This analysis demonstrates room-temperature phosphorescence in π-ternary molecules, highlighting the roles of isomerism and excited states.
The direct observation of thermally-activated intersystem crossing (TA-ISC) processes in room-temperature phosphorescence (RTP) has not been well investigated. Here, we reported four weakly donor-acceptor-donor π-ternary molecules featuring isomerism-dependent phosphorescence behaviors. The isomerism was modulated by changing the substitution position, offering tunable molecular planarity and π-conjugation. As a result, regulated energy levels and orbital configurations of the excited states facilitate additional TA-ISC channels as revealed by theoretical investigations. The temperature-dependent photoluminescence and fs- and ns-transient absorption spectra undoubtedly demonstrate their existence and effectiveness in promoting the efficient and persistent RTP. The ISC rate constant achieves a breakthrough of up to 1.93×10^9 s^(-1) within poly(vinyl alcohol) matrix film, surpassing that in many existing afterglow systems containing heavy or hetero atoms. Abundant triplet excitons are populated and enable remarkable room-temperature phosphorescence performance, facilitating potential applications in constructing thermosensitive glasses and anti-counterfeiting patterns. This study offers a practical mechanism for developing novel RTP materials.
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Huang et al. (2025) studied this question.
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