Femtosecond stimulated Raman spectroscopy

被引:511
|
作者
Kukura, Philipp [1 ]
McCamant, David W. [1 ]
Mathies, Richard A. [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
ultrafast spectroscopy; time-resolved vibrational spectroscopy; chemical reaction dynamics; anharmonic coupling; visual photochemistry;
D O I
10.1146/annurev.physchem.58.032806.104456
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
Femtosecond stimulated Raman spectroscopy (FSRS) is a new ultrafast spectroscopic technique that provides vibrational structural information with high temporal (50-fs) and spectral (10-cm(-1)) resolution. As a result of these unique capabilities FSRS studies of chemical and biochemical reaction dynamics are expected to grow rapidly, giving previously unattainable insight into the structural dynamics of reactively evolving systems with atomic spatial and femtosecond temporal resolution. This review discusses the experimental and theoretical concepts behind FSRS, with an emphasis on the origins of its unique temporal and spectral capabilities. We illustrate these capabilities with vibrational studies of ultrafast electronic dynamics as, well as the direct structural observation of nonstationary vibrational wave-packet motion in small molecules and in complex biochemical reaction dynamics.
引用
收藏
页码:461 / 488
页数:28
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