Organoiridium chemistry is the chemistry of organometallic compounds containing an iridium-carbonchemical bond.[2] Organoiridium compounds are relevant to many important processes including olefin hydrogenation and the industrial synthesis of acetic acid. They are also of great academic interest because of the diversity of the reactions and their relevance to the synthesis of fine chemicals.[3]
Organoiridium compounds share many characteristics with those of rhodium, but less so with cobalt. Iridium can exist in oxidation states of −3 to +5, but iridium(I) and iridium(III) are the more common. iridium(I) compounds (d8 configuration) usually occur with square planar or trigonal bipyramidal geometries, whereas iridium(III) compounds (d6 configuration) typically have an octahedral geometry.[3]
Iridium(0) complexes are binary carbonyls, the principal member being tetrairidium dodecacarbonyl, Ir4(CO)12. Unlike the related Rh4(CO)12, all CO ligands are terminal in Ir4(CO)12, analogous to the difference between Fe3(CO)12 and Ru3(CO)12.[4]
This difference between RhCl(PPh3)3 and IrCl(PPh3)3 reflects the generally greater tendency of iridium to undergo oxidative addition. A similar trend is exhibited by RhCl(CO)(PPh3)2 and IrCl(CO)(PPh3)2, only the latter oxidatively adds O2 and H2.[5] The olefin complexes chlorobis(cyclooctene)iridium dimer and cyclooctadiene iridium chloride dimer are often used as sources of "IrCl", exploiting the lability of the alkene ligands or their susceptibility to removal by hydrogenation. Crabtree's catalyst ([Ir(P(C6H11)3)(pyridine)(cyclooctadiene)]PF6) is a versatile homogeneous catalyst for hydrogenation of alkenes.[6]
(η5-Cp)Ir(CO)2 oxidatively adds C-H bonds upon photolytic dissociation of one CO ligand.
As is the case for rhodium(II), iridium(II) is rarely encountered. One example is iridocene, IrCp2.[7] As with rhodocene, iridocene dimerises at room temperature.[8]
Iridium is usually supplied commercially in the Ir(III) and Ir(IV) oxidation states. Important starting reagents being hydrated iridium trichloride and ammonium hexachloroiridate. These salts are reduced upon treatment with CO, hydrogen, and alkenes. Illustrative is the carbonylation of the trichloride:
IrCl3(H2O)x + 3 CO → [Ir(CO)2Cl2]− + CO2 + 2 H+ + Cl− + (x-1) H2O
Oxidation states greater than III are more common for iridium than rhodium. They typically feature strong-field ligands. One often cited example is oxotrimesityliridium(V).[12]
Iridium complexes are highly active for hydrogenation both directly and via transfer hydrogenation. The asymmetric versions of these reactions are widely studied.
Many half-sandwich complexes have been investigated as possible anti-cancer drugs. Related complexes are electrocatalysts for the conversion of carbon dioxide to formate.[9][15] In academic laboratories, iridium complexes are widely studied because its complexes promote C-H activation, but such reactions are not employed in any commercial process.
_Schematic.png){kind=link}
12.svg){kind=link}
3O.svg){kind=link}
