A buffer insertion and simultaneous sizing timing optimization algorithm

A path-based timing optimization algorithm for buffer insertion and simultaneous sizing is proposed. Firstly, candidate buffer insertion location and buffer size for each branch in a given routing path were obtained via localized timing optimization. Then, through evaluating each potential insertion against design objectives, potential optimal buffer insertion locations and sizes for the whole routing tree were determined. At last, by removing redundant buffer insertion operations which do not maximize S （ so ）, given timing requirements are finally fulfilled through minimum number of buffers.     

Li/富锂钒青铜(Li_6V_6O_(15))二次电池正极材料研究

近年来,人们对二次锂电池的正极进行了不少研究。许多过渡金属氧化物或硫化物,如V_6O(13),Li_(1+x)V_3O_8,TiS_2,MoS_2等被认为是较好的正极材料。Pistoia等研究了Li_(1+x)V_3O_8钒青铜的电化学性能得出,当Li浓度高时,由于电子定域作用使电荷屏蔽效应     

微液滴在仿蛛丝结构TiO2纤维表面的定向运动与粘附

制备了具有响应性的仿蛛丝周期纺锤节TiO₂纤维。通过改变纤维表面微观结构、紫外光照和超声波等手段,仿蛛丝结构TiO₂纤维表面浸润性会发生响应性变化。纤维表面的这种浸润性变化,不仅实现了水滴从纺锤节两端到中心处的定向运动,而且可以使得水滴被纤维纺锤节粘附。当仿蛛丝结构TiO₂纤维表面为亲水状态时,无论纺锤节光滑还是粗糙,水都是从纺锤节两端向中心方向运动;当仿蛛丝TiO₂纤维表面疏水时,水滴会被具有粗糙表面的纺锤节两端粘附。     

(NH_4)_2SiF_6预处理改善SBA-15介孔材料的水热稳定性

(NH4)2SiF6 预处理可对 SBA-15 介孔材料的表面缺陷进行补硅修正以及表面疏水化, 从而明显改善 SBA-15 材料的水热稳定性. 结果表明, 用摩尔分数为 5% 的 (NH4)2SiF6 水溶液, 按引入 1% 的 SiO2 计量对 SBA-15 进行处理后, 其水热稳定性明显改善, 在 100 ?C 沸水中处理 14 d, 或在 800 ?C 下用 100% 水蒸气处理 12 h 后, 均保持较好的介观有序度、形貌及六方孔道结构, 比表面积分别高达 310 和 213 m2/g, 但 (NH4)2SiF6 处理量过高, SBA-15 水热稳定性反而下降.     

硅杂六元环化合物的反应

硅杂六元环化合物在有机硅化学中是一类重要的小分子环系化合物,广泛应用于有机化学、高分子化学、金属有机化学以及材料化学等领域。本文综述了环上只含有一个硅原子的硅杂六元环化合物的反应,介绍了硅原子上取代基的反应、立体选择性合成、硅原子α位碳原子上的反应、插入反应、环加成反应、Si—C键的切断反应、硅杂苯衍生物合成以及金属配位反应等,并展望了硅杂六元环化合物反应化学的发展方向。     

计入地面附加衰减的声屏障插入损失估算方法*

基于理论推导和计算,给出了公路声屏障声学设计中,在考虑地面附加衰减情况下计算插入损失的方法。该方法综合考虑了有限长线声源无限长声屏障绕射声衰减量、有限长线声源地面衰减量及遮蔽角对插入损失的影响。通过与《声屏障声学设计和测量规范》（HJ/T90-2004）的计算结果的对比,验证了本文所给方法的精确性及可行性,并对规范所给地面衰减修正量进行了商榷。最后,给出了当预测点位于有限长路段中央法线上时,通过计算线声源地面衰减量得到计算插入损失所需参数值,再计算插入损失的简便方法。本研究为存在地面附加衰减情况下有限长声屏障插入损失计算提供了一个新的参考方法。     

Prediction of sites under adaptive evolution in flavin-containing monooxygenases: Selection pattern revisited

Flavin-containing monooxygenase (FMO), like cytochrome P450 (CYP), is a monooxygenase that uses the reducing equivalents of NADPH to reduce one atom of molecular oxygen to water, while the other atom is used to oxidize the substrate. Recently, it was shown that some CYP isoforms have been subject to positive selection. However, it is unknown whether the highly conserved phase I detoxification enzyme, FMO, has undergone similar positive Darwinian selection. We used maximum-likelihood models of codon substitution, evolutionary fingerprinting, and cross species comparison to investigate the occurrence of adaptive evolution in FMO sequences. We used recent genomic data from a range of species, including vertebrates and invertebrates. We present the evidence for the occurrence of adaptive evolution in mammalian FMO 3, 4, 5, and fugu FMOs but not in mammalian FMO 1, FMO 2, frog FMOs, other fish FMOs and invertebrate FMOs. The sites under adaptive evolution were significantly associated with the insertion domain in mammalian FMO 5. We identified specific amino acid sites in FMOs 3–5 that are likely targets for selection based on the patterns of parallel amino acid change. The most likely role of adaptive evolution is the repair of mutations that permitted optimal NADP+ binding and improved catalytic efficiency. The occurrence of positive selection during the evolution of phase I detoxification enzymes such as FMOs 3–5 and fugu FMO suggests the occurrence of both high selection pressure acting on species within their unique habitats and significant changes in intensity and direction (forms of xenobiotics and drugs) resulting from changes in microhabitat and food.     

SOFM神经网络最近插入法混合算法在TSP问题中应用研究

SOFM神经网络已经成功应用到TSP问题中，但是该算法存在一些缺点，随着学习速度逐步降低，会导致一些城市无法通过。针对这些缺点，尝试在SOFM神经网络中引入最近插入法形成混合算法。通过实验，并与SOFM神经网络该算法对比，结果表明，该算法能够很好地完善该问题。     

Theoretical Prediction on the Germylenoid HB=GeLiF and Its Insertion Reaction with R-H（R = F,OH,NH_2）

In the present work we investigated a novel triplet ground-state germylenoid HB=GeLiF as well as its insertion reactions with RH(R = F,OH and NH2) using the DFT B3LYP and QCISD methods for the first time.Geometry optimization calculations show that the triplet HB=GeLiF has three equilibrium structures,in which the four-membered ring structure is the most stable with the lowest energy.All mechanisms of the three insertion reactions of germylenoid HB=GeLiF with RH(R = F,OH,and NH2) are identical to each other.Based on the calculated results,it is concluded that under the same conditions the insertion reactions should occur easily in the order of H-F > H-OH > H-NH2.In THF solvent the insertion reactions get more difficult than in the gas phase.     

Insertion Reactions of Neutral Phosphidozirconocene Complexes as a Convenient Entry into Frustrated Lewis Pair Territory

Neutral phosphidozirconocene complexes [Cp₂Zr(PR₂)Me] (Cp=cyclopentadienyl; 1a : R=cyclohexyl (Cy); 1b : R=mesityl (Mes); 1c : R=tBu) undergo insertion into the Zr?P bond by non‐enolisable carbonyl building blocks (O=CR′R′′), such as benzophenone, aldehydes, paraformaldehyde or CO₂, to give [Cp₂Zr(OCR′R′′PR₂)Me] ( 3 – 7 ). Depending on the steric bulk around P, complexes 3 – 7 react with B(C₆F₅)₃ to give O‐bridged cationic zirconocene dimers that display typical frustrated Lewis pair (FLP)/ambiphilic ligand behaviour. Thus, the reaction of {[Cp₂Zr(μ‐OCHPhPCy₂)][MeB(C₆F₅)₃]}₂ ( 10a ) with chalcone results in 1,4 addition of the Zr⁺/P FLP, whereas the reaction of {[Cp₂Zr(μ‐OCHFcPCy₂)][MeB(C₆F₅)₃]}₂ ( 11a ; Fc=(C₅H₄)CpFe) with [Pd(η³‐C₃H₅)Cl]₂ yields the unique Zr?Fe?Pd trimetallic complex 13a , which has been characterised by XRD analysis.