| Autor: |
Knappenberger Jr., K. L., Castleman Jr., A. W. |
| Předmět: |
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| Zdroj: |
Journal of Chemical Physics; 8/22/2004, Vol. 121 Issue 8, p3540-3549, 10p, 1 Diagram, 2 Charts, 6 Graphs |
| Abstrakt: |
A femtosecond pump-probe technique was employed to study the dissociation dynamics of sulfur dioxide and sulfur dioxide clusters in real time. Dissociation is initiated by a multiphoton scheme that populates the E state. The SO2+ transient is fit to a biexponential decay comprising a fast and a slow component of 230 fs and 8 ps, respectively. The SO+ transient consists of a growth component of 225 fs as well as a subsequent decay of 373 fs. The pump-probe response obtained from the monomer clearly shows the predissociative cleavage of a S–O bond. Upon cluster formation, a sequential increase in the fast decay component is observed for increasing cluster size, extending to 435 fs for (SO2)4+. The transient response of cluster dissociation products SO(SO2)n+, where n=1–3, reflects no growth component indicating that formation proceeds through the ion state. Therefore, cluster formation results in a caging effect, which impedes the dissociation process. Further direct evidence for our proposed mechanism is obtained by a technique that employs a comparison of the amplitude coefficients of each respective component of the fit. This method makes possible the determination of branching ratios of competing relaxation processes and thereby the influence of cluster formation on each can be resolved. The caging effect is attributed to a steric hindrance placed on the SO2 chromophore, preventing it from attaining a linear geometry necessary for dissociation. © 2004 American Institute of Physics. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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