Metal tetranorbornyl
In organometallic chemistry, metal tetranorbornyls are compounds with the formula M4 and are one of the largest series of tetraalkyl complexes derived from identical ligands. Metal tetranorbornyls display uniform stoichiometry, low-spin configurations, and high stability, which can be attributed to their +4 oxidation state metal center. The stability of metal tetranorbornyls is predominately considered to be derived from the unfavorable β-hydride elimination. Computational calculations have determined that London dispersion effects significantly contribute to the stability of metal tetranorbornyls. Specifically, Fe4 has a stabilization of 45.9 kcal/mol−1. Notable metal tetranorbornyls are those synthesized with metal centers of cobalt, manganese, or iron.
Preparation
Traditionally, metal tetranorbornyls are prepared by a reaction of 1-norbornyllithium, with transition-metal halides. Alternative methods have been proposed. Specifically, the tetrakischromium complex can be prepared in inert atmosphere conditions with 1-norbornyllithium dissolved in hexane.The tetrakis(1-norbornyl)cobalt(IV) complex can be prepared by the following:
The tetrakismolybdenum complex was prepared by the following:
Structure
The stability of metal tetranorbornyls is generally considered to be a result of unfavorable β-hydrogen elimination. Metal alkyl species with β-hydrogen atoms present on the alkyl group are disfavored due to β-hydrogen migration to the metal center, which results in an olefin being eliminated and the production of the corresponding metal hydride. 1-norbornyl does not undergo β-hydrogen migration even though it possesses 6 β-hydrogen atoms due to the unfavorable formation of the olefin, 1-norbornene. According to Bredt's rule, one of the sp2 carbons of the double-bonded carbon atoms would be located at the bridgehead, which would cause 1-norbornene to be highly strained. β-hydrogen elimination does not explain the formation of metal tetranorbornyls complexes that are synthesized from lower valent metal center precursors, shortened bond lengths between the metal center and 1-norbornyl ligand carbons, or the resulting low-spin tetrahedral molecular geometry.Quantum mechanical calculations have elucidated that London dispersion forces between the norbornyl ligands are accountable for the stability and molecular geometry of the homoleptic tetranorbornyl metal complexes.
Metal tetranorbornyls complexes consisting of the divalent and trivalent metal center species of Cr, Mn, Fe and Co halides undergo formation of negatively charged complexes followed by oxidation that is induced by other transition-metal species in the reaction. Factors that lead to disproportionation are traditionally considered to be derived from the tertiary carbanion ligand, 1-norbornyllithium, and the lack of potential for the pentane solvent to act as a ligand. Therefore, metal tetranorbornyls composed of first-row transition metals are not accessible to be penetrated by small reagents due to the metal center's coordination sphere.
Tetrakis(1-norbornyl)cobalt(IV)
Tetrakis(1-norbornyl)cobalt(IV) is a thermally stable homoleptic complex observed with σ-bonding ligands. The metal tetranorbornyl complex was the first isolated low-spin complex with tetrahedral molecular geometry. The tetrakiscobalt complex was first synthesized by Barton K. Bower and Howard G. Tennent in 1972.The tetrakis(1-norbornyl)cobalt(IV) oxidation state is a reversible reaction using O2 as the oxidizing agent. The coordination environment of the cobalt metal center has a distorted tetrahedron structure. When examined by x-ray crystallography, the metal tetranorbornyl has a crystallographic Cs symmetry due to the presence of six carbons laid on the mirror plane. However, the four carbons atoms bonded to the cobalt metal center resembled a tetragonally compressed tetrahedron, which appeared as a pseudo D2d symmetry.
The cobalt metal center in the +4 oxidation state has a d5 configuration. Typically, the d5 configuration is expected to result in the high spin complex containing 5 unpaired electrons and only 1 unpaired electron in the low spin tetrahedral complex. The single unpaired electron resides in the antibonding t2 orbital, which would cause the structure to experience a Jahn-Teller distortion. However, Theopold and co-workers speculated that the slight tetragonal compression could have been a result of steric interactions between norbornyl ligands and crystal packing forces.
Tetrakis(1-norbornyl)iron(IV)
The tetrakisiron complex was first synthesized by Barton K. Bower and Howard G. Tennent in 1972. The 1-norbornyl ligands on the complex have a strong dispersion attraction and high ring strain, which as a consequence hinders the α- and β-hydride elimination reactions. Additionally, the identical ligands cause a reduced chemical reactivity due to a crowded chemical environment that impedes the interaction of small molecules with the Fe-C bonds.Synthesized complexes
Barton K. Bower and Tennent characterized the following metal tetranorbornyls:- tetrakishafnium
- tetrakiszirconium
- tetrakistitanium
- tetrakisvanadium
- tetrakischromium
- tetrakismanganese
- tetrakisiron
- tetrakismolybdenum