冷蒿挥发油化学成分的分离和鉴定

采用水蒸气蒸馏法提取了冷蒿挥发油,气相色谱-质谱联用结合计算机检索对其化学成分进行了分析和鉴定,共分离出106个峰,确定了101种化合物,它们主要是二甲基-甲撑基环庚（17.67%）、3,3,6-三甲基-1,5-庚二烯醇-2（16.40%）、3,3,6-三甲基-1,4-庚二烯醇-6（8.55%）、桉树脑（5.57%）、3,7-二甲-基2,6-辛二烯醇-1（3.85%）、神圣亚麻三烯（3.73%）、1-甲基-3-异丙基苯（3.26%）、桥环[2,2,1]萜烯（2.91%）、樟脑（2.26%）、香叶烯（2.20%）,以上10种化合物占挥发油总量的66.40%。

唐古特大黄的离体快速繁殖

1植物名称唐古特大黄(Rheum tanguticum),又名鸡爪大黄.2材料类别无菌种子苗.3培养条件种子萌发培养基:(1)MS无激素培养基.前期分化培养基:(2)MS+2,4-D 1 mg?L-1(单位下同)+KT 1+ZT 0.5+6-BA 0.5.后期分化培养基:(3)MS+2,4-D 1+KT 2+ZT 0.5+6-BA 1.以上3种培养基均附加CH 300、肌醇200、3%蔗糖、5 g?L-1琼脂粉.生根培养基:(4)MS+NAA 1+3%蔗糖;(5)1/2MS+NAA 1+3%蔗糖;(6)1/2MS+NAA0.5+1.5%蔗糖;(7)1/2MS+NAA 0.5+3%蔗糖;(8)1/2MS+NAA 1+1.5%蔗糖.pH 5.8.培养温度为(25±1)℃,光源为日光灯,光照度为2 000～3 000 lx,光照时间12 h?-1

乌江流域不同演化阶段水库汞的输入输出通量研究

北欧和北美的研究发现水库是典型的汞敏感生态系统，新建水库而引起的鱼体甲基汞污染问题已受到科学家的高度重视，而我国在这方面的研究比较薄弱。本论文选择乌江流域的6个水库作为研究对象，并根据年龄把这些水库划分为3个演化阶段，洪家渡、引子渡、索风营水库为初级演化阶段，普定、东风水库为中级演化阶段，乌江渡水库为高级演化阶段。对这6个水库总汞和甲基汞的输入和输出通量进行了研究，探讨了不同演化阶段的水库对总汞和甲基汞的“源/汇”作用，主要研究内容有以下三个方面：(1)各水库入出库河流中汞的分布特征；(2)大气降水中汞浓度及沉降通量的分布；(3)乌江流域不同水库汞的输入输出通量。通过本论文的研究，得出以下主要结论： 1. 乌江流域河流中总汞、颗粒态汞、溶解态汞、活性汞、总甲基汞、溶解态甲基汞的年均浓度分别为3.41±1.98、2.05±1.73、1.36±0.44、0.24±0.11、0.15±0.06、0.08±0.03 ng•L-1。与国内外其它河流的比较发现，总汞的浓度明显低于国外受污染的河流，略高于国外未受污染的河流。溶解态汞、活性汞、甲基汞的浓度略低于受污染的河流，与未受污染的河流基本相当。与同处在贵州喀斯特地区的阿哈湖、红枫湖、百花湖的入出库河流相比，总汞、溶解态汞、活性汞、甲基汞、溶解态甲基汞的浓度均明显偏低。 2. 水库的修建显著降低了出库河流中总汞、颗粒态汞的浓度，使总甲基汞和溶解态甲基汞的浓度升高，而且增加了出库河流中溶解态汞、活性汞、总甲基汞占总汞的比例。不同形态汞的沿程分布显示，梯级水库的修建改变了河流原有的汞的生物地球化学过程，使乌江多个河段的甲基汞升高，并且随着水库生态系统的不断演化，水库输出的甲基汞将增加，下游河流水体中甲基汞有继续升高的趋势。 3. 大气降雨中总汞、溶解态汞、颗粒态汞、活性汞、总甲基汞的浓度分别为7.49~149 ng•L-1、1.23~10.0 ng•L-1、5.76~142 ng•L-1、0.56~2.94 ng•L-1、0.08~0.82 ng•L-1，且以颗粒态汞为主，约占总汞比例的87%。总汞、溶解态汞、颗粒态汞、甲基汞的浓度有明显的季节变化趋势，冬春季高于夏秋季，而空间分布特征不明显。2006年总汞、甲基汞的年湿沉降通量为34.7±5.80 µg•m-2•yr-1、0.18±0.03 µg•m-2•yr-1，且主要受降雨量的影响。乌江流域降雨中总汞的浓度及其湿沉降通量远高于北美和日本，低于中国的一些城市地区（如长春和北京），而甲基汞的浓度和通量与其它地区相当。 4. 在乌江流域的不同水库中，降雨输入总汞和甲基汞的通量主要受降雨量和水库面积的影响，而与降雨的汞浓度间没有相关性。河流向水库输入总汞的量主要受河流流量的控制，而输入甲基汞和颗粒物的量受河流流量和浓度的影响。下泄水输出总汞、甲基汞、颗粒物的通量受浓度和流量的影响。由于流域面积/水面面积的比值较大，水库水量、总汞、甲基汞、颗粒物的输入以河流为主，分别占总输入的87%、80%、85%、86%。输出以下泄输出为主，下泄水输出的水量、总汞、甲基汞、颗粒物分别占总输出的80%、77%、86%、79%。 5. 从输入-输出通量的结果发现，各水库均表现为河流颗粒物输送的“汇”；除乌江渡水库外，其它水库均表现为总汞的“汇”；对甲基汞而言，引子渡、洪家渡、索风营水库表现为“汇”，而普定、东风、乌江渡水库则表现为“源”。 6. 普定和洪家渡水库中总汞的贮存率为56%和57%，明显高于其它水库，说明在上游有水库存在的情况下，水库对总汞“汇”的作用将降低。普定、东风、乌江渡水库中甲基汞的净通量分别为+69.4 g•yr-1、+368 g•yr-1、+857 g•yr-1，转化率为13%、73%、84%，说明甲基汞的净通量和转化率与水库的演化阶段有关，随着水库演化阶段的升高而增加，并且随着水库的不断演化，甲基汞将从“汇”变成“源”。

小学学习不良儿童对言语交际策略的理解与运用

[Abstract] Verbal communication strategy (VCS) refers to a programmed knowledge applied by individuals to understand and express intentions via language symbols in their realization of communicative objectives according to social conventions. As an important index of social development, verbal communication strategy has provided a new perspective for social skill studies. However, more work has to be done in the investigation of LD children’s VCS developmental pattern and affecting mechanism. Through contextual test, structured interview and role-play, the present study, by adopting integrated measurements of instrumental and interpersonal effectiveness, explored the developmental characteristics of Chinese learning-disabled primary school children across 3-6th grades at both comprehension and application levels. Then, their social perspective-taking performance and verbal retelling competence of each participant were examined, on the basis of which, path analysis was conducted, with social perspective-taking, verbal retelling and verbal communication strategy comprehension as independent variables, to reveal the inner mechanism affecting LD children’s application of verbal communication strategy. Finally, an intervention study was carried out through a combination of polite request strategy understanding lessons and social perspective-taking training dramas. The results indicate that:(1) No significant grade differences were found in LD group for polite request strategy, while significant differences were reported across different grades of non-LD children. For indirect reply strategy, significant grade and gender differences were found among LD children, but the developmental trajectory between the two groups was different. For both polite request and indirect reply strategies, the strategy comprehension level of LD children was significantly lower than those without learning disabilities. (2) No significant grade and gender differences were found in LD group in their application of polite request strategy, while for non-LD children, significant differences were reported across different grades. For indirect reply strategy, both LD and non-LD groups exhibited similar developmental characteristics. Significant group differences only exist in the over-all application level of polite request strategies, not in indirect reply strategies. However, the differences of the latter between the two groups were found at significant level only among the 11-12 year olds. (3) LD children’s perspective-taking and verbal retelling competence were significantly lower than those of non-LD group. For polite request strategy, the influence of social perspective-taking to strategy application was indirect and must be via strategy comprehension, while for indirect reply strategy, strategy comprehension was found to play as a partial mediator between social perspective-taking and strategy application. The influence of verbal retelling to strategy application was indirect on both types of strategies. (4) LD children’s strategy comprehension and social perspective-taking level can be improved, and the improvement of these two competences has significant positive impact on the increase of their strategy application level. Key Words: learning disabilities, verbal communication strategy, social perspective- taking

Visual C++ 6.0学习教程

MicrosoftVisualC十十6.0作为Microsoft Visual Studio的重要组成部分，包含了迄今为止功能最为强大的基于Windows的应用框架，在同类产品中处于领先地位。VisualC十十6.0是Microsoft迄今为止最全面、最完善的程序开发工具，为了适应各种编程风格，该软件提供了各种各样的辅助工具，在发挥编程能力和提高灵活性方面达到了空前的水平。与以往VisualC十十的各种版本相比较，VisualC十十6.0在编程环境、程序语言技术等方面做了许多改进，从而使VisualC十十更加适合专业程序员快速进行应用程序的开发。

本书内容丰富、图文并茂，是一本适合各种读者学习VisualC十十6.0的优秀参考书。

目 录
第一章 VisualC十十6.0简介及安装
1.1VisualC十十6.0新特性
1.2viSualC十十6.0开发环境简介
1.3如何学习使用VisualC十十6.0
1.4VisualC十十6.0的安装
第二章 走进C十十的世界
2.1类和对象的简介
2.2继承和多态性――一个具体的例子
2.3内嵌对象
2.4在栈中申请对象
2.5全程对象的申请
2.6对象之间的相互关系――指针数据成员
2.7this指针的使用
2.8对指针的引用
2.9友元类和友元函数
2.10静态类成员
2.11重载运算符
2.12从代码中分离出类定义
2.13匈牙利表示法
第三章 VisualC十十6.0的编程环境
3.1VisualC十十6.0主窗口
3.2VisualC十十6.0工具栏
3.3VisualC十十6.0菜单栏
3.4项目与项目工作区
3.5资源与资源编辑器
第四章 编一个最简单的VC十十程序
4.1什么是AppWizard？
4.2迎接你的第一个AppWizard程序
4.3“Iamaprogrammer.”在哪儿？
第五章 程序框架入门
5.1一个简化过的程序框架
5.2WinMain（）：第一个动作
5.3登记窗口类
5.4创建一个窗口
5.5显示窗口
5.6显示出那条消息
5.7窗口类与窗口对象
第六章 消息循环
6.1在消息循环中兜圈子
6.2对事件做出响应：WindowFun（）
6.3响应不同的消息
6.4现在你还跟得上吗？
6.5设备界面进行交互
第七章 精通程序框架
7.1WinMain（）函数在哪儿？
7.2应用程序框架和源文件
7.3工具条、状态条和打印等选项
7.4程序的控制流程
第八章 使用classWizard编程
8.1使用ClassWizard添加消息处理函数
8.2classWizard功能介绍
8.3传送鼠标消息
8.4保存鼠标绘图的信息
第九章 视图与文档
9.1Document－View模式
9.2从视图中分离出文档
9.3保存文档
9.4再访MyProg2.cpp
第十章 对象连接与嵌入（OLE）及其自动化
10.1公共对象模式（COM）
10.2类厂（classfactory）
10.3OLE自动化
10.4IDispatch接口
第十一章 动态连接库（DLLs）
11.1为什么使用DLL
11.2传统的DLL
11.3MFC库DLL
11.4MyProg4A――编写自己的类库扩展DLL
11.5MyProg4B――使用MFC库扩展DLL
11.6资源访问
第十二章 图形设备接口
12.1设备环境类
12.2GDI对象
12.3Windows的颜色映射
12.4映射方式
12.5字体
12.6MyProg3例程序
12.7MyProg3B程序
12.8MyPr0g3C例程序――使用CScrollView
第十三章 对话框
13.1在状态条上显示对话控件的帮助信息
13.2利用Fi1eOpen通用对话框打开多个文件
13.3定制通用文件对话框
13.4扩展和缩减一个对话框
13.5显示一个模式或无模式对话框
13.6编写定制的DDX/DDV例程
第十四章 剖析工具Spy十＋
14.1窗体
14.2消息
14.3进程与线程
第十五章 代码调试
15.1TRACE
15.2调试框架
15.3自我诊断
15.4调试代码的作用
15.5用Dump（）显示对象的信息
15.6检查内存

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.

Blue amplified spontaneous emission from 2, 1, 3-benzothiadiazole attached polyfluorene semiconductor polymer with high photoluminescence efficiency

The amplified spontaneous emission properties of a 2, 1, 3-benzothiadiazole attached polyfluorene semiconductor polymer were studied. The conjugated polymer shows a high photoluminescence quantum efficiency of 67% and emits a narrowed blue emissive spectrum with a full width at half-maximum of 3.6 nm when optically pumped, indicating better lasing action. A threshold energy as low as 0.22 mJ pulse(-1) cm(-2), a net gain of 40.54 cm(-1) and a loss of 7.8 cm(-1) were obtained, demonstrating that this conjugated polymer could be a promising candidate as the gain medium for the fabrication of blue polymer lasers.

成核剂1,3:2,4-二(亚苄基)-D山梨醇对PET/PEN共混体系结构和结晶形态影响

利用差示扫描量热仪、X射线衍射仪、正交偏光显微镜研究了成核剂 1,3 :2 ,4-二 (亚苄基 ) -D山梨醇(DBS)对聚对苯二甲酸乙二醇酯 (PET) /聚 2 ,6-萘二甲酸乙二醇酯 (PEN)共混体系的结构及结晶形态的影响。结果表明 :成核剂的加入 ,使PET/PEN共混体系熔融起始温度升高 10℃左右 ,结晶峰形变尖锐 ,说明加入成核剂后有效促进了PET/PEN共混体系的结晶。实验结果表明 :成核剂含量低于 1%时 ,PET/PEN共混体系晶体的球晶完整。成核剂含量大于 3 %时 ,PET/PEN /DBS共混体系晶体的球晶碎小。成核剂的加入 ,能够有效地减小球晶尺寸和降低球晶的完善性

H-1 NMR analysis for metabolites in serum and urine from rats administrated chronically with La(NO3)(3)

H-1 NMR spectroscopy has been used to assess long-term toxicological effects of a rare earth. Male Wistar rats were administrated orally with La(NO3)(3) at doses of 0.1, 0.2, 2.0, 10, and 20 mg/kg body wt, resp., for 3-6 months. Urine was collected at 1, 2, and 3 months and serum samples were taken after 6 months. Numerous low-M-r metabolites in rats serum and rats urine, including creatinine, citrate, glucose, ketone bodies, trimethylamine N-oxide (TMAO), and various amino acids, were identified on 400- and 500-MHz H-1 NMR spectra. La3+-induced renal and liver damage is characterized by an increase in the amounts of the excreted ketone bodies, amino acids, lactate, ethanol, succinate, TMAO, dimethylamine, and taurine and a decrease in citrate, glucose, urea, and allantoin. Information on the molecular basis of the long-term toxicity of La(NO3)(3) was derived from the abnormal patterns of metabolite excretions. An assay of some biochemical indexes and analysis of some enzymes in plasma supported NMR results.

Studies on the structure of tricyclohexyltin-2-(1,2-dithioethylene)methylene-3-oxo-5-aryl-4-pentenicate

Three title compounds were prepared and the structure of title compound 2 was characterized by IR, H-1 NMR, C-13 NMR, Sn-119 NMR spectroscopy and the crystal structure of compound 2a was determined by X-ray analysis with the final R indices[I >2 sigma (I)] R-1 = 0.0350 and R-2,R-omega = 0.0888. The crystal of compound 2a belongs to triclinic system, space group P1 with a = 1.0598(6) nm, b = 1.307 4(10) nm, c = 1.378 6(10) nm, alpha = 62.666(7)degrees, beta = 72.530(2)degrees, gamma = 80. 680(2)degrees, V = 1.618 0 nm(3), D-x = 1. 444 g (.) cm(-3), Z = 1, F (000) = 728. The bond length of Sn1-O1 is 0. 2076 nm and Sn1 . . . O2 distance is 0.301 3 nm. The coordination about the tin atom can be considered as a distorted tetrahedral. The detail values of H-1 NMR, C-13 NMR, Sn-119 NMR, (2)J(119Sn-1H) and J(119Sn-13C) were obtained. delta (119Sn) = 23.836, (2)J(119Sn-1H) = 88.0 Hz, (1)J(119Sn-13C) = 347.1 Hz, (2)J(119Sn-13C) = 45.6 Hz.

YP_xV_(1-x)O_4(0≤x≤1):Dy~(3+)的合成及其光谱性质的研究

本文报道了不同组成的YP_xV_(1-x)O_4(0≤x≤1):Dy~(3+)的合成和结构。YP_xV_(1-x)O_4(0≤x≤1)为四方晶系,晶胞参数随x的增大呈线性减小。基质的Stokes位移随x的增大逐渐变大,而激发光谱峰值则向短波方向移动。在YP_xV_(1-x)O_4:0.006Dy~(3+)体系中,x>0.4时出现的基质发射是由P0_4~(3-)引起的。基质及Dy~(3+)的发光效率和Dy~(3+)的发光强度的黄蓝比均与x有关。同时探讨了Bi~(3+)和温度对Dy~(3+)的发光强度的影响。

α-羰基烯酮式环二硫代缩醛化学(V)——β,β-1,3-亚丙二硫基-α,β-不饱和芳酮类化合物的合成

β,β-二烷硫基-α,β-不饱和酮类化合物作为一类具多反应中心的活泼中间体在有机合成中的应用,近20年来已引人注目并进行了深入广泛的研究~[1,2].以往的研究大多是针对β,β-二甲硫基-α,β-不饱和酮类化合物1进行的,而对结构相近的β,β-1,3-亚丙二硫基-α,β-不饱和酮类化合物2的研究较少.对于1类的合成,所用碱的选择至关重要~[1].实验证明叔丁醇钠和叔丁醇钾~[3～5]在1类的合成中效果较好.前文~[6]曾以六甲基二硅氨基锂(LHMDS)为碱高

两种新的手性1,6-双膦的合成

由D-甘露醇出发合成了两种新型的手性1,6-双膦:1,6-双(二苯膦基)-2,3,4,5-二亚(艹卡)基-D-甘露醇和1,6-双(二苯膦基)-3,4-亚(艹卡)基-2,5-亚甲基-D-甘露醇。 以这两种手性配位体的Rh(Ⅰ)配合物为催化剂用于α-乙酰氨基肉桂酸的不对称氢化反应,但都未观察到对映选择性,而且由第一种配位体参加的反应,也未显示氢化活性,对此本文也作了初步的说明。

Hymeniacidon perleve associated bioactive bacterium Pseudomonas sp NJ6-3-1

Among marine bacteria isolated from the cytotoxic sponge Hymeniacidon perleve, one strain NJ6-3-1 classified as Pseudomonas sp. showed both cytotoxic and antimicrobial activities. Fatty acid analysis indicated that the bacterial strain consists mainly of C16:1, C16:0, C18:1, C18:0, C15:0, C14:0. One unusual 9,10-cyclopropane-C17:0 fatty acid and C26:0 also constitute major components, as well as the existence of squalene, the precursor of triterpenoids. The major metabolites in the culture broth were identified as alkaloids, including diketopiperazines and indole compounds, namely 3,6-diisopropylpiperazine-2,5-dione, 3-benzyl-3-isopropylpiperazine-2,5-dione, 3,6-bis-(2-methylpropyl)-piperazine-2,5-dione, indole-3-carboxaldehyde, indole-3-carboxylic acid methyl ester, indole-3-ethanol, and quinazoline-2,4-dione.

Structural and up-conversion luminescence properties in Tm (3+)/Yb3+-codoped heavy metal oxide-halide glasses

Tm3+/Yb3+-codoped heavy metal oxide-halide glasses have been synthesized by conventional melting and quenching method. Structural properties were obtained based on the Raman spectra, indicating that halide ion has an important influence on the phonon density and maximum phonon energy of host glasses. Intense blue and weak red emissions centered at 477 and 650 nm, corresponding to the transitions (1)G(4) -> H-3(6) and (1)G(4) -> H-3(4), respectively, were observed at room temperature. The possible up-conversion mechanisms are discussed and estimated. With increasing halide content, the up-conversion luminescence intensity and blue luminescence lifetimes of Tm3+ ion increase notably. Our results show that with the substitution of halide ion for oxygen ion, the decrease of phonon density and maximum phonon energy of host glasses both contribute to the enhanced up-conversion emissions. (c) 2005 Elsevier B.V. All rights reserved.