BEPCⅡ高频发射机和环流器的调整和测试

北京正负电子对撞机升级改造工程(BEPCⅡ)将采用的频率500MHz、输出功率250kW的高频发射机和环流器已安装、调整、测试和验收完毕,这是国内建立的第一套500MHz/250kW发射机系统.本文将详细介绍机器的调测试的原理和各项测量内容及结果, 并比较设计指标和要求,来阐述此发射机的实际技术指标和测试性能.     

Explicit formula of holomorphic automorphism group on complex homogeneous bounded domains

We known that the maximal connected holomorphic automorphism group Aut (D)(0) is a semi-direct product of the triangle group T(D) and the maximal connected isotropic subgroup Iso(D)(0) of a fixed point in the complex homogeneous bounded domain D and any complex homogeneous bounded domain is holomorphic isomorphic to a normal Siegel domain D(VN,F). In this paper, we give the explicit formula of any holomorphic automorphism in T(D(VN, F)) and Iso(D(VN,F))(0), where G(0) is the unit connected component of the Lie group G.     

用于二聚物三能级蒸气激光系统的环形谐振腔设计

针对二聚物三能级蒸气激光系统增益相对于泵浦光方向显著的不对称特性,本文设计了一种稳定的能够充分利用介质增益特性的环形谐振腔,给出了象散和慧差补偿及泵浦激光与谐振腔匹配的条件。文中还给出了Na_2B~1Ⅱ_u-X~1∑_g~+跃迁激光谐振腔设计数据。     

线列阵甚宽频带恒定束宽的数字实现方法

线性嵌套阵可以很好地在很宽的频率（N个倍频程，N=7）上实现恒定束宽。这种方法设计简单，又节省线阵阵元。本文给出了线性嵌套阵具体的数字化实现方法，解决了FIR滤波器设计，滤波器时间延迟等问题。由于数字化实现过程中使用了很多组FIR滤波器，计算量很大，文章采用了DSP信号处理板实现数字化算法，利用DSP处理板可以多任务同时处理优势，解决了计算量大的问题。经过实验验证，在DSP上实现的数字化的线性嵌套阵宽带恒定束宽方法满足了工程上实时处理的需要。     

Enantioseparation of Dencichine and D-Isomer on L-Cysteine Derivative Phase by Ligand-exchange Chromatography

Dencichine (β-N-oxalyl-L-α, β-diaminopropionic acid, L-ODAP), a nonprotein amino acid, is a haemostatic agent present in important Chinese medicinal herbs such as Panax notoginseng, as well as other Panax species1. It was first isolated from the seeds …     

高抗冲聚丙烯序列结构的综合表征

用高分辨＾１３Ｃ ＮＭＲ、ＦＴＩＲ等手段获得了高抗冲聚丙烯的组成和序列分布等链结构方面的信息。用ＤＳＣ、ＷＡＸＤ等方法研究了它们的结晶行为、熔融转变及晶体结构，多种方法相结合有效地表征了高抗冲聚丙烯的序列结构。     

同输入M/M/∞排队群的联合队长过程

本提出一个偏微分方程方法，用这一方法研究同输入M/M／∞排队群中的联合队长分布。在任意初始条件下，给出了瞬时联合队长分布的多元母函数，也讨论了稳态队长的联合分布及各排队系统之间的相关性。     

Study on Inhibitors of Methionine Synthase Ⅷ: Synthesis of 2,5-Diamino-4-oxo-6- (3-butenyl) pyrimidine

Cobalamin-dependent methionine synthase plays a crucial role in folate metabolism and such would appear to be an excellent target for rational antifolate drug design. However, to date, no anticancer agents directed at this enzyme are available, but the enzyme is efficiently and specifically inhibited by N2O and this has proven invaluable for evaluating the biochemical consequence of enzyme inhibition and for mechanistic studies. [1,2] 2,5-Diamino-4-oxo-6-(3-butenyl) pyrimidine, a key intermediate in synthetic inhibitors of methionine synthase, was first synthesized using γbutenyl-β-ketoester and guanidine carbonate (Scheme 1). [3]     

Triterpenoid Constituents of Huperzia miyoshiana

Thirteen triterpenoids, including three new ones, miyoshianois A (1), B (2) and C (3), were isolated from Huperzia miyoshiana. The structures of these new compounds were established as 3-O-dihydroferuloyltohogenol (1), 16-oxo-3β,21β-dihydrox-y-serrat-14-en-24-ferulate (2) and 16-oxo-3a, 21β-dihydroxy-serrat-14-en-24-ferulate (3), respectively, on the basis of their spectroscopic analysis.