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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。

The substituted group on the bipyridyl ligand in complex 2 could lose C2H4 neutral molecule under a higher CID fragmentation (such as CID 110 V), and its single charge ion is more stable than its double charge ion.

而络合物2在较高的CID电压下(1l0V)会发生联吡啶环上取代基的中性C2H4小分子丢失,其单电荷离子比二价电荷离子稳定。

Using pyridine-2, 6-dicarboxylic acid as starting material, a novel ligand N^2, N^6-bis(3-methyl-pyridine-2-yl)-pyridine-2, 6-dicarboxamide was synthesized, which contained multidentate and large conjugative system.

以吡啶-2,6-二甲酸为原料,合成含有多个共轭体系多齿配体N^2,N^6-二(3-甲基吡啶)-2-取代吡啶-2,6-二甲酰胺;同时制备它与稀土离子Tb和Eu的配合物,并培养出单晶。

Three isomorphic pendant derivatives based on monovacant Keggin heteropolytungstate [SiW11O39]8- as building block have been synthesized through the decoration of Co-Im complexes using bench method:5Na_4H_2[SiW_(11)O_(39)CoIm]_(0.63)[SiW_(11)O_(39)Co(H_2O)]_(0.37)·7H_2O (1)_6[SiW_(11)O_(39)NiIm]_(0.8)[SiW_(11)O_(39)Ni(H_2O)]_(0.2)·7H_2O (2)_4Na_6[SiW_(11)O_(39)MnIm]_(0.69)[SiW_(11)O_(39)Mn(H_2O)]_(0.31)·7.5H_2O (3) Complexes 1–3 are the first examples of crystallographically characterized 3d-transition metal mono-substituted POMs with an antenna organic ligand synthesized under normal bench conditions.

以单缺位Keggin型杂多钨硅酸盐[SiW11O39]8-为建筑单元,在水溶液中通过过渡金属-咪唑配合物的修饰,成功地获得了三个同构的悬臂式衍生物:5Na_4H_2[SiW_(11)O_(39)CoIm]_(0.63)[SiW_(11)O_(39)Co(H_2O)]_(0.37)·7H_2O (1)_6[SiW_(11)O_(39)NiIm]_(0.8)[SiW_(11)O_(39)Ni(H_2O)]_(0.2)·7H_2O (2)_4Na_6[SiW_(11)O_(39)MnIm]_(0.69)[SiW_(11)O_(39)Mn(H_2O)]_(0.31)·7.5H_2O (3)它们是第一例在常规水溶液条件下合成得到的X-射线表征的3d-过渡金属取代的悬臂式多酸衍生物。

A soluble polymer analogue was realized by using a 1,2,4,5-tetralkoxy benzene in the place of dialkyl benzenes, and its properties are compared to a nonfluorinated analogue.

一种可溶性聚合物模拟实现用1,2,4,5- tetralkoxy苯取代烷基苯,其性能相对于非氟类似物。

The disubstituted ureas and the catalyst could be separated by addition of water and the catalyst could be reused without deactivation.

新型高效的菲咯啉钯-离子液体含氮化合物羰化催化剂体系,以苯胺为反应物时该体系的转化频率可以达到6000mol/mol/h;氢氧化铯-离子液体催化剂体系,可以在不加入化学计量脱水剂的条件下活化二氧化碳与脂肪族胺反应得到二取代脲,反应结束后可以通过加入水实现产品和催化剂体系的分离,催化剂体系可以重复使用。

For a disubstituted complex, MA4B2, the planar arrangement gives three isomers, the familiar ortho, meta, and para arrangement s of organic chemistry.

对于双取代络合物MA4B2,其平面排列有三个异构体,常见的为有机化学中的邻位、间位和对位排列。

For a disubstituted complex, MA4B2, the planar arrangement gives three isomers, the familiar ortho, meta, and para arrangements of organic chemistry.

对于双取代络合物 MA4B2,其平面排列有三个异构体,常见的为有机化学中的邻位、间位和对位排列。

Four new salicylaldehyde derivatives with a glucose or mannose moiety were synthesized with 2-tert-butylphenol or 4-tert-butylphenol as the starting material, followed by the formylation, chloromethylation, nucleophilic substitution reaction with the desired carbohydrate. The salicylaldehyde derivatives condensed with ethylenediamine to give the Schiff bases, which coordinated with Mn to afford four novel sugar-based Salen Mn complexes.

首先,分别以2-叔丁基苯酚和4-叔丁基苯酚为起始原料,经过甲酰化反应、氯甲基化反应、和糖类衍生物的亲核取代反应制得了四种新型并入葡萄糖基或甘露糖基的水杨醛衍生物,将它们与乙二胺缩合生成希夫碱配体,得到的配体与过渡金属Mn~(3+)配位制备出四种新型含糖基的Salen Mn配合物。

It solves the problem of water soluble iminazole and other low molecular easy runs off slowly following water vapor in sulfonated polymeric compound or iminazole composite film, can be used for moderate temperature proton exchange film fuel cell.

采用齐聚物取代咪唑等小分子,可解决磺化聚合物/咪唑复合膜中水溶性的咪唑等小分子易随水汽慢性流失的问题,可应用于中温质子交换膜燃料电池。

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然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。

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