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There will be many astigmatism veins in the process of expiating new motor lamps using Reverse Engineering such as side astigmatism veins pole astigmatism veins triangle astigmatism veins, yuyan astigmatism veins pyramid astigmatism veins four-corner astigmatism veins six-corner fake astigmatism veins six-corner changed stigmatism veins and etc.

利用逆向工程技术进行汽车车灯新产品的开发过程中经常遇到各种各样的光纹,常见的有侧光纹、柱状光纹、三角形光纹、鱼眼光纹、金字塔光纹、四角电铸纹、六角伪电铸纹和六角变形电铸纹等。

The novel complex (1) in which both benzylic nitrogens and heteroaromatic ones to the same metal ion with the rigid ligand imposed by the large heteroaromatic moiety first time was synthesized; a 2: 1 (ligand: metal ions) type complex which has steric resistance and strong thermochemical driving force was obtained. The crystal structures of characteristic ligand (LA4) and complexes (4, 7, 10), in which one cell includes two moieties: there exist minute difference in coordinated bonds and angles despite the same metal ions with the same ligand, were obtained. It shows that several stable conformation in one complex cell.

首次合成了含邻菲罗啉的具有较大刚性的四氮体中四个氮原子全部与同一金属离子位的合物的晶体结构;得到了一个在空间上存在位阻作用的体与金属离子2:1结构的晶体;解析了具有特色的一个体(LA4)和三个合物(4、7和10)的晶体结构,其中的体与金属离子的位作用显示出细微的差异,表明在同一金属合物的晶胞中,可以同时存在着多个稳定的构象。

The copper ions showed four different coordination numbers and geometrical structures. 4 coordination, planar quadrangle; 5 coordination, tetragonal pyramid; 6 coordination, octahedron; 7 coordination, triagonal bipyramid.

晶体结构分析表明,该合物中存在 [Cu2]2+、[Cu2(H2O)]2+和[Cu6(H2O)65Cu24]4-三种位离子,铜原子呈现四种不同的位数和几何构型,它们是:4位的平面四边形;5位的四方锥型;6位的八面体型;7位的三角双锥型。

From the structural analysis of three praseodymium complexes, we could draw a conclusion that as the dentate arms of carboxyl group on ligands elongating, the coordination numbers of Pr and the coordination modes of ligands increase, and the mean distances between metallic atoms of metallic helices existing in these complexes augment.2. By altering 5-substituting group of isophthalic acid three series of lanthanide complexes 8~19 with 5-methylisophthalic acid and 5-nitroisophthalic acid have been prepared.

从得到的三个体的镨合物的结构分析可以看出,随体的羧基齿臂的增长,Pr的位数逐渐增大,体的位模式增多,合物中存在的螺旋金属链中的金属间平均距离增大。2、通过改变间苯二甲酸体的5位取代基,制备了5-甲基间苯二甲酸和5-硝基间苯二甲酸的三个系列稀土羧酸合物8~19。

In the thesis, a series of novel single and multi-armed oxadiazole bridging ligands and pyridyl-4, 5-imidazole dicarboxylic acid ligands have been synthesized. The coordination chemistry of these novel ligands with transition metal ions was investigated. In addition, two 1, 3, 4-oxadiazole bridging ligands end-capped by chelating Schiff-base coordination sites have been designed and synthesized. The coordination chemistry based on one of the two ligands with metal ions was primarily investigated.

本文报道了一系列新颖的含1, 3, 4-Oxadiazole杂环的单臂及多臂有机体,研究了它们与过渡金属离子的位反应化学;合成了吡啶基-4,5-咪唑二羧酸有机体,研究了它们在水热条件下与过渡金属离子的位反应化学;另外,还合成了1, 3, 4-Oxadiazloe杂环桥联的双Schiff-base有机体,初步探讨了其与过渡金属离子的位反应化学。

The main contributions of this thesis are:(1) Seven mononuclear complexes of tetradentate ligand NTB have been obtained using N〓 or SCN〓 as the additional ligand;(2) Seventeen binuclear complexes of Fe , Zn , Co , Cu have been designed and the complexes of Co , Cu exhibit antiferromagnetic properties;(3) Changing the bridged-ligand such as PO〓, CO〓, o-phth, mai, Ag (CN 〓, Au 〓, etc , fourteen tetranuclear complexes of polypridine ligand have been synthesized;(4) Two antiferromagnetic 1D chain complexes of KH〓pdc ligand have been prepared from hydrothermal reactions; in addition, one ferromagnetic 1D chain copper complex of tpdp which is bridged by oxalate has been obtained.

本论文的主要贡献为:(1)合成了体NTB的七个新型单核合物;(2)合成了十七个铁、锌、钴及铜系列混桥双核合物,其中双核钴和双核铜合物为反铁磁偶合;(3)选用多吡啶体tpdp和TPA,改变桥联体,合成了十个四核合物;(4)选择体KH〓pdc,采用水热合成方法得到了反铁磁性一维链状锰、铜合物;以草酸根为桥联体,合成了体tpdp的一维链状铜合物,该化合物为铁磁偶合,文献较少报道。

L acted as tridentate ligand to chelate with metal atom in enol and ketone form respectively; In complex anion Co atom reside in tetrahedral coordination environment.

钴原子位于八面体位环境中,体L分别以烯醇式和酮式充当三齿体与金属原子位,阴离子中Co原子位于四面体位环境中。

The result notes that dynamic triaxial test preferably simulate the actual stress state of grading macadam, and Uzan model which considers the shear performance of material can better reflect stress states of grading macadam. Regression coefficients of the model obviously present nonlinear characteristic with moisture changed, and to further influence dynamic resilient module.More the module is larger, more diminishing rate of maximum tensile stress on pavement Bottom is smaller. To enhance draining function and strength, the gradation should been rigid controlled, and which the content of less than 0.075mm is controlled between 5~7% and spring-back is controlled between200~300MPa are appropriate.

结果表明,动三轴试验较好地模拟了级碎石层的实际受力状态;Uzan模型考虑了材料的剪切性能,更能反映了级碎石在隧道路面中应力状态;随含水量的变化,Uzan模型中回归系数变化呈明显的非线性特征,进而显著影响级碎石的动态回弹模量的变化;级碎石模量越大,路面层底的最大拉应力减小率越小;为了兼顾到级碎石层的排水渗透功能和强度,应严格控制级,特别是0.075mm以下的含量宜控制在5%~7%,级碎石的回弹模量宜控制在200~300MPa之间。

The complexing properties of compounds 10a, 10b, 11a and 11b toward alkali metal ions were studied by 〓H NMR titration, ESI-MS, UV-Vis spectra, Fluoresence spectra and liquid-liquid extraction. The results show:(1) the 1:1 complexes were formed.(2) The calix-crown 10a, 11a have a higher selectivity for Na〓 ions, whereas 10b, 11b for K〓 ions.(3) The complexing ability toward alkali metal ions was enhanced when the calix-crown have side arm carbonyl.(3) The coordination of alkali metal ions toward phenoxy, carbonyl and crown ethereal oxygens take place by rotation around the carbon-carbon bond of carbonyl and methylene.

六,用〓H NMR滴定,ESI-MS,UV-Vis,Fluorescence,液-液萃取实验研究了10a,10b,11a和11b对金属离子的位性质,研究结果表明:1)杯芳烃冠醚衍生物同碱金属离子形成了1:1合物,化合物10a、11a对Na〓具有较高的位能力,化合物10b、11b对K〓具有较高的位能力;2)在杯冠醚环的旁边引入带有羰基氧原子的基团作为侧臂参与位可以加强对碱金属离子的位能力;3)金属离子分别同苯酚氧,羰基氧,聚氧醚链氧发生了位,位过程中侧链基团涉及到了羰基碳与亚甲基碳的碳碳键的旋转过程。

Complexes 7-12, 16, 22 and 23 are dimeric molybdatesor dimeric tungstates, the central metal with citrate or malate in a molar ratio of 1:1. Theanions of these complexes have two metal atoms and two ligands. Each ligand acts as atridentate fashion via theirα-alkoxy,α-carboxy andβ-carboxy groups coordinated to eachmetal atom. Complex 13 is a monomeric molybdate. The citrate ligand coordinates tomolybdenum with itsα-alkoxy,α-carboxy andβ-carboxy groups in a tridentate mode.

阴离子中都含有2个金属原子和2个体,且体均以α-烷氧基、α-羧基和β-羧基氧与中心金属三齿位。13是单核柠檬酸钼合物,柠檬酸也以α-烷氧基、α-羧基和β-羧基氧与钼三齿位。17和21分别为苹果酸钼、柠檬酸钨单核合物,其中苹果酸、柠檬酸体均以α-烷氧基氧和α-羧基氧与金属双齿位。

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