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.^[1]

Stable organorhodium compounds and transient organorhodium intermediates are used as catalyst such as in olefin hydroformylation, olefin hydrogenation, olefin isomerization and the Monsanto process.^[2]

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(I) and rhodium(III) are the more common. Rhodium(I) compounds (d⁸ configuration) usually occur with square planar or trigonal bipyramidal geometries, while rhodium (III) compounds (d⁶ configuration) typically have an octahedral geometry.^[2]

Rhodium(0) complexes are binary carbonyls, the principal examples being tetrarhodium dodecacarbonyl, Rh₄(CO)₁₂, and hexadecacarbonylhexarhodium, Rh₆(CO)₁₆. These compounds are obtained by reductive carbonylation of rhodium(III) salts or Rh₂Cl₂(CO)₄. In contrast to the stability of the homologous Co₂(CO)₈, Rh₂(CO)₈ is very labile.

Rhodium(I) complexes are important homogeneous catalysts. Common complexes include bis(triphenylphosphine)rhodium carbonyl chloride, chlorobis(ethylene)rhodium dimer, cyclooctadiene rhodium chloride dimer, chlorobis(cyclooctene)rhodium dimer, dicarbonyl(acetylacetonato)rhodium(I), and rhodium carbonyl chloride. Although not formally organometallic, Wilkinson's catalyst (RhCl(PPh₃)₃), is included in the list of important catalysts. The simple olefin complexes chlorobis(ethylene)rhodium dimer, chlorobis(cyclooctene)rhodium 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. (η⁵-Cp)RhL₂ are derived from Rh₂Cl₂L₄ (L = CO, C₂H₄).

Unlike the prevalence of cobalt(II) complexes, compounds of rhodium(II) are rare. The sandwich compound rhodocene is one example, even it exists in equilibrium with a dimeric Rh(I) derivative. Although not organometallic, rhodium(II) acetate (Rh₂(OAc)₄) catalyzes cyclopropanations via organometallic intermediates. Rhodium(II) porphyrin complexes react with methane.^[3]

Rhodium is usually supplied commercially in the Rh(III) 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(I). Cyclopentadienyl complexes of rhodium include the half-sandwich compound pentamethylcyclopentadienyl rhodium dichloride dimer.

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

Cyclometalated rhodium compounds constitute an important class of organometallic chemistry. Although such compounds are well documented in the literature rhodium(III) cyclometalates with azo function are spare. A typical example of this category viz. novel hexacoordinated orthometalated rhodium(III) thiolato complex trans-[Rh(C^∧N^∧S)Cl(PPh₃)₂] was synthesized from benzyl 2-(phenylazo)phenyl thioether and RhCl₃·3H₂O in the presence of excess PPh₃ via in situ C(sp²)−H and C(sp³)−S bond scissions. This is the first example for a coordination compound of (phenylazo)thiolate ligand. The mechanism of formation of orthometalated azobenzene derivative was described to proceed via initial coordination of azo-nitrogen followed by electrophilic substitution at the pendant phenyl ring. PPh₃ plays a crucial role in the C(sp³)−S cleavage process. Reductive cleavage by single electron transfer (SET) mechanism is likely to be operative for the C−S bond cleavage. Unlike analogous (phenylazo)phenolato compound the orthometalated thiolato complex exhibits a fully reversible oxidative wave at 0.82 V vs Ag/AgCl and this response is supposed to be primarily centered on the thiolato sulfur atom.^[4]

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

The Monsanto process is an industrial method for the making of acetic acid by catalytic carbonylation of methanol,^[5] although it has largely been supplanted by the iridium-based Cativa process.

The catalytically active species is the anion cis-[Rh(CO)₂I₂]⁻.^[6] which undergoes oxidative addition with methyl iodide. The related Tennessee Eastman acetic anhydride process affords acetic anhydride by carbonylation of methyl acetate.^[7]

CH₃CO₂CH₃ + CO → (CH₃CO)₂O

Hydroformylations often rely on rhodium-based catalysts. Water-soluble catalysts have also been developed. They facilitate the separation of the products from the catalyst.^[8]

${\displaystyle {\ce {{\overset {alkene}{RHC=CH2}}+{CO}+H2->[{\ce {HRh(CO)(PPh3)3}}][{\text{hydroformylation}}]{\overset {aldehydes}{RCH2CH2CHO}}}}}$

Wilkinson's catalyst is used as a homogeneous catalyst for the hydrogenation of olefins.^[9] The mechanism of catalysis involves oxidative addition of H₂, π-complexation of alkene, migratory insertion (intramolecular hydride transfer or olefin insertion), and reductive elimination.

Cationic organorhodium(I) catalysts are useful for asymmetric hydrogenations, which are applied to bioactive products such as pharmaceutical agents and agrochemicals.^[10]

Nitrobenzene reduction is another reaction catalysed by this compound type:

${\displaystyle {\ce {{\overset {nitrobenzene}{PhNO2}}+ {C6H6}+ 3CO ->[{\ce {Rh6(CO)16}}] {PhNHCOPh}+ {2CO2}}}}$