The gas-phase methylation of benzene and toluene
| Autor: | Marin S. Robinson, Ditte L. Thomsen, Edwin L. Motell, Rustam Garrey, Zhe Chen Wang, Charles H. DePuy, Veronica M. Bierbaum |
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| Rok vydání: | 2018 |
| Předmět: |
Hydride
010401 analytical chemistry 010402 general chemistry Condensed Matter Physics Photochemistry 01 natural sciences Toluene Medicinal chemistry Dissociation (chemistry) 0104 chemical sciences Adduct Electron transfer chemistry.chemical_compound chemistry Physical and Theoretical Chemistry Benzene Instrumentation Spectroscopy Gas-phase ion chemistry Methyl group |
| Zdroj: | International Journal of Mass Spectrometry. 429:6-13 |
| ISSN: | 1387-3806 |
| DOI: | 10.1016/j.ijms.2017.03.009 |
| Popis: | The reactions of the methyl cation with benzene and toluene in the gas phase have been examined using the flowing afterglow-selected ion flow-drift tube technique. With benzene four product ions are formed, C 6 H 6 + by electron transfer, C 6 H 5 + by addition and loss of CH 4 , C 7 H 7 + by addition and loss of H 2 , and an adduct C 7 H 9 + . Deuterium and carbon-13 labeling experiments were carried out to provide mechanistic insights. In agreement with earlier work, deuterium labeling (CD 3 + with C 6 H 6 or CH 3 + with C 6 D 6 ) shows that partial H/D scrambling between the methyl group and the ring occurs during the formation of C 6 H 5 + and C 7 H 7 + . However, in contrast to earlier work, no carbon-13 scrambling was observed between the methyl and ring carbons, thus ruling out a ring expansion and contraction mechanism to account for the H/D scrambling. Nor did we find H/D scrambling in the electron transfer product ion, C 6 H 6 + . When collision-induced dissociation (CID) was carried out on the adduct ion, extensive H/D and carbon-13 scrambling was found, indicating that at least some ring expansion occurs during its formation. Reaction of C 6 H 5 + with methane at room temperature exclusively forms the adduct ion; in a drift field, this adduct ion fragments by loss of CH 4 and H 2 . Mechanisms are proposed which account for our results, and these are supported by ab initio calculations. Similar studies were carried out with toluene as the neutral reagent. Besides the four analogous product ions, we found hydride transfer from the methyl group of toluene to be a major reaction channel and addition with loss of ethylene to be a minor channel. |
| Databáze: | OpenAIRE |
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