Highly Substituted Δ3 -1,2,3-Triazolines: Solid-State Emitters with Electrofluorochromic Behavior.

Highly substituted Δ3 -1,2,3-triazolines can be prepared by reaction of triarylvinyl Grignard reagents with functionalized organic azides. The heterocycles are fluorescent in the solid state, and-depending on the substituents-they can display aggregation-induced emission. Upon oxidation, the triazolines form stable radical cations with altered photophysical properties. Therefore, they represent rare examples of solid-state emitters with intrinsic electrofluorochromic behavior.