ADSORPTION OF MACROPOROUS PHOSPHONIC ACID RESIN FOR INDIUM

1. INTRODUCTION The research papers about synthesis characterization and adsorption property of polymeric materials have been reported in recent years [1~8]. Macroporous phosphonic acid resin (PAR) is a novel polymeric material which contains a functional group of [-PO(OH)2]. It has quite a lot of advantages such as high adsorption capacity, easy regeneration and convenient operation. PAR can be effectively used in the adsorption of metal ions. So far, however, there is no report abo…     

Synthesis,Biological Evaluation,and Crystallographic Studies of Extended Guanine‐Based (lin‐Benzoguanine) Inhibitors for tRNA‐Guanine Transglycosylase (TGT)

This paper describes the rational design, synthesis, and biological evaluation of a new generation of inhibitors of the bacterial enzyme tRNA‐guanine transglycosylase (TGT), which has been identified as a new target in the fight against bacillary dysentery (Shigellosis). The enzyme catalyzes the exchange of guanine in the anticodon wobble position of tRNA by the modified base preQ₁, a guanine derivative, according to a ping‐pong mechanism involving a covalent TGT‐tRNA intermediate (Fig. 2). Based on computer modeling (Fig. 3), lin‐benzoguanine (6‐aminoimidazol[4,5‐g]quinazolin‐8(7H)‐one ( 2 )) was selected as an extended central scaffold, to form up to seven in‐plane intermolecular H‐bonds with the protein while sandwiching between Tyr106 and Met260. Versatile synthetic protocols were developed for the synthesis of 2 , and derivatives with phenyl, benzyl, and 2‐phenylethyl side chains (i.e., 16, 17a , and 12a, 12b, 13, 17 , resp.) to reach into the lipophilic pocket lined by Val282, Val45, and Leu68 (Schemes 1–3). To account for the limited solubility of the new ligands and in consequence of a recently developed detailed understanding of the mechanism of TGT catalysis (Fig. 2), the enzyme kinetic assay was completely redesigned, providing competitive (K_ic) and uncompetitive (K_iu) inhibition constants with respect to tRNA binding by TGT. The modifications of the various parameters in the new assay are described in detail. Binding affinities of the new inhibitors were found to be in the single‐digit micromolar range (K_ic values, Fig. 8). Decoration of the lin‐benzoguanine scaffold with lipophilic residues only gave a modest improvement in biological activity which was explained on structural grounds with the help of four crystal structures (Fig. 10) obtained by soaking the protein with inhibitors 2 and 12a – 12c . Both biochemical and biostructural analyses reported in this paper provide a fertile basis for the development of more potent future generations of TGT inhibitors.     

碳酸盐碳,氧稳定同位素微量测试方法的研究

本文简要叙述了微量碳酸盐样品碳，氧稳定同位素测试对于古海洋学研究的重要性，着重介绍了该方法的原理，制样过程以及质谱测量，同时还介绍了微量测试几个方面的试验工作，并对影响微量测试的几种因素进行了探讨。     

A New Cyclic Bisdesmoside from Tubers of Bolbostemma paniculatum

The structure of tubeimoside V (1), a new cyclic bisdesmoside, isolated from tubers of Bolbostemma paniculatum (Tu Bei Mu), was established by means of 2D NMR spectral and chemical methods. Compound 1 has inter-saccharide chain bridging by a dicrotalic acid to form aunique macrocyclic structure.     

石墨炉原子吸收法连续测定气溶胶中重金属

提出了用石墨炉原子吸收法连续测定气溶胶中六种重金属的方法.气溶胶样品经处理后,直接用石墨炉原子吸收法测定其中的铜、钴、镍、镐、铅和铬.其检出限在 1.9×10~(-12)～1.6×10~(-10)g,仪器的精密度(RSD)<6.1%,标准加入回收率为90.4%～106.5%,已用于大批气溶胶样品的测定,结果令人满意.     

λ-卡拉胶有限水解物在蛋白质置换层析分离中的应用研究

λ－卡拉胶经过有限酸水解得到不同平均分子量的组分，选用平均分子量为21kDa的组分，作为蛋白质置换层析的置换制，用于纤维素酶的分离纯化。经过置换层析，使黑色葡萄状穗霉S607发酵液中难以通过常规的分子筛和离子交换层析分离的一个内切酶组分（EGⅢ）和一个β－葡萄糖苷酶组分得到较好的分离。     

PIV measurements of turbulent jets issuing from triangular and circular orifice plates

The present study experimentally investigated the near-field flow mixing characteristics of two turbulent jets issuing from equilateral triangular and circular orifice plates into effectively unbounded surroundings,respectively.Planar particle image velocimetry(PIV) was applied to measure the velocity field at the same Reynolds number of Re=50,000,where Re = UeDe /with Ue being the exit bulk velocity and the kinematic viscosity of fluid,D e the equivalent diameters.The instantaneous velocity,mean velocity,Reynolds stresses were obtained.From the mean velocity field,the centreline velocity decay rate and half-velocity width were derived.Comparing the mixing characteristics of the two jets,it is found that the triangular jet has a faster mixing rate than the circular counterpart.The triangular jet entrainments with the ambient fluid at a higher rate in the near field.This is evidenced by a shorter unmixed core,faster Reynolds stress and centreline turbulence intensity growth.The primary coherent structures in the near field are found to break down more rapidly in the triangular jet as compared to the circular jet.Over the entire measurement region,the triangular jet maintained a higher rate of decay and spread.Moreover,all components of Reynolds stress of the triangular jet appear to reach their peaks earlier,and then decay more rapidly than those of the circular jet.In addition,the axis-switching phenomenon is observed in the triangular jet.     

Moisture driven aging mechanism of LiFePO4 subjected to air exposure

The impact of air exposure on LiFePO₄–C nanocomposites has been investigated at moderate temperature. We show here that the storage in 120 °C hot air for 30 days leads not only to the material delithiation but also to the formation of an amorphous ferric phosphate side-phase, accounting for 38% of the total iron. The formed phase is found to be partially hydrated, suggesting a water-driven aging mechanism and a proposed hypothetic formula: Li_xFePO₄(OH)_x. The side-phase displays new electrochemical activity but poor cyclability and the overall battery performance is thus deteriorated. The regeneration of pristine structure, together with the performance recovery can be achieved by a simple thermal treatment under inert atmosphere.     

A practical mild, one-pot, regiospecific synthesis of 2,3-disubstituted indoles via consecutive Sonogashira and Cacchi reactions

[Structure: see text] A practical one-pot, regiospecific three-component process for the synthesis of 2,3-disubstituted indoles was developed via consecutive Pd-catalyzed Sonogashira coupling, amidopalladation, and reductive elimination.