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新配合物
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  new complex
     Synthesis and Crystal Structure of the New Complex [Cd(H_2O)_2(phen)_2](PA)_2
     新配合物[Cd(H_2O)_2(phen)_2](PA)_2的制备及晶体结构
短句来源
     A new complex,[Co(PHEN)2(EA)](ClO4)2.H2O. CH3OH(1),was synthesized from PHEN(1,10-phenanthroline) and EA(2-aminoethanol).
     以2-氨基乙醇(EA)和邻菲咯啉(PHEN)为配体合成了新配合物[Co(PHEN)2(EA)](ClO4)2.H2O.
短句来源
     A new complex of Cr(Ⅲ), Cr_2(Inic)_3Cl_3(H_2O)_3·5H_2O, where Inic denotes isonicotinate,was prepared.
     合成了铬(Ⅲ)的一个新配合物物Cr_2(Inic)_2Cl_3(H_2O)_3·5H_2O,这里Inic ̄-表示异烟酸根。
短句来源
     A new complex Cr(Nica) 3 (H2 O) 3 (NO3 ) 3 · H2 O(Nica denotes nicotinamide) was pre- pared,and its kinetics of thermal decomposition was studied undrnon- isothermal condition.
     合成了铬 ( )的一个新配合物 Cr(Nica) 3 (H2 O) 3 (NO3 ) 3 ·H2 O(Nica表示烟酰胺 ) ,并对其进行了热分解非等温动力学研究。
短句来源
     A new complex,[(C_(6)H_(6)N_(2)O)_(2)Co(H_(2)O)_(2)] Br_(2) was prepared from picolinamide,Co(NO_(3))_(2 )and benzyl bromide,and characterized by X-ray diffraction.
     用皮考林酰胺、六水合硝酸钴和苄基溴反应制得一种新配合物[(C6H6N2O)2Co(H2O)2]. B r2,通过红外光谱、元素分析及X射线晶体衍射对化合物进行了表征.
短句来源
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  new complexes
     New complexes (Me3CCOO)3 Ln (Ln=SM, Gd, Yb)are synthesized fromLn(NO3)3· nH2O (n =6 or 7) and Me3CCOONa in aleohol.
     以Ln(NO3)3·n(H2O)(Ln=Sm.Gd.Yb.n=6或7)与Me3CCOONa在乙醇溶剂中反应,合成了新配合物(Me3CCOO)3Ln。
短句来源
     Four trans-PtHX(AsPh_3)_2(X=Cl~-,Br~-,I~-,SCN~-)complexes were synthesized. Except trans-PtHCl(AsPh_3)_2 complexes,others are new complexes.
     合成了 trans-PtHX(AsPh_3)_2(X=Cl~-、Br~-、I~-、SCN~-)四个配合物,除 trars-PtHCl(AsPh_3)_2外,其余三个为新配合物
短句来源
     Two new complexes: Zn(T(4-MOP)P and Co(T(4-MOP)P has been synthesized and characterized by elemental analysis, electronic spectra. IR. H NMR.
     合成了两种新配合物:Zn[T(4-MOP)P]及co[T(4-MOP)P],进行了元素分析,电子光谱,红外光谱和质子核磁共振波谱研究。
短句来源
     The weak interactions in the crystals are discussed. (3)Two new complexes, [Cr(DMSO)6]Cl3 and [Fe(DMSO)4Cl2]Cl, were synthesized.
     (3)合成了两个以DMSO为配体的新配合物[Cr(DMSO)_6]Cl_3和[Fe(DMSO)4Cl_2]Cl。
短句来源
     A series of new complexes [LnCl2(Ph3PO)4][CuCl3] were prepared (Ln = La, Ce,Pr,Nd, Sm,Eu, Gd, Tb, Dy, Ho, Er, Y). X-ray diffraction crystallographic structural analysis for [GdCl2 (Ph3PO)4] [CuCl3] reveals Gd(Ⅲ) is of hexa- coordinated distorted octahedral configuration and Cu(Ⅱ ) is of tri-coordinated trigonal planar configuration.
     合成了通式为[LnCl_2(Ph_aPO)_4][CuCl_3](Ln=La,Ce,Pr,Nd,Sm,Eu,Gd,Tb,Dy,Ho,Er,Y)的12种新配合物,X射线衍射结构分析证实[GdCl_2(Ph_2PO)_4][CuCl_3]中Gd(Ⅲ)为六配位畸变八面体形,Cu(Ⅱ)为三配位平面三角形.
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  “新配合物”译为未确定词的双语例句
     The results indicate that their compositions are LaL(H2O)2NO3and Ce2L3 nH2O (L=MSEA or MSPA,n = 0,4) , respectively.
     这些新配合物的组成可表示为:[LaL(H_2O)_2]NO_3和Ce_2L·nH_2O(L=MSEA或MSPA,n=0或4)。
短句来源
     The three new coordination compounds that they are La(NO 3) 3·4Im·2HNO 3·H 2O,Nd(NO 3) 3·4Im·HNO 3·H 2O and Eu(NO 3) 3·3Im·HNO 3·H 2O have been prepared,where Im is a abbreviation of imidazole.
     合成了 L a( NO3 ) 3 · 4Im· 2 HNO3 · H2 O,Nd( NO3 ) 3 · 4Im· HNO3 · H2 O,Eu( NO3 ) 3 ·3 Im· HNO3 · H2 O三种新配合物
短句来源
     On the basis of elemental analysis and molar conductance, the general formula of the complexes, [REL_2NO_3 ]·nH_2O (RE=La, Pr, Eu, Y, n=2; RE=Nd, Sm, n=1; RE=Tb, Dy, Er, Yb, n=3), is given.
     元素分析及摩尔电导值表明新配合物的组成为[REL2NO3]·nH2O(RE=La,Pr,Eu,Y,n=2;RE=Nd,Sm,n=1;RE=Tb,Dy,Er,Yb,n=3)。
短句来源
     A new manganese (Ⅲ) compound, [Mn(napn)(CH3OH)2]ClO4 (C26H26ClN2O8Mn, Mr = 584.88, napn2- = N,N-ethylenebis(1-naphtholideneaminato) dianion), was synthesized and characterized by IR spectroscopy and single-crystal X-ray diffraction analysis.
     合成了一个新配合物[Mn(napn)(CH3OH)2]ClO4 (C26H26 Cl N2O8Mn,Mr = 584.88,H2napn = 双a-萘酚醛缩乙二胺),并测定了其晶体结构。
短句来源
     There were two complexes La(Gly)3(ClO4)3·2H2O(I) and La(Gly)4(ClO4)3(II) occurring in the system.
     体系中形成了2个新配合物La(Gly)_3(ClO_4)_(3)·2H_2O(Ⅰ)和La(Gly)_4(ClO_4)_3(Ⅱ).
短句来源
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  new complex
During the experiment of preparing ITO (Indium Tin Oxide) nanopowder, a new complex salt crystal K3[InCl6] was found and synthesized using a solution growth method.
      
Gilyarov's scientific school in the development of the subject and methodology of a new complex discipline formed in the mid 20th century-soil zoology-was considered.
      
In addition, a new complex (B3 band) was for the first time detected under induction by PB, TPD, and TCPOPOB.
      
Synthesis and study of new complex Pu(V) and Np(V) acetates
      
New complex plasticizing additives for mortars based on Portland cement, increasing the mobility of the cement paste and improving some technological properties of the resulting materials, were prepared.
      
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  new complexes
Increase in the incubation time up to 2 h facilitated the formation of other new complexes (B4 and B5 bands), which were detected only in the presence of TPD.
      
Synthesis and Spectral Study of New Complexes of Eu3+, Am3+, and Cm3+ with GaMo6O18(OH)63- Polyanion
      
New complexes of Np(V) and Pu(V) with α,α'-bipyridine of the composition AnO2(bipy) · OOCC2H5·H2O (An = Np, Pu) were synthesized.
      
New complexes of bivalent Co, Ni, and Cu with isatin aminoguanisone (HL) and nitroaminoguanisone (HL1) of the composition ([Co(HL)2]Cl2 (I), [Ni(HL)2]Cl2 (II), [Cu(L)Cl] (III), [Co(L1)2] (IV), [Ni(L1)2] (V), and [Cu(L1)2] (VI) are synthesized.
      
Four new complexes of pentavalent bismuth are synthesized: Ph3Bi[OC6H2(Br3-2,4,6)]2, Ph3Bi[OC6H2(Cl3-2,4,6)]2, Ph4BiOC6H2(Br3-2,4,6), and Ph4BiOC6H2(Cl3-2,4,6).
      
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Monocyanoethyl-β-diketone ( monocyanoethyl acetone, monocyanoeth-yl propionylacetone , monocyanoethyl benzoylacetone , monocyanoethyl

本文通过一氰乙基化β-二酮与醋酸铜作用合成了五个双-[一氰乙基化β-二酮基]合铜(Ⅱ)配合物,并进行了元素定量分析,红外光谱分析、紫外光谱分析,这些配合物是未知的新的配合物。

Two new Coordinetion Compounds tri (1-methylimidazole)cobalt(Ⅱ) sulfate and hexaimidazolecobalt(Ⅱ) were Synthesized. Their composition and properties have been explored with the aid of elemental analysis, TGA, DTA, IR, UV, NMR, x-ray powder pattern, magnetic susceptiblity and electrolytic conductivity. And what is more, the reasons for the coordination number of cobalt (Ⅱ) in tri(1-methylimidazole)cobalt(Ⅱ) smaller than that in the another Coordination Compounds of cobalt(Ⅱ) have also been discussed.

合成了硫酸三(1-甲基)咪唑合钴和硫酸六咪唑合钴两种新的配合物。通过元素分析、热重、差热分析、红外光谱、紫外光谱、核磁共振谱、x射线粉末衍射图、磁化率和电导测定等研究了这两配合物的组成和性质,探讨了1-甲基咪唑钴(Ⅱ)配合物中Co(Ⅱ)配位不饱和的原因。

Heteronuclear Clusters[Ni(Mo_nS_(4-n))_2]~(2-)(M=Mo or W,n=0-2)and 0 0 were prepared by the reaction of NiCl_2 with (NH_4)_2Mo_nS_(4-n)(M=Mo or W,n=0-2)in the basic methanol solution.13 Comdounds(including 10 new ones)Were Characterized on the basis of chemical analysis,electronic spectra,IR spectra and magnetic susoptibility. The thermal decomposition of[(n-Bu)_4N]_2[Ni(MoS_4)_2]and[(n-Bu)_4N]_2 -[Ni(WS_4)_2]by DTA and TG was also studied.

本文提出在甲醇溶剂,碱性条件下,合成杂核原子蔟状配合物[Ni(Mo_nS_(4-n))_2]~(2-)(M=Mo,W,n=0-2)和[Ni(WOS_2)_2]~(2-)的方法。共合成出13个化合物,其中10个为新配合物,3个为新骨架结构。用元来分析,红外光谱,电子光谱对化合物进行了表征,得出化合物中阳离子的变化会影响簇阴离子 M—S 链的红外吸收。此外还用差热和热重法,研究了部分化合物的热分解。

 
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