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171.
The present article deals with M-soliton solution and N-soliton solution of the (2 + 1)-dimensional asymmetrical Nizhnik–Novikov–Veselov equation by virtue of Hirota bilinear operator method. The obtained solutions for solving the current equation represent some localized waves including soliton, breather, lump, and their interactions, which have been investigated by the approach of the long-wave limit. Mainly, by choosing the specific parameter constraints in the M-soliton and N-soliton solutions, all cases of the one breather or one lump can be captured from the two, three, four, and five solitons. In addition, the performances of the mentioned technique, namely, the Hirota bilinear technique, are substantially powerful and absolutely reliable to search for new explicit solutions of nonlinear models. Meanwhile, the obtained solutions are extended with numerical simulation to analyze graphically, which results in localized waves and their interaction from the two-, three-, four-, and five-soliton solutions profiles. They will be extensively used to report many attractive physical phenomena in the fields of acoustics, heat transfer, fluid dynamics, classical mechanics, and so on.  相似文献   
172.
The incorporation of allylic monomers into highly reactive vinyl polymerizations provides a means to control molecular weight, conversion, and Trommsdorff effect to produce copolymers with desirable performance characteristics. The copolymerization behavior of styrene with sec‐butenyl acetate, whose copolymerization properties have not been reported, is investigated. Copolymers were produced via semicontinuous emulsion polymerization and characterized via NMR, gel permeation chromatography, differential scanning calorimetry, dynamic light scattering, and atomic force microscopy. A high degree of chain termination due to allylic hydrogen abstraction was observed, as expected, with resultant decreases in molecular weight and in monomer conversion. However, high conversions were achieved, and it was possible to incorporate high percentages of the allylic acetate comonomer into the polymer chain. Copolymer thermal properties are reported. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3191–3203, 2007  相似文献   
173.
The beat pattern produced by nuclear resonant scattering of synchrotron radiation scattered from two stainless steel foils in constant relative motion has been measured at 3-ID beamline at the Advanced Photon Source. Contrary to theoretical prediction and different from the result in glassy material, the scattering in Bragg directions from single crystal of CoGa diffusional smoothening of the quantum beats was absent within the statistical errors. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   
174.
175.
Multiarm star polymers containing thiol‐reactive maleimide groups at their core have been synthesized by utilization of atom transfer radical polymerization (ATRP) of various methacrylates using a masked maleimide containing multiarm initiator. One end of the initiator contains multiple halogen groups that produce the star architecture upon polymerization and the other end contains a masked maleimide functional group. Unmasking of the maleimide group after the polymerization provides the thiol reactive maleimide core that is widely used in bioconjugation. Functionalization of the core maleimide group with a thiol containing tripeptide was used to demonstrate facile reactivity of the core of these multiarm polymers under reagent‐free conditions. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2546–2556, 2010  相似文献   
176.
Azide end‐functionalized polyhedral oligomeric silsesquioxane (POSS‐N3) was incorporated into the periphery of well‐defined alkyne‐polystyrene50‐poly(divinyl benzene) (alkyne‐PS50‐polyDVB) and alkyne‐poly(tert‐butyl acrylate)43‐poly(divinyl benzene) (alkyne‐PtBA43‐polyDVB) multiarm star polymers via highly efficient azide‐alkyne click reaction, resulting in POSS‐PS50‐polyDVB and POSS‐PtBA43‐polyDVB multiarm star block copolymers respectively, in the solution of tetrahydrofuran/N,N‐dimethyl formamide, CuBr/N,N,N,N,N″‐pentamethyldiethylenetriamine (PMDETA) at room temperature for 24 h. Linear precursors and star polymers obtained in this study were characterized 1H NMR, gel permeation chromatography (GPC), and triple detection GPC (TD‐GPC). Absolute molecular weight, hydrodynamic radius, and intrinsic viscosity ([η]) values for all star polymers were determined by TD‐GPC. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010  相似文献   
177.
Two different oxanorbornene monomers were prepared and copolymerized with butyl-functionalized oxanorbornene monomer through the ring-opening metathesis polymerization. The resulting polymers were then subjected to the aminolysis reactions with propylamine (PA) in the presence of methyl acrylate (MA) to capture, in situ, the latent thiol. It was found that the polymer, in which the thiolactone unit is close to the polymer backbone, did not undergo an efficient aminolysis reaction even an excess amount of PA was utilized, while the other polymer, in which the thiolactone unit away from the polymer backbone, did efficiently undergo aminolysis reaction even PA was used in low amounts. Besides, a variety of primary amine compounds along with MA were reacted with the polymer, in which the thiolactone group away from the polymer backbone, to test their reactivity toward the aminolysis reactions. All modified polymers were characterized by using conventional instruments such as gel permeation chromatography, nuclear magnetic resonance, and differential scanning calorimetry. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 2145–2153  相似文献   
178.
In this study, a new benzoin-based multi-arm star polymer was synthesized by using ATRP, and characterization was achieved by spectrophotometric and chromatographic methods. Obtained multiarm (Benzoin-PS)m-polyDVB star polymer was employed as a polymeric photoinitiator for polymerization of methacrylates and acrylates. Photophysical properties of this initiator were determined by fluorescence and phosphorescence measurements, the phosphorescence lifetime was calculated as 29 ms hence the lowest triplet state nature was n-π* character, and laser flash photolysis technique was additionally used to get more information about triplet state and triplet lifetime which was calculated as 1.34 ms. Photokinetics of difunctional acrylate such as HDDA was studied with a multi-arm (Benzoin-PS)m-polyDVB star polymeric initiator using Photo-DSC.  相似文献   
179.
In this study, two types of hyperbranched (HB) polythioether could readily be achieved in a short time at ambient temperature through a thiol-Michael addition reaction. Dimethyl acetylenedicarboxylate (DMADC) or methyl propiolate (A2) and trimethylolpropane tris(3-mercaptopropionate) (B3) monomers were reacted using an organobase 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as a catalyst in chloroform at room temperature to provide subsequent HB polythioethers. The effect of TBD concentration on the polymerization was studied for the DMDAC case monitoring the molecular weight evolution against time. HB polythioethers were characterized using spectroscopic (nuclear magnetic resonance) and chromatographic (gel permeation chromatography with refractive index and light-scattering detectors) techniques. © 2020 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 824–830  相似文献   
180.
Achterhold  K.  Sturhahn  W.  Alp  E. E.  Parak  F. G. 《Hyperfine Interactions》2002,141(1-4):3-12
Hyperfine Interactions - Proteins are involved in nearly all aspects of function and control of life. For many proteins, the structure alone cannot explain the function. Proteins often have to...  相似文献   
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