Water-catalyzed hydrolysis of the radical cation of ketene in the gas phase: theory and experiment |
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Authors: | Orlova Galina Blagojevic Voislav Bohme Diethard K |
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Institution: | Department of Chemistry, Centre for Research in Mass Spectrometry, Centre for Research in Earth and Space Science, York University, Toronto, Ontario, Canada M3J 1P3. |
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Abstract: | Both theoretical and experimental investigations are reported for the gas-phase hydrolysis of the radical cation of ketene, H(2)CCO(*+). Density functional theory (DFT) with the B3LYP/6-311++G(d,p) method indicates that a second water molecule is required as a catalyst for the addition of water across the C=O bond in H(2)CCO(*+) by eliminating the activation barrier for the conversion of H(2)CCO.H(2)O](*+) to H(2)CC(OH)(2)](*+). Theory further indicates that H(2)CC(OH)(2).H(2)O](*+) may recombine with electrons to produce neutral acetic acid. Experimental results of flow-reactor tandem mass spectrometer experiments in which CH(2)CO(*+) ions were produced either directly from ketene by electron transfer or by the chemical reaction of CH(2)(*+) with CO are consistent with formation of an (C(2),H(4),O(2))(*+) ion in a reaction second-order in H(2)O. Furthermore, comparative multi-CID experiments indicate that this ion is likely to be the enolic CH(2)C(OH)(2)(*+) cation. The results suggest a possible mechanism for the formation of acetic acid from ketene and water on icy surfaces in hot cores and interstellar clouds. |
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