Ortho-hydroxyl effect and proton transfer via ion-neutral complex: the fragmentation study of protonated imine resveratrol analogues in mass spectrometry

The fragmentation pathways of protonated imine resveratrol analogues in the gas‐phase were investigated by electrospray ionization–tandem mass spectrometry. Benzyl cations were formed in the imine resveratrol analogues that had an ortho‐hydroxyl group on the benzene ring A. The specific elimination...

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Veröffentlicht in:	Journal of mass spectrometry. 2016-07, Vol.51 (7), p.518-523
Hauptverfasser:	Yue, Lei, Li, Jing, Xie, Xiaodong, Guo, Cheng, Yin, Xinchi, Yin, Qi, Chen, Yinjuan, Pan, Yuanjiang, Ding, Chuanfan
Format:	Artikel
Sprache:	eng
Schlagworte:	benzyl cation Cations Chlorination Congeners Fragmentation imine resveratrol analogue Imines ion-neutral complex Mass spectrometry ortho-hydroxyl effect Pathways proton transfer Rings (mathematics)
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