Different reactivities of H3 O+ (H2 O)n with unsaturated and saturated aldehydes: ligand-switching reactions govern the quantitative analytical sensitivity of SESI-MS
Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články
Grantová podpora
Praemium Academiae
Akademie Věd České Republiky
21-25486S
Czech Science Foundation GACR
Czech Academy of Sciences
PubMed
36807598
DOI
10.1002/rcm.9496
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
RATIONALE: The detection sensitivity of secondary electrospray ionisation mass spectrometry (SESI-MS) is much lower for saturated aldehydes than for unsaturated aldehydes. This needs to be understood in terms of gas phase ion-molecule reaction kinetics and energetics to make SESI-MS analytically more quantitative. METHODS: Parallel SESI-MS and selected ion flow tube mass spectrometry (SIFT-MS) analyses were carried out of air containing variable accurately determined concentrations of saturated (C5, pentanal; C7, heptanal; C8 octanal) and unsaturated (C5, 2-pentenal; C7, 2-heptenal; C8, 2-octenal) aldehyde vapours. The influence of the source gas humidity and the ion transfer capillary temperature, 250 and 300°C, in a commercial SESI-MS instrument was explored. Separate experiments were carried out using SIFT to determine the rate coefficients, k73 , for the ligand-switching reactions of the H3 O+ (H2 O)3 ions with the six aldehydes. RESULTS: The relative slopes of the plots of SESI-MS ion signal against SIFT-MS concentration were interpreted as the relative SESI-MS sensitivities for these six compounds. The sensitivities for the unsaturated aldehydes were 20 to 60 times greater than for the corresponding C5, C7 and C8 saturated aldehydes. Additionally, the SIFT experiments revealed that the measured k73 are three or four times greater for the unsaturated than for the saturated aldehydes. CONCLUSIONS: The trends in SESI-MS sensitivities are rationally explained by differences in the rates of the ligand-switching reactions, which are justified by theoretically calculated equilibrium rate constants derived from thermochemical density functional theory (DFT) calculations of Gibb's free energy changes. The humidity of SESI gas thus favours the reverse reactions of the saturated aldehyde analyte ions, effectively suppressing their signals in contrast to their unsaturated counterparts.
Zobrazit více v PubMed
Martínez-Lozano Sinues P, Rus J, Fernández de la Mora G, Hernández M, Fernández de la Mora J. Secondary electrospray ionization (SESI) of ambient vapors for explosive detection at concentrations below parts per trillion. J Am Soc Mass Spectrom. 2009;20(2):287-294. doi:10.1016/j.jasms.2008.10.006
Dillon LA, Stone VN, Croasdell LA, Fielden PR, Goddard NJ, Paul Thomas CL. Optimisation of secondary electrospray ionisation (SESI) for the trace determination of gas-phase volatile organic compounds. Analyst. 2010;135(2):306-314. doi:10.1039/b918899a
Rioseras AT, Gaugg MT, Martinez-Lozano Sinues P. Secondary electrospray ionization proceeds via gas-phase chemical ionization. Anal Methods. 2017;9(34):5052-5057. doi:10.1039/C7AY01121K
Dryahina K, Som S, Smith D, Španěl P. Reagent and analyte ion hydrates in secondary electrospray ionization mass spectrometry (SESI-MS), their equilibrium distributions and dehydration in an ion transfer capillary: Modelling and experiments. Rapid Commun Mass Spectrom. 2021;35(7):e9047. doi:10.1002/rcm.9047
Dryahina K, Polášek M, Smith D, Španěl P. Sensitivity of secondary electrospray ionization mass spectrometry to a range of volatile organic compounds: Ligand switching ion chemistry and the influence of Zspray™ guiding electric fields. Rapid Commun Mass Spectrom. 2021;35(22):e9187. doi:10.1002/rcm.9187
Spesyvyi A, Lacko M, Dryahina K, Smith D, Španěl P. Ligand switching ion chemistry: An SIFDT case study of the primary and secondary reactions of protonated acetic acid hydrates with acetone. J Am Soc Mass Spectrom. 2021;32(8):2251-2260. doi:10.1021/jasms.1c00174
Martinez-Lozano Sinues P, Criado E, Vidal G. Mechanistic study on the ionization of trace gases by an electrospray plume. Int J Mass Spectrom. 2012;313:21-29. doi:10.1016/j.ijms.2011.12.010
de la Mora JF. Ionization of vapor molecules by an electrospray cloud. Int J Mass Spectrom. 2011;300(2-3):182-193. doi:10.1016/j.ijms.2010.09.009
Kaeslin J, Wuthrich C, Giannoukos S, Zenobi R. How soft is secondary electrospray ionization? J Am Soc Mass Spectrom. 2022;33(10):1967-1974. doi:10.1021/jasms.2c00201
Liu C, Zeng J, Sinues P, Fang M, Zhou Z, Li X. Quantification of volatile organic compounds by secondary electrospray ionization-high resolution mass spectrometry. Anal Chim Acta. 2021;1180:338876. doi:10.1016/j.aca.2021.338876
Martinez-Lozano Sinues P, de la Mora JF. Electrospray ionization of volatiles in breath. Int J Mass Spectrom. 2007;265(1):68-72. doi:10.1016/j.ijms.2007.05.008
Lan J, Kaeslin J, Greter G, Zenobi R. Minimizing ion competition boosts volatile metabolome coverage by secondary electrospray ionization orbitrap mass spectrometry. Anal Chim Acta. 2021;1150:338209. doi:10.1016/j.aca.2021.338209
Midey AJ, Williams S, Arnold ST, Viggiano AA. Reactions of H3O+(H2O)(0,1) with alkylbenzenes from 298 to 1200 K. J Phys Chem a. 2002;106(48):11726-11738. doi:10.1021/jp014141e
Španěl P, Smith D. Reactions of hydrated hydronium ions and hydrated hydroxide ions, with some hydrocarbons and oxygen-bearing organic-molecules. J Phys Chem. 1995;99(42):15551-15556. doi:10.1021/j100042a033
Viggiano AA, Dale F, Paulson JF. Proton transfer reactions of H+(H2O)n=2-11 with methanol, ammonia, pyridine, acetonitrile, and acetone. J Chem Phys. 1988;88(4):2469-2477. doi:10.1063/1.454027
Španěl P, Smith D. Selected ion flow tube mass spectrometry analyses of stable isotopes in water: Isotopic composition of H3O+ and H3O+(H2O)(3) ions in exchange reactions with water vapor. J Am Soc Mass Spectrom. 2000;11(10):866-875. doi:10.1016/S1044-0305(00)00157-4
Španěl P, Smith D. Progress in SIFT-MS: Breath analysis and other applications. Mass Spectrom Rev. 2011;30(2):236-267. doi:10.1002/mas.20303
Španěl P, Smith D. Advances in on-line absolute trace gas analysis by SIFT-MS. Curr Anal Chem. 2013;9(4):525-539. doi:10.2174/15734110113099990017
Smith D, Pysanenko A, Španěl P. Ionic diffusion and mass discrimination effects in the new generation of short flow tube SIFT-MS instruments. Int J Mass Spectrom. 2009;281(1-2):15-23. doi:10.1016/j.ijms.2008.11.007
Španěl P, Dryahina K, Smith D. A general method for the calculation of absolute trace gas concentrations in air and breath from selected ion flow tube mass spectrometry data. Int J Mass Spectrom. 2006;249:230-239. doi:10.1016/j.ijms.2005.12.024
Neese F. Software update: The ORCA program system, version 4.0. Wiley Interdiscip Rev Comput Mol Sci. 2018;8(1). doi:10.1002/wcms.1327
Hanwell MD, Curtis DE, Lonie DC, Vandermeersch T, Zurek E, Hutchison GR. Avogadro: An advanced semantic chemical editor, visualization, and analysis platform. J Chem. 2012;4(1):17. doi:10.1186/1758-2946-4-17
Caldeweyher E, Bannwarth C, Grimme S. Extension of the D3 dispersion coefficient model. J Chem Phys. 2017;147(3):034112. doi:10.1063/1.4993215
Španěl P, Smith D. On-line measurement of the absolute humidity of air, breath and liquid headspace samples by selected ion flow tube mass spectrometry. Rapid Commun Mass Spectrom. 2001;15(8):563-569. doi:10.1002/rcm.265
Smith D, Chippendale TWE, Španěl P. Reactions of the selected ion flow tube mass spectrometry reagent ions H3O+ and NO+ with a series of volatile aldehydes of biogenic significance. Rapid Commun Mass Spectrom. 2014;28(17):1917-1928. doi:10.1002/rcm.6977
Španěl P, Ji YF, Smith D. SIFT studies of the reactions of H3O+, NO+ and O2+ with a series of aldehydes and ketones. Int J Mass Spectrom. 1997;165:25-37. doi:10.1016/S0168-1176(97)00166-3
Španěl P, Van Doren JM, Smith D. A selected ion flow tube study of the reactions of H3O+, NO+, and O2+ with saturated and unsaturated aldehydes and subsequent hydration of the product ions. Int J Mass Spectrom. 2002;213(2-3):163-176. doi:10.1016/S1387-3806(01)00531-0
Su T, Chesnavich WJ. Parametrization of the ion-polar molecule collision rate constant by trajectory calculations. J Chem Phys. 1982;76(10):5183-5185. doi:10.1063/1.442828