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agostic interaction
Agostic interaction is a term in organometallic chemistry for the interaction of a coordinatively-unsaturated transition metal with a C-H bond, when the two electrons involved in the C-H bond enter the empty d-orbital of a transition metal, resulting in a three-center two-electron bond. Many catalytic transformations, e.g. oxidative addition and reductive elimination, are proposed to proceed via intermediates featuring agostic interactions. Agostic interactions are observed throughout organometallic chemistry in alkyl, alkylidene, and polyenyl ligands.
==History==
The term agostic, derived from the Greek word for "to hold close to oneself", was coined by Maurice Brookhart and Malcolm Green, on the suggestion of the Classicist Jasper Griffin, to describe this and many other interactions between a transition metal and a C-H bond. Often such agostic interactions involve alkyl or aryl groups that are held close to the metal center through an additional σ-bond.〔.〕
Short interactions between hydrocarbon substituents and coordinatively unsaturated metal complexes have been noted since the 1960s. For example, in tris(triphenylphosphine) ruthenium dichloride, a short interaction is observed between the ruthenium(II) center and a hydrogen atom on the ortho position of one of the nine phenyl rings. Numerous borohydride complexes were also described crystallographically that were described using the three-center two-electron bonding model.
The nature of the interaction was foreshadowed in main group chemistry in the structural chemistry of trimethylaluminium.
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