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211.
为了实现基于磁畴壁运动的自旋电子学装置, 掌握磁畴壁动力学行为是重要争论之一.研究了在外磁场驱动下L-型纳米铁磁线磁畴壁的动力学行为. 通过微磁学模拟,在各种外磁场的驱动下考察了纳米铁磁线磁畴壁的动力学特性; 在较强外磁场的驱动下, 在不同厚度纳米线上考察了纳米线表面消磁场对磁畴壁动力学行为的影响. 为了进一步证实消磁场对磁畴壁动力学的影响, 在垂直于纳米线表面的外磁场辅助下分析了磁畴壁的动力学行为变化. 结果表明, 随着纳米线厚度和外驱动磁场强度的增加, 增强了纳米线表面的消磁场的形成, 使得磁畴壁内部自旋结构发生周期性变化, 导致磁畴壁在纳米线上传播时出现Walker崩溃现象. 在垂直于纳米线表面的外磁场辅助下, 发现辅助磁场可以调节消磁场的强度和方向. 这意味着利用辅助磁场可以有效地控制纳米铁磁线磁畴壁的动力学行为. 相似文献
212.
在介质阻挡放电体系中产生辉光放电可以有效的提高放电体系产生高能电子的性能, 为等离子体化学反应提供更加丰富的活性粒子.本文对针-板介质阻挡放电体系下的放电模式进行了研究,实验发现放电正负半周期表现出不同的放电模式, 激励电压为3 kV时放电正负半周期分别为微流注放电和电晕放电(或者Trichel脉冲放电),激励电压为6 kV时放电正负半周期分别为微流注放电和微辉光放电.微辉光放电形貌具有与典型辉光放电相同的分层次放电结构, 分析了激励电压6 kV时的放电过程,认为足够强的阴极电场强度和裸露针状电极形成的有效的二次电子发射过程是形成微辉光放电的主要因素,绝缘介质层的存在避免了微辉光放电向弧光放电过渡. 相似文献
213.
Gravitational field equations in Randers-Finsler space of approximate Berwald type are investigated. A modified Friedmann equation and a new luminosity distance-redshift relation is proposed. A best-fit to the Type Ia supernovae (SNe) observations yields that the ΩΛ in the Λ-CDM model is suppressed to almost zero. This fact indicates that the astronomical observations on the Type Ia SNe can be described well without invoking any form of dark energy. The best-fit age of the universe is given. It is in agreement with the age of our galaxy. 相似文献
214.
研究了算子空间的原子性.证明了算子空间V是原子当且仅当V是正合且有限内射; V内的任意一个有限维算子子空间是原子当且仅当V是原子且V内任意有限维算子子空间足V的完全补.因此作为推论,得到了无限维箅子空间V的任意有限维子空间是原子,则V是1-Hilbertian和1-齐次. 相似文献
215.
Haijing Liang Lixia Ma Changwei Li Qiang Peng Zhaoyan Wang Zhan-xin Zhang Lan Yu Huanxiang Liu Fengli An Weihua Xue 《Tetrahedron letters》2019,60(1):84-87
Glycosylation reactions are significant as they provide access to model compounds that are useful for elucidating biochemical pathways. Herein, we describe the development of glycosyl ortho-alkynylbenzoates as novel, bench-top stable, and readily available glycosyl donors. Glycosylation is promoted by inexpensive trimethylsilyl triflate (TMSOTf) in combination with N-iodosuccinimide (NIS) under mild reaction conditions; hence, the novel glycosyl donors are promising reagents for the synthesis of glycosides. 相似文献
216.
本文合成了四种新配合物:二氯化双苯甲醛缩氮基硫脲合铜(Ⅱ)(Cu~Ⅱ(Betsc—H)_2Cl_2),三氯化水杨醛缩氨基硫脲合铁(Ⅲ)(Fe~Ⅲ(Satsc—H_2)Cl_3,二氯化双对二甲氨基苯甲醛缩氨基硫脲合钴(Ⅱ)(Co~Ⅱ(Dmabtsc—H)_2Cl_2·H_2O)及双对硝基苯甲醛缩氨基硫脲合钴(Ⅱ)醋酸盐(Co~Ⅱ(Nitsc—H)(Nitsc)(Ac))。用元素分析和IR测定了化合物的组成,并进行了吸放O_2和CO的试验。 相似文献
217.
Xu Z Yao S Wei Y Zhou J Zhang L Wang C Guo Y 《Journal of the American Society for Mass Spectrometry》2008,19(12):1849-1855
A matrix-assisted laser desorption/ionization Fourier transform mass spectrometry (MALDI-FTMS)-based assay was developed for
kinetic measurements and inhibitor screening of acetylcholinesterase. Here, FTMS coupled to MALDI was applied to quantitative
analysis of choline using the ratio of choline/acetylcholine without the use of additional internal standard, which simplified
the experiment. The Michaelis constant (K
m) of acetylcholinesterase (AChE) was determined to be 73.9 μmol L−1 by this approach. For Huperzine A, the linear mixed inhibition of AChE reflected the presence of competitive and noncompetitive
components. The half maximal inhibitory concentration (IC50) value of galantamine obtained for AChE was 2.39 μmol L−1. Inhibitory potentials of Rhizoma Coptidis extracts were identified with the present method. In light of the results the
referred extracts as a whole showed inhibitory action against AChE. The use of high-resolution FTMS largely eliminated the
interference with the determination of ACh and Ch, produced by the low-mass compounds of chemical libraries for inhibitor
screening. The excellent correlation with the reported kinetic parameters confirms that the MS-based assay is both accurate
and precise for determining kinetic constants and for identifying enzyme inhibitors. The obvious advantages were demonstrated
for quantitative analysis and also high-throughput characterization. This study offers a perspective into the utility of MALDI-FTMS
as an alternate quantitative tool for inhibitor screening of AChE. 相似文献
218.
Within an extended Su-Schrieffer-Heeger model including interchain interactions and the extended Hubbard model, the dynamical relaxation of photoexcitations in two coupled conjugated polymer chains is investigated by using a nonadiabatic evolution method. Initially, one of the two chains is photoexcited and the other chain is in the dimerized ground state. Due to the interchain interactions, the electron and/or the hole can be transferred from one chain to the other chain. For weak interchain coupling, the dynamical evolution of the lattice on the photoexcited chain is similar to that found in an isolate single chain case. With interchain interactions increasing, the amplitude of the distortions on the photoexcited chain decreases, and simultaneously, that on the other chain gradually increases. Until stronger interchain coupling, the deformations of the two chains have almost the same amplitude. Besides intrachain polaron-excitons and intrachain oppositely charged polaron pairs as found in single chain case, interchain polaron-excitons and interchain separated charged polaron pairs are obtained. The results show that the yield of interchain products increases and that of intrachain products decreases with interchain coupling increasing. Totally, the yield of charged polarons (including intrachain oppositely charged polaron pairs and interchain oppositely charged polaron pairs) is about 25%, in good agreement with results from experiments. 相似文献
219.
Honglan Cai Chang Yi Xueqin An Weiguo Shen 《The Journal of chemical thermodynamics》2009,41(5):639-644
To examine the critical behavior of the microemulsion, we have determined the coexistence curves for two ternary microemulsion systems of {water + sodium di(2-ethylhexyl) sulfosuccinate (AOT) + n-decane} with the molar ratios ω = (45.2 and 50.0) of water to AOT, respectively, by measuring refractive index at a constant pressure in the critical region. The critical exponent β and the critical amplitude B have been deduced from the coexistence curves. It was found that the values of β for both systems were consistent with the 3D-Ising exponent in a critical region. By increasing ω, i.e. the droplet size, the critical temperature and, to a lesser extent, the critical concentration decrease. The region of coexisting two phases was drastically reduced by an increase in the droplet size. 相似文献
220.
The field of supramolecular assemblies has developed rapidly in the last few decades, thanks in a large part to their diverse applications. These assemblies have been mostly based on Werner-type coordination motifs in which metal centres are coordinated by nitrogen or oxygen donors. Recently, N-heterocyclic carbene(NHC) ligands have been employed as carbon donors not only because of their appealing structures but also due to the extensive applications in catalysis, biomedicine and material science of the resulting assemblies. During the last decade, NHC-based supramolecular assemblies have witnessed rapid growth and extensive application in molecular recognition, luminescent materials and catalysis. For different topological systems, a diverse selection of poly-NHC precursors and synthetic strategies is crucial to precisely control the synthesis of supramolecular architectures. Several synthetic strategies have been developed to synthesise two-dimensional(2D) molecular metallacycles and three-dimensional(3D) metallacages from a wide range of poly-NHC precursors, including a straightforward one-pot strategy,supramolecular transmetalation, stepwise synthesis, an improved one-pot strategy involving self-sorting behaviour of 3D metallacages and a subtle variation strategy of poly-NHC ligand precursors. This review offers a summary of the synthetic strategies applied for the construction of different poly-NHC-based supramolecular assemblies, particularly emphasizes recent progress in the synthesis of large and complex supramolecular assemblies from poly-NHC precursors, and further attention is given to their application in postsynthetic modifications(PSMs), host-guest chemistry, luminescent properties and biomedical applications. 相似文献