluble resin (ASR) is detailed. According to this process, latexes with a high solid content and low viscosity are obtained using a substantially lower amount of ASR when compared with existing techniques. Similar rewet properties were found for the latexes obtained by a standard process and for the one obtained by the process described in this work.
Comparison of the particle size distributions obtained by conventional emulsion polymerization (○) and by miniemulsion polymerization (□). 相似文献
