Insights into the Photochemical Disproportionation of Transition Metal Dimers on the Picosecond Time Scale

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• 作者：Justin P. Lomont ; Son C. Nguyen ; Charles B. Harris
• 刊名：The Journal of Physical Chemistry A
• 出版年：2013
• 出版时间：May 9, 2013
• 年：2013
• 卷：117
• 期：18
• 页码：3777-3785
• 全文大小：355K
• 年卷期：v.117,no.18(May 9, 2013)
• ISSN：1520-5215

文摘

The reactivity of five transition metal dimers toward photochemical, in-solvent-cage disproportionation has been investigated using picosecond time-resolved infrared spectroscopy. Previous ultrafast studies on [CpW(CO)₃]₂ established the role of an in-cage disproportionation mechanism involving electron transfer between 17- and 19-electron radicals prior to diffusion out of the solvent cage. New results from time-resolved infrared studies reveal that the identity of the transition metal complex dictates whether the in-cage disproportionation mechanism can take place, as well as the more fundamental issue of whether 19-electron intermediates are able to form on the picosecond time scale. Significantly, the in-cage disproportionation mechanism observed previously for the tungsten dimer does not characterize the reactivity of four out of the five transition metal dimers in this study. The differences in the ability to form 19-electron intermediates are interpreted either in terms of differences in the 17/19-electron equilibrium or of differences in an energetic barrier to associative coordination of a Lewis base, whereas the case for the in-cage vs diffusive disproportionation mechanisms depends on whether the 19-electron reducing agent is genuinely characterized by 19-electron configuration at the metal center or if it is better described as an 18 + 未 complex. These results help to better understand the factors that dictate mechanisms of radical disproportionation and carry implications for radical chain mechanisms.