| Literature DB >> 28389984 |
Thyago S Rodrigues1, Denis Lesage2, Wender A da Silva1, Richard B Cole2, Günter Ebeling3, Jaïrton Dupont3, Heibbe C B de Oliveira1, Marcos N Eberlin4, Brenno A D Neto5.
Abstract
Negatively charge-tagged N-heterocyclic carbenes have been formed in solution via deprotonation of imidazolium ions bearing acid side groups and transferred to the gas phase via ESI(-)-MS. The structure of the putative and apparently stable gaseous carbenes formed in such conditions were then probed via reactions with carbon dioxide using a triple quadrupole mass spectrometer particularly optimized for ion/molecule reactions of ESI-generated ions. Complete conversion to imidazolium carboxylates was achieved, which seems to demonstrate the efficiency of the transfer, the gas-phase stability, and the long-lived nature of these unprecedented charge-tagged carbenes and their predominance in the ionic population. Comprehensive studies on the intrinsic reactivity of N-heterocyclic carbenes with silent charge tags are therefore possible. Graphical Abstract ᅟ.Entities:
Keywords: Ion/molecule reactions; Ionic liquids; N-heterocyclic carbenes
Year: 2017 PMID: 28389984 DOI: 10.1007/s13361-017-1637-8
Source DB: PubMed Journal: J Am Soc Mass Spectrom ISSN: 1044-0305 Impact factor: 3.109