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Demonstrates tunable emission from visible to near-infrared in solid-state dyes, indicating potential applications in photonics.
This article reports the synthesis and characterization of cross‐conjugated donor–acceptor dyes based on a N , N , N ’, N ’‐tetraphenyl‐1,4‐phenylenediamine core, substituted at the 2,5‐positions with various electron‐withdrawing groups (carbonyl, imines, nitriles, or electron‐poor heterocycles). Electrochemical studies reveal electronic communication between para ‐substituted donor groups and, in some cases, between acceptor groups. Photophysical studies show tunable absorption and emission properties based on the strength of the electron‐withdrawing groups, a trend that is rationalized through computational analysis. Notably, some compounds exhibit long emission lifetimes in solution, whereas all dyes emit in the solid state, with emission extending into the near‐infrared (up to > 1000 nm).
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Mourot et al. (2026) studied this question.
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