Recent progresses of silicon-based optoelectronic devices for application in fiber communication

Si-based optoelectronic devices, including stimulated emission from Si diode, 1.3 and 1.5mum SiGe photodetector with quantum structures, 1GHz MOS optical modulator, SOI optical switch matrix and wavelength tunable filter are reviewed in the paper.

不同施肥制度下潮棕壤钾素肥力演变

1990～2004年在下辽河平原进行的长期定位试验，对不同施肥制度下作物（玉米、大豆）产量及潮棕壤钾素收支和肥力变化进行了研究；同时用两种不同的方法研究了作物（玉米和大豆）的土壤缺钾临界值。 研究结果表明，不同处理对土壤K素收支状况产生不同的影响：N肥或NP肥并用加剧了土壤K的收支赤字；保持系统中养分的循环再利用，可以缓解但不能从根本上消除土壤K素的收支赤字，只有在K素循环回田的基础上配施K化肥能保持系统内部K素平衡。 未施K肥的各处理土壤速效钾和缓效K浓度均有明显的下降，其中NP和N处理土壤缓效K浓度下降幅度最大；施NPK肥的处理，土壤速效钾和缓效K浓度有所提高；K肥配合循环猪圈肥的施用，能明显提高土壤速效钾和缓效钾浓度。 根据历年试验结果进行统计，用十字交叉法得出玉米的土壤速效K临界值为78mg∙kg-1，大豆的土壤速效K临界值为74mg∙kg-1。将土壤速效K与作物相对产量进行相关分析，根据回归方程计算，玉米和大豆土壤速效K的临界值分别为82.59mg∙kg-1、81.56mg∙kg-1。 K肥对玉米和大豆的增产有一定的效果；施加循环猪圈肥的处理也能在一定程度上提高作物产量，且循环猪圈肥有稳产的作用；化学钾肥配合循环猪圈肥能显著提高玉米和大豆的籽实产量（p<0.01）。

能同时高对映选择性还原酮和亚胺的有机小分子催化体系的设计与合成

不对称催化还原反应是当今有机化学研究中最具活力的研究方向之一。在这一研究领域中，已有不少催化剂体系能够对前手性酮或亚胺进行高对映选择性还原，但极少能够对酮和亚胺同时具有很好的催化效果。本论文从光学纯的哌啶酸出发，设计与合成了一系列结构简单、合成方便的手性有机小分子路易斯碱催化剂，并研究了该系列催化剂在酮和亚胺不对称还原本课题组前期研究中开发出L-哌啶酸和（1S,2R）-1,2-二苯基氨基乙醇衍生的路易斯碱催化剂，在三氯氢硅对亚胺的还原反应中显示出很高的催化活性和对映选择性，但对酮的还原却没有得到很理想的催化效果。本研究对该催化剂进行一定的结构改造和修饰，获得了能够同时高对映选择性催化还原酮和亚胺两类底物的有机小分子催化剂。通过优化条件，取得了很好的收率（高达99%）和对映选择性（高达93%的ee 值）。而且，其底物普适性也是前所未有的，对芳香酮和脂肪酮，芳香亚胺和脂肪亚胺都具有很好的催化效果。通过机理方面的探讨，我们推测该催化体系对酮的还原和对亚胺的还原反应可能分别采用了七配位和六配位过渡态模型。Asymmetric reduction is one of the most active research areas in modernasymmetric synthesis. A number of highly efficient methods have been developed forthe asymmetric reduction of either ketones or ketimines. However, there have beenextremely rare examples of catalytic systems that allow for highly enantioselectivereductions of both ketones and ketimines.In this study, starting from optically pure pipecolinic acid, we designed andsynthesized a series of structurally simple and easily accessible chiral organic Lewisbasic catalysts and employed them in asymmetric reduction of ketones and ketimines.Previously our group has developed a highly enantioselective Lewis basiccatalyst for the asymmetric reduction of ketimines by trichlorosilane starting fromL-piperdine-2-carboxylic acid and (1R,2S)-2-amino-1,2-diphenylethanol. But thiscatalyst was found not to be very effective in the asymmetric reduction of ketones.Slight modifications of this catalyst has led to a new highly enantioselective catalystapplicable for the reduction of both ketones and ketimines by trichlorosilane. Underthe optimal conditions, this catalyst afforded excellent yields (up to 99%) andenantioselectivities (up to 93% ee). Moreover, an unprecedented substrate spectrumwas observed with this catalyst, which are highly effective for aromatic and aliphaticketones as well as aromatic and aliphatic ketimines. A heptacoordinate silicontransition structure and a hexacoordinate one were proposed for the reduction of ketones and ketimines, respectively.

N-烷基氮杂糖及其衍生物的合成

多羟基哌啶类化合物通常称为氮杂糖，由于与糖结构的相似性，亚胺基环醇表现出强的糖苷酶和糖基转移酶抑制活性，可调控在生物识别及酶结构控制中起到重要作用的糖蛋白的生物合成与水解。因此这类抑制剂有望成为与糖代谢紊乱有关的疾病的治疗药物，如：抗糖尿病、抗肿瘤、抗溶酶体贮积症及抗病毒感染（包括艾滋病）等药物。正是由于氮杂糖的重要生物活性及诱人的药用开发前景，近年来，有关氮杂糖及其衍生物的合成、生物活性及应用研究备受关注。 本论文探索了一系列的作为潜在的迈克加成中间体1-C-乙酰甲基/甲氧羰基甲基-5-N-取代呋喃核糖碳苷衍生物在碱的作用下先发生β-消除反应，接着发生分子内的迈克加成反应生成1-C-乙酰甲基-N-取代氮杂吡喃糖碳苷衍生物及1-C-甲氧羰基甲基-N-取代氮杂吡喃糖碳苷衍生物的方法，该转变过程为先通过β-消除得到非环状的α/β不饱和共轭酮或酯的中间体，接着5-N-取代氨基与分子内的α/β不饱和共轭酮或酯发生分子内的1,4-亲核加成，其中，2'-酯的环加成立体选择性的得到β型1-C-乙酰甲基-N-取代氮杂吡喃糖碳苷衍生物，而2'-酮的环加成得到立体异构体1-C-乙酰甲基-N-取代氮杂吡喃糖碳苷衍生物。此外，该类N-取代氮杂吡喃糖碳苷衍生物进一步脱除保护基，得到了一系列新的N-取代氮杂吡喃糖衍生物，拓展了氮杂吡喃糖碳苷分子库。 中间体1-C-(2'-oxoalkyl)-5-N-alkylated glycoribofuranoside的合成是由核糖为原料，通过对其结构修饰，在C-5氮原子上先引入不同的取代基，在C-1上引入乙酰甲基或甲氧羰基甲基。C-5取代氨基的引入通过两种方法：(a) 5-取代链状脂肪氨基可由链状的伯胺直接与5-甲磺酰基发生SN2亲核取代得到；(b) 5-取代芳香氨基可通过芳香醛与C-5氨基缩合再由硼氢化钠还原得到。2'-酰基的引入通过烯丙基氧化得到：2'-酮羰基由醋酸汞和琼斯试剂氧化得到；2'-酯基由高锰酸钾氧化再碘甲烷的作用下得到。 The polyhydroxylated piperidines, commonly be called azasugars. Iminocyclitols and their derivatives have exhibited remarkable biological activity to inhibit glycosidase-processing enzymes, with resulting potential chemotherapeutic applications against diabetes, cancer, lysosomal storage disorders and viral infections including AIDS. Recently, because of the important biological activity and excellent foreground on pharmaceutical application, great attention has been attracted to the synthesis of the new derivatives and analogues. In this dissertation, 1-C-(2'-oxoalkyl)-5-N-substituted-glycoribofuranosides, which used as latent substrates for intramolecular hetero-Michael addition, were converted to 2-ester and 2-ketone aza-C-glycopyranosides by base treatment. The transformation was achieved through β-elimination to an acyclic α/β-conjugated ketone or ester, followed by an intramolecular hetero-Michael addition by the 5-N-alkylated amino group. The 2-ester cycloaddition was highly stereoselective in favor of an equatorial 1-C-substitution while the 2-ketone cycloaddition was produced a pair of stereoisomers of 2′-ketonyl aza-C-glycoside. Additionally, the resultant different N-alkylated aza-C-glycopyranosides could be further prepared for various azasugar library constructions by removal of protecting groups. Synthesis of the key intermediate 1-C-(2'-oxoalkyl)-5-N-alkylated glycoribo- furanoside involved the introduction of 5-substituted amino and 1-C-2′-oxoalkyl groups from D-ribose. The 5-alkylated amino was introduced through two methods: (a) the 5-aliphatic series amino synthesized by the nucleophilic substitution of 5-mesylate using neat ethylamine, propylamine, butylamine, and hexylamine, (b) the 5-aromatic series amino synthesized by various aromatic aldehydes with C-5 amino under NaBH4 reduction. The 1-C-2′-oxoalkyl groups were introduced through oxidation of the ally group: the 1-C-allyl group was oxidized with Hg(OAc)2 and Jones reagent to the 2-ketonyl C-glycoside; the 1-C-allyl group was oxidized with KMnO4 and CH3I/NaHCO3 to 1-C-methyl acetate glycoside.

中国蔷薇属芹叶组（Rosa Sect. Pimpinellifoliae DC. ex Ser.）的分类学研究

本研究通过我国CDBI、 KUN、PE、SZ等主要标本馆约3, 500份馆藏标本的研究和野外考察相结合，对我国蔷薇属（Rosa L.）芹叶组(Sect. pimpinellifoliae DC. ex Ser.）植物以及相关组的一些种进行了性状特征、形态和微形态的研究，对该组的一些种的形态特征描述进行了补充，同时给出详细的地理和海拔范围分布图。综合花粉以及种子（瘦果）形态的研究结果重新制订了分种检索表，同时，对该组一些形态相近容易混淆的种进行了对比研究，特别对一直存在争议的绢毛复合体（绢毛蔷薇R. sericea Lindl.和峨眉蔷薇R. omeiensis Rolfe）进行了大量宏观形态特征的研究，并用光学显微镜（LM）和扫描电镜(SEM)对二者的花粉及种子形态、微形态进行对比研究和分析，主要研究内容包括： 1. 芹叶组孢粉研究 对芹叶组的10个种及相关的4个组共17个种（18个样品）的植物花粉进行了光镜和扫描电镜观察和比较研究。研究结果表明：蔷薇属植物花粉粒大小为中等偏小，极轴长23.98[21.82(R. graciliflora Rehd. et Wils.)～29.18(R. tsinglingensis Pax. et Hoffm.)] μm，赤道轴长28.65[24.15（R. graciliflora）～34.70(R. davidii Crép.)] μm；花粉属辐射对称等极单花粉，花粉形态赤道面观呈球形到超长球形；极面观为三裂圆形或近圆形,三孔沟，孔缘加厚,具中部突起的桥状盖。花粉外壁纹饰为条纹状，光镜下形态特征相差不大；在电镜下外壁条纹和脊沟内穿孔的形状、大小和频度等特征，常具组至种水平上的可见变异，可作为组至种水平划分的依据。 根据花粉外壁条纹特征及穿孔形状和数目等特征，本研究将这些植物的花粉归为5个类型，并编制了分组检索表。同时，根据条纹状的清晰度，排列方式、条纹形状、穿孔大小及其频度等方面的差异，各有特点，对该组的10个种编制了分种检索表。 2. 芹叶组种子形态研究 应用光学显微镜和扫描电镜对我国蔷薇属芹叶组14个种及相关组5个组共36种植物的种子宏观形态及种皮微形态特征进行了观察研究。结果显示，蔷薇属种子形态多样,形状分别为肾形、卵形或锥形等；种子颜色以淡棕色、褐色以及土黄色为主；种子大小种间相差悬殊，相对体积为（长×宽×厚）36.66（4.79～114.47) mm3。光镜下，种子宏观形态特征具组内一致性，在扫描电镜下种子表面结构特征因种而异，其纹饰以网纹为主，可分为3种类型，即近平滑型、负网纹型和网纹型。研究结果表明，蔷薇属种子表面纹饰与地理分布关系不大,具有组及种内稳定性。其种子形态、大小、表而纹饰类型等特征可作为蔷薇属组及种水平上的分类依据。 结合蔷薇属花粉形态研究结果，得出蔷薇属种皮微形态特征与花粉外壁纹饰特征相吻合，在代表组及种的特征上具相关性的结论。同时根据种子形态、微形态结构特征的组间区别和种间差异编制了分组及芹叶组14个种的分种检索表。 3. 绢毛蔷薇复合体的研究 通过对大量标本的研究、野外观察以及扫描电镜对绢毛蔷薇复合体的花粉形态和种皮表面结构进行研究，通过对小叶、花粉及种子的形态定量分析结果支持Rowley (1959)的观点，将峨眉蔷薇处理为绢毛蔷薇的一个变种。 综上研究结果得出，蔷薇属植物的小叶片数目、花被基数以及花粉及种子形态等性状是较为稳定的，这些特征可很好的作为分类学依据。 The morphology, pollen exine sculpture and seed coat structure of the species of Rosa sect. Pimpinellifoliae and related sections were studied.About 3,500 herbarium specimens at CDBI, KUN, PE, and SZ were examined. Field work in Sichuan and Yunnan were conducted. Revisions of some species were carried out and a new key to species of sect. Pimpinellifoliae was proposed based on morphology, pollen exine sculpture and seed coat structure, Detailed morphological descriptions, geographical distributions and the altitudinal ranges of some taxa are given. The systematics of the species complex, the Rosa sericea complex (R. sericea Lindl. & R. omeiensis Rolfe), was emphasized. This thesis focused on the following three aspects: 1. Pollen morphology of Rosa sect. Pimpinellifoliae The pollen morphology of 18 samples representing 10 species of the Eurasian Rosa sect. Pimpinellifoliae and 7 additional species of related sections was investigated under LM and SEM. The pollen grains are monadic, actinomorphic, equipolar, medium-sized, spheroidal to perprolate in equatorial view, 3-lobed circular or semi-circular in polar view, crassimarginate, pontoperculate, and with striate exine sculpture. The striate sculpture varies among sections and species. The equatorial axis ranges from 17.97 μm (R. sikangensis) to 29.18 μm (R. tsinglingensis) with an average of 23.98 μm in length, while polar axis varies from 24.15 μm (R. gracilifolra) to 34.70 μm (R. davidii) with an average of 28.65 μm in length. The pollens can be divided into five types based on striate sculpture and a key to the sections sampled was proposed accordingly. The pollen morphology of species of sect. Pimpinellifoliae is more homogeneous and different from other sections sampled and did not support the two-series subdivisions in sect. Pimpinellifoliae. A key is also provided based on characers of pollen morphology among species in sect. Pimpinellifoliae. 2. Seed coat structure of Rosa sect. Pimpinellifoliae The seed coat structure of 39 samples representing 14 species of Rosa sect. Pimpinellifoliae and 12 additional species of related sections was investigated under LE and SEM. The seed relative volume (Length × width × thickness) ranges from 4.79 to 114.47 mm3 with an average of 36.66. mm3. The seeds are reniform, ovate or oblong in shape, with orange-brown, light brown or deep brown color. Seed coat sculpture was reticulate or striate-like reticulate. There was no difference in sculpture character of various speices under LM, while three types of seed coat sculpture were identified under SEM and a key to species based on the seed coat sculpture was provided. The three types of seed coat sculpture were nearly smooth, areolate and reticulate. The study of the seed coat sculpture of same species sampled from different populations showed that characters on the seed coat are stable, and thus the size, shape and seed coat sculpture can be used in species level identification. Interestingly, characters in the seed coat sculpture and the pollen morphology in sect. Pimpinellifoliae are consistent at in specific or sectional levels. A key to the 14 species sampled was given based on seed coat sculpture. 3. The study on Rosa sericea complex The Rosa sericea complex contains R. omeiensis and R. sericea. They are morphologically similar to one another and the systematic status of R. omeiensis has been controversial. In this study we examined large numbers of herbarium specimens of R. omeiensis and R. sericea and conducted field observations in the Hengduan Mts.. We also performed SEM study of pollen morphology and seed coat structure of R. omeiensis and R. sericea. We further carried out intensive morphometric study on the leaflet, pollen, and seed morphology. Our results showed that R. omeiensis should be sunk to be a variety of R. sericea, just as Rowley’s treatment in 1959. In conclusion, the features in the number of leaflet and petal, and the morphological character on pollen and seed are relatively stable. Therefore these characters are very useful in taxon delimition.

~(12)C与~(133)Cs反应中Ba同位素的Q_(gg)产额依赖

使用47MeV/u12C离子轰击133Cs靶,由多核子转移反应产生Ba同位素。使用放射化学方法,从133Cs和反应产物中分离出产物Ba,再使用高纯Ge探测器测量Ba放射性同位素的γ活性,根据Ba同位素的活度和其他相关数据,确定Ba同位素的产生截面。通过分析测得的Ba同位素的厚靶平均产生截面,发现缺中子Ba同位素的独立截面不遵从规则的Qgg系统性。该结果可用重离子碰撞中的次级过程加以解释。

流域水土资源优化配置的几种方法比较

目前关于流域水土资源优化配置研究的特点表现为:对单项的水、土资源优化配置研究较多,把两者结合起来的研究较少;分别从宏观和微观两个尺度研究的较多,将两种尺度结合起来研究的较少;越来越重视资源配置模式下的生态系统服务功能状况及其能否满足特定区域可持续发展的需要;研究方法逐渐由定性向定量化转变,在定量研究中,较多使用一般线性规划、灰色线性规划、动态规划、多目标决策和系统动力学等方法;越来越重视以3S技术为基础,结合专业模型进行模拟,为水土资源配置和管理提供高质量的科学决策支持,但目前还没有建立完善的区域性的支持

catena-Poly[diammonium [diaquabis(pyridine-2,4-dicarboxylato-kappa N-2,O-2)cuprate(II)] [[diaquacopper(II)]-mu-pyridine-2,4-dicarboxylato-kappa N-3,O-2:O-2 '-[tetraaquacadmium(II)]-mu-pyridine-2,4-dicarboxylato-kappa O-3(2):N,O-2 '] hexahydrate]

The title mixed-metal complex, {(NH4)(2)[Cu(C7H3NO4)(2)(H2O)(2)][CdCu(C7H3NO4)(2)(H2O)(6)]center dot 6H(2)O}(n), contains one octahedrally coordinated Cd-II center and two octahedrally coordinated Cu-II centers, each lying on an inversion center. The two Cu-II atoms are each coordinated by two O atoms and two N atoms from two 2,4-pydc (2,4-H(2)pydc = pyridine-2,4-dicarboxylic acid) ligands in the equatorial plane and two water molecules at the axial sites, thus producing two crystallographically independent [Cu(2,4-pydc)(2)(H2O)(2)](2-) metalloligands. One metalloligand exists as a discrete anion and the other connects the Cd(H2O)(4) units, forming a neutral chain.

Uniform Ln(OH)(3) and Ln(2)O(3) (Ln = Eu, Sm) Submicrospindles: Facile Synthesis and Characterization

Monodisperse hexagonal Ln(OH)(3) (Ln = Eu, Sm) submicrospindles with uniform morphology and size have been Successfully synthesized in a large scale via a Facile aqueous solution route from the mixture of aqueous solutions or LnCl(3) and NaOH at 5 degrees C without using any surfactant or template. The as-synthesized products are characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA), energy-dispersive X-ray (EDX) spectra, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM). The SEM and TEM images show that the as-formed Ln(OH)(3) samples have a spindlelike shape with an equatorial diameter of 80-200 nm and a length of 500-900 nm, which are aggregates of even smaller nanoparticles.

Spindle-like Lanthanide Orthovanadate Nanoparticles: Facile Synthesis by Ultrasonic Irradiation, Characterization, and Luminescent Properties

A general and facile ultrasonic irradiation method has been established for the synthesis of the lanthanide orthovanadate LnVO(4) (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) nanoparticles from an aqueous solution of Ln(NO3)(3) and NH4VO3 without any surfactant or template. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), and photoluminescence (PL) spectra as well as kinetic decays were employed to characterize the as-prepared products. Ultrasonic irradiation has a strong effect on the morphology of the LnVO(4) nanoparticles. The SEM and TEEM images illustrate that the as-formed LnVO(4) particles have a spindle-like shape with an equatorial diameter of 30-70 nm and a length of 100-200 am, which are the aggregates of even.

Sonochemical synthesis and photoluminescent property of YVO4 : Eu nanocrystals

YVO4 nanocrystals doped with 10.0 mol% Eu3+ have been synthesized from an aqueous solution of ( Y, Eu)( NO3) (3) and NH4VO3 with or without ultrasonic irradiation. The ultrasonic irradiation has a strong effect on the morphology of the YVO4: Eu particles. The spindle-like particles with an equatorial diameter of 90 - 150 nm and a length of 250 - 300 nm could be obtained with ultrasonic irradiation, whereas only nanoparticles were produced without ultrasonic irradiation. The photoluminescence intensity of YVO4: Eu of the spindle-like particles was largely improved compared with that of the nanoparticles. The possible formation mechanism of the spindle-like particles of YVO4: Eu with the application of ultrasonic irradiation was discussed in this paper.

生物酶催化大豆油制备的脂肪酸比例协调食用油及制法

一种生物酶催化大豆油制备的脂肪酸比例协调食用油，其特征在于它是用生物酶催化Ｎ３系列多不饱和脂肪酸与大豆油酯化反应，其脂肪酸组成的重量百分含量为：饱和脂肪酸８－１２％，单不饱和脂肪酸２０－２６％，多不饱和脂肪酸６２－６８％，其中Ｎ６系列多不饱和脂肪酸５０－５５％，亚麻酸１０－１５％，酸价０．１－４．０ｍｇＫＯＨ／ｇ。本发明具有以酶催化方式合成脂肪酸比例协调的大豆油，脂肪酸结合均匀稳定，不含化学残留，工艺过程绿色环保。通过酶催化酯化反应，提高了大豆油中亚麻酸的含量，使其脂肪酸组成更加合理的优点。

Microwave-assisted synthesis of high-molecular-weight poly(ether imide)s by phase-transfer catalysis

A facile and rapid polycondensation reaction of disodium bisphenol A with bis(chlorophthalimide)s was preformed with a domestic microwave oven in o-dichlorobenzene by phase-transfer catalysis. The polymerization reactions, in comparison with conventional heating polycondensation, proceeded rapidly and were completed within 25 min. The polymerizations gave the corresponding poly(ether imide)s with inherent viscosities of 0.55-0.92 dL g(-1). The effects of various factors on the polymerization, such as the amount of the catalyst, the reaction time, and the microwave power were studied. The properties of the polymers were briefly characterized.