激发态
发色团
单重态裂变
光子上转换
紧身衣
光化学
分子内力
化学
猝灭(荧光)
三重态
量子产额
单重态
荧光
系统间交叉
分子物理学
原子物理学
物理
立体化学
光学
离子
有机化学
作者
Zhangrong Lou,Yuqi Hou,Kepeng Chen,Jianzhang Zhao,Shaomin Ji,Fangfang Zhong,Yavuz Dede,Bernhard Dick
标识
DOI:10.1021/acs.jpcc.7b10466
摘要
It is well-known that the fluorescence of a chromophore can be efficiently quenched by the free rotor effect, sometimes called intramolecular rotation (IMR), i.e. by a large-amplitude torsional motion. Using this effect, aggregation induced enhanced emission (AIE) and fluorescent molecular probes for viscosity measurements have been devised. However, the rotor effect on triplet excited states was rarely studied. Herein, with molecular rotors of Bodipy and diiodoBodipy, and by using steady state and time-resolved transient absorption/emission spectroscopies, we confirmed that the triplet excited state of the Bodipy chromophore is not quenched by IMR. This is in stark contrast to the fluorescence (singlet excited state), which is significantly quenched by IMR. This result is rather interesting since a long-lived excited state (triplet, 276 μs) is not quenched by the IMR, but the short-lived excited state (singlet, 3.8 ns) is quenched by the same IMR. The unquenched triplet excited state of the Bodipy was used for triplet–triplet annihilation upconversion, and the upconversion quantum yield is 6.3%.
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