Jv. Headley et al., COLLISION-INDUCED DISSOCIATION MASS-SPECTROMETRY OF THE HERBICIDE DICLOFOP-METHYL, Rapid communications in mass spectrometry, 8(6), 1994, pp. 484-486
The collision-induced dissociation (CID) spectra of positive ions of t
he herbicide diclofop-methyl are reported. The results indicate that f
or relatively low collision energies (<75 eV, laboratory frame of refe
rence), the distribution of the CID ions of the molecular ion correlat
es in a qualitative manner with the occurrence of transformation produ
cts arising from the degradation of the herbicide in geologic or biofi
lm materials. At low collision energies (30-45 eV, laboratory frame of
reference), the CID spectra contained a preponderance of product ions
at m/z 281 and 253. These product ions correspond to prevalent transf
ormation products in soil, 4-(2,4-dichlorophenoxy)dehydrophenetole (mo
lecular ion 282) and 4-(2,4-dichlorophenoxy)phenol (molecular ion 254)
respectively. At higher collision energies (>45 eV), product ions wer
e observed for up to three bond cleavages. The high energy CID product
ions correspond to transformation products observed in mature biofilm
materials cultivated on the parent herbicide as the sole carbon sourc
e.