Calculation of Valence Subband Structures for Strained Quantum-Wells by Plane Wave Expansion Method Within 6 * 6 Luttinger-Kohn Model

The valence subband energies and wave functions of a tensile strained quantum well are calculated by the plane wave expansion method within the 6 * 6 Luttinger-Kohn model. The effect of the number and period of plane-waves used for expansion on the stability of energy eigenvalues is examined. For practical calculation, it should choose the period large sufficiently to ensure the envelope functions vanish at the boundary and the number of plane waves large enough to ensure the energy eigenvalues keep unchanged within a prescribed range.

In_(0.4)Ga_(0.6)As/GaAs自组织量子点的光伏谱温度特性

采用无需在样品上制备电极的电容耦合的光伏谱方法,实验测量了In_(0.4)Ga_(0.6)As/GaAs自组织量子点在不同的温度下的光伏谱,对测量谱峰进行了指认,研究了量子点谱峰能量位置随温度的依赖关系。实验结果表明,量子点具有与体材料及二维体系不同的温度特性,对实验所测样品,其激子峰能量随温度增加而红移的速率约为GaAs体材料带隙变化的1.4倍。

GaAs/Al（0.4）Ga（0.6）As多量子肼红外探测器光吸收计算

于2010-11-23批量导入

涡动相关法估算森林生产力及与测树学方法的比较

大气中CO2、CH4和其它温室气体浓度升高导致的全球气候变化引起了人们对全球碳循环和碳收支的关注，植被与大气间CO2通量的长期测定能够加深对陆地生态系统在全球碳循环作用的科学理解。本文以我国北方典型的温带植被类型长白山阔叶红松林为研究对象，利用观测塔上的涡动相关系统对长白山阔仆卜红松林进行长期的CO2通量监测，并分析CO2通量的周年动态，估算森林净生态系统生产力；同时基于测树学方法，进行群落调查，根据已有的经验公式，估算森林净生态系统生产力，综合评价长白山阔汗卜红松林碳收支，为森林碳收支的研究提供基础。主要结论有：（1）FSAM模型的分析结果表明，观测塔上40m高度的涡动相关仪器测量的信息中，76％来自于西北至西南方相对均质的阔叶红松原始林，其中footprint最大的源区在塔西南方100m-400m范围内。因此，森林群落调查选择在此区内进行，使得涡动相关法和测树学方法估算的生产力具有可比性。（2）2003-2004年碳通量季节变化趋势基本一致，从年初到4月上旬该森林生态系统保持较弱的正的碳通量（释放CO2），5月开始表现为净的碳吸收，且吸收量迅速增加，到6月达到最大值，然后又逐渐减小；9月末到10月末随着生长季的结束，净生态系统COZ交换（NEE）开始由负转为正，11-12月NEE为正，生态系统以呼吸为主。净生态系统COZ交换的年累计量表明长白山阔叶红松林为明显的碳汇，2003年和2004年净生态系统生产力NEP分别为-217±75gcm-2a-1和-190±85gcm-2a-1，相当于-2.17±0.75tCha-1a-1和-1.90±0.85tCha-1a-1。（3）根据经验公式和材积法得到阔汗卜红松林的生物量在343．9-362．3tha－l之间，应用两种方法得到2003一2004年群落的净初级生产力在10.22-10.40tCha-1a-1之间，净生态系统生产力在2.50±1.12tCha-1a-1-2.68±1.20tCha-1a-1之间。（4）测树学方法与涡动相关法测得的净生态系统生产力略有差异，但在误差有效范围内基本一致。

2-C-支链-1,6-脱水吡喃葡萄糖的开环反应及吡喃烯糖的合成研究

在糖化学合成中，1,6-脱水吡喃糖不仅是合成具有生物活性低聚糖、糖共体、抗原、抗体以及天然产物等化合物重要原料，而且还是许多具有生物活性的天然产物的结构单元。同时，它还具有[3,2,1]的双环缩醛结构，使其在糖化学合成中具有高的立体选择性和区域选择性，同时减少了C-1 和C-6 位的保护和去保护的优点。此外，环内的缩醛开环后，又可以相应地在C-1 和C-6 位进行官能团转化以及糖苷化反应。 本文报道了一种新的1,6-脱水吡喃糖的合成方法，并设计合成了2-C-支链-1,6-脱水吡喃葡萄糖1-195、1-197、1-198 以及2-C-支链-6-硫代1,6-脱水吡喃葡萄糖1-225。到目前为止，1,6-脱水糖开环并进行糖苷化反应，存在选择性较差、产率低的缺点。我们发现，在乙腈做溶剂的条件下，NiCl5 能高立体选择性高产率地催化化合物1-195、1-197、1-198 开环并与ROH、RSH 发生糖苷化反应。在NiCl5-乙腈条件下，合成了一系列2-C-支链-α-糖苷和2-C-支链-β-硫代糖苷，并对2-C-支链1,6-脱水吡喃葡萄糖的生成机理以及开环机理进行了探讨。 烯糖在糖化学合成中是重要的起始原料，从Fischer 首次合成烯糖至今，一直不断地有新的合成方法出现。但目前文献报道的方法存在所用试剂有毒、价格贵和操作繁琐等缺点。我们对Fischer-Zach 方法进行了改进， 发现Zn-NaH2PO4-H2O 和Zn-PEG600-H2O 体系都能很好地合成烯糖。该方法具有条件温和、绿色环保、操作简单的优点。在Zn-NaH2PO4 溶液或Zn-PEG600 条件下，以溴代糖为原料，高产率地合成一系列的烯糖。 The 1,6-anhydrohexopyranoses are crucial subunits of myriad bioactive nature products, as well as important syntons of carbohydrate chemistry which have been extensively used to prepare the biologically potential oligosaccharides, glycoconjugates, antibiotics, and structurally varied nature products. Their particular [3.2.1] bicyclic skeleton makes them have high regio- and stereo-control in a variety of reactions, and such structure avoids protecting hydroxyl groups at C1 and C6.Additionally, the cleavage of the internal acetal under acidic conditions could be beneficial for further transformations of functional group and glycosylation of the corresponding pyranosyl sugar at the C6 or C1 site. Herein we developed a novel approach to prepare the 1,6-anhydrohexopyranose, and synthesized the 2-C-branched-1,6-anhydrohexopyranose 1-195, 1-197, 1-198 and 2-C-branched-6-thio-1,6-anhydrohexopyranose 1-225. Until now, glycosylation of 1,6-anhydrohexopyranoses has been limited because of the low yields and low stereoselectivity. In this paper, we found that NiCl5-MeCN system could selectively cleave the ring of 1,6-anhydrohexopyranoses with alcohols and thiols at room temperature in high yields. A series of 2-C-branched-α-glycosides and 2-C-branched-β-thioglycosides have been synthesized via NiCl5-catalyzed. Furthermore, we investigated the formation and ring-opening mechanism of 2-C-acetylmethyl-1,6-anhydrohexopyranose. Glycals are significant starting material in carbohydrate chemistry. After the Fischer-Zach method for forming glucal was reported for the first time, the numerous synthetic methods for glycals have been explored. However, there are several drawbacks in the existing methods, such as the usage of very expensive and toxic reagents, intricate operation, and the influence of acid-sensitive and base-sensitive functional group. We improved the Fischer-Zach method and developed a facile, mild and environmentally benign methodology towards the synthesis of the glycals in Zn-NaH2PO4-H2O or Zn-PEG600-H2O system. Our method involves the treatment of glycosyl bromides with Zn in NaH2PO4 aqueous solution or PEG600-H2O at room temperature, affording various glycals in excellent yields.