任意两态叠加多模泛函叠加态光场的等幂次差压缩

构造了任意两态叠加多模泛函叠加态光场|ψ(2)f>q,利用多模辐射场广义非线性等幂次高次差压缩的一般理论,研究了态|ψ(2)f>q的广义磁场分量的非线性等幂次N次方差压缩特性.得到了一般理论结果,讨论了两种特殊两态叠加多模泛函叠加态光场的差压缩特性.结果表明:1)当qN为偶数时,第一类两态叠加多模泛函叠加态光场和虚相干两态叠加多模泛函叠加态光场都不出现广义磁场分量的非线性差压缩效应,也不处于N-j最小测不准态;2)当qN为奇数时,在一定条件下,任意两态叠加多模泛函叠加态光场中,广义磁场分量呈现出周期性变化的广义非线性N次方差压缩效应.     

基于宽光谱干涉系统的拼接主镜共相位检测技术

 针对拼接式大口径望远镜主镜,提出一种基于迈克尔逊干涉原理基础上的宽带光谱（白光）干涉检测方法,对拼接子镜间相位误差进行实时检测,进而对失调子镜进行相应校正,以实现拼接子镜的共面排布。子镜间相位误差通过干涉图形间的不匹配性进行提取。应用双中心波长组合白光源来提高白光中心条纹的可见度,通过理论仿真,对不同中心波长组合的白光中心条纹可见度进行比较,结果表明：该双中心波长组合白光源系统的应用,可以提高白光干涉中心条纹的信号分辨能力,借以提高检测精度,使得该白光干涉检测系统对拼接子镜间的相位失调误差进行高精度提取。     

用于拼接子镜相位误差检测的低相干光谱干涉系统分析

针对大口径望远镜拼接式主镜,提出一种基于迈克尔逊干涉原理的低相干光谱干涉检测系统.应用该系统对拼接子镜间相位失调误差进行实时检测,进而对失调子镜进行相应校正,以实现拼接子镜的共面排布.子镜间相位误差通过干涉图形间的不匹配性进行提取.给出了该低相干光谱干涉检测系统的具体结构,叙述了该干涉检测系统的检测原理.针对该系统的干涉条纹对比度V及系统的最低信噪比SNRdBmin进行了分析,论证了通过该低相干光谱干涉检测系统进行子镜间相位误差检测的可行性.     

Enhanced <Emphasis Type="SmallCaps">l</Emphasis><Emphasis Type="Italic">-</Emphasis>(+)-Lactic Acid Production by an Adapted Strain of <Emphasis Type="Italic">Rhizopus oryzae</Emphasis> using Corncob Hydrolysate

Corncob is an economic feedstock and more than 20 million tons of corncobs are produced annually in China. Abundant xylose can be potentially converted from the large amount of hemicellulosic materials in corncobs, which makes the crop residue an attractive alternative substrate for a value-added production of a variety of bioproducts. Lactic acid can be used as a precursor for poly-lactic acid production. Although current industrial lactic acid is produced by lactic acid bacteria using enriched medium, production by Rhizopus oryzae is preferred due to its exclusive formation of the l-isomer and a simple nutrition requirement by the fungus. Production of l-(+)-lactic acid by R. oryzae using xylose has been reported; however, its yield and conversion rate are poor compared with that of using glucose. In this study, we report an adapted R. oryzae strain HZS6 that significantly improved efficiency of substrate utilization and enhanced production of l-(+)-lactic acid from corncob hydrolysate. It increased l-(+)-lactic acid final concentration, yield, and volumetric productivity more than twofold compared with its parental strain. The optimized growth and fermentation conditions for Strain HZS6 were defined.     

Hydrothermal synthesis and characterization of two novel tungstovanadophosphate derivatives

Two novel tungstovanadophosphate derivatives, namely [Fe(phen)₃]₂[PW₈^VIV^VV₅^IVO₄₂] · H₂O (1) and [Fe(phen)₃]₂[PW₉V₃O₄₀] (2), were synthesized under hydrothermal conditions, and characterized by elemental analysis, IR, ESR, XPS, TGA, and single-crystal X-ray diffraction analysis. The crystal structure analyses reveal that the ‘mixed-addenda’ Keggin polyoxoanion in 1 is decorated with VO²⁺ units, such that four V atoms are disordered over eight metal sites; the anion in compound 2 has a typical Keggin structure with three V atoms disordered over 12 metal sites. The two compounds are ionic crystals with slightly different packing modes for the polyoxoanions and [Fe(phen)₃]³⁺ cations. π–π stacking interactions between phen molecules, weak hydrogen bonding interactions between phen ligands and polyoxoanions, and electrostatic forces lead to an extended 3D supramolecular framework. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Switchable antenna: a star-shaped ruthenium/osmium tetranuclear complex with azobis(bipyridine) bridging ligands

A star-shaped Ru/Os tetranuclear complex, in which a central Os unit is linked to three peripheral Ru units by 4,4'-azobis(2,2'-bipyridine) (azobpy) bridging ligands, was prepared to examine the unique photodynamics regulated by its redox state. The Ru/Os tetranuclear complex exhibits Ru-based luminescence at 77 K, whereas the three-electron reduction (one for each azobpy) of the Ru/Os complex results in luminescence from the Os unit. The photoexcited state of the Ru/Os complex rapidly decays into low energy metal-to-ligand charge-transfer states, in which the excited electron is localized in the azobpy ligand in the form of azobpy(.-). Upon the one-electron reduction of the azobpy ligands, the above-mentioned low-energy states become unavailable to the photoexcited complex. As a result, an energy transfer from the Ru-based excited state to the Os-based excited state becomes possible. Ultrafast transient absorption measurements revealed that the energy transfer process consists of two steps; intramolecular electron transfer from the terminal bipyridine ligand (bpy(.-)) to form azobpy(2-) followed by a metal-to-metal electron transfer. Thus, the Ru/Os tetranuclear complex collects light energy into the central Os unit depending on the redox state of the bridging ligands, qualifying as a switchable antenna.     

A Method for Quantifying Azoxystrobin Residues in Grapes and Soil Using GC with Electron Capture Detection

A relatively simple method for the determination of azoxystrobin residues in grapes and soil using gas chromatography equipped with electron capture detector (GC-ECD) is described. Samples were extracted with acetone, and further partitioned with dichloromethane and petroleum ether. The extracts were then cleaned up in a glass clean-up column filled with active charcoal and silica gel, and eluted with dichloromethane/ethyl acetate (70:30, v/v). The eluate was collected and concentrated for GC-ECD analysis. The results showed good linearity (r ² = 0.9998) over the concentration range of 6.25–400 ng mL^?1. The limits of detection (LOD) and quantification (LOQ) of azoxystrobin were 3 and 10 ng mL^?1. Recovery from soil and grape samples was in the range of 83.52–107.36 and 82.21–107.31%, with corresponding relative standard deviations (RSD) of 5.21–9.11 and 4.53–5.90% for the three fortified levels. Inter- and intra-day RSDs were in the range of 0.87–6.76 and 2.01–5.46%. The accuracy and sensitivity of the GC-ECD method was independently confirmed by LC and GC-MS. It was demonstrated that the proposed method was simple and efficient, and particularly suitable for detecting azoxystrobin residues in grapes and soil.     

Study of michael-michael-retro michael addition catalyzed by 9-amino-9-deoxyepiquinine using ESI-MS

The Michael-Michael-retro Michael addition catalyzed by 9-amino-9-deoxyepiquinine was monitored and the major intermediates and catalyst in the catalytic cycle were detected and characterized using ESI-MS/MS for the first time. Some important isomeric intermediates including isomeric enamine and imine structures were tentatively differentiated and further studied by theoretical calculations. Fragment ions of protonated catalyst indicate that proton possibly influences the conformation of the catalyst.     

Practical and efficient synthesis of various meso-functionalized porphyrins via simple ligand-free nickel-catalyzed C-O, C-N, and C-C cross-coupling reactions

Various meso-functionalized porphyrins were conveniently synthesized by direct reactions of meso-bromoporphyrins with oxygen-, nitrogen-, and carbon-based nucleophiles in moderate to high yields via practical, efficient, and ligand-free nickel-catalyzed C-O, C-N, and C-C bond-forming reactions. The central metal ions of the substrate porphyrin have much effect on the reactions. Introduction of Ni(II) as a central metal ion into the substrate porphyrin markedly accelerated the cross-coupling.     

5-取代丙二酸亚异丙酯的结构研究 II: 5-(α-异丙基)-2,2-二甲基-1,3-二氧杂环乙烷-4,6-二酮的晶体结构及量子化学计算

5-(α-异丙基)-2,2-二甲基-1,3-二氧杂环己烷-4,6-二酮C9H14O4, MT=186.21, 正交晶系, 空间群为P212121, 晶胞参数为: a=5.228(1), b=11.079(4), c=16.955埃.V=892.1(5)埃^3, Dc=1.286g.cm^-^3. Z=4, μ(MoKa)=0.92cm^-^1. 用直接法解出结构, 经最小二乘法修正, 最后的偏离因子R=0.062. 结构 测定表明, 分子内六元环具有扭曲船式结构. 对5-(α-苯乙基)-2,2-二甲基-1,3-二氧杂环己烷-4,6-二酮的CNDO/2计算表明, 最稳定构型是扭曲船式结构, 与X射线晶体分析 结果相一致.