二(2,4,4-三甲基戊基)膦酸萃取分离稀土元素(Ⅲ)的研究

本文研究了二(2,4,4-三甲基戊基)磷酸(Cyanex 272)的煤油溶液在不同介质(HCI,HNO_3)中对三价混合稀土的萃取分离性能.观测了平衡水相酸度对萃取平衡的影响,由酸度曲线求出相邻元素的平均分离系数,并考察了酸度对反萃取平衡的影响.比较了HCI和HNO_3介质中,Cyanex 272对混合稀土(Ⅲ)的萃取性能.     

Sesquiterpene esters from the fruits of Celastrus orbiculatus

Three new beta-dihydroagarofuran sesquiterpene esters, 6 alpha-acetoxy-9 beta-benzoyloxy-1 beta-cinnamoyloxy-8 beta-butanoyloxy-beta-dihydroagarofuran (1), 6 alpha-acetoxy-9 beta-benzoyloxy-1 beta-cinnamoyloxy-8 beta-(2-methylbutanoyloxy)-beta-dihydroagarofuran (2), and 6 alpha-acetoxy-1 beta,8 beta-dibenzoyloxy-9 beta-hydroxy-beta-dihydroagarofuran (6), together with three known compounds (3-5) were isolated from the fruits of Celastrus orbiculatus THUNB. Their structures were elucidated on the basis of spectroscopic methods. Compound 4 showed moderate activity in inhibiting LPS-induced nitric oxide production in murine macrophage RAW264.7 cells with an IC(50) value of 43.7 microM.     

菲林B近红外分光光度法测定维生素C

在pH 3的三氯乙酸酸性介质中,菲林B可以定量地将还原型维生素C氧化成脱氢型维生素C,利用脱氢型维生素C在920 nm处有最大吸光度,测定其含量,建立了一种测定维生素C的新方法,并研究了影响反应的各种因素。该方法对维生素C的检出限为0.17 mg/L;线性范围为0.5~10 mg/L,对水果中维生素C含量测定的RSD<2.31%;回收率为99.7%~101.1%,比2,4-二硝基苯肼分光光度法测定结果的相对偏差<±1.6%。     

新的不对称双Schiff碱镍配合物

乙二胺中2个氨基具有相同的反应活性,易同时反应形成对称的双Schiff碱,随着不对称配合物的设计和金属酶模型化合物的不断开发,业已发现严格控制反应条件和改变反应物摩尔比,可以有效地实现单个氨基的选择性反应,例如,在低温、稀的反应液中,乙酰丙     

链状[NH3CH2CH2NH3]AgAsS4的溶剂热合成及表征

利用溶剂热方法合成了链状[NH3CH2CH2NH3]AgAsS4,通过单晶X射线衍射技术对其进行了晶体结构分析,该化合物晶体属单斜晶系,空间群C2/c,晶胞参数a=1.35805(8)nm,b=0.65331(3)nm,c=2.27711(9)nm,β=106.42(3)°,Z=8.化合物具有有趣的梯子状双链结构,该阴离子链由AsS4与AgS3共用顶点交替连接而成,有机阳离子在阴离子链之间存在较强的N—H…S氢键.DSC和Tg分析结果表明化合物在200℃以下是稳定的.     

手性配体的空间结构与产物对映选择性的关系

首次采用4－烷氧羰基噻唑烷、E唑烷作为手性配体，诱导烷基锌对醛类的亲核加成反应，获得产物是烷基化的醛，最高达90％ee，产率98％的（S）－二级醇。系统地考察了该类手性配体三维空间结构变化与产物对映选择性的关系，当配体4－位烷氧羰基上的R、2－位R′基和环体上原子X发生变化时都会引起产物（S）－二 级醇的对映选择性发生规律性变化。对五种不同结构的底物醛在同一手性配体催化下，诱导烷基锌对醛类的亲核加成反应，底物结构变化也会引起（S）－二级醇对映选择性变化。     

铅、汞、镉离子的荧光传感器研究进展

化学传感器提供了方便、快捷、廉价的分析检测有毒重金属离子的方法,并具有很高的灵敏度和选择性.它在环境科学、分析化学以及生命科学等领域有广泛的应用前景.本文分别综述了pb²⁺、Hg²⁺、Cd²⁺几种有毒重离子化学传感器的最新研究进展,并展望了该领域的发展趋势.     

Light- and temperature-assisted spin state annealing: accessing the hidden multistability

Among responsive multistable materials, spin crossover (SCO) systems are of particular interest for stabilizing multiple spin states with various stimulus inputs and physical outputs. Here, in a 2D Hofmann-type coordination polymer, [Fe(isoq)₂{Au(CN)₂}₂] (isoq = isoquinoline), a medium-temperature annealing process is introduced after light/temperature stimulation, which accesses the hidden multistability of the spin state. With the combined effort of magnetic, crystallographic and Mössbauer spectral investigation, these distinct spin states are identified and the light- and temperature-assisted transition pathways are clarified. Such excitation-relaxation and trapping-relaxation joint mechanisms, as ingenious interplays between the kinetic and thermodynamic effects, uncover hidden possibilities for the discovery of multistable materials and the development of multistate intelligent devices.

Two new two-stage manipulation protocols, namely light- and temperature-assisted spin state annealing (LASSA/TASSA), are applied to a spin crossover coordination polymer, [Fe(isoq)₂{Au(CN)₂}₂], revealing the hidden multistability of spin states.     

Two salts of 5‐sulfosalicylic acid and 3‐aminopyridine

5‐Sulfosalicylic acid (5‐SSA) and 3‐aminopyridine (3‐APy) crystallize in the same solvent system, resulting in two kinds of 1:1 proton‐transfer organic adduct, namely 3‐aminopyridinium 3‐carboxy‐4‐hydroxybenzenesulfonate monohydrate, C₅H₇N₂⁺·C₇H₅O₆S⁻·H₂O or 3‐APy·5‐SSA·H₂O, (I), and the anhydrous adduct, C₅H₇N₂⁺·C₇H₅O₆S⁻ or 3‐APy·5‐SSA, (II). Both compounds have extensively hydrogen‐bonded three‐dimensional layered polymer structures, with interlayer homo‐ and heterogeneous π–π interactions in (I) and (II), respectively.