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Ultrafast intersystem crossing in thiophene oligomers investigated by fs-pump-probe spectroscopy

机译:FS泵探针光谱法研究噻吩低聚物中的超快系统间穿越

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Exciting the shortest members of thiophene oligomers, we observed ultrafast triplet formation on a time scale of 1.5-3 ps. From the time resolved transient spectra in terthiophene at different excitation wavelengths, we concluded the existence of an intermediate state within the S-1 manifold. This state is populated during the relaxation of the structure of the excited molecule to a planar conformation and can be the key for understanding the high triplet of about 0.95 in dioxane. In bithiophene, using two-photon excitation, we found excited state absorption, triplet-triplet absorption and radical cation absorption. The time constant for triplet formation was estimated to amount to 1.5 ps. [References: 6]
机译:激发噻吩低聚物的最短成员,我们在1.5-3 ps的时间尺度上观察到超快三重态的形成。根据不同激发波长下噻吩的时间分辨瞬态光谱,我们得出结论,S-1流形内存在中间状态。该状态在被激发的分子的结构松弛为平面构象期间填充,并且可能是理解二恶烷中约0.95的高三重态的关键。在联噻吩中,使用双光子激发,我们发现了激发态吸收,三重态-三重态吸收和自由基阳离子吸收。三重态形成的时间常数估计为1.5 ps。 [参考:6]

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