| Literature DB >> 25146595 |
G K Surya Prakash1, Fang Wang, Zhe Zhang, Ralf Haiges, Martin Rahm, Karl O Christe, Thomas Mathew, George A Olah.
Abstract
The trifluoromethanide anion is the postulated key intermediate in nucleophilic trifluoromethylation reactions. However, for more than six decades, the trifluoromethanide anion was widely believed to exist only as a short-lived transient species in the condensed phase. It has now been prepared in bulk for the first time in THF solution. The trifluoromethanide anion with the [K(18-crown-6)](+) cation was unequivocally characterized by low-temperature (19)F and (13)C NMR spectroscopy. Its intermediacy in nucleophilic trifluoromethylation reactions was directly evident by its reaction chemistry with various electrophilic substrates. Variable-temperature NMR spectroscopy, along with quantum mechanical calculations, support the persistence of the trifluoromethanide anion.Entities:
Keywords: NMR spectroscopy; carbanions; fluorine; reaction mechanisms; reactive intermediates
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Year: 2014 PMID: 25146595 DOI: 10.1002/anie.201406505
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336