Investigation of the unusual behavior of metolachlor under chemical ionization in a hybrid 3D ion trap mass spectrometer.

Pierre Henri Goulden (1) , Sarah Coffinet (1) , Christophe Genty (1) , Sophie Bourcier (1) , Michel Sablier (1) , Stephane Bouchonnet (1)

1 DCMR - Laboratoire des mécanismes réactionnels

This article describes the strange behavior of the widely used herbicide metolachlor under chemical ionization conditions in a hybrid source ion trap mass spectrometer in gas chromatography/mass spectrometry (GC/MS) coupling. With the use of ammonia as the reagent gas, metolachlor provides a chlorinated ion at m/z 295/297, almost as abundant as the protonated molecule at m/z 284/286, which cannot be isolated to perform tandem mass spectrometry (MS(n)) experiments. Curiously, this ion at m/z = M + 12 is not observed for the herbicides acetochlor and alachlor, which present very similar chemical structures. The chemical structure of the m/z 295/297 ions and the explanation of the observed phenomenon based on the metastable behavior of these ions were elucidated on the basis of experiments including isotopic labeling and modifications of the operating conditions of the ion trap mass spectrometer. This work allows one to give new recommendations for an optimized use of hybrid source ion trap mass spectrometers. © 2011 American Chemical Society

Domains: Theoretical and/or physical chemistry

Pierre Henri Goulden, Sarah Coffinet, Christophe Genty, Sophie Bourcier, Michel Sablier, et al.. Investigation of the unusual behavior of metolachlor under chemical ionization in a hybrid 3D ion trap mass spectrometer.. Analytical Chemistry, 2011, 83 (20), pp.7587-7590. ⟨10.1021/ac201563w⟩. ⟨hal-00904587⟩