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Organocobalt chemistry is the chemistry of organometallic compounds containing a carbon to cobalt chemical bond. Organocobalt compounds are involved in several organic reactions and the important biomolecule vitamin B₁₂ has a cobalt-carbon bond. Many organocobalt compounds exhibit useful catalytic properties, the preeminent example being dicobalt octacarbonyl.

Alkyl complexes

Most fundamental are the cobalt complexes with only alkyl ligands. Examples include Co(4-norbornyl)₄ and its cation.

Alkylcobalt is represented by vitamin B₁₂ and related enzymes. In methylcobalamin the ligand is a methyl group, which is electrophilic. in vitamin B12, the alkyl ligand is an adenosyl group. Related to vitamin B12 are cobalt porphyrins, dimethylglyoximates, and related complexes of Schiff base ligands. These synthetic compounds also form alkyl derivatives that undergo diverse reactions reminiscent of the biological processes. The weak cobalt(III)-carbon bond in vitamin B12 analogues can be exploited in a type of Cobalt mediated radical polymerization of acrylic and vinyl esters (e.g. vinyl acetate), acrylic acid and acrylonitrile.

Carbonyl complexes

Dicobalt octacarbonyl is produced by the carbonylation of cobalt salts. It and its phosphine derivatives are among the most widely used organocobalt compounds. Heating Co₂(CO)₈ gives Co₄(CO)₁₂. Very elaborate cobalt-carbonyl clusters have been prepared starting from these complexes. Heating cobalt carbonyl with bromoform gives methylidynetricobaltnonacarbonyl. Dicobalt octacarbonyl also reacts with alkynes to give dicobalt hexacarbonyl acetylene complexes with the formula Co₂(CO)₆(C₂R₂). Because they can be removed later, the cobalt carbonyl centers function as a protective group for the alkyne. In the Nicholas reaction an alkyne group is also protected and at the same time the alpha-carbon position is activated for nucleophilic substitution.

Cp, allyl, and alkene compounds

Sandwich compounds

Organocobalt compounds are known with alkene, allyl, diene, and Cp ligands. A famous sandwich compound is cobaltocene, a rare example of low-spin Co(II) complex. This 19-electron metallocene is used as a reducing agent and as a source of CpCo. Other sandwich compounds are CoCp(C₆Me₆) and Co(C₆Me₆)₂, with 20 electrons and 21 electrons, respectively. Reduction of anhydrous cobalt(II) chloride with sodium in the presence of cyclooctadiene gives Co(cyclooctadiene)(cyclooctenyl), a synthetically versatile reagent.

CpCo(CO)₂ and derivatives

The half-sandwich compounds of the type CpCoL₂ have been well investigated (L = CO, alkene). The complexes CpCo(C₂H₄)₂ and CpCo(cod) catalyze alkyne trimerisation, which has been applied to the synthesis of a variety of complex structures.

Applications

Dicobalt octacarbonyl is used commercially for hydroformylation of alkenes. A key intermediate is cobalt tetracarbonyl hydride (HCo(CO)₄). Processes involving cobalt are practiced commercially mainly for the production of C7-C14 alcohols used for the production of surfactants. Many hydroformylations have switched from cobalt-based processes to rhodium-based processes, despite the great expense of that metal. Replacing H₂ by water or an alcohol, the reaction product is a carboxylic acid or an ester. An example of this reaction type is the conversion of butadiene to adipic acid. Cobalt catalysts (together with iron) are relevant in the Fischer–Tropsch process in which it is assumed that organocobalt intermediates form.

Cobalt complexes have been applies to the synthesis of pyridine derivatives starting from alkynes and nitriles.

Aspirational applications

Although really only dicobalt octacarbonyl has achieved commercial success, many reports have appeared promising applications. Often these ventures are motivated by the use of "earth abundant" catalysts.

References

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v t e Compounds of carbon with other elements in the periodic table
CH He CLi CBe CB CC CN CO CF Ne CNa CMg CAl CSi CP CS CCl CAr CK CCa CSc CTi CV CCr CMn CFe CCo CNi CCu CZn CGa CGe CAs CSe CBr CKr CRb CSr CY CZr CNb CMo CTc CRu CRh CPd CAg CCd CIn CSn CSb CTe CI CXe CCs CBa CLu CHf CTa CW CRe COs CIr CPt CAu CHg CTl CPb CBi CPo CAt Rn Fr CRa Lr Rf Db CSg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og   CLa CCe CPr CNd CPm CSm CEu CGd CTb CDy CHo CEr CTm CYb Ac CTh CPa CU CNp CPu CAm CCm CBk CCf CEs Fm Md No
Legend	Chemical bonds to carbon Core organic chemistry Many uses in chemistry Academic research, no widespread use Bond unknown

• Organocobalt compounds