A Versatile Strategy for the Generation of Air‐stable Radical‐functionalized Materials

Abstract The exploration of a facile approach to create structurally versatile substances carrying air‐stable radicals is highly desired, but still a huge challenge in chemistry and materials science. Herein, a non‐contact method to generate air‐stable radicals by exposing pyridine/imidazole ring‐bearing substances to volatile cyanuric chloride vapor, harnessed as a chemical fuel is reported. This remarkable feat is accomplished through a nucleophilic substitution reaction, wherein an intrinsic electron transfer event transpires spontaneously, originating from the chloride anion (Cl − ) to the cationic nitrogen (N + ) atom, ultimately giving rise to pyridinium/imidazolium radicals. Impressively, the generated radicals exhibit noteworthy stability in the air over one month owing to the delocalization of the unpaired electron through the extended and highly fused π‐conjugated pyridinium/imidazolium‐triazine unit. Such an approach is universal to diverse substances, including organic molecules, metal–organic complexes, hydrogels, polymers, and organic cage materials. Capitalizing on this versatile technique, surface radical functionalization can be readily achieved across diverse substrates. Moreover, the generated radical species showcase a myriad of high‐performance applications, including mimicking natural peroxidase to accelerate oxidation reactions and achieving high‐efficiency near‐infrared photothermal conversion and photothermal bacterial inhibition.