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Mode-selective O-H stretching relaxation in a hydrogen bond studied by ultrafast vibrational spectroscopy

机译:超快振动光谱研究氢键中模式选择的O-H拉伸弛豫

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The ultrafast relaxation of the excited O-H stretching vibration is studied by ultrafast infrared-pump/infrared-probe and infrared-pump/Raman-probe spectroscopy. We demonstrate a 200 fs lifetime of the hydrogen-bonded O-H stretching mode in 2-(2(')-hydroxy-5(')-methyl-phenyl)benzotriazole (TINUVIN P). O-H stretching relaxation occurs through a few major channels that all involve combination and overtone bands of modes with considerable in-plane O-H bending character. In particular, the mode, which contains the largest O-H bending contribution, plays a prominent role for primary processes of intramolecular vibrational energy redistribution. Theoretical calculations of vibrational energy transfer rates based on a Fermi golden rule approach account for the experimental findings. (c) 2006 American Institute of Physics.
机译:通过超快红外泵/红外探针和红外泵/拉曼探针光谱研究了激发的O-H拉伸振动的超快弛豫。我们证明了在2-(2(')-羟基-5(')-甲基-苯基)苯并三唑(TINUVIN P)中氢键O-H拉伸模式的200 fs寿命。 O-H拉伸松弛是通过一些主要通道发生的,这些通道都涉及具有大量O-H面内弯曲特性的模态的组合和泛音带。尤其是,包含最大O-H弯曲贡献的模式对于分子内振动能量重新分配的主要过程起着重要作用。基于费米黄金法则的振动能量传递速率的理论计算说明了实验结果。 (c)2006年美国物理研究所。

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