| Literature DB >> 11192090 |
W Sander1, R Hübert, E Kraka, J Gräfenstein, D Cremer.
Abstract
The 4-oxocyclohexa-2,5-dienylidenes are an interesting class of highly electrophilic carbenes. We investigated the reactivity of the 2,3,5,6-tetrafluorinated and -tetrachlorinated derivatives 1b and 1c with small molecules under conditions of matrix isolation. The reactions with molecular oxygen and with carbon monoxide produce the expected carbonyl O-oxides and ketenes, respectively. As a result of the extreme electrophilicity of 1b and c both carbenes insert with no or very small activation barriers into H2 or the CH bonds of hydrocarbons. Obviously, spin restrictions for these formally spin-forbidden reactions do not result in substantial thermal activation barriers.Entities:
Year: 2000 PMID: 11192090 DOI: 10.1002/1521-3765(20001215)6:24<4567::aid-chem4567>3.0.co;2-a
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236