کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1324007 | 977316 | 2006 | 6 صفحه PDF | دانلود رایگان |
The rate constant for the methyl abstraction reaction of CpFe(CO)2Me has been measured with the benzyl radical clock as (1.1 ± 0.2) × 105 M−1 s−1 at room temperature. Time-resolved Fourier-transform Infrared (FTIR) absorption spectroscopy pointed towards the formation of the CpFe(CO)2 radical upon benzyl abstraction. The main stable product has been established by a linear scan of the reaction mixture as Cp2Fe2(CO)4 produced by the dimerization of the CpFe(CO)2 radicals. The transition state structure for the abstraction process was also found at UB3LYP/6-311+G* level of theory to contain a planar CH3 group.
Measurement of the rate constant for the methyl abstraction reaction of CpFe(CO)2Me has been accomplished using a benzyl radical clock and yielding a value of (1.1 ± 0.2) × 105 M−1 s−1 at room temperature.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 691, Issue 4, 1 February 2006, Pages 687–692