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Transition metal complexes of aldehydes and ketones

Transition metal complexes of aldehydes and ketones describes coordination complexes with aldehyde (RCHO) and ketone (R2CO) ligands. Because aldehydes and ketones are common, the area is of fundamental interest. Some reactions that are useful in organic chemistry involve such complexes.

Structure of an η2-formaldehyde complex.

Structure and bonding

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Structure of [ZnBr3(η1-acetone)]−.

In monometallic complexes, aldehydes and ketones can bind to metals in either of two modes, η1-O-bonded and η2-C,O-bonded. These bonding modes are sometimes referred to sigma- and pi-bonded. These forms may sometimes interconvert.

The sigma bonding mode is more common for higher valence, Lewis-acidic metal centers (e.g., Zn2+).[1] The pi-bonded mode is observed for low valence, electron-rich metal centers (e.g., Fe(0) and Os(0)).[2]

For the purpose of electron-counting, O-bonded ligands count as 2-electron "L ligands": they are Lewis bases. η2-C,O ligands are described as analogues of alkene ligands, i.e. the Dewar-Chatt-Duncanson model.[3]

η2-C,O ketones and aldehydes can function as bridging ligands, utilizing a lone pair of electrons on oxygen. One such complex is [(C5H5)2Zr(CH2O)]3, which features a Zr3O3 ring.[4]

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Related to η1-O-bonded complexes of aldehydes and ketones are metal acetylacetonates and related species, which can be viewed as a combination of ketone and enolate ligands.

Reactions

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(Benzylideneacetone)iron tricarbonyl is an organoiron compound with an η2 ketone ligand.

Some η2-aldehyde complexes insert alkenes to give five-membered metallacycles.[5]

η1-Complexes of alpha-beta unsaturated carbonyls exhibit enhanced reactivity toward dienes. This interaction is the basis of Lewis-acid catalyzed Diels-Alder reactions.

References

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  1. ^ Andreev, V. P.; Sobolev, P. S.; Tafeenko, V. A. (2017). "Coordination of Zinc Tetraphenylporphyrin with Pyridine Derivatives in Chloroform Solution and in the Solid Phase". Russian Journal of General Chemistry. 87 (7): 1572–1579. doi:10.1134/S1070363217070210. S2CID 102539549.
  2. ^ Berke, Heinz; Huttner, Gottfried; Weiler, Gertrud; Zsolnai, Laszlo (1981). "Struktur und Reaktivität eines Formaldehydeisen-Komplexes". Journal of Organometallic Chemistry. 219 (3): 353–362. doi:10.1016/S0022-328X(00)90020-2.
  3. ^ Huang, Yo Hsin; Gladysz, J. A. (1988). "Aldehyde and Ketone Ligands in organometallic complexes and catalysis". Journal of Chemical Education. 65 (4): 298. Bibcode:1988JChEd..65..298H. doi:10.1021/ed065p298.
  4. ^ Kropp, Kurt; Skibbe, Volker; Erker, Gerhard; Krueger, Carl (1983). "Fischer-Tropsch intermediates: Tris[(.eta.2-formaldehyde)zirconocene] from the carbonylation of a zirconium hydride". Journal of the American Chemical Society. 105 (10): 3353–3354. doi:10.1021/ja00348a075.
  5. ^ Hoshimoto, Yoichi; Ohashi, Masato; Ogoshi, Sensuke (2015). "Catalytic Transformation of Aldehydes with Nickel Complexes through η2-Coordination and Oxidative Cyclization". Accounts of Chemical Research. 48 (6): 1746–1755. doi:10.1021/acs.accounts.5b00061. PMID 25955708.
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