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tetrahedral complex
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  四面体配合物
     In absolute alcohol,the experiment condition of synthesis of tetrahedral complex (Bu 4N) 4NiBr 4 was concluded. Two-type solid complexes were prepared:tetrahedral complex (Bu 4N) 2NiBr 4 and octahedral complex Ni(NH 3) 6Br 2.The properties of complexes(electronic spectrum,in spectrum,molar conductivity etc.)
     以无水乙醇为反应介质 ,找出合成四面体配合物 (Bu4N) 2 NiBr4的适宜实验条件 ,制备出四面体(Bu4N) 2 NiBr4和八面体Ni(NH3) 6 Br2 二种固体配合物 ,并研究了配合物的电子光谱、红外光谱、摩尔电导等 .
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  “tetrahedral complex”译为未确定词的双语例句
     Modeling results showed that in soluble Zn2 + complex, NT of imidazole ring of His 14, O of carbonyl of main-chain, and two O of water occupy the four ligand positions of the tetrahedral complex;
     计算结果显示在可溶键合模式中,锌离子被包容在由组氨酸残基Hisl4的咪哇N:、肤链主链上的拨基氧以及两个水分子氧形成的四面体络合物中:在纤维化过程中,锌离子可能通过Hisl3(N劝一znZ十一HIS14(N劝桥键将相邻的、不同Ap多肤交叉连接形成纤维束。
短句来源
     The results indicate that both complexes 4 and 5 are monomeric. The central metal atom Yb was coordinated by two cyclopentadienes and two nitrogen atoms of p-diketiminate to form a eight-coodinate distorted tetrahedral complex.
     X射线晶体结构表明,配合物4,5都是以单分子形式存在,中心金属镱分别与两个环戊二烯墓和β-二酮亚胺配体的两个氮原子配位,形成了配位数为8的稳定结构。
短句来源
     At 1170°C SiO2 separated out. (3) The broad absorption band in the wavelength range of 1200-1600nm of 0.2CoO-5Li2O-6Al2O3-89SiO2 sample in the range of 850-1000°C was observed, and the intensity of the absorption band increased with heat-treatment temperature. The broad absorption band in the NIR region is due to tetrahedral complex of [COO4].
     1、Li_2O-Al_2O_3-SiO_2及CoO-Li_2O-Al_2O_3-SiO_2体系纳米复合氧化物玻璃陶瓷材料的制备、微结构与性能研究
短句来源
     The equilibrium constants of addition reaction of alcohol to tetrahedral complex of cobalt with organophosphorus monobasic acids in octane are established by spectrophotometry.
     用光度法测算了醇与有机磷一元酸四面体钴配合物加合反应的平衡常数。
短句来源
     It is concluded that tendency of alcohol addition to the tetrahedral complex is affected by hindrance and electron effects of the hydrocarbonyl in acid and alcohol,and substituent effect of acid is more important.
     试验结果表明 ,酸和醇的烃基的位阻效应与电子效应影响醇与四面体钴配合物的加合趋势 ,并且酸的取代基效应更重要
短句来源
  相似匹配句对
     On Complex Reality
     复杂的实在
短句来源
     On the Confidant Complex
     《聊斋志异》中的知己情结
短句来源
     the tetrad is tetrahedral;
     四面体型四分体;
短句来源
     The tetra is tetrahedral.
     四面体型四分体;
短句来源
     Asymmetric Tetrahedral Cadmium Complex:Bis[triphenylphosphine]cadmium(Ⅱ) Diiodide
     Asymmetric Tetrahedral Cadmium Complex:Bis[triphenylphosphine]cadmium(Ⅱ)Diiodide
短句来源
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  tetrahedral complex
HgI2(tzdtH)2 exists as a mononuclear tetrahedral complex with two long Hg-S [2.672(1) ?] and two short Hg-I bond distances [2.688(1) ?] related by a twofold axis.
      
It is shown that the polarizing effects of cations on anions gives rise to considerable changes in electric charge distribution, which, in particular, results in the formation of a tetrahedral complex LiO4.
      
The structure was built from cations of aminoguanidinium and tetrahedral complex anions [ZnCl4]2-.
      
The resultingcomplex, Fe(H2O)5(HS)+, thentransforms to a tetrahedral complex on further addition of sulfide.
      
The excitation spectra of tetrahedral complex compounds of manganese(II) bromide with hydrobromides of some derivatives of pyrid
      
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In absolute alcohol,the experiment condition of synthesis of tetrahedral complex (Bu 4N) 4NiBr 4 was concluded.Two-type solid complexes were prepared:tetrahedral complex (Bu 4N) 2NiBr 4 and octahedral complex Ni(NH 3) 6Br 2.The properties of complexes(electronic spectrum,in spectrum,molar conductivity etc.)were studied.The result of magnetic susceptibility showed tetra-coordination complex(Bu 4N) 2NiBr 4 was tetrahedral configuration.

以无水乙醇为反应介质 ,找出合成四面体配合物 (Bu4N) 2 NiBr4的适宜实验条件 ,制备出四面体(Bu4N) 2 NiBr4和八面体Ni(NH3) 6 Br2 二种固体配合物 ,并研究了配合物的电子光谱、红外光谱、摩尔电导等 .磁化率测定结果证实 ,四配位的 (Bu4N) 2 NiBr4化合物为四面体构型

The equilibrium constants of addition reaction of alcohol to tetrahedral complex of cobalt with organophosphorus monobasic acids in octane are established by spectrophotometry. The acids invole n octyl,2ethylhexyl and l methylheptyl hydrogen styrylphosphonates,2 ethylhexyl hydrogen 2 ethylhexyl phosphonate and di 2 ethylhexyl hydrogen phosphate.The alcohols studied are n ,iso and sec octanol,ethanol,tert butanol and benzyl alcohol.It is concluded that tendency of alcohol addition to...

The equilibrium constants of addition reaction of alcohol to tetrahedral complex of cobalt with organophosphorus monobasic acids in octane are established by spectrophotometry. The acids invole n octyl,2ethylhexyl and l methylheptyl hydrogen styrylphosphonates,2 ethylhexyl hydrogen 2 ethylhexyl phosphonate and di 2 ethylhexyl hydrogen phosphate.The alcohols studied are n ,iso and sec octanol,ethanol,tert butanol and benzyl alcohol.It is concluded that tendency of alcohol addition to the tetrahedral complex is affected by hindrance and electron effects of the hydrocarbonyl in acid and alcohol,and substituent effect of acid is more important.

用光度法测算了醇与有机磷一元酸四面体钴配合物加合反应的平衡常数。试验的有机磷酸是苯乙烯膦酸的单正辛基酯 ,单 2乙基己基酯和单 1甲基庚基酯 ,以及 2乙基己基膦酸单 2乙基己基酯和二 (2乙基己基 )磷酸。研究的醇的烃基分别为正辛基、2乙基己基、1甲基庚基、叔丁基和苯甲基。试验结果表明 ,酸和醇的烃基的位阻效应与电子效应影响醇与四面体钴配合物的加合趋势 ,并且酸的取代基效应更重要

 
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