| Literature DB >> 25257391 |
Marcileia Zanatta1, Anne-Lise Girard, Nathalia M Simon, Gunter Ebeling, Hubert K Stassen, Paolo R Livotto, Francisco P dos Santos, Jairton Dupont.
Abstract
1-n-Butyl-2,3-dimethylimidazolium (BMMI) ionic liquids (ILs) associated with different anions undergo H/D exchange preferentially at 2-Me group of the imidazolium in deuterated solvents. This process is mainly related to the existence of ion pairs rather than the anion basicity. The H/D exchange occurs in solvents (CDCl3 and MeCN for instance) in which intimate contact ion pairs are present and the anion possesses a labile H in its structure, such as hydrogen carbonate and prolinate. In D2 O, separated ion pairs are formed and the H/D exchange does not occur. A plausible catalytic cycle is that the IL behaves as a neutral base in the course of all H/D exchange processes. NMR experiments, density functional calculations, and molecular dynamics simulations corroborate these hypotheses.Entities:
Keywords: NMR spectroscopy; contact ion pairs; density functional calculations; ionic liquids; molecular dynamics
Year: 2014 PMID: 25257391 DOI: 10.1002/anie.201408151
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336