Cyclopentadienyl complex

Biscyclopentadienyl complexes are called metallocenes. A famous example of this type of complex is ferrocene (FeCp₂), which has many analogues for other metals, such as chromocene (CrCp₂), cobaltocene (CoCp₂), and nickelocene (NiCp₂). When the Cp rings are mutually parallel the compound is known as a sandwich complex. This area of organometallic chemistry was first developed in the 1950s. Bent metallocenes are represented by compounds of the type [MCp₂L_x]. Some are catalysts for ethylene polymerization.[2] Metallocenes are often thermally stable, and find use as catalysts in various types of reactions.

Mixed-ligand Cp complexes containing Cp ligand and one or more other ligands. They are more numerous. One widely studied example is the Fp dimer, (Cp₂Fe₂(CO)₄). Monometallic compounds featuring only one Cp ring are often known as half sandwich compounds or as piano stool compounds, one example being cyclopentadienylmanganese tricarbonyl (CpMn(CO)₃).

All 5 carbon atoms of a Cp ligand are bound to the metal in the vast majority of M–Cp complexes. This bonding mode is called η⁵-coordination. The M–Cp bonding arises from overlap of the five π molecular orbitals of the Cp ligand with the s, p, and d orbitals on the metal. This π bonding is significant, hence these complexes are referred to as π-complexes. Almost all of the transition metals, that is, group 4 to 10 metals, employ this coordination mode.[1]

In relatively rare cases, Cp binds to metals via only one carbon center. These types of interactions are described as σ-complexes because they only have a σ bond between the metal and the cyclopentadienyl group. Typical examples of this type of complex are group 14 metal complexes such as CpSiMe₃. An example of both is (Cp₂Fe(CO)₂).. It is probable that η¹-Cp complexes are intermediates in the formation of η⁵-Cp complexes.

Still rarer, the Cp unit can bond to the metal via a three-carbons. In these η³-Cp complexes, the bonding resembles that in allyl ligands. Such complexes, sometimes called "slipped Cp complexes", are invoked as intermediates in ring slipping reactions.

The compounds are generally prepared by salt metathesis reactions of alkali-metal cyclopentadienyl compounds with transition metal chlorides. Sodium cyclopentadienide (NaCp) and lithium cyclopentadienide are commonly used. Trimethylsilylcyclopentadiene cyclopentadienylthallium (CpTl) are alternative sources.[1] For the preparation of some particularly robust complexes, e.g. nickelocene, cyclopentadiene is employed in the presence of a conventional base such as KOH. When only a single Cp ligand is installed, the other ligands typically carbonyl, halogen, alkyl, and hydride.

Most Cp complexes are prepared by substitution of preformed Cp complexes by replacement of halide, CO, and other simple ligands.

• Variations of Cyclopentadienyl complexes
• 
  decamethylcobaltocene, a powerful reducing agent
• 
  A constrained geometry organotitanium complex
• 
  An ansa-metallocene

Cp metal complexes are mainly used as stoichiometric reagents in chemical research. Ferrocenium reagents are oxidants. Cobaltocene is a strong, soluble reductant.

Derivatives of Cp₂TiCl₂ and Cp₂ZrCl₂ are the basis of some reagents in organic synthesis. Upon treatment with aluminoxane, these dihalides give catalysts for olefin polymerization. Such species are called Kaminsky-type catalysts.

• Yamamoto, A. (1986). Organotransition Metal Chemistry: Fundamental Concepts and Applications. New York, NY: Wiley-Interscience. p. 105.
• Shriver, D.; Atkins, P. W. (1999). Inorganic Chemistry. New York, NY: W. H. Freeman.
• King, R. B.; Bisnette, M. B. (1967). "Organometallic chemistry of the transition metals XXI. Some π-pentamethylcyclopentadienyl derivatives of various transition metals". J. Organomet. Chem. 8: 287–297. doi:10.1016/S0022-328X(00)91042-8. [Initial examples of the synthesis of Cp*-metal complexes]