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101.
102.
Michele Flammini 《Discrete Applied Mathematics》2009,157(1):98-111
In this paper, we present a new model that combines quality of service and mobility aspects in wireless ATM networks. Namely, besides the hop count and load parameters of the basic ATM layouts, we introduce a new notion of distance that estimates the time needed to reconstruct the virtual channel of a wireless user when he moves through the network. Quality of service guarantee dictates that the rerouting phase must be imperceptible, that is, the maximum distance between two virtual channels must be maintained as low as possible. Therefore, a natural combinatorial problem arises in which suitable trade-offs must be determined between the different performance measures. We first show that establishing the existence of a layout with maximum hop count h, load l and distance d is NP-complete, even in the very restricted case h=2, l=1 and d=1. We then provide optimal layout constructions for basic interconnection networks, such as chains and rings. 相似文献
103.
The noncommutative Singer-Wermer conjecture states that every linear (possibly unbounded) derivation on a (possibly noncommutative) Banach algebra maps into its Jacobson radical. This conjecture is still an open question for more than thirty years. In this paper we approach this question via linear left θ-derivations. 相似文献
104.
本文证明了Cowen-Douglas 算子是强不可约的充要条件,是它的换位代数模去其Jacobson 根同构于$H^{\infty}(D)$中的一个闭子代数,这里$D$表示开单位圆盘, $H^{\infty}(D)$表示$D$上的有界解析函数的全体. 相似文献
105.
3,5-Dicyano-1,4-dihydropyridines underwent ring contraction to give functionalized cyclopentadienes upon treatment with trifluoroacetic anhydride. 相似文献
106.
A series of 5-trichloro-Δ4-1,2,4-oxadiazolines have been synthesised by 1,3-dipolar cycloaddition of nitrones to trichloroacetonitrile. These oxadiazolines rearrange into formamidine derivatives, via ring opening and a 1,2-aryl shift from carbon to the adjacent amino nitrogen. Both cycloaddition and rearrangement are facilitated when electron deficient nitriles and electron rich nitrones are used. 相似文献
107.
The aim of this paper is to characterize those elements in a semiprime ring R for which taking local rings at elements and rings of quotients are commuting operations. If Q denotes the maximal ring of left quotients of R, then this happens precisely for those elements if R which are von Neumann regular in Q. An intrinsic characterization of such elements is given. We derive as a consequence that the maximal left quotient ring
of a prime ring with a nonzero PI-element is primitive and has nonzero socle. If we change Q to the Martindale symmetric ring of quotients, or to the maximal symmetric ring of quotients of R, we obtain similar results: an element a in R is von Neumann regular if and only if the ring of quotients of the local ring of R at a is isomorphic to the local ring of Q at a.
Partially supported by the Ministerio de Educación y Ciencia and Fondos Feder, jointly, trough projects MTM2004-03845, MTM2007-61978
and MTM2004-06580-C02-02, MTM2007-60333, by the Junta de Andalucía, FQM-264, FQM336 and FQM02467 and by the Plan de Investigación
del Principado de Asturias FICYT-IB05-017. 相似文献
108.
Ali Reza Moghaddamfar 《Siberian Mathematical Journal》2006,47(5):911-914
The noncommuting graph ?(G) of a nonabelian finite group G is defined as follows: The vertices of ?(G) are represented by the noncentral elements of G, and two distinct vertices x and y are joined by an edge if xy ≠ yx. In [1], the following was conjectured: Let G and H be two nonabelian finite groups such that ?(G) ? ?(H); then ¦G¦ = ¦H¦. Here we give some counterexamples to this conjecture. 相似文献
109.
本文利用环聚合分子动力学方法对C(1D)+H2反应开展了详细的理论研究. 计算中使用了最近构建的Zhang-Ma-Bian(ZMB)从头算势能面,该势能面对锥形交叉附近区域以及范德华区域均有精确的描述. 环聚合分子动力学计算得到的热反应速率常数与最新实验值吻合很好. 与前人计算结果比较,发现在?1A′电子基态的ZMB-a势能面上获得的反应速率常数远大于前人构建的RKHS势能面上的结果,这是由于ZMB势能面上的范德华鞍具有与之前势能面上的范德华阱完全不同的动态学作用,表明环聚合分子动力学方法能够处理范德华作用引起的势能面拓扑结构所导致的动态学效应. 本文还揭示了b1A′′电子激发态ZMB-b势能面以及量子效应对反应的重要性. 相似文献
110.
Tetraoctyloxy-substituted naphthalenophanedienes were synthesized from tetraoctyloxy-substituted dithia[3.3]naphthalenophanes via sequential benzyne Stevens rearrangement, oxidation, and pyrolysis reactions. Surprisingly, only the pseudo-geminal isomer of tetraoctyloxy-substituted dithia[3.3]naphthalenophane was obtained after cyclization of the corresponding starting materials. The structures of the pseudo-geminal isomers of tetraoctyloxy-substituted dithia[3.3]naphthalenophane and tetraoctyloxy-substituted naphthalenophanediene were fully determined by nuclear magnetic resonance spectroscopy, high resolution mass spectrometry, and X-ray crystallography. The pseudo-geminal and pseudo-meta diastereomers of tetraoctyloxy-substituted naphthalenophanedienes were isolated by multiple fractional recrystallization from hexane at 5 °C. The solid state structure of the pseudo-geminal isomer of tetraoctyloxy-substituted naphthalenophanediene revealed strongly distorted naphthyl rings with high levels of ring strain. 相似文献