Structural Complexity of Glyphosate and Aminomethylphosphonate Metal Complexes

Abstract

Small differences in the structure and subsequent reactivity of glyphosate complexes can have a highly consequential impact due to the enormous quantities of glyphosate used globally. The gas phase metal speciation of glyphosate and its abundant metabolite, aminomethylphosphonic acid (AMPA), were determined using cross-platform electrospray ionisation ion mobility mass spectrometry. Monomeric [M+L−H]⁺ complexes, and both larger, and/or higher order clusters formed with divalent metals (M = Mg²⁺, Ca²⁺, Sr²⁺, Ba²⁺, Mn²⁺, Co²⁺, Cu²⁺, and Zn²⁺; and L = glyphosate and AMPA). Complexation occurred at more than one ligand donor site for [M+L−H]⁺, resulting in multidentate complexes. The type of complex depended on M, with central positions maximizing the interactions of the M with donor sites of the L preferred. The isomers were separated by ion mobility and experimental collisional cross sections (^N2CCS_exp) were derived for all isolated species. An energy threshold DFT approach located the structural families and potential lowest energy forms; these were found to be consistent with confirmed condensed phase (reported crystal structures) and gas phase structures (via infrared multiphoton dissociation, IRMPD). Theoretical nitrogen collisional cross sections (^N2CCS_calc) of these confirmed structures tended to underestimate the ^N2CCS_exp for both [M+glyphosate−H]⁺ and [M+AMPA−H]⁺ complexes. Underestimation ranged between 1 - 20%, and was not uniform between species. By comparison, helium collisional cross sections (^HeCCS_exp and ^HeCCS_calc) were in better agreement (within 1-3%). These findings suggest further refinements are needed to collisional cross section modelling for metal containing species, in particular for nitrogen drift gas.