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甲基吡啶

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Part two, Three analogue compounds of actamiprid were synthesized by analogue synthesis method through the intermediates which have insecticide activity.

第二部分中,选取本身具有杀虫活性的基团取代吡虫清中的2-氯-5-氯甲基吡啶,采用"类同合成法"合成了3个烟碱类杀虫剂吡虫清的类似物。

The diffusion coefficient of heptachloropyridine in...

求得3,4,5,6-四氯-2-三氯甲基吡啶在乙腈和水的混合溶液(体积比5∶1)中的扩散系数D=3.0 10-5cm2/s。

Reaction conditions are studied, and the result shows that it is better to adopt mercuric oxide or mercuric fluoride as fluorination catalyst with reaction temperature -20~-10℃.

结果表明,采用氧化汞或氟化汞作氟化催化剂、氟化氢作溶剂较好,适宜的反应温度为-20~-10℃,较长的反应时间(48 h)和增加氟化氢和催化剂的量有利于氟化。2-氯-5-三氯甲基吡啶的转化率和选择率均可达到97%以上。

In this thesis, studied the method that adoption air oxidize bandaging synthesize the smoke sour.

在本论文中,研究了采用空气氧化3—甲基吡啶的方法合成烟酸。

It is worthy of noting that different from the pyrolysis of pyrrole and other aroma compounds the products of pyridine pyrolysis is relatively less in number and has low tendency of sooting.

最后第五章研究了取代的六元含氮模型化合物4-甲基吡啶的热解,结合前章吡啶热解反应路径的研究,从产物的分布得出一些普适的定性结论。

In Chapter 5,the pyrolysis of substituted six-membered ring model compound 4-methyl pyridine has been investigated.Instead of detail theoretical analysis of the reaction mechanism,the general results have been proposed from the products distribution and the combination of the pyrolysis investigation of its analogous pyridine.The major products are H_2,C_2H_2,C_4H_2,C_3H_3N and HCN,here HCN is not a primary initial product at low extent of decomposition.The mole fraction profiles of products have been obtained from the near threshold ionization.The pyrolysis of 4-methyl pyridine is initiated from the methyl abstraction and hydrogen abstraction procedures which are associated with the understanding of the soot formation and the NOX precursor correspondingly.

主要产物为H_2,C_2H_2,C_4H_2,C_3H_3N和HCN,其中HCN为非低温时的热解产物;通过近阈值电离并导出物种随温度变化的摩尔分数曲线,更详细地定量地描述了产物随温度的变化。4-甲基吡啶热解主要从母体脱甲基和脱氢两个初始反应出发,一种趋势是形成大质量数的苯并或杂环的多环化合物,有助于了解炭黑形成过程中的复杂化学过程;另一趋势是开环生成小的碳氢和腈类物质,实验得出的含氮物质的种类及随温度变化有助于了解NO_x的前驱物质的形成及其变化规律。

Reactions of 2,6-pyridinedicarboxylic acid or 2,6-dibromomethyl pyridine with 5-(4-hydroxyphenyl)-10,15,20-triphenyl porphyrin, 5-(4-aminophenyl)-10,15,20 triphenyl porphyrin gave three novel bridged diporphyrins 3-5, respectively.

通过将2,6-吡啶二羧酸或2,6-二溴甲基吡啶分别与5-(4-羟基苯基)-10,15,20-三苯基卟啉(1)和5-(4-氨基苯基)-10,15,20-三苯基卟啉(2)反应,合成了3种新型的双卟啉化合物3~5。

The results show that in the protonation process, because of the effect of meso-(p-methylpyridyl), the changes of the structure and bond charge population are obvious; the frontier molecular orbitals have opposite change trend with the case of meso-yridyl, the rapid exchanges of inner hydrogens of the protonated diacid with solvent protons become more difficult.

结果表明,由于m-甲基吡啶的影响,在质子化过程中结构和键电荷布居有明显变化;前沿分子轨道具有与四吡啶基情形相反的变化趋势,质子化二酸与溶液质子的快速交换作用也变得更困难了。

Two novel A-it-A' type benzothiazole-based derivatives with benzothiazolyl, phenyl-acetyl or pyridine cation groups as π electron acceptor, diethenylphenyl as π conjugated bridge: 4-(2-benzothiazolyl) ethenylchalcone (1) and 4-{4-[2-(benzothiazole-2-yl) ethenyl] styryl}-N-methylpyridinium iodide (2) were synthesized.

以苯并噻唑、苯乙酰基和吡啶阳离子为电子受体,二乙烯基苯为共扼桥,合成了两个新的A-π-A'型苯并噻唑衍生物:4-(2-苯并噻唑)-乙烯基查尔酮(1)和4-{4-[2-乙烯基]苯乙烯基}-N-甲基吡啶碘盐(2)。

Two novel A-π-A′ type benzothiazole-based derivatives with benzothiazolyl,phenyl-acetyl or pyridine cation groups as π electron acceptor,diethenylphenyl as π conjugated bridge: 4-(2-benzothiazolyl)ethenylchalcone(1) and 4-{4-[2-(benzothiazole-2-yl)ethenyl]styryl}-N-methylpyridinium iodide(2) were synthesized.

以苯并噻唑、苯乙酰基和吡啶阳离子为电子受体,二乙烯基苯为共轭桥,合成了两个新的A-π-A′型苯并噻唑衍生物:4-(2-苯并噻唑)-乙烯基查尔酮(1)和4-{4-[2-乙烯基]苯乙烯基}-N-甲基吡啶碘盐(2)。

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