M. Abraham, D. Dodd, Michael D. Johnson, E. Lewis, R. O'Ferrall
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引用次数: 2
Abstract
Recent criticisms of well established mechanistic interpretations of isotopic exchange reactions of organomercury-(II) compounds have been shown to be erroneous by consideration of three-dimensional potential-energy surfaces, which show the several possible reaction paths. The method provides a clear understanding of the principle of microscopic reversibility as applied to symmetrical organometallic exchange reactions.
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