Gas phase reaction between chromones and solvent in an electrospray ionization source

• Published in: Journal of mass spectrometry. Vol. 54; no. 1; pp. 66 - 72
• Main Authors: Liu, Zhen, Shao, Yunlong, Zhu, Guizhen, Wang, Xiayan, Chai, Yunfeng, Wang, Lin
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.01.2019
• Subjects: chromones; covalent/noncovalent adduct; Deuterium; Dissociation; electrospray ionization; Electrospraying; High performance liquid chromatography; HPLC; in‐source reaction; Ionization; Ions; Liquid chromatography; Mass spectrometry; Mass spectroscopy; Metabolites; Methanol; Scientific imaging; Solvents; Spectroscopy; Substitutes; Vapor phases; electrospray ionization; in-source reaction; chromones; covalent/noncovalent adduct
• ISSN: 1076-5174; 1096-9888
• DOI: 10.1002/jms.4305

Chromones were measured by using electrospray ionization mass spectrometry in negative mode. Interestingly, in addition to the deprotonated ion ([M − H]−), unexpected [M + 17]− and [M + 31]− ions were observed in high intensity when water and methanol were used as the solvent. Chromones with different substitutes were tested. Compared with the deprotonated ion, [M + 17]− and [M + 31]− ions were observed with higher abundances when the C‐3 site of chromones was substituted by electron withdrawing groups. Based on high performance liquid chromatography‐mass spectrometry (LC‐MS), deuterium‐labeling and collisional‐induced dissociation experiments, a covalent gas‐phase nucleophilic addition reaction between chromone and water, and the formation of a noncovalent complex between chromone and methanol were proposed as the mechanism for the observed [M + 17]− and [M + 31]− ions, respectively. Understanding and using these unique gas phase reactions can avoid misannotation when analyzing chromones and their metabolites.