超声雾化进样微波诱导等离子体原子吸收光谱法测定银的某些影响因素研究

本文将超声雾化技术与MIP-AAS联用,以“L”型吸收管代替“T”型吸收管作为AAS测量的吸收池,采用水冷凝和浓H_2SO_4吸收相结合去溶,研究TUSN-MIP-AAS方法测银时的某些影响因素,讨论了微波前向功率,载气流速、去溶系统、溶液酸度、共存离子及易也离元素等对吸收信号的影响,本法所得的测银的特征浓度为0.01μg/ml(328.1nm)和0.03μg/ml(338.3nm),相对标准偏差为7.5％.     

Electrochemical study on the keto-enol tautomerization of p-hydroxyphenylpyruvic acid in aqueous solution

The keto-enol tautomerization of p-hydroxyphenylpyruvic acid (pHPP) in aqueous solutions and the complexation reaction between enolic pHPP and boric acid have been studied by electrochemical techniques including linear sweep voltammetry (LSV), pulse voltammetry, and cyclic voltammetry (CV), combining with UV spectrometry. Electrochemical techniques reveal that in aqueous solution, there are two tautomers of pHPP: enolic form and ketonic form; the former exists mainly in freshly prepared pHPP solution, and the latter exists mainly in equilibrium solution. Both enolic and ketonic pHPP are electroactive. The electrochemical oxidation of enolic pHPP gives rise to two anodic waves, I(a) and II(a), while the electrochemical oxidation of ketonic pHPP only results in the observation of the second wave II(a). The oxidation process I(a) is revealed to be associated with the quasi-reversible, two-electron two-proton oxidation of "C=C"group at the side chain of enolic pHPP, and the oxidation process II(a) is proposed to result from the irreversible oxidation of phenolic hydroxyl group. It is observed that in aqueous solution, enolic pHPP can quickly complex with boric acid to yield enol-borate complex that can also oxidize at a glassy carbon electrode to yield an anodic wave.     

Phase transition in single crystal Cs2Nb4O11

We studied temperature dependence of complex capacitance, impedance, and polarized Raman spectra of single crystal Cs2Nb4O11. First, we observed a sharp lambda-shaped peak at 165 degrees C in the complex capacitance, then found drastic changes in the Raman spectra in the same temperature range. Utilizing the pseudosymmetry search of structure space group, we attributed the observed anomalies to a structural change from the room temperature orthorhombic Pnn2 to another orthorhombic Imm2. We also measured room temperature polarized Raman spectra in different symmetries of normal vibrations and assigned high wavenumber Raman bands to the internal vibrations of NbO6 octahedra and NbO4 tetrahedra.     

六味地黄丸的精细指纹图谱分析及模式识别分类研究

采用高效液相色谱建立了六味地黄丸的指纹图谱,对两个厂家的16批产品进行了测定,并结合中药相似度软件和主成分分析法对全指纹图谱和其精细指纹图谱进行了模式识别研究。结果表明,中药相似度软件能够对不同厂家的产品进行区分但也可能造成误判;在主成分分析法的投影图中,两个厂家的产品明显聚为两类,而且不同批次产品的差异也能够显示出来。     

Synthesis of a new class of conformationally rigid phosphino-oxazolines: highly enantioselective ligands for Ir-catalyzed asymmetric hydrogenation

[reaction: see text] A new class of conformationally rigid phosphino-oxazoline ligands were synthesized from readily available enantiopure phenyl glycinol. Ir complexes with these ligands are air-stable and highly enantioselective catalysts for asymmetric hydrogenation of aryl alkenes and alpha,beta-unsaturated esters in up to 99% ee.     

牙本质中天冬氨酸消旋化程度的测定——手性毛细管气相色谱法与高效液相色谱法的比较

应用手性毛细管气相色谱法（酸性异丙醇、三氟乙酸酐为衍生试剂）、高效液相色谱法（邻苯二甲醛－Ｎ－乙酰－Ｌ－半胱氨酸为手性衍生试剂）同时测定人类第一磨牙牙本质中天冬氨酸的消旋化程度，结果表明，两者均可有效地用于天冬氨酸对映体的分离测定，但气相色谱检测限（０．２ｐｍｏｌ）低于高效液相色谱（１．０ｐｍｏｌ），而变异系数（７％）、总分析时间（１００ｍｉｎ）均高于高效液相色谱（分别对应为４％，３１ｍｉｎ）。     

Efficient synthesis of p-bis-(chlorodifluoromethyl)benzene

Selective, high yield partial fluorination of p-bis-(trichloromethyl)benzene to p-bis-(chlorodifluoromethyl)benzene has been accomplished by warming a slurry of the p-bis-(trichloromethyl)benzene in anhydrous HF which also contains a small quantity of inert solvent, such as 1,2-dichloroethane.     

化学专业生物化学课程教学内容和教学方法研究

本文是笔者在长期教学实践的基础上，对于化学专业生物化学课程教学内容和教学方法，研究的经济总结。其相关成果曾获陕西师范大学优秀教材一等奖及陕西省教学成果二等奖。     

铋（Ⅲ）—溴邻苯三酚红配合物吸附波及其应用

铋（Ⅲ）－溴邻苯三酚红配合物吸附波及其应用＊刘家欣段友构黄诚朱苗力（吉首大学化学系湖南吉首４１６０００）匡向阳（永州市水文站湖南永州４２５０００）关键词铋溴邻苯三酚红配合物吸附波中图分类号Ｏ６５７．１４近年来，在某些有机试剂存在下用极谱法测定铋已有一...     

低头-头链含量的聚偏氟乙烯合成

研究了偏氟乙烯的聚合条件与其聚合物的头-头链含量的关系。实验表明聚合物的头-头链的含量与聚合温度有关,而与引发剂的种类无关。因而,可以在较低的聚合温度下聚合制得带有低的头-头结构(约3％)的聚偏氟乙烯。将聚合物链的A结构含量对其熔点作图,得一直线,可表示为方程式A=24.8+0.362T_m(％)。