Abstract
AbstractAlkynylferrocenes react with tetracyanoethylene (TCNE) to form 2‐ferrocenyl‐1,1,4,4‐tetracyanobutadienes. These reactions occur under mild reaction conditions in almost quantitative yields if the triple bond is electron‐rich. Systems with more than one triple bond, namely, 1,1′‐dialkynylferrocenes or diynylferrocenes, react once at the more electron‐rich triple bond, and the second reaction cannot be achieved, even under more‐forcing reaction conditions. For a diyne with the reactivity switched by oxidation of the ferrocenyl moiety to the corresponding ferrocenium salt, the addition of TCNE occurred at the less electron‐rich triple bond. This unprecedented reactivity is explained by the resonance stabilization of a diradical intermediate. A push–pull 1,1′‐dialkynylferrocene with a [4‐(dimethylamino)phenyl]ethynyl and a (4‐nitrophenyl)ethynyl substituent reacted exclusively at the [4‐(dimethylamino)phenyl]ethynyl triple bond.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.