Dissociation of gas-phase, doubly-charged uranyl-acetone complexes by collisional activation and infrared photodissociation
| Autor: | Dean Martin, Alexandra Plaviak, Benjamin J. Bythell, Catherine O’Malley, Patricia A. Mihm, John K. Gibson, Jordan Pestok, Michael J. Van Stipdonk, Theodore A. Corcovilos, Cassandra Hanley |
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| Rok vydání: | 2016 |
| Předmět: |
010401 analytical chemistry
Photodissociation Analytical chemistry 010402 general chemistry Photochemistry Mass spectrometry Uranyl Condensed Matter Physics 01 natural sciences Dissociation (chemistry) 0104 chemical sciences chemistry.chemical_compound chemistry Fragmentation (mass spectrometry) Infrared multiphoton dissociation Quadrupole ion trap Physical and Theoretical Chemistry Instrumentation Ion cyclotron resonance Spectroscopy |
| Zdroj: | International Journal of Mass Spectrometry. 396:22-34 |
| ISSN: | 1387-3806 |
| DOI: | 10.1016/j.ijms.2015.12.005 |
| Popis: | Past studies of fragmentation reactions of doubly-charged uranyl (UO22+) complexes have been impeded by very rapid water addition reactions that cause H2O adducts to dominate product ion spectra. The fragmentation of uranyl-acetone (aco) complexes ([UO2(aco)n]2+, n = 1–5), generated by electrospray ionization, is revisited here using: (a) collisional activation in a linear ion trap (LIT) mass spectrometer in which the level of background H2O is significantly lower, and (b) infrared multiple-photon photodissociation (IRMPD, 10.6 μm) in the LIT and a Fourier-transform ion cyclotron resonance (FT-ICR) mass spectrometer. Lower levels of adventitious H2O in the LIT provided access to fragmentation of [UO2(aco)n]2+, n = 1–5. For n = 3–5, direct elimination of aco ligands is the favored fragmentation pathway. For n = 1 and 2, charge reduction reactions are dominant. For [UO2(aco)2]2+, the most abundant product ion is [UO2(aco)]+, while UO2+ is observed following collision-induced dissociation (CID) of [UO2(aco)]2+. Minor peaks corresponding to ligated [UO2OH]+ are also observed. The IRMPD experiments in the FT-ICR yielded highly accurate mass measurements that confirm composition assignments, and shed light on dissociation reactions in a gas-phase environment that is entirely free of adventitious H2O. For [UO2(aco)n]2+, n = 3–5, the primary photodissociation channel is direct aco elimination, along with charge-reduction pathways that involve intra-complex proton transfer and formation of species that contain enolate ligands. Similar pathways are observed for IRMPD measurements in the LIT. |
| Databáze: | OpenAIRE |
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