Počet záznamů: 1
Kinetics of reactions of NH4+ with some biogenic organic molecules and monoterpenes in helium and nitrogen carrier gases: A potential reagent ion for selected ion flow tube mass spectrometry
- 1.
SYSNO ASEP 0558892 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Kinetics of reactions of NH4+ with some biogenic organic molecules and monoterpenes in helium and nitrogen carrier gases: A potential reagent ion for selected ion flow tube mass spectrometry Tvůrce(i) Swift, Stefan James (UFCH-W)
Smith, David (UFCH-W) ORCID
Dryahina, Kseniya (UFCH-W) RID, ORCID
Omezzine Gnioua, Maroua (UFCH-W)
Španěl, Patrik (UFCH-W) RID, ORCIDČíslo článku e9328 Zdroj.dok. Rapid Communications in Mass Spectrometry. - : Wiley - ISSN 0951-4198
Roč. 36, č. 15 (2022)Poč.str. 10 s. Jazyk dok. eng - angličtina Země vyd. GB - Velká Británie Klíč. slova AMMONIA CHEMICAL-IONIZATION ; SIFT-MS ; PROTON AFFINITIES Vědní obor RIV CF - Fyzikální chemie a teoretická chemie Obor OECD Physical chemistry CEP GA21-25486S GA ČR - Grantová agentura ČR Způsob publikování Omezený přístup Institucionální podpora UFCH-W - RVO:61388955 UT WOS 000811538900001 EID SCOPUS 85134179691 DOI 10.1002/rcm.9328 Anotace Rationale To assess the suitability of NH4+ as a reagent ion for trace gas analysis by selected ion flow tube mass spectrometry, SIFT-MS, its ion chemistry must be understood. Thus, rate coefficients and product ions for its reactions with typical biogenic molecules and monoterpenes need to be experimentally determined in both helium, He, and nitrogen, N-2, carrier gases. Methods NH4+ and H3O+ were generated in a microwave gas discharge through an NH3 and H2O vapour mixture and, after m/z selection, injected into He and N-2 carrier gas. Using the conventional SIFT method, NH4+ reactions were then studied with M, the biogenic molecules acetone, 1-propanol, 2-butenal, trans-2-heptenal, heptanal, 2-heptanone, 2,3-heptanedione and 15 monoterpene isomers to obtain rate coefficients, k, and product ion branching ratios. Polarisabilities and dipole moments of the reactant molecules and the enthalpy changes in proton transfer reactions were calculated using density functional theory. Results The k values for the reactions of the biogenic molecules were invariably faster in N-2 than in He but similar in both bath gases for the monoterpenes. Adducts NH4+M were the dominant product ions in He and N-2 for the biogenic molecules, whereas both MH+ and NH4+M product ions were observed in the monoterpene reactions. The monoterpene ratio correlating (R-2 = 0.7) with the proton affinity, PA, of the monoterpene molecule as calculated. The data indicate that this adduct ion formation is the result of bimolecular rather than termolecular association. Conclusions NH4+ can be a useful reagent ion for SIFT-MS analyses of molecules with PA(M) < PA(NH3) when the dominant single product ion is the adduct NH4+M. For molecules with PA(M) > PA(NH3), such as monoterpenes, both MH+ and NH4+M ions are likely products, which must be determined along with k by experiment. Pracoviště Ústav fyzikální chemie J.Heyrovského Kontakt Michaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196 Rok sběru 2023 Elektronická adresa http://hdl.handle.net/11104/0332388
Počet záznamů: 1