Synthesis of differentially protected ribitol derivatives from 3,4-O-benzylidene-d-ribono-1,5-lactone

Several differentially protected ribitol derivatives were synthesised using 3,4-O-benzylidene-d-ribono-1,5-lactone as versatile starting compounds for oligosaccharide synthesis. The obtained ribitol derivatives allow the regiospecific coupling of glycosyl donors to either of the hydroxyl groups of ribitol and can be applied for the preparation of polyhydroxylated compounds.     

主成分回归-紫外光度法同时测定食用香料麦芽酚和乙基麦芽酚

报道了一种快速、简便的同时测定食用香料麦芽酚、乙基麦芽酚光度法,方法基于在pH2.87的B R缓冲溶液中对麦芽酚和乙基麦芽酚两组分混合溶液进行光度测定,所得的重叠波谱数据用主成分回归法(PCR)、经典最小二乘法(CLS)和偏最小二乘法(PLS)等化学计量学方法进行处理,结果表明主成分回归法(PCR)的预报误差最小。对样品进行测定,获得了较好的定量分析结果。麦芽酚和乙基麦芽酚的线性范围均为1.0～20.0mg·L-1;检出限分别为0.4347和0 5589mg·L-1。     

Oxidative Methyl Esterification of Primary Alcohols with Iodine‐Mediated Poly[4‐(Diacetoxyiodo)Styrene]

An operationally simple oxidative methyl esterification of primary alcohols in good yields using an iodine‐mediated poly[4‐(diacetoxyiodo)styrene] in methanol at room temperature is described. The polymeric reagent can be regenerated and reused as an environmentally benign reagent.     

消旋的有机二磺酸三邻菲咯啉锌配合物(英)

Compound [Zn(phen)₃][BDA] (1) (BDA=6,6′-dibromo-2,2′-dimethoxy-1,1′-binaphthylene-4,4′-disulfonate, phen= 1,10-phenanthroline) composes of the anion part (racemic-(R,S)-6,6′-dibromo-2,2′-dimethoxy-1,1′-binaphthylene-4,4′-disulfonate ) and the cation part which consists of a racemic octahedrally coordinated zinc center defined six nitrogen atoms from three phen rings to form an inorganic chirality that can be resolution by chiral organic ligand, the 3D framework was formed through the strong H-bonding interaction between sulfonate and water. CCDC: 277924.     

Structural and characteristic analysis of carbon nanotubes-ionic liquid gel biosensor

The structure and characteristic of carbon nanotubes-ionic liquid gel biosensor were studied by voltammetry, microscopy and spectroscopy. Various biomolecules were electrochemically detected with this gel biosensor such as glucose oxidase and NADH. The excellent electrochemical behavior of this gel biosensor might be due to the following three main factors: (1) the inherently perfect electrochemical characteristic of multi-wall carbon nanotubes (MWNTs); (2) the better solvent effect and conductivity of ionic liquid as well as the proper interactions between MWNTs and ionic liquid; (3) the proper mixing ratio of MWNTs to ionic liquid. Meanwhile, the interactions between MWNTs and ionic liquid were carefully studied as well. It can be concluded that the non-covalent (π–π) interaction between the imidazole loop of ionic liquid and MWNTs side wall should play an important role. This work gives a further understanding of what results in the high sensitivity and selectivity of such a biosensor to some biomolecules, and provides a simple and easy approach to design new biosensors with various nano-particles and versatile ionic liquid.     

Stability analysis of molality-based virial expansion GE-models

A stability analysis of a widely used model of the Gibbs energy of fluid mixtures is presented. In that model, the solutes and the solvent are treated differently (asymmetric normalization). For the solutes, an infinitely dilute reference state is used, the ideal solution is defined using molalities, and a virial expansion in molalities is used for describing the Gibbs excess energy G^E. That model is identical with the well-known Pitzer model if only uncharged molecular species are present. An unusual stability behavior of that model is observed. Instability is predicted for a wide range of concentrations in an important range of model parameters. Despite this, for principal reasons, that model does not allow determining the concentrations in coexisting phases in a physically meaningful way. For example, for binary systems it always predicts that only the pure components are globally stable. To illustrate those findings, the system hydrogen sulfide–water is discussed, for which the Pitzer model is often used in practice. For comparison with the Pitzer model the well-known Margules G^E-model is used that shows no unexpected stability behavior. Conversion rules are presented that allow finding parameters for the well-behaved Margules model from those of the Pitzer model. The application is again demonstrated using the system hydrogen sulfide–water.     

Isobaric vapour–liquid equilibria for binary mixtures of 1,2-dibromoethane with 1,2-dichloroethane,trichloromethane, and 1,1,2,2-tetrachloroethane at atmospheric pressure

Vapour–liquid equilibria at atmospheric pressure have been determined for binary mixtures of 1,2-dibromoethane + 1,2-dichloroethane, +trichloromethane, and +1,1,2,2-tetrachloroethane. These have been shown to be thermodynamically consistent.     

铂电极上异黄樟油和胡椒醛电氧化的SERS研究

采用循环伏安(CV)法和原位表面增强拉曼光谱(SERS)技术, 研究了非水体系中反应物异黄樟油和目标产物胡椒醛在粗糙铂电极上的电氧化行为, 发现胡椒醛在电位≥1.50 V时将进一步氧化, 而且从分子水平证实, 在胡椒醛的氧化电位(≥1.50 V) 下, 波长为632.8 nm的激光对胡椒醛的氧化有助催化作用. 由异黄樟油直接电氧化合成胡椒醛的电位(E)应控制在1.20 V相似文献   

2-溴丙酸气相热消除反应的机理

用密度泛函（DFT）方法,在B3LYP/6-31G**水平上对2-溴丙酸气相消除反应机理进行了研究.计算表明,反应主要是通过半极化五元环结构过渡态进行的,羧基上的氢原子协助溴原子离去,羧基氧原子帮助稳定过渡态.在B3LYP/6-311＋＋G(3df,3pd)水平上对B3LYP/6-31G**优化的几何构型进行了单点能计算,计算所得反应的速度控制步骤的活化能为189.461 kJ•mol－1,偏离实验值((180.3±3.4) kJ•mol－1)5.08％.     

新型含二茂铁有机配合物的合成及其电化学性质

以二茂铁为起始原料,经氯汞化反应、溴代反应、Suzuki偶联反应、水解反应和取代反应等5步反应合成了一种新型的含二茂铁结构单元的有机配合物(7),其结构经1H NMR、13C NMR、IR和HR-MS(ESI-TOF)表征。电化学研究结果表明:化合物6的E1/2小于化合物7,具有较高的氧化还原活性。