Theoretical elucidation reveals bimodality in fluorescent properties of 2,5-diaminopyrimidines, highlighting potential for Pd detection.
Compact organic fluorophores are attractive scaffolds for probe design, yet their emission is often compromised by efficient nonradiative decay. Here, we introduce 2,5-diaminopyrimidine-based C4N4 as an intrinsically emissive, exceptionally small platform, which remains bright without extended π-conjugation. Systematic substitution at 4,6-positions with alkyl, alkenyl, and alkynyl groups reveals robust emission for alkyl and alkynyl derivatives, and a striking bimodality for alkenyls. TDDFT combined with ES/SC-AFIR mapped the S₁→S₀ internal-conversion landscape, providing a rationale for substituent-dependent relaxation behavior. Manipulation at the 5-position allowed for independent trigger-responsive emission behavior. This orthogonal design, where the 4,6-substituted C4N4 core serves as the fluorophore and the 5-position operates as ON/OFF gate, enabled the development of turn-on probes for Pd²⁺.
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Kohei et al. (2026) studied this question.
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