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Dynamics of reactive collisions by optical methods

 

作者: A.González Ureña,   R. Vetter,  

 

期刊: International Reviews in Physical Chemistry  (Taylor Available online 1996)
卷期: Volume 15, issue 2  

页码: 375-427

 

ISSN:0144-235X

 

年代: 1996

 

DOI:10.1080/01442359609353189

 

出版商: Taylor & Francis Group

 

数据来源: Taylor

 

摘要:

This paper reviews recent developments in the study of reactive collisions using optical methods. Although the basic approach is from the experimental viewpoint, attention is paid to the conceptual and theoretical aspects of the physics underlying modern reaction dynamics. After a brief resume of basic concepts and definitions on both scalar and vectorial quantities characterizing the chemical reaction, a significant body of this paper describes the recent achievements using laser techniques, mainly via laser-induced fluorescence, and chemiluminescence. Both high-resolution crossed-beam and high-resolution bulb studies are presented in a complementary fashion, as they provide a detailed picture of reaction dynamics through the measurement of quantum state specific differential cross-sections. Specific examples include the use of Doppler resolved laser-induced fluorescence, multiphoton ionization or Cars studies. Some examples are also included based on the use of product imaging techniques, the novel approach of obtaining quantum state resolved differential cross-sections for chemical reactions. In addition, new data on the collision energy dependence of the collision cross-section, i.e. the excitation function, obtained by highly sensitive collision energy cross-beam techniques is also presented and reviewed. Another part of the paper is dedicated to recent advances in the study of reaction dynamics using electronically excited species. Emphasis is placed not only on the opening of new channels for chemical reactions but also on the possible outcome of the reaction products associated with the different symmetries of the excited potential energy surfaces. Finally, a section is dedicated to recent developments in studies carried out in the area of van der Waals and cluster reactions. The possibility of clocking the chemical act as well as very efficient trapping of reaction intermediates is illustrated with some examples. Throughout the whole paper care is taken to discuss the most significant features of the molecular reaction dynamic observables with reference to simple reaction models and/or theoretical treatments currently used in the field.

 

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