State cyclopentadienyls

Intermediate and Higher Oxidation State Cyclopentadienyl Complexes 392... 

Figure 31 shows the proposed Longuet-Higgins loop for the cyclopentadienyl cation. It uses the type-VI Ai anchors, with the type-VII B structures as transition states between them. This situation is completely analogous to that of the radical (Fig. 23). Since the loop is phase inverting, a conical intersection should be located at its center—as required by the Jahn-Teller theorem.

Cu ( j -C5H5)2] is not. Likewise, Fe and Ni carborane derivatives are extremely stable. Conversely, metallocarboranes tend to stabilize lower oxidation states of early transition elements and complexes are well established for Ti", Zr , Hf , V , Cr and Mn" these do not react with H2, N2, CO or PPh3 as do cyclopentadienyl derivatives of these elements. 

Perhaps because of inadequate or non-existent back-bonding (p. 923), the only neutral, binary carbonyl so far reported is Ti(CO)g which has been produced by condensation of titanium metal vapour with CO in a matrix of inert gases at 10-15 K, and identified spectroscopically. By contrast, if MCI4 (M = Ti, Zr) in dimethoxy-ethane is reduced with potassium naphthalenide in the presence of a crown ether (to complex the K+) under an atmosphere of CO, [M(CO)g] salts are produced. These not only involve the metals in the exceptionally low formal oxidation state of —2 but are thermally stable up to 200 and 130°C respectively. However, the majority of their carbonyl compounds are stabilized by n-bonded ligands, usually cyclopentadienyl, as in [M(/j5-C5H5)2(CO)2] (Fig. 21.8). 

Indeed, it is the cyclopentadienyls which provide the major part of the organometallic chemistry of this group and they are known for metal oxidation states of IV, III and II though III... 

Schrock-type carbenes are nucleophilic alkylidene complexes formed by coordination of strong donor ligands such as alkyl or cyclopentadienyl with no 7T-acceptor ligand to metals in high oxidation states. The nucleophilic carbene complexes show Wittig s ylide-type reactivity and it has been discussed whether the structures may be considered as ylides. A tantalum Schrock-type carbene complex was synthesized by deprotonation of a metal alkyl group [38] (Scheme 7). 

The structure of cyclopentadienylthallium(I) has been the subject of controversy and while the arguments have not been entirely satisfactorily settled, the evidence now available indicates that the compound is primarily ionic in the solid state but possibly mainly covalent in the gaseous phase. The former conclusion at least is reasonable in view of the well-known stability of the cyclopentadienyl anion. Cyclopentadienylthallium(I) has... 

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