三羧基的

基本解释 (translations)

tricarboxylic

与三羧基的相关的网络例句 [注：此内容来源于网络，仅供参考]

The biological activity tests show that some target compounds have a good activity as plant growth regulator, and N-5-(3-carboxy-1H-1,2,4-triazolyl)-N'-o- chlorophenylfonnyl urea, N-5-(3-carboxy-1H-1,2,4-triazolyl)-N'-o- bromophenylformyl urea, N-5-(3-carboxy-1H-1,2,4-triazolyl)-N'-p- methyl-phenyl formyl urea have excellent activity of auxin.

生测试验证明部分酰基脲类化合物具有良好的植物生长调节活性，其中N-5（3-羧基-1，2，4-三唑基）-N'-o-氯苯甲酰基脲、N-5-（3-羧基-1，2，4-三唑基）-N'-o-溴苯甲酰基脲和N-5-3-羧基-1， 2，4-三唑基）-N'-p(或m-甲基苯甲酰基脲具有优良的生长素活性。

The copper atom is in a planar coordination site of [N_2O_2] and it devites from the mean plane by only 0.80 pm. Byπ-πstacking interactions, a alabastrine structure was obtained.(2)Schiff-base complex [Cu(H_2O)]·H_2O, where H3GS is the 3-carboxyl -salicylidene glycine, was synthesized and characterized by elemental analysis, IR spectra and single-crystal analysis. The crystal belongs to monoclinic system, space group P2(1)/c, a=848.46(3)pm, b=681.54(3)pm, c=1967.16(8)pm,β=95.8210(10)°, Z=4, R_1=0.0279, wR_2=0.0724. The copper atom is in a square-pyramidal field with the base

结果表明该晶系属单斜晶系，空间群P2(1)/c，晶胞参数：a=848.46(3)pm，b=681.54(3)pm，c=1967.16(8)pm，α=90°，β=95.8210(10)°，γ=90°，Z=4，R_1=0.0279，wR_2=0.0724，Cu原子位于轻微变形的四方锥场底心，底面被氮原子、酚氧原子、甘氨酸羧基的一个氧原子和一个水分子氧原子占据，而甘氨酸羧基的另一个氧原子占据相邻分子的锥顶，因而形成一维链状结构；合成了单核双聚配合物Na_2[Cu_2_2]·2H_2O ，铜三核配合物Cu_3_2·5H_2O和铜锌异三核配合物ZnCu_2_2·5H_2O，并用元素分析，IR光谱，电子光谱和磁化率测定对配合物的组

A small molecule core (TMP-SK3)with three terminal carboxyl groups was synthesized successfully by the reaction of 1,1,1-trihydroxymethylpropane with the excessive sebacic acid diacetic anhydride.

以1，1，1-三羟甲基丙烷与过量癸二酸二乙酸酐反应，制得了端羧基的三官能度小分子核三癸二酸三羟甲基丙烷酯（TMP-SK3）。

In the structures of these complexes, zinc can act as the vertex of the networks in various styles: single atom; dicarboxylate, tricarboxylate or tetracarboxylate bridged binuclear SBU ; and octacarboxylate bridged trinuclear SBU.

在这些配合物的结构中，锌离子可以按多种形式作为网络结构的顶点：单原子，双羧基、三羧基或四羧基桥连的双核锌次级结构单元，八羧基桥连的三核锌次级结构单元，再与配体组装成不同的配位聚合物网络。

In this thesis, a series of complexes based on aromatic multicarboxylic acids have been successfully synthesized in solutions or under hydrothermal conditions. Their structure and properties are investigated.(1) Eight complex compounds have been synthesized and characterized by X-ray single crystal diffractive technology: The eight complexes are listed as following: [Cu242] complex 1 [Cd22(H2O)4]·4H2O complex 2 [Co(H2btc)(H2O)3] complex 3 [Co2(H2O)2]·H2O complex 4 [Ni22(H2O)4] complex 5 [Cu22(H2O)4] complex 6 [Co(H2biim)2(H2O)2](H2btc) complex 7 [Zn(H2biim)2(H2O)2](H2btc) complex 8 The structure of complex 1 is dinuclear complex resulted from weak interactions（0-D chain）; complex 2 is 1-D chain stucture result from interactions of water molecules; complex 3、4、5、6 are coordination polymers using hydrothermal synthses, where the first kind ligand is H4btc, the second kind ligand is phen and Co2+、Ni2+、Cu2+ as center ions, respectively. While the coordination enviroment of Co2+ is the same in complex 3, the coordination geometries around the Co atoms in complex 4 are obviously different because of the different reaction conditions. In complex 4, the 1-D chains are connected into 2-D layer through carboxy groups of ligand H4btc. The structures of complex 5、6 are 1-D chain stucture result from interactions of carboxy groups in ligand H4btc. Complex 7、8 are homeomorphy compounds. Either of them are linked to the 3-D chains through intermolecular hydrogen bonds. Each H4btc lose two protons and H2btc2- acts as negative electron balance.

合成了8个结构新颖的配合物，并用X-射线单晶结构分析方法确定了晶体结构，分别为： [Cu242] 配合物1 [Cd22(H2O)4]·4H2O 配合物2 [Co(H2btc)(H2O)3] 配合物3 [Co2(H2O)2]·H2O 配合物4 [Ni22(H2O)4] 配合物5 [Cu22(H2O)4] 配合物6 [Co(H2biim)2(H2O)2](H2btc)配合物7 [Zn(H2biim)2(H2O)2](H2btc)配合物8 配合物1是一个依靠弱作用连接的双核铜结构；配合物2借助水分子形成一维链状结构；配合物3、4、5、6是以H4btc为第一配体、phen为第二配体，通过水热法合成的配合物，其中，Co2+、Ni2+、Cu2+为中心离子；配合物3中的二价钴离子具有相同的配位环境，不同反应条件下得到的配合物4中的二价钴离子存在不同的配位环境，在配合物4中，一维链通过H4btc上的羧基形成一个二维层结构；配合物5、6是借助H4btc上的羧基形成的一维链状结构；配合物7、8属于异质同晶结构，它们的分子通过分子间氢键形成三维网状结构，H4btc上的羧基失去2个质子，作为一个二价负离子起到电荷平衡作用。

In - situ photoelectrochemical microscopic method has been used to characterize the spatial variation of the film formed on the copper surface in buffer - borax solutions (pH 9.2) with different concentration of benzotriazole and combined benzotriazole methanoic acid ester .

采用激光扫描微区光电化学显微技术对不同浓度下的苯并三氮唑及其衍生物4-羧基苯并三唑甲酯与5-羧基苯并三唑甲酯的混合物在硼砂缓冲溶液(pH9.2)中对铜电极的缓蚀作用作了比较研究。

When the concentration of zinc nitrite is lower than 0.1 M,(002) is the prior face for zinc oxide. As the concentration raise, the other kinds of crystal face would appear. Among those data,(002) grows the best when the concentration of zinc nitrite is 0.06 M. We add lactic acid and citric acid respectively; there is an carboxyl group on the lactic acid and three carboxyl groups on the citric acid. The monodentate of lactic acid helps the growth of zinc oxide, compared to the tridentate of citric acid which can only produce zinc oxide film under very low concentration, but the growth of (002) face is not that stable as adding the lactic acid and zinc will electrodeposit to substrate.

实验中，当硝酸锌浓度低於0.1 M 时，氧化锌以(002)面为优选位相，当浓度提高，其他晶面将会出现，当硝酸锌为0.06 M，(002)晶面成长最佳，分别加入乳酸和柠檬酸，乳酸结构上有一羧基团而柠檬酸有三个羧基团，单芽基的乳酸有助於氧化锌成长，对照於三芽基的柠檬酸，则必须在极低的浓度下才能制备氧化锌薄膜，但(002)面成长却没有添加乳酸来的稳定而金属锌也会电沉积到基板上。

We have synthesized 4,4'-dinitro-3 4''-dimethyl triphenylamine,(1), in 84% yield in an one-step condensation process between 3,4-dimethyl aniline and 4-fluoro-nitrobenzene. After the auto-oxidation of (1) and the subsequent hydrogenation of the nitro-groups, an AB2 type triphenylamine polyimide intermediate bearing two amine groups and one acid-anhydride group each on individual phenyl ring,{AB2 PI Intermediate}, was prepared successfully. The yields of the autoxidation and the hydrogenation steps are 81% and 90% respectively.

中文摘要本研究以3，4-二甲苯胺及4-氟硝基苯为原料，经一步骤缩合反应得到产率为84 %之4，4'-二硝基-3&，4&-二甲基三苯胺(1)，由(1)经自氧化法后再以氢化法还原硝基，成功地制备出带有二胺基与一羧基的三官能基之AB2型三苯胺中间体(AB2型PI中间体)，自氧化反应与氢化法的产率各为81%及90%。

In this paper,the method for determining the COOH in PET has been introduced by three electrode potential titration .

采用三电极电位法，对以苯酚-四氯乙烷为溶剂测定聚酯中端羧基进行了实验和探讨，并建立了端羧基测定的新方法，此方法的相对标准偏差为 2 78%，可用于聚酯中端羧基测

Six carboxyl acids DEMB was produced with Michael Reaction using triethylamine as alkaline catalyst and solvent, malonic acid and itaconic acid as raw materials.

以三乙胺为催化剂和溶剂，衣康酸和丙二酸为原料，采用迈克尔加成反应合成了含有6个羧基的多元羧酸DEMB。

与三羧基的相关的网络解释 [注：此内容来源于网络，仅供参考]

carboxyl terminal：羧基端

在羧基端(carboxyl terminal)的结合位与铁离子有很高的亲和力,只会与铁离子结合. 在氨基(N-terminal)端的结合位则是可以与其他离子结合,亲和力高低如下:铁>铬>锰>镉>镍. 三价铁离子与运铁蛋白的结合需要一个阴离子的存在,通常是重碳酸盐(bicarbonate).

indigo carmine：靛蓝

化学名称为3-羧基-5-羧基-2-(对-磺苯基)-4-(对-磺苯基偶氮)-邻氮茂的三钠盐,其结构式为如下:日落黄(sunset yellow FCF)的化学名称为1-(4′-磺基-1′-苯偶氮)-2-苯酚-7-磺酸二钠盐,呈橘黄色,化学结构式为:靛蓝(indigo carmine )又名靛胭脂、酸性靛蓝或磺化靛蓝,

glycolysis：醣酵解

确实对代谢作用的集线器的研究表明在RNA世界的重新塑造,例如处于代谢作用网络中最多的连接物质之列的有辅酶A, NAD和GTP,它们是大多数动物的某些代谢通道,例如醣酵解(glycolysis)和三羧基酸周期(tricarboxylic acid cycle)中的元素.

succinate dehydrogenase：琥珀酸脱氢酶

(6)琥珀酸脱氢 琥珀酸脱氢酶(succinate dehydrogenase)催化琥珀酸氧化成为延胡索酸. 该酶结合在线粒体内膜上,而其他三羧酸循环的酶则都是存在线粒体基质中的,这酶含有铁硫中心和共价结合的fad,来自琥珀酸的电子通过fad和铁硫中心,然后进入电子传递链到o2,

tartrazine：柠檬黄

苋菜红(amaranth)即食用红色2号,又名蓝光酸性红,化学名称为1-(4′-磺酸基-1-萘偶氮)-2-萘酚-3,7-二磺酸三钠盐,其化学结构式如下:柠檬黄(tartrazine)又名酒石黄肼,化学名称为3-羧基-5-羧基-2-(对-磺苯基)-4-(对-磺苯基偶氮)-邻氮茂的三钠盐,

malic dehydrogenase：苹果酸脱氢酶

丙二酸是琥珀酸的类似物,是琥珀酸脱氢酶强有力的竞争性抑制物,所以可以阻断三羧酸循环. 在苹果酸脱氢酶(malic dehydrogenase)作用下,苹果酸仲醇基脱氢氧化成羰基,生成草酰乙酸(oxalocetate),nad+是脱氢酶的辅酶,接受氢成为nadh.h+

tricarboxylic ester：三羧酸酯

paper foils [刷]纸基金箔 | tricarboxylic ester 三羧酸酯 | incrustive 结壳的

tricarboxylic acid：三羧酸

单体方面,藉由高产率的硝基取代、水解、脱水以及甲醇加成开环反应,自行制备出具高溶解特性之双羧酸 (bicarboxylic acid) 官能基之反应单体与三羧酸 (tricarboxylic acid) 官能基之反应单体.

tricarboxylic acid cycle：三羧酸循环

TCAC 三羧酸循环(tricarboxylic acid cycle),在有氧条件下丙酮酸在线粒体基质中彻底氧化分解的途径. 三羧酸循环又称柠檬酸循环(citric acid cycle)或 Krebs 循环(Krebs cycle). 它是需氧生物利用糖或其它物质获得能量的最有效方式,

tricarboxylic acid cycle：羧酸循环

图4-4 丙酮酸脱氢酶复合物的作用机制 2.三羧酸循环(tricarboxylic acid cycle) 乙酰coa进入由一连串反应构成的循环体系,被氧化生成h2o和co2. 由于这个循环反应开始于乙酰coa与草酰乙酸(oxaloacetate)缩合生成的含有三个羧基的柠檬酸,