一种新的快速响应的AQM算法

该文应用控制理论,设计了具有快速响应特征的比例积分(Proportional-Integral, PI)控制器,并以此提出了一个新的主动队列管理(Active Queue Management, AQM)算法,称为Active PI算法(简称A-PI)。A-PI用一组参数实现快速响应,用另一组参数保证队长稳定,使用门限值实现两组参数间平滑切换,算法实现简单。理论分析和仿真实验表明,A-PI算法在保证队长稳定的同时实现了对不同网络环境的快速响应。     

离子注入浅结制备技术

根据近年来的文献资料总结报道几种离子注入浅结制备技术，即：大角度偏转注入、分子离子注入、双离子注入，通过介质掩膜注入，注入固体源驱入扩散再分布、等离子体浸没离子注入（ＰＩＩＩ）和反冲离子注入等。     

偏晶向(0001)Si-面衬底上4H-SiC的LPCVD外延生长

化学气相沉积(CVD)是微电子器件用SiC外延材料的主要生长技术.为了获得高质量的4H-SiC外延材料,在偏向<1120>方向8°的4H-SiC(0001)Si-面衬底上,利用台阶控制生长技术进行4H-SiC的同质外延生长.表面形貌是SiC外延材料质量好坏的一个重要参数,为此研究了表面形貌与工艺参数的关系,探讨了4H-SiC外延膜的表面缺陷形成原因.利用Raman散射技术研究了非均匀4H-SiC外延材料的多晶型现象.     

RhⅩⅥ─InⅩⅩ离子n＝4Complex跃迁谱线和振子强度的计算

对类锌等电子序列ＺｎⅠ－ＳｎⅩⅩⅠ离子ｎ＝４Ｃｏｍｐｌｅｘ组态的能级结构和组态相互作用进行了理论分析。通过分析ＨＸＲ方法理论计算值与实验值之差ΔＥ随Ｚｃ的变化关系，找出了用于最小二乘拟合计算的半经验拟合公式，用此公式预测了ＣｄⅩⅠⅩ－ＩｎⅩⅩ离子ｎ＝４Ｃｏｍｐｌｅｘ中至今还没有实验值的部分能级。给出４ｓ２－４ｓ４ｐ，４ｓ４ｐ－４ｓ４ｄ跃迁波长和相应的ＨＸＲ方法计算的振子强度，同时也对预测能级值的可靠性作了说明     

TM掺杂Ⅱ-Ⅳ-Ⅴ2黄铜矿半导体的电磁性质

利用自旋局域密度泛函的第一性原理对3d过渡金属(TM=V，Cr，Mn，Fe，Co和Ni)掺杂的Ⅱ-Ⅳ-Ⅴ2(CdGeP2和ZnGeP2)黄铜矿半导体的电磁性质进行系统计算，结果发现：V和Cr掺杂的CdGeP2和ZnGeP2将出现铁磁状态(FM)，Mn，Fe以及Co掺杂的CdGeB和ZnGeP2将出现反铁磁状态(AFM)，而Ni掺杂时，稀磁半导体(DMS)的磁性比较不稳定，其中Cr掺杂的CdGeP2和ZnGeP2将可能是具有较高居里温度Tc的DMS，当TM-3d电子的t2g态部分被填充时，其掺杂的DMS将出现FM状态；而当TM-3d电子的t2g态全满或者全空时，其掺杂的DMS将出现AFM状态，在(Cd，Mn)GeP，和(Zn，Mn)(GeP2中分别掺入电子和空穴载流子，可以发现载流子是否具有TM-3d电子的巡游特性是。DMS是否出现FM状态的主要原因。     

PCS-环与扩张

结合ACS环和p.q-Baer环的定义,本文将p.q-Baer环推广到PCS环,这样在p.q-Baer环和ACS环之间存在一类新的环,PCS环.环R称为PCS-环,如果R的每个主理想的右零化子作为右理想在一个由幂等元生成的右理想中是本质的.PCS-环包括所有的右p.q-Baer环,所有的右FI-扩展环,以及所有的交换的ACS-环.通过研究环主右理想的零化子的性质和模的本质子模的性质,研究了三种环之间的关系,推广了p.q-Baer环的结果,得到了ACS环所没有的结果,同时研究了环的扩张问题,证明了强PCS性质是Morita等价性质.     

A Hydroxytricyanopyrrole-Based Fluorescent Probe for Sensitive and Selective Detection of Hypochlorous Acid

Hypochlorous acid (HOCl) is a reactive substance that reacts with most biomolecules and is essential in physiological and pathological processes. Abnormally elevated HOCl levels may cause inflammation and other disease responses. To further understand its key role in inflammation, HOCl must be detected in situ. Here, we designed a hydroxytricyanopyrrole-based small-molecule fluorescent probe (HTCP-NTC) to monitor and identify trace amounts of HOCl in biological systems. In the presence of HOCl, HTCP-NTC released hydroxyl groups that emit strong fluorescence covering a wide wavelength range from the visible to near-infrared region owing to the resumption of the intramolecular charge transfer process. Additionally, HTCP-NTC demonstrated a 202-fold fluorescence enhancement accompanied by a large Stokes shift and a low detection limit (21.7 nM). Furthermore, HTCP-NTC provided a rapid response to HOCl within 18 s, allowing real-time monitoring of intracellular HOCl. HTCP-NTC exhibited rapid kinetics and biocompatibility, allowing effective monitoring of the exogenous and endogenous HOCl fluctuations in living cells. Finally, based on fluorescence imaging, HTCP-NTC is a potential method for understanding the relationship between inflammation and HOCl.     

全同超形变带转动惯量的粒子数守恒计算

利用推转壳模型的粒子数守恒方法计算了超形变(SD)转动带¹⁹²Hg和¹⁹⁴Hg(1,2,3)的带首转动惯量.分析了带首附近的组态结构及带首转动惯量随对力强度的变化.带首转动惯量之差δJ₀对对力强度十分敏感,而对Nilsson能级参数K、μ及形变参数并不敏感.对力及堵塞效应是造成带首转动惯量差别的主要因素.但与正常形变核相比,对力强度似有较大程度减弱.     

双(N 氧化吡啶 2-甲醛)缩1,2-丙二胺镍配合物的合成和晶体结构

合成所得双(N-氧化吡啶-2-甲醛)缩1,2-丙二胺的镍(II)配合物[Ni(piopn)(H_2O)_2](ClO_4)_2的晶体属空间群C_s~4-C_c, 晶胞参数a=0.7397(3) nm, b=1.3187(7) nm, c=2.5502(14) nm, β=102.18(4)°. 用分子轨道理论的近似方法分析了该配合物的电子结构和分子轨道, 探讨了分子的结构特征与红外光谱的关系.     

The role of benzoic acid in proline‐catalyzed asymmetric michael addition: A density functional theory study

In asymmetric Michael addition between ketones and nitroolefins catalyzed by L ‐proline, we observed that it was benzoic acid or its derivatives rather than other proton acid that could accelerate the reaction greatly, and different benzoic acid derivatives brought different yields. To explain the experimental phenomena, a density functional theory study was performed to elucidate the mechanism of proline‐catalyzed asymmetric Michael addition with benzoic acid. The results of the theoretical calculation at the level of B3LYP/6‐311+G(2df,p)//B3LYP/6‐31G(d) demonstrated that benzoic acid played two major roles in the formation of nitroalkane: assisting proton transfer and activating the nitro group. In the stage of enamine formation from imine, the energy profiles of benzoic acid derivatives were also calculated to investigate the reasons why different benzoic acid derivatives caused different yields. The results demonstrated that the pK_a value was the major factor for p‐substituted benzoic acid derivatives to improve the yields, whereas for m/o‐substituted benzoic acid derivatives, both pK_a value and electronic and steric effects could significantly increase the yields. The calculated results would be very helpful for understanding the reaction mechanism of Michael addition and provide some insights into the selection of efficient additives for similar experiments. © 2012 Wiley Periodicals, Inc.