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12.4.5: The Kinetic Chelate Effect

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    385514
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    We discussed the increased thermodynamic stability of chelating ligands in a previous section on the chelate effect (Section 10.1.1). This thermodynamic benefit is related to a change in the rate of binding and dissociation events called the kinetic chelate effect. This effect was also mentioned earlier in this chapter (Section 12.2.2).

    Recall that there is a relationship between the equilibrium constant and rate constants of any chemical reaction. The relationship is demonstrated below for a general reaction.

    \[aA+bB \rightleftharpoons cC+dD \nonumber \]

    \[\text{forward rate} = k_f[A]^a [B]^b \nonumber \]

    \[\text{reverse rate} = k_r[C]^c [D]^d \nonumber \]

    At equilibrium, the rate of the forward reactions is equal to the rate of the reverse reaction. Therefore:

    \[ \text{forward rate} = \text{reverse rate} \nonumber \]

    \[k_f[A]^a [B]^b = k_r[C]^c [D]^d \nonumber \]

    Rearrangement of the equation above gives:

    \[\dfrac{k_f}{k_r}=\dfrac{[C]^c [D]^d }{[A]^a [B]^b } = K_{eq} \nonumber \]

    Because chelating ligands have larger values of \(K_{eq}\) than analogous monodentate ligands, there must also be a change in the relative rates of the forward (binding) and reverse (dissociation) reactions. In fact, there is a kinetic benefit that makes a metal bound to a polydentate ligand more inert than the analogous complex with monodentate ligands: this is called the kinetic chelate effect.

    The kinetic chelate effect is a result of a slower first dissociation step and faster re-association step relative to that of a monodentate ligand. The complete dissociation of a bidentate ligand, for example, would require two dissociation steps (see first reaction in figure below). It is the first dissociation step that is slower in a bidentate ligand (\(k_1 < k'_1\) in the figure below). This first dissociation step is slower in part because the chelate would have to rotate to move the free ligand away from the open coordinate site on the metal ion. For the same reason, the reverse of this step (association) is faster than the association of a monodentate ligand (\(k_{-1} > k'_{-1}\)).

    clipboard_ec60e4bb67d021dff05d4bc7281607f38.png
    Figure \(\PageIndex{1}\): Step-wise dissociation of a bidentate ligand and analogous monodentate ligands. (CC-BY-SA; Kathryn Haas)

    (1) Carter, M. J.; Beattie, J. K. Kinetic Chelate Effect. Chelation of Ethylenediamine on Platinum(II). Inorg. Chem.1970, 9 (5), 1233–1238. https://doi.org/10.1021/ic50087a044.

    Curated or created by Kathryn Haas


    This page titled 12.4.5: The Kinetic Chelate Effect is shared under a not declared license and was authored, remixed, and/or curated by Kathryn Haas.