Femtochemistry of hydrogen bonded complexes after electronic excitation in the liquid phase: The case of coumarin 102

被引:76
作者
Nibbering, ETJ [1 ]
Tschirschwitz, F [1 ]
Chudoba, C [1 ]
Elsaesser, T [1 ]
机构
[1] Max Born Inst Nichtlineare Opt & Kurzzeitspektros, D-12489 Berlin, Germany
关键词
D O I
10.1021/jp9937095
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We review our results on hydrogen bonding dynamics in the electronically excited state of coumarin 102 (C102), where we deduced that a hydrogen bond cleavage occurs within 200 fs. We compare the electronic absorption and emission properties of C102 hydrogen bonded to CHCl3, phenol or 2,2-dimethyl-3-ethyl-3-pentanol. We introduce the technique of two-pulse photon echo to show that an optical coherence between the optically coupled electronic ground and excited states survives until 180-200. fs, in the case of C102(phenol)(1,2) complexes, and argue that this is an indication that an electronic state hopping occurs around this time. By comparison with the previous pump-probe and grating scattering results we deduce that this state hopping is accompanied by a hydrogen bond cleavage.
引用
收藏
页码:4236 / 4246
页数:11
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