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Dissociation of doubly charged transition metal/polyether/pyridyl ligand complexes in a quadrupole ion trap mass spectrometer

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Journal of the American Society for Mass Spectrometry

Abstract

The dissociation of a series of doubly charged pyridyl ligand/polyether/transition metal complexes is studied using electrospray ionization and collision activation methods. Both doubly charged mixed-ligand dimer and trimers are observed by electrospray ionization. The mixed-ligand trimer complexes always dissociate by cleavage of one entire ligand, whereas the mixed-ligand dimers show a more diverse array of fragmentation pathways, including charge reduction processes. The fragmentation pathways of these mixed-ligand dimers are influenced by the second ionization energy and electron configuration of the metal and relative coordination strength of the ligands.

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Correspondence to Jennifer Brodbelt.

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Shen, J., Brodbelt, J. Dissociation of doubly charged transition metal/polyether/pyridyl ligand complexes in a quadrupole ion trap mass spectrometer. J Am Soc Mass Spectrom 10, 126–135 (1999). https://doi.org/10.1016/S1044-0305(98)00137-8

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  • DOI: https://doi.org/10.1016/S1044-0305(98)00137-8

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