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lewis base相关的网络例句

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Hydrothermal reactions makes water a Bronsted base-acid and act as an effective catalyst and the metal ions represent Lewis base character. The conversion process occurs in a very complex network of parallel, consecutive and equilibrium reactions, and the last step being the catalyzed Cannizzaro-type reaction of pyruvaldehyde to lactic acid.

nsted酸碱并具有一定的催化作用,金属离子在水热催化降解丙酮醛生成乳酸中表现出Lewis碱的特性,能与丙酮醛生成金属复合物,最终生成乳酸,此反应过程符合Cannizzaro反应特性。

We postulate that this is a Lewis base activating Lewis acid reaction.

我们仔细研究了Lewis碱的变化对反应的影响,并根据实验结果提出了Lewis碱活化Lewis酸的反应机理。

Because substituted anilines have Lewis acid or Lewis base group, extractions with complexing agent was conducted.

由于取代苯胺都具有Lewis酸性或Lewis碱性官能团,采用相应的络合剂进行了络合萃取的研究。

This trend depended on the strength of Lewis base sites M=O and activity of lattice oxygen of catalysts.

这一顺序与各催化剂表面的Lewis碱位M=O碱性的强弱、双键晶格氧活性相一致。

The acidity of Lewis acid sites and the basicity of Lewis base sites influence the intensity between water, 1,2-dichloropropane and catalyst. The specific area of catalyst influences the capacity of adsorption.

催化剂Lewis酸位和Lewis碱位的酸碱强度直接影响水、1,2-二氯丙烷与催化剂的作用强度,而催化剂的表面积直接影响吸附量。

Density functional theory calculations at the B3LYP/6-31G level of theory were employed to study the mechanism and the potential energy surface of Diels-Alder reactions between Lewis base stabilized borabenzene and dienophiles.

采用密度泛函理论方法在B3LYP/6-31G水平上研究了Lewis碱稳定的硼代苯与一些亲二烯体的两种可能的Diels-Alder反应的微观机理和势能剖面,并研究了反应的溶剂效应和取代基效应。

There exist Lewis base sites (M=O and M-O-M or M-O-P) and Lewis acid sites on the surface of these catalysts.

催化剂表面的活性基元由Lewis碱位M=O键的端氧和M-O-M或M-O-P键的桥氧位,Lewis酸位M〓组成。

The results showed that there existed Lewis base sites (M=O and M-O-Fe) and Lewis acid sites on the surface of these catalysts.

研究表明,Fe-V-O、Fe-Mo-O、Fe-P-O和Fe-Al-P-O催化剂表面活性基元都是由Lewis碱位(M=O键的端氧和M-O-Fe键的桥氧位)和Lewis酸位组成。

Nsted acid to activate the carbonyl group of the substrate and iV-oxide as Lewis base to activate TMSCN.

即:催化剂中的酰胺作为Brnsted酸活化羰基,氮氧偶极作为Lewis碱活化TMSCN。

The results showed that C 2H 6 can be adsorbed on the surface terminal oxygen of Lewis base site P=O bonds through H atom in -CH 3 to form a molecular adsorption state, and the adsorption intensity of C 2H 6 increases with the rising of adsorption temperature.

结果表明,乙烷能够以 CH3 中的H原子吸附于催化剂表面P =O键的端氧上形成分子吸附态,并且随着吸附温度的升高,对乙烷的吸附强度逐渐增大;乙烯则主要是以C =C双键吸附在催化剂的Lewis酸位Fe3 +上。

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