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It can beconcluded from the experimental results that in the reaction of flavonoids withα-hydroxy ethyl peroxyl radicals, 2,3-double bond in the C ring plays a moreimportant role than o-dihydroxy in the B ring.

从实验结果来看,在黄酮类化合物与有机过氧自由基反应的过程中,其分子结构中起主要作用的是C环2,3双键,而不是B环的邻二羟基。

Bleaching of rutin was also observedunder 380~490nm, which indicated the destroying of the colorific system of rutinduring its reaction with peroxyl radicals.

在380~490nm观察到了芦丁的褪色反应,这表明在芦丁与有机过氧自由基反应的过程中其发色体系受到了破坏。

The rate constants of the reactions of α-hydroxyl ethyl peroxyl radicalwith quercetin, ruitn, catechin and baicalin were determined through pulse radiolysisstudies to be 〓,〓,〓〓 and 〓, respectively.

用脉冲辐解的方法得到槲皮素、芦丁、儿茶素以及黄芩甙与α-羟乙基过氧自由基的反应速率常数分别为〓;3.4〓;〓和〓。

Spectroscopy ; ion attachment mass spectrometry ; ab initio molecular orbital theory ; density functional theory ; fluoromethyl peroxyl

光谱学;离子附着质谱;分子轨道理论;密度泛涵理论;氟甲基过氧自由基

For flavonoids containing 2,3-doublebond in their C ring, peroxyl radicals mainly add on the double bond, and the adductsmay transfer to the final products through short chain reactions, which results in theincrease of G values of hydrogen peroxide.

根据实验结果我们认为黄酮类化合物与过氧自由基的反应是加成与电子转移的混合反应。

Part Ⅰ: The changing trend of G values of hydrogen peroxide in the reactionsbetween flavonoids and peroxyl radicals is an important parameter in elucidating thereaction mechanisms,γ-Irradiated aqueous solutions (saturated with 〓) andaerated ethanol solutions of several typical flavonoids were eluted through aluminacolumns and the G values of hydrogen peroxide generated in the solutions weremeasured.

第一部分:黄酮类化合物与过氧自由基反应的过程中生成的过氧化氢值的变化是解释机理的主要依据之一。

The synthetic route starts from penicillin G, peroxyacetic acid(8.5%) as Oxidizing Agent to get penicillin G sulfoxide; esterifided with p-nitrobenzyl bromine to synthesize penicillin G sulfoxide ester; we synthesize 3-exomethylenecepham sulfoxide ester with phthalimide potassium and 4A molecular sieve as acid scavenger to open the ring, SnCl_4 as catalyzation to close the ring. The yield is over 60%.

本研究采用的合成路线为:以青霉素G钾盐为原料,选用工业过氧化氢制备的过氧乙酸(22.3%)稀释至8.5%为氧化剂,氧化得青霉素亚砜;采用对硝基溴苄为酯化试剂,制备青霉素亚砜酯;以NCP(N-氯代邻苯二甲酰亚胺)为开环试剂,酞酰亚胺钾和4A型分子筛为酸清除剂,顺利开环;再经无水SnCl_4催化闭环得3-环外亚甲基头孢亚砜酯,最终产率在60%以上。

A diperoxovanadate complex NH4[OV(O2)2{2-(2'-pyridyl)-imidazole}]×4H2O,bpV for short,was investigated at the level of cell and animal based on its proliferation on cancer cells,inhibition on alkaline phosphatase and anti-tumor in animal experiments.

在细胞和动物实验水平上,研究了双过氧钒化合物NH4[OV(O2)2(C8H7N3)]×4H2O简写bpV(Imi-Py对癌细胞的增殖作用,碱性磷酸酶的活性抑制和体内抗肿瘤作用。

The crystal was obtained from the interaction system, NH4VO3/H2O2/ 2-(2′-pyridyl)imidazole, in aqueous solution under the physiological conditions, and the complex was characterized by solution NMR, IR, X-ray crystal diffraction and elementary analysis.

经NMR、IR、X-ray衍射和元素分析等谱学方法或分析手段确定其组成[NH4{OV(O2)2{2-(2′-Py)-Imi}·4H2O}]和结构,其51V的化学位移在单核双过氧钒化合物中是最大的。

A new diperoxovanadate crystal NH4{OV(O2)2{2-(2′-pyridyl)-imidazole}}·4H2O was synthesized.

在相互作用体系NH4VO3/H2O2/2-(2′-Py)Imi中合成了一种新的双过氧钒化合物。

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