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1.
Synthesis and Characterization of Polymeric Acid‐Doped Polyaniline Interpenetrating Polymer Networks
Polyaniline (PANI)/poly(2‐acrylamido‐2‐methylpropane sulfonic acid) (PAMPS) semi‐interpenetrating network polymers (semi‐IPNs) were prepared using the simultaneous method. The formation and properties of the interpenetrating PANI/PAMPS semi‐IPNs were investigated using Fourier transform infrared spectroscopy, X‐ray diffraction, solid‐state 13C‐NMR, differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The interaction of PAMPS with PANI as a polymeric acid dopant was also investigated. These semi‐IPNs had a different microstructure compared to that of pure PANI. Packing structures and several decomposition steps were ordered for each semi‐IPN, while pure PANI exhibits a single amorphous peak and one decomposition step. The NMR spectra show that these peaks broaden and shifted downfield in the semi‐IPNs. A thermal reaction between PANI and PAMPS was observed using DSC and TGA, and the data from the two techniques are in agreement. 相似文献
2.
The motivation of the current work has stemmed from the fact that the selection of suitable stabilizers for nonaqueous emulsions is still challenging because of lack of general knowledge about the underlying stabilization mechanisms. The preparation and surface activity of new amphiphilic gel nanoparticles in organic solvents were investigated. A new bifunctional surfmer was prepared by reacting polyoxyethylene 4‐nonyl‐2‐propylene‐phenol nonionic reactive surfactant with maleic anhydride followed by esterification with poly(ethylene glycol). This surfmer was used as stabilizer to prepare amphiphilic crosslinked N‐isopropylacrylamide (NIPAm) and 2‐acrylamido‐2‐methylpropane sulfonic acid (AMPS) copolymer nanogel on the basis of nonaqueous radical copolymerization temperature modified method in the presence of toluene and formamide (FA) as solvents and N, N‐methylene bisacrylamide as a crosslinker. The chemical structure of the prepared nanogels was determined by Fourier transform infrared spectroscopy analyses. The morphologies of the prepared nanogels were detected by transmission electron microscopy and scanning electron microscopy techniques. The surface tension of colloidal NIPAm/AMPS dispersions was measured in FA as functions of surface age (time), temperature, and the morphology of the NIPAm/AMPS nanogels. The NIPAm/AMPS nanogels reduced the surface tension of FA from 58.2 to about 30.2 mN/m at 25°C, and a little increase in the surface tension was observed at 40°C. The prepared nanogels show great reduction in interfacial tension values between FA and styrene. The NIPAm/AMPS dispersions exhibited high surface activity and used as stabilizers to prepare crosslinked styrene‐co‐AMPS microgel in the presence of divinylbenzene and FA as organic solvents based on nonaqueous emulsion crosslinking polymerization technique. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
3.
S. T. Günday A. Bozkurt W. H. Meyer G. Wegner 《Journal of Polymer Science.Polymer Physics》2006,44(23):3315-3322
Proton transfer reactions under anhydrous conditions have attracted remarkable interest due to chemical energy conversions in polymer electrolyte membrane fuel cells. In this work, 1H‐1,2,4‐triazole (Tri) was used as a proton solvent in different polymer host matrices such as Poly(vinylphosphonic acid) (PVPA), and poly(2‐acrylamido‐2‐methyl‐1‐propane sulfonic acid) (PAMPS). PVPATrix and PAMPSTrix electrolytes were investigated where x is the molar ratio of Tri to corresponding polymer repeat unit. The interaction between polymer and Tri was studied via FTIR spectroscopy. Thermogravimetry analysis and differential scanning calorimetry were employed to examine the thermal stability and homogeneity of the materials, respectively. PVPATri1.5 showed a maximum water‐free proton conductivity of 2.3 × 10?3 S/cm at 120 °C and that of PAMPSTri2 was 9.3 × 10?4 S/cm at 140 °C. The results were interpreted in terms of different acidic functional groups and composition. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 3315–3322, 2006 相似文献
4.
The competitive removal of Pb2+, Cu2+, and Cd2+ ions from aqueous solutions by the copolymer of 2‐acrylamido‐2‐methyl‐1‐propane sulfonic acid (AMPS) and itaconic acid (IA), P(AMPS‐co‐IA), was investigated. Homopolymer of AMPS (PAMPS) was also used to remove these ions from their aqueous solution. In the preparation of AMPS–IA copolymer, the molar percentages of AMPS and IA were 80 and 20, respectively. In order to observe the changes in the structures of polymers due to metal adsorption, FTIR spectra by attenuated total reflectancetechnique and scanning electron microscopy (SEM) pictures of the polymers were taken both before and after adsorption experiments. Total metal ion removal capacities of PAMPS and P(AMPS‐co‐IA) were 1.685 and 1.722 mmol Me2+/gpolymer, respectively. Experimental data were evaluated to determine the kinetic characteristics of the adsorption process. Competitive adsorption of Pb2+, Cu2+, and Cd2+ ions onto both PAMPS and P(AMPS‐co‐IA) was found to fit pseudo‐second‐order type kinetics. In addition, the removal orders in the competitive adsorption of these metal ions onto PAMPS and P(AMPS‐co‐IA) were found to be Cd2+ > Pb2+ > Cu2+ and Pb2+ > Cd2+ > Cu2+, respectively. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
5.
《Macromolecular rapid communications》2017,38(20)
The utility of thermoresponsive hydrogels, such as those based on poly(N‐isopropylacrylamide) (PNIPAAm), is severely limited by their deficient mechanical properties. In particular, the simultaneous achievement of high strength and stiffness remains unreported. In this work, a thermoresponsive hydrogel is prepared having the unique combination of ultrahigh compressive strength (≈23 MPa) and excellent compressive modulus (≈1.5 MPa). This is accomplished by employing a double network (DN) design comprised of a tightly crosslinked, highly negatively charged 1st network based on poly(2‐acrylamido‐2‐methylpropane sulfonic acid (PAMPS) and a loosely crosslinked, zwitterionic 2nd network based on a copolymer of thermoresponsive NIPAAm and zwitterionic 2‐(methacryloyloxy)ethyl]dimethyl‐(3‐sulfopropyl)ammonium hydroxide (MEDSAH). Comparison to other DN designs reveals that this PAMPS/P(NIPAAm‐co‐MEDSAH) DN hydrogel's remarkable properties stem from the intra‐ and internetwork ionic interactions of the two networks. Finally, this mechanically robust hydrogel retains the desirable thermosensitivity of PNIPAAm hydrogels, exhibiting a volume phase transition temperature of ≈35 °C. 相似文献
6.
Min Sup Kim Kwang Min Shin Sun I. Kim Geoffrey M. Spinks Seon Jeong Kim 《Macromolecular rapid communications》2008,29(7):552-556
We have demonstrated that uniform and continuous poly(2‐acrylamido‐2‐methyl‐1‐propane sulfonic acid) (PAMPS) tubular core‐shell nanostructures containing linear features of ferritin nanoparticles can be directly fabricated using two immiscible solutions employing coaxial electrospinning. By adjusting the concentration of PAMPS as the outer solution in the coaxial electrospinning process, the width of a one dimensional (1D) array of ferritin could be accurately controlled. We demonstrate the formation of a nearly linear chain of individual ferritin particles encapsulated in a PAMPS nanofiber of 40 nm diameter. The ability to accurately control the width of the ferritin 1D arrays encapsulated in tubular nanostructures is a key component in determining the efficiency and performance of nanodevices. The demonstrated method of forming tubular nanostructures containing inner 1D particle arrays can also be extended to other materials with potential applications in nanoelectronic devices, such as nanobiosensors and batteries.
7.
Selva Çavuş 《Journal of Polymer Science.Polymer Physics》2010,48(23):2497-2508
Novel poly(methacrylamide‐co‐2‐acrylamido‐2‐methyl‐ 1‐propanesulfonic acid) (poly(MAAm‐co‐AMPS)) hydrogels were synthesized by free radical polymerization of methacrylamide (MAAm) and 2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid (AMPS) in deionized water at 60 °C by using ammonium peroxydisulfate (APS), N,N′‐methylenebisacrylamide (MBAAm) and N,N,N′,N′‐tetramethylethylenediamine (TEMED) as initiator, crosslinker, and activator, respectively. To investigate the effects of feed content on the pH‐ and temperature‐dependent swelling behavior of poly(MAAm‐co‐AMPS), molar ratio of MAAm to AMPS in feed was varied from 90/10 to 10/90. Structural characterization of gels was performed by Fourier transform infrared (FTIR) spectroscopy using attenuated total reflectance (ATR) technique. Thermal and morphological characterizations of gels were performed by thermogravimetric analysis (TGA) and scanning electron microscopy (SEM), respectively. Although an apparent pH‐sensitivity was not observed for the poly(MAAm‐co‐AMPS) gels during the swelling in different buffer solutions, their temperature‐sensitivity became more evident with the increase in AMPS content of copolymer. Thermal stability of poly(MAAm‐co‐AMPS) gels increased with MAAm content. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2010 相似文献
8.
The miscibility and thermal properties of poly(N‐phenyl‐2‐hydroxytrimethylene amine)/poly(N‐vinyl pyrrolidone) (PHA/PVP) blends were examined by using differential scanning calorimetry (DSC), high‐resolution solid‐state nuclear magnetic resonance (NMR) techniques, and thermogravimetric analysis (TGA). It was found that PHA is miscible with PVP, as shown by the existence of a single composition‐dependent glass transition temperature (Tg) in the whole composition range. The DSC results, together with the 13C crosspolarization (CP)/magic angle spinning (MAS)/high‐power dipolar decoupling (DD) spectra of the blends, revealed that there exist rather strong intermolecular interactions between PHA and PVP. The increase in hydrogen bonding and in Tg of the blends was found to broaden the line width of CH—OH carbon resonance of PHA. The measurement of the relaxation time showed that the PHA/PVP blends are homogeneous at least on the scale of 1–2 nm. The proton spin‐lattice relaxation in both the laboratory frame and the rotating frame were studied as a function of the blend composition, and it was found that blending did not appreciably affect the spectral densities of motion (sub‐Tg relaxation) in the mid‐MHz and mid‐KHz frequency ranges. Thermogravimetric analysis showed that PHA has rather good thermal stability, and the thermal stability of the blend can be further improved with increasing PVP content. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 237–245, 1999 相似文献
9.
Dirk Kuckling Pradeep Pareek 《Journal of polymer science. Part A, Polymer chemistry》2003,41(11):1594-1602
A functionalized cyclam was synthesized by the attachment of a polymerizable acryloyl group to one of the four nitrogens on the cyclam molecule. The polymerization of the functionalized cyclam was performed with N‐isopropylacrylamide and N,N′‐methylene bisacrylamide, and the gels obtained were studied in the presence of different transition‐metal‐ion solutions. There was a drastic difference in the phase‐transition temperature (Tc) of the poly(N‐isopropylacrylamide) (PNIPAAm)/cyclam gel in comparison with the pure PNIPAAm gel. For the described system, a Tc shift of 15 °C was obtained. The presence of functionalized cyclam increased the hydrophilicity and Tc of the aforementioned polymer gels in deionized water (at pH 6) because of the presence of protonated amino moieties. The PNIPAAm/cyclam gels showed a dependence of the swelling behavior on pH. Tc of the pure PNIPAAm gel was weakly influenced by the presence of any transition‐metal ions, such as Cu2+, Ni2+, Zn2+, and Mn2+. The addition of Cu2+ or Ni2+ to the PNIPAAm/cyclam gel reduced Tc of the polymer gel, and a shift of approximately 12 °C was observed. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1594–1602, 2003 相似文献
10.
Wen‐Ji Jin Hwang Kyu Lee Eun Hwan Jeong Won Ho Park Ji Ho Youk 《Macromolecular rapid communications》2005,26(24):1903-1907
Summary: Poly(N‐vinylpyrrolidone) (PVP) was used in two methods to prepare polymer nanofibers containing Ag nanoparticles. The first method involved electrospinning the PVP nanofibers containing Ag nanoparticles directly from the PVP solutions containing the Ag nanoparticles. N,N‐Dimethylformamide was used as a solvent for the PVP as well as a reducing agent for the Ag+ ions in the PVP solutions. In the second method, poly(vinyl alcohol) (PVA) aqueous solutions were electrospun with 5 wt.‐% of the PVP containing Ag nanoparticles. The Ag nanoparticles were evenly distributed in the PVA nanofibers. PVP containing Ag nanoparticles could be used to introduce Ag nanoparticles to other polymer nanofibers that are miscible with PVP.
TEM image of a PVA nanofiber electrospun with 5 wt.‐% of the PVP containing Ag nanoparticles. 相似文献
11.
N,N′‐Pyromelliticdiimido‐di‐L ‐alanine ( 1 ), N,N′‐pyromelliticdiimido‐di‐L ‐phenylalanine ( 2 ), and N,N′‐pyromelliticdiimido‐di‐L ‐leucine ( 3 ) were prepared from the reaction of pyromellitic dianhydride with corresponding L ‐amino acids in a mixture of glacial acetic acid and pyridine solution (3/2 ratio) under refluxing conditions. The microwave‐assisted polycondensation of the corresponding diimide‐diacyl chloride monomers ( 5–7 ) with 4‐phenyl‐2,6‐bis(4‐aminophenyl) pyridine ( 10 ) or 4‐(p‐methylthiophenyl)‐2,6‐bis(4‐aminophenyl) pyridine ( 12 ) were carried out in a laboratory microwave oven. The resulting poly(amide‐imide)s were obtained in quantitative yields, and they showed admirable inherent viscosities (0.12–0.55 dlg?1), were soluble in polar aprotic solvents, showed good thermal stability and high optical purity. The synthetic compounds were characterized by IR, MS, 1H NMR, and 13C NMR spectroscopy, elemental analysis, and specific rotation. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
12.
Rosica Mincheva Dilyana Paneva Laetitia Mespouille Nevena Manolova Iliya Rashkov Philippe Dubois 《Journal of polymer science. Part A, Polymer chemistry》2009,47(4):1108-1119
The effect of pH and the ligand nature over the atom transfer radical polymerization (ATRP) of the anionic monomer sodium 2‐acrylamido‐2‐methylpropanesulfonate (AMPSNa) was investigated in aqueous medium by using ω‐halogenated poly(ethylene oxide) and CuBr, as macroinitiator and catalyst, respectively. The stability of both catalytic complexes and macroinitiator was investigated in function of pH, that is, fixed between 7.5 and 12. UV‐VIS spectroscopy confirmed a good catalytic complex stability in the studied conditions. Hydrolysis of the macroinitiator ester group at pH higher than 7.5 was detected by 1H NMR and GPC, yielding ill‐defined polymer samples when ATRP is performed in alkaline conditions. 2,2′‐Bipyridyl (Bpy), 1,1,4,7,10,10‐hexamethyltriethylenetetramine (HMTETA), and tris(2‐methylaminoethyl)amine (Me6‐TREN)‐based complexes were compared at the optimal pH (pH 7.5). When polymerization was carried out in the presence of CuBr · 2Me6‐TREN complex block copolymers with narrow molecular weight distribution (1.1 ≤ M W/M n ≤ 1.3), and good agreement between theoretical and experimental molar masses was obtained. Moreover, increasing the PAMPSNa polymerization degrees (n) did not affect the control over the polymerization. Preliminary characterization of the diblock copolymers behavior in aqueous medium revealed a strong polyelectrolyte effect independently of n. Interestingly, occurrence of interactions between the PEO and PAMPSNa‐blocks was also evidenced by differential scanning calorimetry and thermogravimetric analyses. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1108–1119, 2009 相似文献
13.
Masamichi Inoue Kyohei Noda Shin‐ichi Yusa 《Journal of polymer science. Part A, Polymer chemistry》2012,50(13):2596-2603
Water‐soluble crosslinked hollow nanoparticles were prepared using pH‐responsive anionic polymer micelles as templates. The template micelles were formed from pH‐responsive diblock copolymers (PAMPS‐PAaH) composed of the poly(sodium 2‐(acrylamido)‐2‐methylpropanesulfonate) and poly(6‐(acrylamido)hexanoic acid) blocks in an aqueous acidic solution. The PAMPS and PAaH blocks form a hydrophilic anionic shell and hydrophobic core of the core‐shell polymer micelle, respectively. A cationic diblock copolymer (PEG‐P(APTAC/CEA)) with the poly(ethylene glycol) block and random copolymer block composed of poly((3‐acrylamidopropyl)trimethylammonium chloride) containing a small amount of the 2‐(cinnamoyl)ethylacrylate photo‐crosslinkable unit can be adsorbed to the anionic shell of the template micelle due to electrostatic interaction, which form a core‐shell‐corona three‐layered micelle. The shell of the core‐shell‐corona micelle is formed from a polyion complex with anionic PAMPS and cationic P(APTAC/CEA) chains. The P(APTAC/CEA) chains in the shell of the core‐shell‐corona micelle can be photo‐crosslinked with UV irradiation. The template micelle can be dissociated using NaOH, because the PAaH blocks are ionized. Furthermore, electrostatic interactions between PAMPS and PAPTAC in the shell are screened by adding excess NaCl in water. The template micelles can be completely removed by dialysis against water containing NaOH and NaCl to prepare the crosslinked hollow nanoparticles. Transmission electron microscopy observations confirmed the hollow structure. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
14.
Hyun Jeong Jeon Young Chang You Ji Ho Youk 《Journal of polymer science. Part A, Polymer chemistry》2009,47(12):3078-3085
An amphiphilic block copolymer of poly(N‐vinyl pyrrolidone)‐b‐poly(ε‐caprolactone) (PVP‐b‐PCL) was synthesized by a combination of cobalt‐mediated radical polymerization (CMRP) and ring‐opening polymerization (ROP). The micellar characteristics of this copolymer were subsequently investigated. PVP (Mn = 11,400, Mw/Mn = 1.32) was synthesized at 20 °C via CMRP using a molar ratio of [VP]0/[V‐70]0/[Co]0 = 150/8/1. The PVP was then reacted with 2,2′‐azobis[2‐methyl‐N‐(2‐hydroxyethyl)propionamide] (VA‐086) to modify its cobalt complex chain end to a hydroxyl group. The cobalt (Co) content in the resulting PVP‐OH was 1.2 ppm, indicating that all of the covalent Co? C bonds were cleaved and reacted with VA‐086, and that the separated cobalt complexes were successfully removed. The ROP of CL was subsequently carried out using the produced PVP‐OH as a macroinitiator at 110 °C. The GPC trace of PVP‐b‐PCL was monomodal without any tailing caused by the residual PVP‐OH, indicating that the initiation efficiency was very high. The critical micelle concentration (CMC) of PVP‐b‐PCL (Mn = 18,000, Mw/Mn = 1.35) was 0.015 mg/mL. The PVP‐b‐PCL micelles were spherical in shape with an average diameter of 105 nm. The nanosized PVP‐b‐PCL micelles show promise as novel drug carriers in biomedical and pharmaceutical applications. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3078–3085, 2009 相似文献
15.
Stela Dragan Demetra Dragan Mariana Cristea Anton Airinei Luminita Ghimici 《Journal of polymer science. Part A, Polymer chemistry》1999,37(4):409-418
We report on the formation of the polycation/dye/polyanion (PC/D/PA) complexes by the interaction between nonstoichiometric polycation/dye (PC/D) complexes with polyanions. Polycations differed in their content of the (N,N‐dimethyl‐2‐hydroxypropylene ammonium chloride) units in the main chain. Poly(sodium acrylate) (NaPA), poly(sodium 2‐acrylamido‐2‐methylpropane sulfonate) (NaPAMPS) and poly(sodium styrenesulfonate) (NaPSS) were used as polyanions. Crystal Ponceau 6R (CP6R) and Ponceau 4R (P4R) with two or three sulfonic groups were used as anionic dyes. The interaction between nonstoichiometric PC/D complexes and polyanions was followed by UV‐VIS spectroscopy, viscometry, and conductometry measurements. Formation of PC/D/PA complexes takes place mainly by the electrostatic interaction between the polyanion and the free positive charges of the nonstoichiometric PC/D complex. The stoichiometry and the stability of the tricomponent complexes depended on the polycation structure, the structure and molecular weight of polyanion, the dye structure, and the P/D molar ratio. A high amount of the dye was excluded from the complex before the end point when a branched polycation was used. The higher the solubility of the dye the lower the stability of the PC/D/PA complexes. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 409–418, 1999 相似文献
16.
Zhiping Peng Guangzhao Li Xinxing Liu Zhen Tong 《Journal of polymer science. Part A, Polymer chemistry》2008,46(17):5869-5878
A doubly hydrophilic triblock copolymer of poly(N,N‐dimethylamino‐2‐ethyl methacrylate)‐b‐Poly(ethylene glycol)‐b‐poly(N,N‐dimethylamino‐2‐ethylmethacrylate) (PDMAEMA‐b‐PEG‐b‐PDMAEMA) with well‐defined structure and narrow molecular weight distribution (Mw/Mn = 1.21) was synthesized in aqueous medium via atom transfer radical polymerization (ATRP) of N,N‐dimethylamino‐2‐ethylmethacrylate (DMAEMA) initiated by the PEG macroinitiator. The macroinitiator and triblock copolymer were characterized with 1H NMR and gel permeation chromatography (GPC). Fluorescence spectroscopy, dynamic light scattering (DSL), transmittance measurement, and rheological characterization were applied to investigate pH‐ and temperature‐induced micellization in the dilute solution of 1 mg/mL when pH > 13 and gelation in the concentrated solution of 25 wt % at pH = 14 and temperatures beyond 80 °C. The unimer of Rh = 3.7 ± 0.8 nm coexisted with micelle of Rh = 45.6 ± 6.5 nm at pH 14. Phase separation occurred in dilute aqueous solution of the triblock copolymer of 1 mg/mL at about 50 °C. Large aggregates with Rh = 300–450 nm were formed after phase separation, which became even larger as Rh = 750–1000 nm with increasing temperature. The gelation temperature determined by rheology measurement was about 80 °C at pH 14 for the 25 wt % aqueous solution of the triblock copolymer. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 5869–5878, 2008 相似文献
17.
《高分子科学杂志,A辑:纯化学与应用化学》2013,50(10):1087-1094
Abstract Copolymers of methacryl‐N,N′‐diisopropylurea (MA‐DiPrU) with ethylene glycol dimethacrylate (EDMA) at monomer‐to‐monomer ratios in the feed: 0.3/0.7; 0.5/0.5; 0.7/0.3; 0.8/0.2 were prepared in butanone in the presence of 2% of dibenzoyl peroxide (Bz2O2) at 70°C for 48?hr. Copolymers regardless of the ratio of comonomers in the feed decompose thermally at 200–250°C under the separation of isopropylisocyanate (iPrNCO). Residues after the removal of iPrNCO are thermally stable nanoporous crosslinked copolymers of methacryl‐isopropylamide (MA‐iPrA) with EDMA which decompose by a one‐step mechanism between 280°C and 450°C. Nonporous model copolymers poly(MA‐iPrA‐co‐EDMA) of similar composition, prepared by copolymerization of MA‐iPrA with EDMA, also decomposed by a one‐step mechanism as shown by TGA measurements. 相似文献
18.
Peng‐Fei Gou Wei‐Pu Zhu Ning Zhu Zhi‐Quan Shen 《Journal of polymer science. Part A, Polymer chemistry》2009,47(11):2905-2916
Novel amphiphilic eight‐arm star triblock copolymers, star poly(ε‐caprolactone)‐block‐poly(acrylic acid)‐block‐poly(ε‐caprolactone)s (SPCL‐PAA‐PCL) with resorcinarene as core moiety were prepared by combination of ROP, ATRP, and “click” reaction strategy. First, the hydroxyl end groups of the predefined eight‐arm SPCLs synthesized by ROP were converted to 2‐bromoesters which permitted ATRP of tert‐butyl acrylate (tBA) to form star diblock copolymers: SPCL‐PtBA. Next, the bromide end groups of SPCL‐PtBA were quantitatively converted to terminal azides by NaN3, which were combined with presynthesized alkyne‐terminated poly(ε‐caprolactone) (A‐PCL) in the presence of Cu(I)/N,N,N′,N″,N″‐pentamethyldiethylenetriamine in DMF to give the star triblock copolymers: SPCL‐PtBA‐PCL. 1H NMR, FTIR, and SEC analyses confirmed the expected star triblock architecture. The hydrolysis of tert‐butyl ester groups of the poly(tert‐butyl acrylate) blocks gave the amphiphilic star triblock copolymers: SPCL‐PAA‐PCL. These amphiphilic star triblock copolymers could self‐assemble into spherical micelles in aqueous solution with the particle size ranging from 20 to 60 nm. Their micellization behaviors were characterized by dynamic light scattering and transmission electron microscopy. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2905–2916, 2009 相似文献
19.
Shidi Xun Quanguo Zhou Hongchao Li Dongge Ma Lixiang Wang Xiabin Jing Fosong Wang 《Journal of polymer science. Part A, Polymer chemistry》2008,46(5):1566-1576
Three series of poly(phenylene vinylene) (PPV) derivatives containing hole‐transporting triphenylamine derivatives [N‐(4‐octoxylphenyl)diphenylamine, N,N′‐di(4‐octyloxylphenyl)‐N,N′‐diphenyl‐1,4‐phenylenediamine, and N,N′‐di(4‐octoxylphenyl)‐N,N′‐diphenylbenzidine] (donor) and electron‐transporting oxadiazole unit (2,5‐diphenyl‐1,3,4‐oxadiazole) (acceptor) in the main chain were synthesized by improved Wittig copolymerization. The resulting donor–acceptor (D‐A) polymers are readily soluble in common organic solvents, such as chloroform, dichloroethane, THF, and toluene. The polymers containing oxadiazole group exhibit good thermal stability with 5% weight loss above 400 °C. The intramolecular charge‐transfer was observed in these D‐A polymers. In comparison with corresponding polymers without oxadiazole unit, the single‐layer devices based on the D‐A polymers showed much improved electroluminescent properties, because of the balanced charge injection and transport. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1566–1576, 2008 相似文献
20.
Jong‐Beom Baek Frank W. Harris 《Journal of polymer science. Part A, Polymer chemistry》2003,41(15):2374-2389
Two new extended self‐polymerizable AB monomers, N‐(4‐fluorobenzoyl)‐4‐amino‐4′‐hydroxydiphenylether and N‐(4‐fluorobenzoyl)‐4‐amino‐4′‐hydroxybiphenyl, were prepared. The monomers were homopolymerized and copolymerized to high‐molecular‐weight, linear poly(arylether amides) in N‐methylpyrrolidone (NMP)/toluene in the presence of potassium carbonate at elevated temperature. The polymers retained NMP up to 200 °C. Samples containing small amounts of the solvent (5–10 wt %) were soluble in polar aprotic solvents. However, after complete removal of the NMP, the polymers were only soluble in strong acids such as sulfuric acid and methanesulfonic acid (MSA). The polymers, which had intrinsic viscosities of 0.57–1.49 dL/g (30.1 ± 0.1 °C in MSA), were semicrystalline with melting temperatures above 400 °C. Two new self‐polymerizable AB2 amide monomers, N,N′‐bis(4‐fluorobenzoyl)‐3,4‐diamino‐4′‐hydroxydiphenylether and N,N′‐bis(4‐fluorobenzoyl)‐3,5‐diamino‐4′‐hydroxybenzophenone, were also prepared and polymerized to give a hyperbranched poly(arylether amide) and a hyperbranched poly(aryletherketone) amide. The arylfluoride‐terminated, amorphous polymers had intrinsic viscosities of 0.34 and 0.24 dL/g (30.0 ± 0.1 °C in m‐cresol), glass‐transition temperatures of 210–269 °C, and were soluble in a wide variety of organic solvents. Matrix‐assisted laser desorption/ionization time‐of‐flight analysis indicated that the components of the low‐molecular‐weight fractions contained cyclic structures. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2374–2389, 2003 相似文献