Connecting chemical dynamics in gases and liquids

被引:123
作者
Elles, Christopher G. [1 ]
Crim, F. Fleming
机构
[1] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
[2] Argonne Natl Lab, Div Chem, Argonne, IL 60439 USA
[3] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
关键词
chemical reaction dynamics; ultrafast spectroscopy; molecular energy transfer; photodissociation; bimolecular reactions;
D O I
10.1146/annurev.physchem.57.032905.104538
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 [物理化学]; 081704 [应用化学];
摘要
Modern ultrafast spectroscopic techniques provide new opportunities to study chemical reaction dynamics in liquids and hold the possibility of obtaining Much of the same detailed information available in gases. Vibrational energy transfer studies are the most advanced of the investigations and demonstrate that it is possible to observe state-specific pathways of energy flow within a vibrationally excited molecule (intramolecular vibrational relaxation) and into the surrounding solvent molecules (intermolecular energy transfer). Energy transfer in liquids and gases share many common aspects. but the presence of the solvent also alters the relaxation in both obvious and Subtle ways. Photodissociation is amenable to similarly detailed Study in liquids, and there are informative new measurements. Bimolecular reactions have received the least attention in state-resolved measurements in liquids, but the means to carry them much further now exist. Studying photodissociation and bimolecular reaction of molecules prepared with initial vibrational excitation in liquids is a realistic, but challenging, goal.
引用
收藏
页码:273 / 302
页数:30
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