羰基镍分析报警仪

羰基镍分析报警仪运用化学发光原理构成，不仅适用于羰基镍生产车间现场的检测和报警，也适于实验室的研究工作。检出限达0.037mg/m^3(0.5ppb），响应时间2min。     

The particular role of radiopharmacy within bioorganometallic chemistry

This article will emphasize the particular role of organometallic radiopharmaceutical chemistry, namely the need for syntheses from water and the emerging implications for other (bio)organometallic fields. After some basic insights into the different directions of bioorganometallic chemistry, some facets of the [M(CO)₃]⁺ (M = Tc, Re) moiety are reviewed and discussed in the respective context. The mechanism for the synthesis of [M(OH₂)₃(CO)₃]⁺ which is still little understood, will be touched. The formation of additional M-C bonds is exemplified with cyclopentadienyl chemistry, the potential impact on targeted molecular imaging with the labelling of amino acids and the reactivity towards essential biomolecules such as guanine is shown. Future perspectives and implications for organometallic radiopharmaceutical chemistry will close this article.     

分子筛笼内金属羰基簇合物的热稳定性研究

本实验采用戊马比妥钠诱发豚鼠和家兔急性心力衰竭模型，观察了舒心丸的治疗作用。结果表明，舒心丸ｉｖ能明显升高心衰豚鼠的心脏收缩幅度和心衰家兔的Ｂｐ，ＬＶＰ，ＬＶ±ｄｐ／ｄｔ和ＣＯ。其作用与哇巴因相似。     

助熔剂N_aCl－CdCl_2对CdS∶Cu，In结晶状态作用规律研究

发现在确定的热处理温度和时间下，随炉料中助熔剂ＮａＣｌ－ＣｄＣｌ２，总含量的增加，ＣｄＳ：Ｃｕ，Ｉｎ多晶的粒度分布变窄，数均粒径具有最大值，晶粒外型趋于规整且表面平滑．进而证明，多晶的结晶状态对其光电性能具有显著的影响．     

简便快速的硫化氢测定法

本文提出了有一种简易快速测定剂来测定水样中的硫化氢的方法。该法的检出限为０．１ｍｇ／Ｌ，对１．０１ｍｇ／Ｌ的Ｈ２Ｓ样品７次测定的相对标准偏差＜４．１％，１ｈ能测定１２个样品。用本测定了几种水样中的Ｈ２Ｓ含量，回收率为８４％－１０５％。应用它可上标准法的４ｈ左右缩短到５ｍｉｎ；使分析成本降低９／１０；不需配制一系列分析试剂和仪器，只需一支小型塑料管和几片药片，便于渔业水质和环境水质的野外现场监测。     

碱改性γ－Al_2O_3催化剂表面碱强度分布与COS水解活性的研究

用非水滴定法和Ｈａｍｍｅｔｔ系列指示剂测定了ＣＯＳ水解碱改性γ－Ａｌ_２Ｏ_３催化剂的表面碱强度分布．发现表面碱强度分布不均匀与表面能量分布不均匀相呼应．采用零点酸碱强度（Ｈ_（０，ｍａｘ））及碱中心区域分析法，Ｂｒｏｎｓｔｅｄ催化定律，进一步证实ＣＯＳ水解反应具有明显碱催化特征，较高活性催化剂的Ｈ_（０，ｍａｘ）一般为１０左右，对ＣＯＳ水解反应起主要作用的碱性中心的碱强度（Ｈ_０）为４．８≤Ｈ_０≤９．８．对碱金属氧化物改性后的γ－Ａｌ_２Ｏ_３催化剂，Ｂｒｏｎｓｔｅｄ规律在每个碱强度分区域内是适用的．     

Chiral Recognition in π Complexes of Alkenes,Aldehydes, and Ketones with Transition Metal Lewis Acids; Development of a General Model for Enantioface Binding Selectivities

Prochiral alkenes, aldehydes, and ketones constitute the most frequently used starting materials for enantioselective organic syntheses. Protocols often involve chiral binding agents or Lewis acids that can give two diastereomeric adducts, the ratios of which are measures of chiral recognition. With π adducts, the diastereomers differ in the enantioface of the C?C or O?C group bound to the Lewis acid. This review provides the first comprehensive analysis of such equilibria and related binding phenomena with chiral transition metal Lewis acids. An extensive body of data from the authors' laboratory for complexes of the pyramidal rhenium fragment [(η⁵?C₅H₅)Re(No)(PPh₃)]⁺ ( I ) affords particular insight. Literature data for other complexes are also summarized. A general model for chiral recognition based upon the relative steric properties of four quadrants is presented. This enables binding selectivities to be individually and rationally optimized for different classes of ligands. Electronic effects are also identified and correlated with specific structural properties. Relationships between binding equilibria, reactivity, and product configurations are discussed.     

聚-4,7-二硫杂壬基倍半硅氧烷铑配合物的合成与催化硅氢化性能

本文叙述了一种新型有机硅聚合物负载配位催化剂——聚-4,7-二硫杂壬基倍半硅氧烷铑配合物的合成、结构及其对烯烃硅氢化反应的催化性能.标题配合物在用量为烯烃摩尔量的十万分之一时仍具有良好的催化活性,烯烃的转化数达到80,000.     

选择性氧化含氰基的对硝基苯硫醚

选择性氧化含氰基的对硝基苯硫醚岳国仁，王建华，张正（南京大学化学系南京２１０００８）关键词含氰基硫醚，选择性氧化，四水合过硼酸钠据报道［１］对硝基苯磺酰基乙腈的合成，反应时间长，可采用四水合过硼酸钠（ＮａＢＯ３·４Ｈ２Ｏ）作为氧化剂，受到重视［２，３...     

Kinetics and mechanism of gold dissolution in thiourea solutions: Effect of sulfide ions

Chronoamperograms for gold in solutions containing 0.1 M thiourea, 0.5 M H₂SO₄, and catalytically active sulfide ions at the concentration c ₁ from 1 × 10^?5 to 4 × 10^?5 M are obtained at different potentials with the aid of an automated setup intended for renewing the electrode surface directly in the solution by cutting off a thin surface layer of the metal. It is shown that the results of measurements of the current practically coincide at a constant value of the product c ₁ t, where t is the time period elapsed after the renewal of the electrode surface. Such a coincidence testifies to a diffusion nature of processes that hamper accumulation of sulfide ions at the gold surface. This fact permitted the use of a procedure developed previously for the calculation of polarization curves at constant values of surface coverage θ by catalytically active ions. At θ = const, the voltammetric curves for gold in sulfide-containing thiourea solutions are shown to correspond to the Tafel equation. With the surface coverage increasing, the effective values of the exchange current i ₀, transfer coefficient α, and anodic reaction order with respect to thiourea P _a increase from the values i }~ 10^?5 A cm^?2, α }~ 0.12, and P _a = 0.2, which are characteristic of pure solutions, to 2 × 10^?4 A cm^?2, α }~ 0.5, and P _a = 1.1 (at θ }~ 0.5). An interpretation to the established regularities is given.