Organorhodium chemistry


Organorhodium chemistry is the chemistry of organometallic compounds containing a rhodium-carbon chemical bond, and the study of rhodium and rhodium compounds as catalysts in organic reactions.
Stable organorhodium compounds and transient organorhodium intermediates are used as catalyst such as in olefin hydroformylation, olefin hydrogenation, olefin isomerization and the Monsanto process

Classification based on principal oxidation states

Organometallic rhodium compounds share many characteristics with those of iridium, but less so with cobalt. Rhodium can exist in oxidation states of -III to +V, but rhodium and rhodium are the more common. Rhodium compounds usually occur with square planar or trigonal bipyramidal geometries, while rhodium compounds typically have an octahedral geometry.

Rhodium(0)

Rhodium complexes are binary carbonyls, the principal examples being tetrarhodium dodecacarbonyl, Rh410, and hexadecacarbonylhexarhodium, Rh616. These compounds are obtained by reductive carbonylation of rhodium salts or Rh2Cl24. In contrast to the stability of the homologous Co28, Rh28 is very labile.

Rhodium(I)

Rhodium complexes are important homogeneous catalysts. Common complexes include bisrhodium carbonyl chloride, chlorobisrhodium dimer, cyclooctadiene rhodium chloride dimer, chlorobisrhodium dimer, dicarbonylrhodium, and rhodium carbonyl chloride. Although not formally organometallic, Wilkinson's catalyst, is included in the list of important catalysts. The simple olefin complexes chlorobisrhodium dimer, chlorobisrhodium dimer, and cyclooctadiene rhodium chloride dimer are often used as sources of "RhCl", exploiting the lability of the alkene ligands or their susceptibility to removal by hydrogenation. RhL2 are derived from Rh2Cl2L4.

Rhodium(II)

Unlike the prevalence of cobalt complexes, compounds of rhodium are rare. The sandwich compound rhodocene is one example, even it exists in equilibrium with a dimeric Rh derivative. Although not organometallic, rhodium acetate catalyzes cyclopropanations via organometallic intermediates. Rhodium porphyrin complexes react with methane.

Rhodium(III)

Rhodium is usually supplied commercially in the Rh oxidation state, the main starting reagent being hydrated rhodium trichloride. The latter reacts with olefins and with CO to give organometallic complexes, often concomitant with reduction to Rh. Cyclopentadienyl complexes of rhodium include the half-sandwich compound pentamethylcyclopentadienyl rhodium dichloride dimer.

Rhodium(V)

Strong donor ligands - hydride, silyl, boryl - are required to stabilize Rh. This oxidation state is invoked in borylation reactions.

Major applications

Despite its high cost, rhodium is heavily relied on as a commercial catalyst.

Acetic acid and acetic anhydride syntheses

The Monsanto process is an industrial method for the manufacture of acetic acid by catalytic carbonylation of methanol, although it has largely been supplanted by the iridium-based Cativa process.
for production of acetic acid.
The catalytically active species is the anion cis-−. which undergoes oxidative addition with methyl iodide. The related Tennessee Eastman acetic anhydride process affords acetic anhydride by carbonylation of methyl acetate.

Hydroformylation

s often rely on rhodium-based catalysts. Water-soluble catalysts have also been developed. They facilitate the separation of the products from the catalyst.

Hydrogenation

Wilkinson's catalyst is used as a homogeneous catalyst for the hydrogenation of olefins. The mechanism of catalysis involves oxidative addition of H2, π-complexation of alkene, migratory insertion, and reductive elimination.
Cationic organorhodium catalysts are useful for asymmetric hydrogenations, which are applied to bioactive products such as pharmaceutical agents and agrochemicals.
File:IBOZABcationDownC2.png|thumb|left|Structure of +, a precatalyst for asymmetric hydrogenation.

Other reactions

reduction is another reaction catalysed by this compound type: