State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology , E-208 West Campus, 2 Ling-Gong Road, Dalian 116024, P. R. China.
J Am Chem Soc. 2014 Jul 2;136(26):9256-9. doi: 10.1021/ja504211y. Epub 2014 Jun 24.
Reversible photoswitched triplet-triplet annihilation upconversion (TTA UC) was demonstrated with dithienylethene (DTE) derivatives as the photochromic units, 2,6-diiodoBodipy as the triplet photosensitizer, and perylene as the triplet acceptor/emitter. The TTA UC is undisturbed by the open-form DTE but can be switched OFF upon photoirradiation of the mixture of the three components at 254 nm, i.e., by the closed-form DTE. Subsequent visible light irradiation restores the TTA UC. By studying the competitive triplet-state energy-transfer processes with nanosecond time-resolved transient difference absorption and fluorescence spectroscopy, we confirmed that the quenching of the perylene triplet excited state by closed-form DTE is dominant among the four possible quenching processes.
可逆光致变色三重态-三重态湮灭上转换(TTA UC)得到了证明,其中二噻吩乙烯(DTE)衍生物作为光致变色单元,2,6-二碘 Bodipy 作为三重态光敏剂,苝作为三重态受体/发射器。TTA UC 不受开环 DTE 的干扰,但可以在 254nm 光辐照三种组分的混合物时关闭,即通过闭环 DTE。随后的可见光辐照恢复 TTA UC。通过使用纳秒时间分辨瞬态差分吸收和荧光光谱研究竞争三重态能量转移过程,我们证实了闭环 DTE 对苝三重态激发态的猝灭在四个可能的猝灭过程中占主导地位。