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. 2024 Feb 1;29(3):680.
doi: 10.3390/molecules29030680.

Fragmentation Pathway of Organophosphorus Flame Retardants by Liquid Chromatography-Orbitrap-Based High-Resolution Mass Spectrometry

Kangcong Li  1   2 , Yan Gao  1   3 , Xiuqin Li  1   3 , Yan Zhang  1   4 , Benfeng Zhu  2 , Qinghe Zhang  1   3
Affiliations

Fragmentation Pathway of Organophosphorus Flame Retardants by Liquid Chromatography-Orbitrap-Based High-Resolution Mass Spectrometry

Kangcong Li et al. Molecules. .

Abstract

Organophosphorus flame retardants (OPFRs) have been widely used in polymeric materials owing to their flame retardant and plasticizing effects. Investigating the fragmentation pathway of OPFRs is of great necessity for further discovering and identifying novel pollutants using orbitrap-based high-resolution mass spectrometry (HRMS). A total of 25 OPFRs, including alkyl, halogenated, and aromatic types, were analyzed in this study. The fragmentation pathways of the OPFRs were investigated using orbitrap-based HRMS with high-energy collision dissociation (HCD) in positive mode. The major fragmentation pathways for the three types of OPFRs are greatly affected by the substituents. In detail, the alkyl and halogenated OPFRs underwent three McLafferty hydrogen rearrangements, wherein the substituents were gradually cleaved to form the structurally stable [H4PO4]+ (m/z = 98.9845) ions. In contrast, the aromatic OPFRs would cleave not only the C-O bond but also the P-O bond, depending on the substituents, to form fragment ions such as [C6H7O]+ (m/z = 95.0495) or [C7H7]+ (m/z = 91.0530), among others. Using HRMS improved the accuracy of fragment ion identification, and the pathway became more evident. These fragmentation laws can provide identification information in pollutant screening work and theoretical references for the structural characterization of compounds with diverse substituent structures.

Keywords: fragmentation pathway; high resolution mass spectrometry; liquid chromatography; organophosphorus flame retardant.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Possible fragmentation pathway of TnPP.
Figure 2
Figure 2
MS2 spectra of 5 alkyl OPFR compounds.
Figure 2
Figure 2
MS2 spectra of 5 alkyl OPFR compounds.
Figure 3
Figure 3
Possible fragmentation pathway of TCPP.
Figure 4
Figure 4
MS2 spectra of two halogenated OPFR compounds.
Figure 5
Figure 5
Possible fragmentation pathway of dBPhP.
Figure 6
Figure 6
MS2 spectra of two aromatic OPFR compounds.
Figure 7
Figure 7
Mass spectra of TMP under two instruments.
Figure 8
Figure 8
Matching of MS2 spectra of (a) TEP and (b) CDPP in standard solutions and rice samples.
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