Abstract The dicyanomethylene derivative of a benzophenone analog significantly alters the fragmentation pattern observed during electron impact ionization of the underivatized parent compound. A double bond connecting the dicyanomethylene moiety to the parent compound is cleaved during a major fragmentation pathway for many of these compounds. A mechanism involving rearrangement of two hydrogen atoms is proposed to rationalize ...
[Shibuya, Isao; Taguchi, Yoichi; Tsuchiya, Tohru; Oishi, Akihiro; Katoh, Eisaku Bulletin of the Chemical Society of Japan, 1994 , vol. 67, # 11 p. 3048 - 3052]