Reactivity of Functionalized Ynamides with Tetracyanoethylene: Scope, Limitations and Optoelectronic Properties of the Adducts

The reactivity of functionalized ynamides and arylynamines with tetracyanoethylene at room temperature was evaluated. In most cases, the corresponding 1,1,4,4‐tetracyanobutadienes (TCBDs) were obtained in good to excellent yields through a [2+2]‐cycloaddition/[2+2]‐retro‐electrocyclization sequence. The influence of diverse functional groups on the yield of the reaction was investigated, in particular concerning multiple ynamides. These TCBDs were characterized by various spectroscopic techniques and electrochemistry and X‐ray diffraction in some cases. Sequence of events: The reactivity of functionalized ynamides and arylynamines towards tetracyanoethylene at room temperature is evaluated. In most cases, the corresponding 1,1,4,4‐tetracyanobutadienes are obtained in good to excellent yields through a [2+2]‐cycloaddition/[2+2]‐retro‐electrocyclization sequence. The influence of diverse functional groups on the yield is investigated, in particular concerning multiple ynamides.