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Polyaniline nanodisks have been synthesized successfully by the chemical oxidation polymerization of aniline by a self‐assembly process without the use of any acid. The thickness and lateral dimensions of the polyaniline nanodisks are in the range of 20–30 nm and 1–2 µm, respectively. The influence of synthetic parameters, such as the concentration of ammonium peroxydisulfate and pH, on the morphologies of polyaniline nanostructures have been investigated.
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Synthesis of Peptide‐Based Hybrid Nanobelts with Enhanced Color Emission by Heat Treatment or Water Induction 下载免费PDF全文
Xingcen Liu Pengli Zhu Jinbo Fei Jie Zhao Prof. Dr. Xuehai Yan Prof. Dr. Junbai Li 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(26):9461-9467
We demonstrate that an inorganic lanthanide ion (Tb3+) or organic dye molecules were encapsulated in situ into diphenylalanine (FF) organogels by a general, simple, and efficient co‐assembly process, which generated peptide‐based hybrid nanobelts with a range of colored emissions. In the presence of a photosensitizer (salicylic acid), the organogel can serve as an excellent molecular‐donor scaffold to investigate FRET to Tb3+. More importantly, heat treatment or water induction instigated a morphology transition from nanofibers to nanobelts, after which the participation of guest molecules in the FF assembly was promoted and the stability and photoluminescence emission of the composite organogels were enhanced. 相似文献
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Haibin Zhang Jixiao Wang Zhi Wang Fengbao Zhang Shichang Wang 《Macromolecular rapid communications》2009,30(18):1577-1582
Polyaniline (PANI) micro/nanosheets are successfully synthesized by a template‐free method without using any conventional oxidants. Scanning electron microscopy, transmission electron microscopy, and FT‐IR spectroscopy are applied to characterize the products. By investigating the morphologies and chemical structures of the PANI micro/nanosheets, a possible formation mechanism is proposed. In addition, the influences of experimental parameters, such as the kind of dopant, concentration of aniline, and acidity of reaction system, on the morphologies of the PANI micro/nanosheets have been systematically investigated.
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Summary: We report an artful method to form a stable pattern of chiral polyaniline nanocomposites (CPANs). It consists of the preparation of a diazoresin (DR)/poly(acrylic acid) (PAA) thin buffer layer on an Si substrate by self‐assembly, followed by the deposition of a multi‐layer film by spin‐assembly, leading to the formation of a (DR/PAA)2DR/(CPAN/DR)n film on the substrate. After selective exposure to UV light through a photomask and the development process, a defined pattern is formed.
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Xiaomiao Feng Gang Yang Qin Xu Wenhua Hou Jun‐Jie Zhu 《Macromolecular rapid communications》2006,27(1):31-36
Summary: Polyaniline (PANI)/Au composite nanotubes and nanofibers are synthesized through a self‐assembly process in the presence of camphorsulfonic acid and hydrochloric acid, as dopants, respectively. The PANI/Au composites are characterized by FT‐IR, UV‐vis, and thermogravimetric analysis to verify the incorporation of the Au nanoparticles and determine the Au content. Structural characterization is performed using SEM, TEM and X‐ray diffraction. The presence of the Au nanoparticles results in an increased conductivity and improved crystallinity of the PANI. The self‐assembly method employed here is a simple and inexpensive route to synthesize multifunctional nanotubes and nanofibers and could be extended to prepare other inorganic nanoparticle/PANI composites.
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Junsheng Wang Jixiao Wang Zhi Wang Fengbao Zhang 《Macromolecular rapid communications》2009,30(8):604-608
Urchin‐like PANI microspheres with an average diameter of 5–10 µm have been successfully prepared. Their surfaces consist of highly oriented nanofibers of ≈30 nm diameter and 1 µm length. The solvent composition plays an important role in the formation process of urchin‐like PANI microspheres. The structure of the products has been characterized by FT‐IR, UV‐vis, and XRD. To investigate the self‐assembly of urchin‐like PANI microspheres, the effect of polymerization time on the morphology of the products has been studied. The morphological evolution process indicates that the urchin‐like microspheres originate from the self‐assembly of nanoplates, which then grow into urchin‐like microstructures with nanofibers on the surface.
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Zhaoyuan Liu Ying Zhu Liang Wang Chunmei Ding Nü Wang Meixiang Wan Lei Jiang 《Macromolecular rapid communications》2011,32(6):512-517
Polyaniline (PANI) microtubes with a hexagonal cross‐section are successfully synthesized by a self‐assembly process in the presence of 8‐hydroxyquinoline‐5‐sulfonic acid (HQS) as a dopant and FeCl3 as an oxidant. The wall thickness of the PANI/HQS microtubes can be adjusted by the content of the oxidant. It is proposed that the aniline/HQS salts serve as a hard template for the formation of the hexagonal‐cross‐section microtubes. Moreover, PANI/HQS microtubes combined with ZnSO4 show pH‐dependent fluorescence. PANI hexagonal‐cross‐section microtubes combined with a pH‐sensitive fluorescence may promise potential applications in fields such as chemical sensors and confined reaction vessels.
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Dr. Nina McGrath Dr. Avinash J. Patil Dr. Scott M. D. Watson Dr. Benjamin R. Horrocks Dr. Charl F. J. Faul Prof. Andrew Houlton Prof. Mitchell A. Winnik Prof. Stephen Mann Prof. Ian Manners 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(39):13030-13039
Stable colloidal dispersions of polyaniline (PAni) nanofibers with controlled lengths from about 200 nm–1.1 μm and narrow length distributions (Lw/Ln<1.04; Lw=weight average micelle length, Ln=number average micelle length) were prepared through the template‐directed synthesis of PAni using monodisperse, solution‐self‐assembled, cylindrical, block copolymer micelles as nanoscale templates. These micelles were prepared through a crystallization‐driven living self‐assembly method from a poly(ferrocenyldimethylsilane)‐b‐poly(2‐vinylpyridine) block copolymer (PFS25‐b‐P2VP425). This material was initially self‐assembled in iPrOH to form cylindrical micelles with a crystalline PFS core and a P2VP corona and lengths of up to several micrometers. Sonication of this sample then yielded short cylinders with average lengths of 90 nm and a broad length distribution (Lw/Ln=1.32). Cylindrical micelles of PFS25‐b‐P2VP425 with controlled lengths and narrow length distributions (Lw/Ln<1.04) were subsequently prepared using thermal treatment at specific temperatures between 83.5 and 92.0 °C using a 1D self‐seeding process. These samples were then employed in the template‐directed synthesis of PAni nanofibers through a two‐step procedure, where the micellar template was initially stabilised by deposition of an oligoaniline coating followed by addition of a polymeric acid dopant, resulting in PAni nanofibers in the emeraldine salt (ES) state. The ES–PAni nanofibers were shown to be conductive by scanning conductance microscopy, whereas the precursor PFS25‐b‐P2VP425 micelle templates were found to be dielectric in character. 相似文献
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Superhydrophobic dandelion‐like 3D microstructures self‐assembled from 1D nanofibers of PANI were prepared by a self‐assembly process in the presence of perfluorosebacic acid (PFSEA) as a dopant. The dandelion‐like microspheres (about 5 µm) are composed of uniform Y‐shaped junction nanofibers of about 210 nm average diameter and several micrometers in length, as measured by SEM. The dandelion‐like microstructure is coreless with a hollow cavity, and the shell thickness is about one third of the sphere diameter, as measured by TEM. Since PFESA dopant has a low surface energy perfluorinated carbon chain and two hydrophilic COOH end groups, it has dopant, is a “soft‐template” and brings about superhydrophobic functions at the same time. Moreover, it is proposed that the self‐assembly of PANI 1D nanofibers, driven by a combined interaction of hydrogen bonding, π‐π stacking and hydrophobic interactions, leads to the formation of the 3D microstructures.
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William B. Tucker Aaron M. McCoy Samantha M. Fix Melissa F. Stagg Matt M. Murphy Sandro Mecozzi 《Journal of polymer science. Part A, Polymer chemistry》2014,52(23):3324-3336
Linear, dibranched, and miktoarm amphiphiles containing both hydrophobic and fluorophilic moieties were synthesized and characterized in an attempt to elucidate the relationship between semifluorinated amphiphile structure and aggregate behavior in aqueous solution. For the linear and dibranched amphiphiles, there was an exponential decrease in critical aggregation concentration (CMC) and a logarithmic increase in core microviscosity with increasing length of the fluorocarbon segments; while the miktoarm architecture produced no notable trend in microviscosity or CMC. Furthermore, the linear and dibranched surfactants showed enhanced kinetic stability, dissociating more slowly in the presence of human serum than did either the dibranched or miktoarm amphiphiles. Finally, encapsulation studies with the hydrophobic drug paclitaxel (PTX) showed that the ability to solubilize and retain PTX increased with the presence and with the increasing size of the fluorocarbon moiety for both the linear and dibranched amphiphiles, while no such trend was observed for the miktoarm amphiphiles. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3324–3336 相似文献
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Summary: Polyaniline (PANI) is successfully self‐assembled with poly(N‐vinylpyrrolidone) (PVP) into aqueous nanocolloids. The typical morphology of the colloids is studied by atomic force microscopy (AFM), which reveals spherical nanoparticles with a diameter of 80–150 nm. A possible mechanism for such a post‐synthetic self‐assembly process is proposed.
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Wenbin Zhong Xianhong Chen Shoumei Liu Yongxin Wang Wantai Yang 《Macromolecular rapid communications》2006,27(7):563-569
Summary: Polyaniline (PANI) nanowires and sub‐micro/nanostructured dendrites are synthesized and immobilized on PP‐g‐PAA film surfaces via routine oxidative polymerization of aniline under different conditions, where grafting poly(acrylic acid) (PAA) served as a template and dopant, and SDS as a surfactant. The immobilized PANI enhances the surface hydrophilicity of the poly(propylene) (PP) films, and a superhydrophilic surface is obtained in this way. The mechanism of forming different morphologies of PANI and of correspondingly obtaining a superhydrophilic surface are briefly discussed.
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Polyaniline (PANI) nanotubes with rectangular cross section, which had 90–500 nm in outer diameter and 30–400 nm in inner diameter, were synthesized via a self‐assembly process in the presence of chiral acid (1S)‐(+)‐10‐camphorsulfonic (D‐CSA) and non‐chiral hydrochloric acid (HCl) coordinating with sodium dodecylbenzenesulfonate (SDBS), respectively. By using SEM, TEM, OM, FTIR, and WAXD, the as‐prepared PANI nanotubes with diversified morphologies were also characterized so as to investigate the formation mechanism of such tubular nanostructures with square cross sections. The results showed that the bilayer‐lamellar micelles formed by anilinium cations and CSA anions acted as the primary templates in the formation of the flat oligomer flakes, and the flakes finally united together to form rectangular nanotubes initiated by the reaction of the active centers on their edges. This study sheds light on the formation process of the PANI nanotubes with rectangular holes and outer contours and may be instructive to the controllable growth of certain nanostructures with unique morphologies. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
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Conducting polyaniline doped with polymeric acids was synthesized by a in situ chemical polymerization method. The synthesized polymers were characterized by using UV‐Visible, FT‐IR spectroscopy and SEM analysis. Thermal stability of these polymers was evaluated by using TGA/DSC analysis. Among the three polymeric acids used for doping purpose, poly(vinyl sulphonic acid) doped polyaniline is found to be more conducting than those doped with other acids. From the temperature dependent conductivity measurements, an increase in conductivity with increase in temperature was observed. 相似文献
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Guohua Jiang Li Wang Tao Chen Xiaochen Dong Haojie Yu Jianfeng Wang Chang Chen 《Journal of polymer science. Part A, Polymer chemistry》2005,43(22):5554-5561
Hyperbranched polyesters (HPs) with a variable content of benzoyl terminal groups were synthesized through the chemical modification of the HPs' cores by substituting a controlled fraction of the terminal hydroxyl groups with benzoyl chloride. The resulting hyperbranched polymers that were modified by benzoyl groups (HPs‐B) were characterized by 1H NMR, FTIR, differential scanning calorimetry (DSC), and gel permeation chromatography (GPC). Research results revealed that self‐assembled structures could be formed in selected solvents (acetone/n‐hexane). It was found that the morphologies of self‐assembled structures could be adjusted by controlling the content of outside benzoyl terminal groups in the hyperbranched polymers, the volume ratio of acetone with n‐hexane, and the concentration of the hyperbranched polymers with benzoyl terminal arms. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5554–5561, 2005 相似文献
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Poly(ethylene glycol) (PEG) was modified with aniline groups at both the end, and then PEG‐PANI rod‐coil block polymers have been synthesized by polymerization of the aniline with the aniline‐modified PEG. FTIR, NMR, and elemental analysis provided the chemical strucutre of the as‐prepared polymers. The achiral rod‐coil copolymer could form different superstructures by means of self‐assembly when adding diethyl ether into its THF solution and the length of PANI segments is a key factor to the superstructures. AFM measurements revealed that they form spring‐like helical superstructures from the short PANI‐containing copolymers while these form fibrous helical superstructures from the longer PANI‐containing copolymer. A possible mechanism of the helical superstructures is suggested in this article and the driving force is believed the π–π stacking of the rigid segment of the copolymers. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 12–20, 2008 相似文献