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7.1.4: Sigma Bond Metathasis

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    Metal compounds with \(d^0\) electron count are able to activate C-H bonds through \(\sigma\) bond metathesis reactions. \(\sigma\)-bond metathesis is a chemical reaction wherein a metal-ligand \(\sigma\) bond undergoes metathesis (exchange of parts) with the sigma bond in some other reagent. The reaction is illustrated by the exchange of lutetium(III) methyl complex with a hydrocarbon (R-H) (Figure \(\PageIndex{1}\)). The oxidation state of the metal ion does not change during the reaction. This reactivity was first observed by Patricia L. Watson, a researcher at duPont.

    clipboard_e5e3a016c5b9395063bdf34844162404c.png
    Figure \(\PageIndex{1}\): Example of \(\sigma\) bond metathesis; exchange of lutetium(III) methyl complex with a hydrocarbon. The R-H bond is activated and a new C-H bond is created. (CC-BY-SA; Kathryn Haas)

    The reaction is mainly observed for complexes of metals with \(d^0\) electron configuration, e.g. complexes of Sc(III), Zr(IV), Nb(IV), Ta(V), etc. Complexes of the f-block elements also participate, regardless of the number of f-electrons. For metals unsuited for redox, sigma bond metathesis provides a pathway for introducing substituents.

    The details of the reaction mechanism are somewhat a matter of debate, however a currently accepted model is that it precedes through a cycloaddition and via a "kite-shaped" transition state (Figure \(\PageIndex{2}\)). Indeed, the rate of the reaction is characterized by a highly negative entropy of activation, indicating an ordered transition state.

    clipboard_e2c17b04422bd66540af6e4369e54d29d.png
    Figure \(\PageIndex{2}\): The currently accepted mode for the mechanism of \(\sigma\) bond metathesis involving a kite-like transition state. (CC-BY-SA; Kathryn Haas)

    The reaction attracted much attention because hydrocarbons are normally unreactive substrates, whereas some sigma-bond metatheses are facile. Unfortunately the reaction does not readily allow the introduction of functional groups. It has been suggested that dehydrocoupling reactions proceed via sigma-bond metathesis.

    Sources:


    This page titled 7.1.4: Sigma Bond Metathasis is shared under a not declared license and was authored, remixed, and/or curated by Kathryn Haas.

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