Abstract
The H/D exchange of arenes in acidic media by transition-metal and main-group-metal complexes and common inorganic salts was studied. The influence of Lewis acidity, anions, charge, and ligands was evaluated. The results indicate that the determination of H/D exchange activity in acidic media is not related to the formation of metal-carbon bonds (i.e., C-H activation). The combined experimental data (regioselectivity, activation energy, kinetics, isotope effects, solvent effects) and DFT calculations point toward a proton catalysis mechanism. Thus, highly Lewis acidic metal compounds, such as aluminum(III) triflate, were extraordinarily active for the H/D exchange reactions. Indeed, the degree of H/D exchange reactivity allows for a comparative measurement of Lewis acidities. (Chemical Equation Presented).
| Original language | English |
|---|---|
| Pages (from-to) | 769-775 |
| Number of pages | 7 |
| Journal | ACS Catalysis |
| Volume | 5 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 6 Feb 2015 |
| Externally published | Yes |
Keywords
- CH activation
- H/D exchange
- Lewis acid
- acids
- benzene
- toluene
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