posted on 2013-10-14, 00:00authored byAnnika Liske, Kathrin Verlinden, Hannes Buhl, Klaus Schaper, Christian Ganter
A new method for the assessment of
the π-acceptor strength
of N-heterocyclic carbenes is presented. The 77Se chemical
shifts of the easily available selenium carbene adducts 1·Se–7·Se correlate with the π-acceptor
character of the respective carbenes. The observed δ(77Se) values cover a range of almost 800 ppm, with increasing π-acidity
leading to a downfield shift of the signal.