Infrared spectroscopy to probe structure and dynamics in metal ion-molecule complexes

被引:314
作者
Duncan, MA [1 ]
机构
[1] Univ Georgia, Dept Chem, Athens, GA 30602 USA
基金
美国国家科学基金会;
关键词
D O I
10.1080/0144235031000095201
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
Vibrational spectroscopy measurements are described for mass-selected metal cation-molecular complexes using the technique of infrared resonance-enhanced photodissociation (REPD) spectroscopy. We discuss the mechanism of the REPD process in the infrared and how multiphoton techniques or rare gas tagging can be employed to facilitate dissociation processes in strongly bound complexes. Spectra are reported for Fe+(CO2)(n) complexes that demonstrate the formation of coordination spheres around the metal cation and for Mg+(CO2)(n) complexes, where the interaction with theory makes it possible to obtain structures for small clusters. Both of these studies investigate the asymmetric stretch region of CO2. Ni+(C2H2)(n) complexes are studied in the C-H stretch region, demonstrating evidence for intracluster cyclization reactions. Finally, experiments are described for metal ion-benzene (M = V, Al) complexes excited in the benzene ring distortions and C-H bending region. These experiments confirm the pi-bonded configuration of these complexes.
引用
收藏
页码:407 / 435
页数:29
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