Caught in the act: Observation of the solvent response triggered by excited-state proton transfer in real time

C. Hoberg, T. Ockelmann, J. Shee, P. Balzerowski, Debasish Das Mahanta, F. Novelli, M. Head‐Gordon, M. Havenith
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Abstract

Real-time observation of the solvent response following Excited State Proton Transfer (ESPT) of the photoacid HPTS into water using Optical Pump THz Probe (OPTP) spectroscopy from 0.1 ps up to 300 ps is reported. Subsequent to an instantaneous (< 0.2 ps) electronic response of the solute to photoexcitation, an oscillation with a period of 4 ps involving an intermolecular H (pyranine) - O (water) mode is observed. While for the methylated derivative, MPTS, and the deprotonated photoacid this oscillation relaxes on a time scale of 1.5 – 2 ps, for HPTS the oscillation decays more rapidly within 0.4 ps, which marks the onset of proton transfer. Energy transfer from the excited solute to the solvent takes place on a time scale of 120 ps and is proportional to the Stokes shift associated with energetic relaxation from the Franck-Condon region to the ground state of the photoexcited HPTS.
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当场:实时观察激发态质子转移引发的溶剂反应
利用光泵太赫兹探针(OPTP)在0.1 ~ 300ps范围内实时观察了光酸HPTS在激发态质子转移(ESPT)过程中的溶剂响应。在溶质对光激发的瞬时(< 0.2 ps)电子响应之后,观察到一个周期为4 ps的振荡,涉及分子间H (pyranine) - O (water)模式。而对于甲基化衍生物,MPTS和去质子化光酸,这种振荡在1.5 - 2ps的时间尺度上松弛,对于HPTS,振荡在0.4 ps内衰减得更快,这标志着质子转移的开始。从被激发的溶质到溶剂的能量转移发生在120ps的时间尺度上,并且与Stokes位移成正比,Stokes位移与从Franck-Condon区到光激发HPTS的基态的能量松弛有关。
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