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Fragmentation characteristics of hydroxycinnamic acids in ESI-MSn by density functional theory.
- Source :
-
Journal of Mass Spectrometry . Jul2017, Vol. 52 Issue 7, p427-433. 7p. - Publication Year :
- 2017
-
Abstract
- This work aims to analyze the electrospray ionization multistage mass spectrometry (ESI-MSn) fragmentation characteristics of hydroxycinnamic acids (HCAs) in negative ion mode. The geometric parameters, energies, natural bond orbitals and frontier orbitals of fragments were calculated by density functional theory (DFT) to investigate mass spectral fragmentationmechanisms. The results showed that proton transfer always occurred during fragmentation of HCAs; their quasi-molecular ions ([M - H]-) existed inmore than one form and weremainlywith the lowest energy. The fragmentation characteristics included the followings: (1) according to the different substitution position of phenolic hydroxyl group, the ring contraction reaction by CO elimination from benzene was in an increasingly difficult order: m-phenolic hydroxyl > p-phenolic hydroxyl > o-phenolic hydroxyl; and (2) ortho effect always occurred in o-dihydroxycinnamic acids (o-diHCAs), i.e. one phenolic hydroxyl group offered H+, which combined with the other one to lose H2O. In addition, there was a nucleophilic reaction during ring contraction in diHCAs that oxygen atom attacked the carbon atom binding with the other phenolic hydroxyl to lose CO2. The fragmentation characteristics andmechanismof HCAs could be used for analysis and identification of such compounds quickly and effectively, and as reference for structural analogues by ESI-MS. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10765174
- Volume :
- 52
- Issue :
- 7
- Database :
- Academic Search Index
- Journal :
- Journal of Mass Spectrometry
- Publication Type :
- Academic Journal
- Accession number :
- 123795123
- Full Text :
- https://doi.org/10.1002/jms.3945