Zirconocene
Zirconocene is a hypothetical compound with 14 valence electrons, which has not been observed or isolated. It is an organometallic compound consisting of two cyclopentadienyl rings bound on a central zirconium atom. A crucial question in research is what kind of ligands can be used to stabilize the Cp2ZrII metallocene fragment to make it available for further reactions in organic synthesis.
Structure
In contrast to sandwich compounds that have parallel cyclopentadienyl rings bound on opposite sides of the metal atom, such as ferrocene, zirconocene and other group 4 metallocenes are bent. Without stabilizing ligands, the Cp2ZrII fragment is unstable and dimerizes to form a fulvalene complex.History
In 1954, Wilkinson and Birmingham described zirconocene dihalides Cp2ZrX2 with X=Cl or Br, as some of the earliest examples of organozirconium compounds. The chemistry of Cp2ZrII-compounds was explored more extensively in the 1980s by Negishi, Takahashi, Buchwald, and others. In the 1990s, Rosenthal synthesized zirconocene reagents using bis(trimethylsilyl)acetylene as stabilizing ligand. This novel zirconocene source offers a number of compelling advantages over previously used reagents and broadens the range of possible reactions. The chemistry of Cp2ZrII-compounds is still a rapid growing area with zirconium being ranked among the most widely used transition metals in organic synthesis.Synthesis
The unstable 14-electron Cp2ZrII-compound is generally non-existent, but can be generated using ligands that stabilize the metallocene fragment. Optimally, these ligands can be quantitatively released under mild conditions.One option is the usage of π-acceptor ligands like carbon monoxide. Furthermore, a reaction with trimethylphosphine yields Cp2ZrII-complex as illustrated below.
In the synthesis of the Negishi reagent, treatment of zirconocene dichloride in tetrahydrofuran with two equivalents of n-butyllithium at −78 °C gives zirconocene, which is represented by the resonance structures A and B.
If bisacetylene is used instead of n-butyllithium, a higher yield is can be obtained. In this case, zirconocene complexes are synthesized to Rosenthal's reagent, represented by the resonance structures A and B. This reagent is stable at room temperature, can be stored under an inert atmosphere and allows a more precise control over the stoichiometry of reactions as it can be formed quantitatively. A fine tune of the general reaction shown below is feasible by using different substituted cyclopentadienyl ligands as well as additional ligands. Instead of zirconium used as central atom, an analogous reaction with titanium is possible, too.