吡啶

The reactivities of the phenyl boronic acids containing di-, tri-fluoro substituents with pyridyl bromide were investigated in different catalyst system.

利用钯催化的SUZUKI偶联反应，以氟取代的苯硼酸与2-溴吡啶为原料合成了系列新的邻吡啶芳香化合物，研究了二及三氟取代的苯硼酸与溴代吡啶在不同催化体系中的反应性质。

Using pyridine-2, 6-dicarboxylic acid as starting material, a novel ligand N^2, N^6-bis(3-methyl-pyridine-2-yl)-pyridine-2, 6-dicarboxamide was synthesized, which contained multidentate and large conjugative system.

以吡啶－2，6-二甲酸为原料，合成含有多个共轭体系多齿配体N^2，N^6-二（3-甲基吡啶）－2-取代吡啶－2，6-二甲酰胺；同时制备它与稀土离子Tb和Eu的配合物，并培养出单晶。

In this paper, a series of thermal stable PTC based on dimethylamino pyridinium salts were synthesized and characterized by 〓HNMR, mp, IR, and MS.

由于4-二烷基氨基吡啶中供电子的二烷基与吡啶环共振，使正电荷分散于多个原子中，稳定性比吡啶增加。

Three novel hemicyanine derivatives,-N-(4-sulfopropyl)-4-[2-(4- N, N-diethylaminophenyl)-ethenyl]pyridinium,-N-(4-suMbbutyl)- 4-[2-(4-N, N-diethylaminophenyl)ethenyl]pyridinium (EPS4), and-N-(4- su)fobutyl-4-[2-(4-N, N-diethylaminophenyl)ethenyl]quinolinium (EQS4) with different length of alkyl chains between the adsorbing group (RSO3-) and the chromophore group, were synthesized and their photophysical and photoelectrochemical properties were studied.

设计合成了具有不同空间位阻的吡啶盐类和喹啉盐类半菁染料-N-(4—磺酸根丙基)-4-[2-4（4-N，N-二乙基氨基苯基）乙烯基]吡啶鎓盐，-N-4-磺酸根丁基）-4-[2-(4-N，N-二乙氨基苯基）乙烯基]吡啶鎓盐（EPS4）和-N-（4-磺酸根丁基）-4-2-（4-N，N-二乙基氨基苯基）喹啉鎓盐（EQS4），研究了它们的光物理性质，并将它们用作TiO2纳米晶电极的光敏化剂引入光电化学电池中。

The outward rectifier K+ current current was the dominant K+ current in the whole cell currents in Deiters' cells. In the presence of 200μ M linopirdine, the Ik current was not significantly effected. Our findings demonstrated that the KCNQ heteromeric or homomeric potassium channel may be the molecular basis for the peak outward K+ current and testified that the inward IKn current is mediated by KCNQ potassium channel.

在细胞外液中，加入100 μmol/L利诺吡啶后，OHCs中的四乙基二乙胺敏感的钾电流峰电流成分被抑制，稳态电流幅值减小，且电流的失活时间常数明显延长；在细胞外液中加入100 μmol/L和200 μmol/L利诺吡啶后，OHCs的内向性钾电流IKn被完全抑制；而细胞外液中利诺吡啶终浓度为200 μmol/L 时，Deiters细胞的外向整流性钾电流幅值无明显变化。

Using pyridine-2, 6-dicarboxylic acid as starting material, a novel ligand N2,N6-bis(3-methyl- pyridine-2-yl)-pyridine-2, 6-dicarboxamide was synthesized,which contained multidentate and large conjugative system.

摘 要：以吡啶-2， 6-二甲酸为原料，合成含有多个共轭体系多齿配体N2，N6-二(3-甲基吡啶)-2-取代吡啶-2， 6-二甲酰胺；同时制备它与稀土离子Tb和Eu的配合物，并培养出单晶。

Moreover, seven ruthenium phenanthroline derivatives were also synthesized. The synthesis of Ru3Cl2 and Ru2AqphenCl2 have not yet been reported, and a new and effective method for the synthesis of Ru32 was also investigated.

本文第二章主要内容是以邻菲咯啉为原料，合成四种刚性结构强的邻菲咯啉衍生物：二吡啶基吩嗪，四吡啶基吩嗪， 10.11-1.4-萘酮－2，3；2'，3'－二吡啶基吩嗪，对羟基苯基并[4，5]-邻菲咯啉。

Picolinic acid∶Eu3+ complex synthesized in aqueous solution was determined by DTATG, ultraviolet absorption spectra and infrared spectra.

通过差热－热失重、红外光谱和紫外光谱等测试手段，对溶液中合成的吡啶－2－羧酸∶Eu3＋配合物进行了表征，并且通过原位合成方法在SiO2凝胶中合成了吡啶－2－羧酸∶Eu3＋配合物，与溶液中合成的吡啶－2－羧酸∶Eu3＋配合物进行了对比。

For three different reaction paths leading to ortho, meta, para-chloropyridine, two transition states have been located by PM3 on each reaction path, while only one transition state by ab initio, however both methods give the same results: the energy of transition state and activation barrier on producing 2-chloropyridine are the lowest among three reaction paths, so 2-chloropyridine is obtained priorly, which agrees with the experimental results.

生成邻、间、对氯代吡啶三条不同反应途径PM3方法优化得到两个过渡态，而从头算方法中只优化得到一个过渡态。但两种方法的研究结果均表明：三条反应途径中生成2-氯吡啶的过渡态能量和活化能最低，因此反应优先生成2-氯吡啶，与实验结果一致。

Adjacent helical chains are racemic. The Ag atom is linked to two nitrogen atoms of the 2-pyridyl and 4'-pyridyl groups from two different 2,4'-bpy ligands as well as to the oxygen atom of the counterion. In 17 and 19, the adjacent helical chains are linked to wavy two-dimensional network structures by the nitrate counterions.

相邻的螺旋链间是外消旋的，Ag 原子与分别来自两个不同2，4'-联吡啶的2-吡啶基和4'-吡啶基的氮原子以及阴离子的氧原子配位，在配合物17和19中，相邻聚合螺旋链被硝酸根离子桥连接起来，变成了一个波浪形的二维网络结构；配合物18是首次通过无桥连配体支持的Ag ××× Ag键将相邻螺旋链连接成二维非穿插的网络结构。

Fancy gold-plated dangling earrings with facetted White Opal crystals.

花式镀金悬垂耳环与facetted白欧泊水晶。

This essay chooses the study aim from biology teachers in middle school in Shi Jiazhuang which tells us that most of the middle school biology teachers in Shi Jiazhuang have the"burnout", lower successfulness, individualize.

本文选取石家庄市初中生物教师作为研究对象，运用问卷调查的方法对石家庄市初中生物教师职业倦怠的现状进行调查，调查结果发现，石家庄市初中生物教师这一群体普遍存在职业倦怠，情感枯竭程度偏高，成就感偏低，去个性化程度最为严重。