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Putting the Bite on Metals - Chelation

Free and coordinated ammonia and water molecules. The second lone pair of water is oriented in a direction prohibiting its interaction with the same metal centre as the first. However, it does have the potential, in principle, to use this lone pair to bind to a second metal centre in a bridging coordination mode. (Other groups bound to the metals are left off to simplify the views.) [Pg.18]

Diaminomethane, a molecule with two amine groups. Once the first is coordinated, the second lone pair from the other amine can be oriented in a direction more appropriate for bonding than is the case for two lone pairs on a single atom, with limited bond angle distortion permitting both to coordinate, illustrated at right, in a chelated coordination mode. [Pg.18]

Metal ion binding options for a carboxylate group, featuring various monodentate and didentate coordination modes. [Pg.19]

O returning us to the M, so four atoms are involved in the continuous ring, meaning it is a four-membered chelate ring. [Pg.19]

The stepwise process for chelation of diaminoethane. This features initial monodentate formation, rearrangement and orientation of the second lone pair, and its subsequent binding to form the chelate ring. s [Pg.19]


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