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锌配合物     
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  zinc complex
     DNA Hydrolysis by the Di Zinc Complex Zn_2(DTPB)Cl_4
     双锌配合物Zn_2(DTPB)Cl_4水解DNA
短句来源
     Synthesis and Crystal Structure of Binuclear Zinc Complex Zn_2(dhaash)_2(py)_4
     一个新的双核锌配合物Zn_2(dhaash)_2(py)_4的合成及晶体结构
短句来源
     Synthesis,Crystal Structure and Theoretical Study of One-dimensional Binuclear Zinc Complex [Zn_2(SHSH)_2(2-Me-py)_2]
     一维双核锌配合物[Zn_2(SHSH)_2(2-Me-py)_2]的合成、晶体结构及理论研究
短句来源
     The Characteristics Study of Zinc Complex with S 2- 6 and 3-Methylpyridine Ligands
     含多硫基S~(2-)_6及3-Mep_y配体的锌配合物性能的研究
短句来源
     The Synthesis and Properties of Zinc Complex with S_6 ̄(2-) and Pyridine Ligands
     含多硫基S_6~(2-)及吡啶配体的锌配合物的合成及表征
短句来源
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  zinc complexes
     Three zinc complexes with dithiocarbamate were synthesized. They are [Zn 2(S 2CNBu n 2) 4](1), [Zn (S 2CNBy 2) 2] (2) and [Zn(S 2CNBy 2) 2Py] (3) (where By=benzyl, Py=pyridine).
     合成了 3个二硫代氨基甲酸锌配合物 [Zn2 (S2 CNBun2 ) 4 ] ( 1) ,[Zn(S2 CNBy2 ) 2 ] ( 2 )和 [Zn(S2 CNBy2 ) 2 Py] ( 3 ) (Bun=正丁基 ,By =苄基 ,Py =吡啶 ) .
短句来源
     In the mononuclear zinc complexes, [Zn(PTPY)_2](ClO_4)_2 ( 1 ) and [Zn(MPTPY)_2](ClO_4)_2 ( 2 ), weak hydrogen bonding interaction, C-H.
     在单核锌配合物[zn(PTPY)_2](ClO_4)_2(1)和[Zn(MPTPY)_2](ClO_4)_2(2)中,有CIO_4~-与吡啶H形成的C-H…O弱氢键作用。
短句来源
     Synthesis and Structures of Mannich Ligands and Zinc Complexes
     Mannich碱类配体及其锌配合物的合成与结构研究
短句来源
     The electrochemical property of 5-o-[N-(L-alanine)-ethoxy]phenyl-10,15,20-triphenylporphyrin(o-AlaNC 2-OTPP)and its zinc complexes(o-AlaN-C 2-OTPP·Zn)have been investigated with cyclic voltammetry in CH 2Cl 2 using TBPA as electrolyte.
     本文采用循环伏安法研究了 5 -邻 [N - (L -丙氨酸 ) -乙氧基 ]苯基 - 10 ,15 ,2 0 -三苯基卟啉及其锌配合物在CH2 Cl2 为溶剂和TBPA为电解质条件下的电化学性质 .
短句来源
     The TG-DTG curve of a series of octaalkoxy naphthalocynine zinc complexes Zn(RO) 8NPc (NPc=C 48 H 16 N 8,R=C 4H 9,C 8H 17 ,C 12 H 25 ) and electronic absorption spectra of these complexes in different organic solvents are measured. The relation between structure and properties of these complexes are studied.
     测定了一组八烷氧基2,3-萘酞菁锌配合物Zn(RO)8NPc(R=C4H9,C8H17,C12H25,NPc=C48H16N8)的热稳定性及其在5种有机溶剂(DMSO、DMF、Py、CH2Cl2、C6H12)中的电子吸收光谱,并研究了配合物结构与这些性质之间的关系.
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  zn complex
     The results showed Mn and Ni complexes possibly bind to DNA by the mode of interaction, whereas Zn complex possibly bind to DNA by the modes of interaction and electrostatic binding.
     结果表明,镍、锰配合物与DNA可能只有插入结合,而锌配合物与DNA的结合方式极有可能不止一种,除插入方式结合以外还伴随有静电结合。
短句来源
     meso Tetrakis( p methoxyl)phenylporphyrin(T( p OCH 3)PP) and its Zn complex (Zn T( p OCH 3)PP) were synthesized and characterized by elemental analysis, 1H NMR, UV and fluorescence spectra. The electrochemical properties of the complex have been investigated by cyclic voltammetry, electrocapillary method in DMSO and a tentative mechanism of reduction on the mercury electrode has been proposed.
     合成了 meso-四 -(对甲氧基 )苯基卟啉 [T(p-OCH3) PP]及其锌配合物 [Zn T(p-OCH3) PP],用核磁共振法对配合物进行了表征 ,用紫外可见光谱法 ,荧光光谱法及循环伏安法研究了配合物的光谱学和电化学性质 ;
短句来源
  “锌配合物”译为未确定词的双语例句
     Syntheses and Crystal Structures of Two Mononuclear Complexes M(2-SC5H3NH-3-SiM63)2Cl2(M=Cd,Zn)
     两个单核镉、锌配合物M(2-SC_5H_3NH-3-SiMe_3)_2Cl_2(M=Cd,Zn)的合成与晶体结构
短句来源
     These two complexes have the formulas Zn(L2)Cl2(Zn2) and Zn(L3)Cl2·CH3CN(Zn3), respectively.
     合成了两个吡啶二亚胺锌配合物,两个配合物分子式分别为Zn(L2)Cl2 (Zn2)和 Zn(L3)Cl2·CH3CN(Zn3)。
短句来源
     Synthesis and crystal structure of the complex Zn(p-HPO)_2Cl_2 with 4-pyridone ligand
     4-吡啶酮锌配合物Zn(p-HPO)_2Cl_2的合成与晶体结构
短句来源
     Zn complexs of 1,4,7,10,13,16-hexaazacyclooctadecene: synthesis and characterization
     1,4,7,10,13,16,-六氮杂-十八环四烯合锌配合物的合成与表征
短句来源
     The new complexes of [VO(Mbiim)(H2O)3]SO4 (2) and [Zn(Mbiim)2SO4] 4H2O (3)has been designed, characterized by elemental analyses, IR spectroscopy and melting point.
     以它为配体合成了钒配合物[VO(Mbiim)(H_2O)_3]SO_4(2)和锌配合物[Zn(Mbiim)_2SO_4]·4H_2O(3),并得到了3的单晶。 晶体属单斜晶系,C2/c空间群,所得晶体学参数为a=25.713(5)(?)
短句来源
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  zinc complex
Meanwhile, the fluorescence lifetime of 2-[2-(9-ethyl-9H-carbazol-2yl)-vinyl]-quinolin-8-ol and its zinc complex showed long lifetime in benzene solution.
      
The corrosion and electrochemical behavior of CT3 steel and Armco iron in soft corrosive water at 20 and 80°C in the presence of a zinc complex with hydroxyethylidenediphosphonic acid (HEDPZn) and sodium nitrite and m-nitrobenzoate was studied.
      
A zinc complex of hydroxyethylidenediphosphonic acid (OEDP-zinc) is the most effective inhibitor of the anodic reaction.
      
This work is devoted to studying the passivating ability of the zinc complex of the 1-hydroxyethane-1,1-diphosphonic acid (HEDP) in a borate buffer solution.
      
Sorption of zinc complex ions from chloride solutions with ion exchangers
      
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  zinc complexes
All results considered, make us conclude that the function of cyanide ions is not to form electroinactive zinc complexes, but to change the properties of difficultly soluble compounds formed on the cathode's interface in the course of electrolysis.
      
The interaction of meso-tetra(4-N-hydroxyethylpyridyl)porphyrin, meso-tetra(3-N-hydroxyethylpyridyl)porphyrin, and their zinc complexes with bovine serum albumin (BSA) was studied by electronic spectroscopy, CD, and equilibrium dialysis at pH 7.2.
      
Extra coordination of zinc complexes of bromo-substituted tetraphenylporphyrins was studied by spectrophotometry.
      
Dissociation of Zinc Complexes in a Series of Phenyltetrabenzoporphyrins with Varying Macrocycle Rigidity
      
Kinetic stability of zinc complexes with meso-phenyltetrabenzoporphyrins in DMSO-HOAc mixture and in glacial acetic acid was studied.
      
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  zn complex
Zn complex with N-(4'-Benzo-15-crown-5)-2-(amino-N-tosyl)-phenylaldimine: Synthesis, crystal structure, and vibration spectrum
      
It was found that the catecholase activity of the Cu,Zn complex increased considerably upon immobilization on silica gel via hydrogen bonds and intercalation by ion exchange among the layers of montmorillonite.
      
The thermal stability of ATS is better than that of Ca-Zn complex and basic lead stabilizers, and equal to that of dibutyltin dilaurate.
      
The thermal stability of this product is better than that of Ca-Zn complex and basic lead salt stabilizers, and equal to that of dibutyltin diaurate.
      
The results show that decomposition takes place at 180°±5°C for lactic acid-Zn complex, 200°±5°C for EDTA-Zn, 240°±5°C for quinone-Zn and 190°±5°C for fulvic acid-Zn.
      
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