三苯基膦

As to the catalytic coupling of aryl bromides, when triphenylphosphine as ligand and malononitrile as subtracts, their isolated yields were generally in 72-88%; While using cyanoacetate instead of malononitrile, the yields were in 67-84%.

当采用常见的三苯基膦为配体、对取代溴苯而言，以丙二腈为底物时，偶联产物的分离产率一般都在72-88％之间；以腈基乙酸乙酯为底物时，分离产率在67-84％之间。

Also, the type of dispersion of four gasliquid-liquid systems: air-decane-aqueous solution of sodium sulfite and surfactant, airmixture of decane and dodecene-aqueous solution of rhodium complex, ligand, and surfactant, air-mixture of decane, dodecene and tridecyl aldehyde-aqueous solution of rhodium complex, ligand and surfactant, and air-mixture of decane and dodeceneaqueous solution of trisodium salt of tri (m-sulfophenyl) phosphine, and surfactant is determined by electric conductivity.

本文采用电导率测量的方法实验研究了空气—正癸烷—亚硫酸钠和十六烷基三甲基溴化铵水溶液、空气—正癸烷和1-十二碳烯混合物—铑膦络合物催化剂和十六烷基三甲基溴化铵水溶液、空气—正癸烷、1-十二碳烯和十三醛混合物—铑膦络合物催化剂和十六烷基三甲基溴化铵水溶液、空气—正癸烷和1-十二碳烯混合物—三间磺化苯基膦三钠盐和十六烷基三甲基溴化铵水溶液四个三相体系的液液分散特性。当有机相与水相体积比分别为7／3、1／1和3／7时，前三个体系均形成水包油型分散，并有稳定的乳状液生成。

Hydroesterification of tert-butyl alcohol with ethanol catalyzed by transition metal triphenylphosphine complexes was first investigated in room temperature ionic liquids.

反应温度为100～140 ℃，CO初始压力为2～6 MPa条件下，研究了室温离子液体与过渡金属三苯基膦配合物构成的催化反应体系中，叔丁醇与乙醇的氢酯基化反应。

In this article, three novel cyclopalladated ferrocenylimine triphenylphosphine complexes 2-4 were easily synthesized and characterized by elemental analysis, IR, 1H NMR, 31P NMR and X-ray single crystal diffraction.

为筛选高效催化Suzuki反应的催化剂，合成了3种新的环钯化二茂铁亚胺-三苯基膦配合物2~4，经元素分析、红外光谱和核磁共振谱对其结构进行了表征，并通过X射线单晶衍射测定了化合物3的晶体结构。

Tungsten\|silver\|sulfur cluster ; crystal structure ; triphenylphosphine

钨银硫簇合物；晶体结构；三苯基膦

Methods 2-(piperazin-1-yl)-1-(pyrrolidin-1-yl)ethanone (2) was synthesized from pyrrolidine via amidation and substitution, followed by treating with chloroacetyl chloride and triphenylphosphine in a "one pot" manner to give the corresponding phosphonium chloride 3 in a stable and pure form after crystallization from isopropanol.

以四氢吡咯为原料，先与氯乙酰氯成酰胺，再与哌嗪发生取代反应制得中间体［（1-四氢吡咯基）甲基］哌嗪(2)；化合物2与氯乙酰氯和三苯基膦反应，经异丙醇重结晶得到稳定的有机鏻盐(3)；化合物3与3，4，5-三甲氧基苯甲醛发生Wittig反应，再与马来酸成盐得目标化合物马来酸桂哌齐特(1)。

A series of lanthanide complexes (Ln = Er, Nd, Yb) with infrared emission properties were designed and synthesized by using different anionic ligands [1 -phenyl-3-methyl-4-(4-tertbutylbenzoyl)-5-pyrazolone and l-phenyl-3-methyl-4--5-pyrazolone and 2-naphtoyl trifluoroacetone] and netural ligands (2,2-dipyridine, phenanthroline, triphenylphosphine oxide and water). Three crystal structures of these complexes were obtained and structure studied, and the properties of photoluminescence and fluorescent lifetime were studied in detail.

我们通过选用不同的第一配体[1-苯基-3-甲基-4-(4-异丁酰基)-5-吡唑酮，1-苯基-3-甲基-4-(4-叔丁基苯甲酰基)-5-吡唑酮和2-萘基三氟乙酰丙酮]和第二配体(2，2-联吡啶，邻菲啰啉，三苯基氧膦)合成了16个稀土红外配合物(Ln=Er，Nd，Yb)，获得了其中三个配合物的单晶结构，研究了这些稀土红外配合物的光致发光和荧光寿命等性质。

In this dissertation, preparation of polysubstituted ethene and heterocyclic compounds based on 2-hydroxyalkyl phenyl selenides andα-phenylselenopropionic acid reagents were further investigated as follow: Firstly, O-ethyl-O-vinyl phosphonates were prepared in a one-pot, two-step transformation by Mitsunobu reaction of 2-hydroxyalkyl phenyl selenides with monoethyl esters of phosphonic acid in the presence of diethyl azodicarboxylate and triphenyl phosphine (PPh3) followed by oxidation-eliminatio...

中文摘要：本文主要进一步探索了2-羟基烷基苯基硒醚、α-苯硒基丙酸试剂在制备多取代乙烯和杂环化合物反应中的应用，具体研究内容和结果如下：一、在偶氮二羧酸乙酯和三苯膦(PPh3)存在下，苯基-2-羟基烷基硒醚和O-乙基膦酸单酯发生Mitsunobu反应，无需分离和纯化反应中间体，直接使用30 %的双氧水进行氧化-消除反应，提供了&两步、一锅&合成O-乙基-O-乙烯基膦酸酯的新方法，该方法反应条件温和，操作简便，产物收率良好(76-82 %)。

A series of sulfonated poly(phthalazinone ether phosphine oxide)s were prepared via polycondensation of 4-(4-hydroxyphenyl) phthalazinone with sBFPPO and BFPPO.

通过将4-(4-羟基苯基)-2，3-二氮杂萘酮与二(4-氟苯)苯基氧膦和磺化二(4-氟苯)苯基氧膦单体共聚，制备了一系列磺化聚二氮杂萘酮醚三苯基氧膦。

On the contrary, sulfonated poly(arylene thioether phosphine oxide)s, with a IEC of 1.60 meq/g, even denote a swelling of 70.1% at 80oC and thus lose most of the mechanical strength.

而前述IEC为1.60 meq/g的磺化聚芳硫醚三苯基氧膦在80oC下的溶胀率为70.1%，已经出现溶胀突变，显著丧失力学强度，其耐溶胀性能比磺化聚二氮杂萘酮醚三苯基氧膦差得多。

What would he tell Judith and the children?

他将怎样告诉朱迪丝和孩子们呢？

I this is at that time, the opinion with peacockish true girl is full of in a heart.

这就是当时的我，一个心中布满虚荣的女孩子真实的想法。