负催化吸光光度法测定锌

研究了在乙醇介质中Ｚｎ＾２＋对过氧化氢氧化甲基红褪色反应的负催化作用,提出了测定痕量Ｚｎ＾２＋的新方法,通过实验确定了最佳条件,方法简单,灵敏度高,用于水样中痕量Ｚｎ＾２＋的测定,结果满意。     

西加毒素(CTX)的电子结构及构效关系研究

应用MNDO方法对CTX衍生物进行了量子化学计算 ,得到了它们的电子结构信息.根据构象分析研究了它们的空间结构.推测出它们的活性部位 ,探讨了与受体结合时的作用方式 ,讨论了结构 -活性关系 ,解释了活性差异的原因.研究结果表明该类化合物的D、E、F环和A环及其支链等部位的不饱和键对活性有重要影响     

气相色谱法分析季戊四醇的一溴代、二溴代产物

 采用BPX 70毛细管色谱柱对季戊四醇的一溴代、二溴代和三溴代产物进行了分离 ,并对一溴代物、二溴代物进行了定量分析。方法快速、简便、准确度高。     

Synthesis of 3‐[5‐methyl‐1‐(4‐methylphenyl)‐1,2,3‐triazol‐4‐yl]‐6‐substituted‐s‐triazolo[3,4‐b]‐1,3,4‐thiadiazoles

Several 3‐[5‐methyl‐1‐(4‐methylphenyl)‐1,2,3‐triazol‐4‐yl]‐6‐substituted‐1,3,4‐triazolo[3,4‐b]‐1,3,4‐thiadiazoles have been synthesized and the structures of these compounds were established by elemental analysis, MS, IR and ¹H NMR spectral data.     

钨磷酸催化H2O2氧化降解壳聚糖

钨磷酸催化H2O2氧化降解壳聚糖;壳聚糖;钨磷酸;H2O2;催化降解     

General Formalism for Setting Up Unitary Transform Operators from Classical Transforms via IWOP Technique

We present a general formalism for setting up unitary transform operators from classical transforms via the technique of integration within an ordered product of operators, their normally ordered form can be obtained too.     

Raman microspectroscopic mapping or thermal system used to investigate milling‐induced solid‐state conversion of famotidine polymorphs

Confocal Raman microspectroscopy was used to nondestructively determine the polymorphic conversion of famotidine in the course of the milling process. A mapping system was applied to assess the blending uniformity of each polymorphic component in the milled mixture. Raman microspectroscopy combined with a thermal analyzer was also used to investigate the synergistic co‐effects of milling and heating on the polymorphic conversion of famotidine polymorphs. Famotidine has two polymorphs, forms A and B, the raw material of famotidine used was proved to be of form B. The Raman peak intensity ratio of the 2920 cm⁻¹ band for form A and 2897 cm⁻¹ band for form B was used to act as an indicator to evaluate the polymorphic conversion of famotidine form B to form A after different milling courses. The results indicate that the peak intensity at 2897 cm⁻¹ gradually decreased with the milling time, whereas the peak intensity at 2920 cm⁻¹ slowly enlarged, suggesting the polymorphic conversion of famotidine from form B to form A. The longer milling process might strongly induce and promote this polymorphic conversion of famotidine. Both polymorphic forms of famotidine were found to be well uniformly distributed within the milled samples due to their smaller varieties by using the Raman microscopic mapping system. The temperature effect could synergistically accelerate the polymorphic conversion of famotidine from form B to form A in the milled sample. The thermal‐dependent critical temperature for sharply enhancing the content of famotidine form A in each milled sample was also identified. Copyright © 2007 John Wiley & Sons, Ltd.     

尿素共沉淀法制备纤维状羟基磷灰石/壳聚糖复合粉料

尿素共沉淀法制备纤维状羟基磷灰石/壳聚糖复合粉料;壳聚糖; 羟基磷酸钙; 尿素共沉淀     

Preparation, Crystal Structure and Thermal Behaviour of a One-dimensional Coordination Polymer [Mn（m-CPOAH）2（H2O）2]n

1 INTRODUCTION Supramolecular chemistry of manganese(II) car- boxylate coordination polymers has been inten- sively studied in recent years, within which ligand design is an important aspect in adjusting the coordi- nation framework and functionalities of the complexes formed[1～4]. Carboxyphenoxyacetic acids (CPOAH2), which have been known to show biological activities and are widely used in agriculture, are a family of multidentate flexible ligands with versatile binding abilities. …     

锆对低温液相合成甲醇Cu-Cr催化剂性能的影响

Cu-Cr and Cu-Cr-Zr catalysts for the low temperature methanol synthesis slurry phase, with the surface area of 77.9 and 113.2 m2/g respectively, were prepared by the co precipitation approach. The activity and selectivity of these catalysts were evaluated in a stainless steel autoclave at 5.5 MPa and at different temperatures of 383 and 423 K separately. It was found that the activity of Cu-Cr-Zr catalyst was obviously higher than that of Cu-Cr catalyst, whereas the methanol selectivity of Cu-Cr-Zr catalyst was a little lower. The concentration of sodium compounds in the solution after reaction was also measured. The results showed that the concentration of sodium formate after reaction is much lower than that before reaction, which is quite different from the observations from the Cu-Cr catalyst previously. This implies that the conversion of sodium methoxide to sodium formate has been completely suppressed in the presence of zirconia in Cu-Cr-Zr catalyst. This finding is more beneficial to improve the performance of Cu-Cr catalyst and to increase the life of catalyst system as well.