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Haibin Zhang Jixiao Wang Zhibin Zhou Zhi Wang Fengbao Zhang Shichang Wang 《Macromolecular rapid communications》2008,29(1):68-73
PANI nanofibers are prepared electrochemically by template‐free method on a stainless steel electrode. Both the hydrophilicity and the lipophilicity of the modified SS surface are enhanced by the nanostructured PANI, and a super‐amphiphilic surface is obtained in this way. The influence of polymerization conditions, such as polymerization potentials, polymerization time, the acidity, and the dopants on the super‐amphiphilic property, has been systematically investigated. In addition, the mechanisms of obtaining a super‐amphiphilic surface are briefly discussed.
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Ryszard Szymanski 《Macromolecular theory and simulations》2011,20(1):8-12
The IUPAC recommended factor 2 preceding rate coefficients in the radical termination kinetic equations is claimed to be incorrect and confusing. This recommendation can lead to incorrect analysis of experimental data, especially while applying kinetic Monte Carlo simulations. The statement is based on the derivation of the corresponding relationships.
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Wu Aik Yee Shanxin Xiong Guoqiang Ding Chien Anh Nguyen Pooi See Lee Jan Ma Masaya Kotaki Ye Liu Xuehong Lu 《Macromolecular rapid communications》2010,31(20):1779-1784
A reverse‐barrier technique is used to enable the treatment of electrospun poly(vinylidene fluoride) nanofibrous membranes with supercritical carbon dioxide. The treatment induces the formation of nanopores and extended‐chain β crystallites of small lateral dimensions in the nanofibers. It also creates interfiber junctions, resulting in a remarkable improvement in mechanical properties of the membranes. The treated membranes are able to retain their shape very well after loading with an ionic liquid (IL). The ionic conductivity of the IL‐loaded membrane is very close to that of the neat IL.
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Qianqian Li Gui Yu Jing Huang Haijie Liu Zhen Li Cheng Ye Yunqi Liu Jingui Qin 《Macromolecular rapid communications》2008,29(10):798-803
Two new “H” type of indole‐based chromophores were designed and successfully introduced to the polymeric system, the resultant polymers demonstrated enhanced NLO effects, good processability, thermal stability and nearly excellent transparency, indicating the advantages of “H” type chromophore moieties. And they could be promising candidates for the practical applications as new photonic materials.
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Liang Song Chunlai Tu Yunfeng Shi Feng Qiu Lin He Yi Jiang Qi Zhu Bangshang Zhu Deyue Yan Xinyuan Zhu 《Macromolecular rapid communications》2010,31(5):443-448
A simple approach to tune the optical properties of the hyperbranched conjugated polymers by only adjusting the terminal‐backbone interactions has been reported in this article. Hyperbranched conjugated polyazomethines have been successfully prepared by the reaction of tetramine and dialdehyde. Not only varying the monomer feed ratio to change the quantity of terminal amino groups, but also adopting protonation or complexion with proper dopants (SnCl2 and β‐cyclodextrin), can alter the interactions between amino terminals and imine bonds in the backbone. Correspondingly, the optical properties of the resulting hyperbranched polymers are controlled.
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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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Jixiao Wang Junsheng Wang Xiaoyan Zhang Zhi Wang 《Macromolecular rapid communications》2007,28(1):84-87
Polyaniline nanostructures (nanosheets, nanofibers, and nanoparticles) can be assembled at the organic/aqueous interface or in solution by controlling the diffusion rate and the polymerization induction time of aniline. The quality of polyaniline nanostructures is determined by the polymerization solution conditions. Polyaniline nanosheets formation mechanism was proposed. Under certain polymerization conditions, polyaniline nanofibers or/and nanoparticles were obtained.
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This paper highlights the powerful combination of reversible addition–fragmentation chain transfer (RAFT) radical polymerization and various click/coupling chemistries. This is not an exhaustive review but rather an overview demonstrating the impressive possibilities that the “marriage” of these two synthetic approaches offers in modern macromolecular design and synthesis.
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Ping Xu Xijiang Han Chao Wang Bin Zhang Xiaohong Wang Hsing‐Lin Wang 《Macromolecular rapid communications》2008,29(16):1392-1397
Polyaniline‐polypyrrole (PANI‐PPy) nanofibers with high aspect ratios have been synthesized by a one‐step, surfactant‐assisted chemical oxidative polymerization from mixtures of aniline (An) and pyrrole (Py) monomers. PANI‐PPy nanofibers synthesized with an excess of either PANI or PPy show similar spectral (UV‐vis and FT‐IR) characteristics as the individual homopolymers, whereas nanofibers from an equimolar mixture of An and Py display unique spectral characteristics. PANI‐PPy nanofibers undergo a spontaneous redox reaction with metal ions to produce metal nanoparticles with various morphologies and/or sizes. These findings may open new opportunities for synthesizing functional polymer nanofibers and metal nanoparticles with controllable sizes and/or morphologies.
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The gecko adhesion phenomenon has stimulated efforts to produce synthetic patterned dry adhesives. Besides introducing surface patterns on dry adhesives, it is also highly desirable to understand their intrinsic material properties. This communication reports the viscoelastic behavior of non‐patterned epoxy elastomers exhibiting intrinsic adhesion that is much higher than that of elastomers typically used for structure patterning. The diverse molecular origin of the adhesion is revealed through the study of adhesion against various substrates.
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Udo Schmidt Philip C. Zehetmaier Bernhard Rieger 《Macromolecular rapid communications》2010,31(6):545-548
Poly(dimethylsiloxane) copolymers were synthesized directly from AA/BB monomers employing a CuAAC reaction (click chemistry) in a polyaddition approach. Using organic dialkynes and oligo(siloxane)s end‐functionalized with azide moieties it was possible to obtain siloxane‐based copolymers with TPE properties by click chemistry for the first time. As seen from DSC experiments, properties were strongly dependent on the incorporated organic comonomer.
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Summary: A water‐soluble gold nanoparticle aggregate 2 was prepared by chloroauric acid and a polypseudorotaxane 1 of mono‐6‐thio‐β‐cyclodextrin with poly(propylene glycol) bis(2‐aminopropyl ether) ( ≈ 2 000) in the presence of sodium borohydride in N,N‐dimethylformamide (DMF) solution. The investigative results indicated that the gold nanoparticle aggregate 2 might act as an efficient DNA‐cleavage reagent.
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Kathrin Isenbügel Helmut Ritter Robert Branscheid Ute Kolb 《Macromolecular rapid communications》2010,31(24):2121-2126
Stable nanoparticle vesicles were for the first time prepared from adamantyl‐ and cyclodextrin (CD)‐modified silica nanoparticles forming host–guest interactions in aqueous solution. Adamantyl‐functionalized nanoparticles were obtained from thiol‐isocyanate reaction of thiol‐modified nanoparticles with 1‐adamantyl isocyanate. The CD modified silica particles were isolated from a reaction of mono‐6‐para‐toluenesulfonyl‐β‐cyclodextrin with the thiol functionalized silica under microwave conditions in basic media. The obtained particles were characterized in respect of agglomeration and self‐assembly behavior in aqueous solution by dynamic light scattering and transmission electron microscopy. The found vesicle structures are exceptionally stable even after evaporation of water. Such inorganic hollow spheres formed through self‐assembly processes may be important for chemical storage and transport. The technique of chemically‐driven assembly is an attractive option to form useful complex structures by tunable agglomeration.
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Summary: Transcrystallinity in UHMWPE fiber‐reinforced HDPE composites promotes a significant β transition that is untypical of high‐density polyethylene. Surface profiling by atomic force microscopy identifies two distinct morphologies in the composite without a boundary phase between them, which coincide with the transcrystalline layer and with the bulk spherulitic matrix. As a result, the claim that attributes this transition to loose chain folds at the lamella surface is favored.
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Woo‐Sik Jang Tomonori Saito Michael A. Hickner Jodie L. Lutkenhaus 《Macromolecular rapid communications》2010,31(8):745-751
Poly(ethylene glycol) (PEG)‐based films, nanotubes, and nanotube arrays were successfully made using layer‐by‐layer (LbL) assembly ion‐containing PEO derivatives on porous templates and planar substrates. PEG nanotubes are challenging to produce because PEG dissolves into solutions and solvents used during nanotube processing, but our techniques circumvent the issue. Nanotube dimensions were verified using microscopy and the average observed diameter was 155 nm. The PEG‐based structures showed remarkable stability in water, salt water, and sodium hydroxide solution.