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首页> 外文期刊>European journal of mass spectrometry >The influence of the C'-4' substituent on the formation of benzoyl ions during electron ionization-induced decomposition of some 2-phenyl-1,3,4-oxadiazoles
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The influence of the C'-4' substituent on the formation of benzoyl ions during electron ionization-induced decomposition of some 2-phenyl-1,3,4-oxadiazoles

机译:C'-4'取代基对电子电离诱导的某些2-苯基-1,3,4-恶二唑分解过程中苯甲酰离子形成的影响

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The effect of the C-4' substituent for the formation of benzoyl ions during electron ionization-induced decomposition of some 2-phenyl-1,3,4-oxadiazoles is studied. The formation of these ions occurs via an azirane ion. The sums of the abundances of benzoyl ions and abundances of fragment ions derived from them, expressed as a percentage of total-ion current, were compared with the calculated charge density on both C-4' atoms and atoms connected with C-4' atoms. Linear correlations were found for both molecular and intermediate azirane ions. In the case of substituents which are less likely to be positively charged, the peaks of benzoyl ions have higher relative intensities. It is deduced that ionization in the phenyl ring strongly affects the formation of benzoyl ions from molecular ions of the studied compounds.
机译:研究了C-4'取代基对电子电离诱导的某些2-苯基-1,3,4-恶二唑分解过程中苯甲酰离子形成的影响。这些离子的形成通过叠氮基离子发生。将苯甲酰基离子丰度的总和和由它们衍生的碎片离子的丰度之和(以总离子流的百分比表示)与C-4'原子和与C-4'原子相连的原子的电荷密度进行比较。分子和中间叠氮离子均具有线性相关性。在取代基不太可能带正电的情况下,苯甲酰基离子的峰具有较高的相对强度。可以推断出,苯环中的电离强烈地影响了所研究化合物分子离子中苯甲酰离子的形成。

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