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Mass Spectrometry of 2a,4-Disubstituted 5-Benzoyl-2a,3,4,5-tetrahydro-2-phenoxy-azeto[1,2-a][1,5]benzodiazepin-1(2H)-ones Under Electron Impact Ionization Conditions

Mass Spectrometry of 2a,4-Disubstituted 5-Benzoyl-2a,3,4,5-tetrahydro-2-phenoxy-azeto[1,2-a][1,5]benzodiazepin-1(2H)-ones Under Electron Impact Ionization Conditions
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摘要 The mass spectrometric fragmentation of 2a,4-disubstituted 5-benzoyl-2a,3,4,5-tetrahydro-2-phenoxy-azeto{[1,2-a]}[1,5]benzodiazepin-1(2H)-ones has been investigated by means of mass-analyzed ion kinetic energy spectrometry under electron impact ionization conditions. All compounds tend to lose different moieties, such as phenoxy, phenoxy and H, and phenoxyketene. Both [M +-PhO] and [M +-PhOH] ions could further lose CO, and the [M +-PhOCHCO] ions could lose propene or styrene, PhCON, PhCOHN, and other fragments. The mass spectrometric fragmentation of 2a,4-disubstituted 5-benzoyl-2a,3,4,5-tetrahydro-2-phenoxy-azeto{[1,2-a]}[1,5]benzodiazepin-1(2H)-ones has been investigated by means of mass-analyzed ion kinetic energy spectrometry under electron impact ionization conditions. All compounds tend to lose different moieties, such as phenoxy, phenoxy and H, and phenoxyketene. Both [M +-PhO] and [M +-PhOH] ions could further lose CO, and the [M +-PhOCHCO] ions could lose propene or styrene, PhCON, PhCOHN, and other fragments.
出处 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2005年第4期452-456,共5页 高等学校化学研究(英文版)
基金 SupportedbytheNationalNaturalScienceFoundationofChina(Nos.20272002and20472005),theExcellentYoungTeachersProgram,theScientificResearchFoundationfortheReturnedOverseaChineseScholarsofMinistryofEducationofChina,andthePresidentGrantofPekingUniversity.
关键词 Azeto[1 2-a][1 5]benzodiazepin-1(2H)-one Mass spectrometry FRAGMENTATION Mechanism Azeto[1,2-a][1,5]benzodiazepin-1(2H)-one, Mass spectrometry, Fragmentation, Mechanism
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