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ligand相关的网络例句

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与 ligand 相关的网络例句 [注:此内容来源于网络,仅供参考]

The effect of different second ligand on the flourescent properties of polymers were studied. Then AxByEu/HTTA/PMMA was prepared using the best second ligand HTTA.

考察了不同的第二配体(咔唑、二甲基-联吡啶、邻菲罗啉、噻吩甲酰三氟丙酮HTTA)对脂肪酸铕聚合物发光性能的影响,选择出合适的第二配体HTTA,进而合成了A3Eu/HTTA/PMMA聚合物。

Mathematical analysis predicts that constant rate shedding of autocrine ligands into a collapsing lateral intercellular space leads to increased local ligand concentrations that are sufficient to account for the observed receptor signalling; direct experimental comparison of signalling stimulated by compressive stress versus exogenous soluble ligand supports this prediction.

数学分析预测自分泌配体以常数频率脱落入萎陷的侧面胞间隙可以引起足以解释观察到的信号转导的局部配体浓度增加;直接实验比较由压力和外源可溶性配体刺激产生的信号转导也支持这个预测。

The biological activities of the metal complexes of derivatives of benzaldehyde nitrogen mustard were investigated against 〓,〓 and SMMC-7721 cell lines. The interesting results were found. When the non-activity ligand combines with cobalt and nickel , the complexes have good antitumor activity, while active ligand binds to the metal, the complex has no activity, indicating there are synergic effect and counteraction between the metals and the ligands.

对所获得苯甲醛氮芥衍生物的金属配合物进行研究,观察它们对SMMC-7721、〓细胞株的作用,发现某些有趣的实验结果,无活性的配体,当与钴,镍形成配合物后,具有很好的抗肿瘤活性,而有活性的配体形成配合物后无活性,揭示在它们存在有协同作用及拮抗作用。

NHC ligand was found to be more efficient than phosphine ligand in this reaction.

该反应体系大为拓展了此类反应亲电试剂的范围。

Mn-complexes in which Mn atom ligand with the N atom within ligand can stimulate the recovery of electron transfer and oxygen evolution. The trinuclear Mn-complex is extremely sensitive to the addition of CaCl2. It is suggested that there is an interaction between Ca2 and carboxyl within the trinuclear Mn-complex during photoactivation and this interaction benefits the ligation of Mn atom to the apo-WOC and form an active WOC. Binuclear MnMn complex shows slightly higher efficiency than binuclear MnMn complex in restoration of O2 evolution activity. It is suggested from our results that recovery of electron transport and O2 evolution with synthetic Mn-complexes is affected by different factors. Cl- can stimulate the reconstitution of WOC at the concentration of over 100mM;the maximal recovery of O2 evolution activity requires the presence of CaCl2 and 33 kDa protein polypeptide together. Bicarbonate can stimulate the reconstitution of WOC.

锰配合物中锰原子与配体中的氮原子配位连接时,能显著恢复电子传递活性和放氧活性;三核锰化合物在重组时对CaCl2的存在非常敏感,我们认为Ca2 与三核锰化合物中的羧基之间存在一定的相互作用,而这种作用有助于锰原子的光配位进而使三核锰化合物易于组装成有活性的水氧化复合物:双核锰化合物MnMn比双核锰化合物MnMn在恢复放氧活性方面更有效;影响锰化合物电子传递能力恢复的因素与影响锰化合物放氧活性恢复的因素不同;在锰蔟重组过程中,氯离子的浓度必须在100mM以上,才能有效进行光重组;最大光重组效率的获得必须有钙离子和33kDa多肽同时存在;碳酸氢根离子促进锰化合物与去锰光系统II的光组装。

In complex 1,Cucan be described as a four-coordinated square planar geometry.Compound 8 is the sodium salt of plumbagin and exists as ionic compound.Compounds 9-16 are the rare earth complexes of plumbagin with La,Y,Dy,Sm,Gd,Nd,Erand Eu.Compound 17 is binuclear Y complex.18 is mononuclear Ycomplex with plumbagin and another ligand from Plumbago Zeylanica.Compounds 19-21 are the ternary complexes with plumbagin and 2,2\'-bpy and phen as assistant ligand.In 19, the geometry of Cucan be described as five-coordinated distorted square pyramid that exists in a dimer through the weak bonding,and 1-D chain structure is formed by intermolecular hydrogen bonds.

化合物1的单晶结构分析表明1具有四配位平面四边形结构,化合物8是白花丹素的Na盐,以离子化合物形式存在;化合物9~16为白花丹素的La,Y,Dy,Sm,Gd,Nd,Er,Eu的稀土金属配合物;化合物17是白花丹素的双核钇结构;化合物18为白花丹素的单核钇结构,该配合物除了含白花丹素外,还有来自白花丹植物中的另一个单体化合物也参与配位;化合物19~21是以2,2\'-联吡啶和邻菲咯啉等含N配体为辅助配体,具有白花丹素—含N配体—金属离子的三元配合物,化合物19是白花丹素和2,2\'-联吡啶与Cu的配合物,具有五配位的四方锥构型,通过Cu…O弱的成键作用形成二聚体,再通过分子间的氢键作用进一步形成一维链状结构,化合物20和化合物21是白花丹素分别与2,2\'-联吡啶和邻菲咯啉的Zn配合物,都具有六配位八面体构型的双核锌配合物,呈一维链状结构,化合物20中链与链之间的大量氢键将一维链扩展成二维层,分子间的π-π堆积作用进一步形成三维结构。

OPG belongs to the TNF superfamily and its ligand, RANKL, is a member of TNF ligand family.

OPG的配体是一个已知的TNF配体家族的成员RANKL。

The present research work focuses on two aspects. On one hand, the most successful alkaloid-derived ligands have been attached to a soluble or insoluble support covalently, but additional OsO〓 is necessary to maintain the consistent catalytic activity during the reuse of supported chiral ligand in the next AD reaction. On the other hand, immobilization of osmium tetroxide based on microencapsulation, ion-exchange techniques, and osmylation of resins has made it possible to recover and reuse of the osmium, but failed to recover the chiral ligand at the same time.

目前的研究主要集中在两个方面:一方面,将手性配体共价键合到不溶或可溶性载体上制成负载手性配体,但在重复使用负载配体时必须补充OsO〓,才能保证催化活性不降低;另一方面,将OsO〓包裹在高聚物微囊内,或运用离子交换技术或共价键合的方法将OsO〓固载在树脂、硅胶或层状双金属氢氧化物材料上,但手性配体却不能同时回收。

Benzylidene[1,3-bis(2,6-dimethylphenyl)-4,5-dihydroimidazol-2-ylidene]dichloro(2-methylpyridine)ruthenium (62), benzylidene[1,3-bis(2,6-dimethylphenyl)-4,5-dihydroimidazol-2-ylidene] dichloro(2,4-dimethylpyridine)ruthen ium (63) introduce ortho substituted pyridine as dissociating ligand to weaken Ru-N bondand accelerate dissociation of pyridine derivative ligand through steric hindrance.

在钌卡宾配合物[1,3-二-(2,6-二甲苯基)-4,5-二氢咪唑基]-苯亚甲基-(2-甲基吡啶)-二氯合钌(62),1,3-二-(2,6-二甲苯基)-4,5-二氢咪唑基1-苯亚甲基-(2,4-二甲基吡啶)-二氯合钌(63)中,邻位取代的吡啶作为解离配体,通过邻位基团的空间效应削弱钌-氮配位键,使配体更易解离,提高了催化剂的初活性。

Of bidentate ligand DABCO is added exactly as axial ligand to the catalytic system.

以双齿配体DABCO作为轴向配体,双核铁双卟啉催化环己烷羟化反应

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