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991.
In this article, we show the existence of intertwined basins of attraction for a class of prey-predator systems, which improves the extant results by deleting some crucial and hard testing conditions. 相似文献
992.
Let f:I→I be a unimodal map on I without homtervals. We characterize the α-limit set of each point in I by considering the consecutive renormalization process of f. 相似文献
993.
994.
JPC – Journal of Planar Chromatography – Modern TLC - Two new types of reversed-phase sintered plate have been prepared used in planar electrochromatography (PEC). One was bonded with... 相似文献
995.
An efficient and convenient three‐component A3 coupling reaction of aldehyde, amine and alkyne via C? H activation with CuI alone as the catalyst in PEG is developed, providing a wide range of propargylamines with yields ranging from moderate to excellent. Additionally, the catalyst system was recovered and reused several times without evident loss in activity. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
996.
Haiyang Zhang Lei Ding Yu Chen Wantai Yang Jianping Deng 《Journal of polymer science. Part A, Polymer chemistry》2012,50(21):4415-4422
This article reports on optically active core/shell nanoparticles constituted by chiral helical polymers and prepared by a novel approach: using self‐assembled polymer micelles as reactive nanoreactors. Such core/shell nanoparticles were composed of optically active helical‐substituted polyacetylene as the core and thermosensitive poly(N‐isopropylacrylamide) as the shell. The synthetic procedure is divided into three major steps: (1) synthesis of amphiphilic diblock copolymer bearing polymerizable C[tbond]C bonds via atom transfer radical polymerization, followed by (2) self‐assembly of the diblock copolymer to form polymer micelles; and (3) catalytic emulsion polymerization of substituted acetylene monomer conducted using the polymer micelles as reactive nanoreactors leading to the core/shell nanoparticles. The core/shell nanoparticles simultaneously exhibited remarkable optical activity and thermosensitivity. The facile, versatile synthesis methodology opens new approach toward preparing novel multifunctional core/shell nanoparticles.© 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
997.
In this paper, a general solution for three-dimensional static piezothermoelastic problems of crystal class 6mm solids is
presented. The general solution involves four piezoelastic potential functions and a piezothermoelastic potential function,
of which four piezoelastic potential functions are governed by weighted harmonic differential equations. Compared with the
general solution given by Ashida et al., in which seven potential functions are introduced, the general solution proposed
in the present paper is more rigorously derived. Moreover, it has a simple form and is convenient for application. As an illustrative
example, the problem of a pyroelectric half-space subjected to axisymmetric heating is studied. Numerical results of displacements
stresses, electric potential and electric displacements are obtained for a cadmium selenide half-space. Thermally induced
displacements and stress distribution are compared with those obtained for the same material without piezoelectric and pyroelectric
effects.
Project supported by the National Natural Science Foundation of China (19872060). 相似文献
998.
Li‐Ying Li Wei‐Dong He Wen‐Tao Li Ke‐Ren Zhang Ting‐Ting Pan Zong‐Lei Ding Bo‐Yu Zhang 《Journal of polymer science. Part A, Polymer chemistry》2010,48(22):5018-5029
Well‐defined H‐shaped pentablock copolymers composed of poly(N‐isopropylacrylamide) (PNIPAM), poly(N,N‐dimethylaminoethylacrylamide) (PDMAEMA), and poly(ethylene glycol) (PEG) with the chain architecture of (A/B)‐b‐C‐b‐(A/B) were synthesized by the combination of single‐electron‐transfer living radical polymerization, atom‐transfer radical polymerization, and click chemistry. Single‐electron‐transfer living radical polymerization of NIPAM using α,ω azide‐capped PEG macroinitiator resulted in PNIPAM‐b‐PEG‐b‐PNIPAM with azide groups at the block joints. Atom‐transfer radical polymerization of DMAEMA initiated by propargyl 2‐chloropropionate gave out α‐capped alkyne‐PDMAEMA. The H‐shaped copolymers were finally obtained by the click reaction between PNIPAM‐b‐PEG‐b‐PNIPAM and alkyne‐PDMAEMA. These copolymers were used to prepare stable colloidal gold nanoparticles (GNPs) in aqueous solution without any external reducing agent. The formation of GNPs was affected by the length of PDMAEMA block, the feed ratio of the copolymer to HAuCl4, and the pH value. The surface plasmon absorbance of these obtained GNPs also exhibited pH and thermal dependence because of the existence of PNIAPM and PDAMEMA blocks. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
999.
1000.