Mengyuan Song, Meng Liu, Xue Zhang, Haijuan Qin, Jinglu Sun, Juanjuan Wang,* Qian Peng, Zhiwei Zhao, Xianchang Yan, Yongxin Chang, Yahui Zhang, Dongdong Wang, Junhui Wang,* Jianzhang Zhao,* and Guangyan Qing.*

Chem. Sci., 2025, 10.1039/D4SC08197H

https://pubs.rsc.org/en/content/articlelanding/2025/sc/d4sc08197h

    Excitation wavelength-dependent (Ex-De) chromophores, which exhibit changes in spectral composition with varying excitation wavelengths, have garnered significant interest. However, the pursuit of novel photoluminescence (PL) mechainsims and high luminescence quantum yields is facing huge challenges. Here, we discover that the introduction of a spinacine moiety to 2-(2-Hydroxy-5-methylphenyl)benzothiazole, a traditional excited-state intramolecular proton transfer (ESIPT) fluorophore, results in a novel Ex-De PL molecule. The luminescent color of this compound could be effectively modulated from greenish-blue to yellow-green by adjusting either the excitation wavelength or temperature. Transient absorption and spectroelectrochemistry spectra elucidate the underlying mechanism, demonstrating the roles of ESIPT and proton-coupled electron transfer (PCET). When embedded in a poly(vinyl alcohol) film, the composite exhibits remarkable Ex-De PL behavior, achieving absolute fluorescence quantum yields of 55.6% (λex: 396 nm) and 69.6% (λex: 363 nm), as well as phosphorescence at room temperature. These properties highlight its potential for multiple encryption features, enhancing its application in anti-counterfeiting technologies.