Iridium catalysis ligands

With iridium catalysis, the -rr-allyl intermediate is attacked by the nucleophile at the more-substituted terminus. Again, the inclusion of a chiral ligand yields an optically active product (Scheme 9.66). 

Keywords Alcohols Amides Amines Carbon dioxide Catalysis Dehydrogenative coupling Esters Hydrogen Imines Iridium Metal-ligand cooperation O-H activation Pincer complexes PNN PNP Ruthenium... 

Reactivity studies of organic ligands with mixed-metal clusters have been utilized in an attempt to shed light on the fundamental steps that occur in heterogeneous catalysis (Table VIII), although the correspondence between cluster chemistry and surface-adsorbate interactions is often poor. While some of these studies have been mentioned in Section ll.D., it is useful to revisit them in the context of the catalytic process for which they are models. Shapley and co-workers have examined the solution chemistry of tungsten-iridium clusters in an effort to understand hydrogenolysis of butane. The reaction of excess diphenylacetylene with... 

Today, iridium compounds find so many varied applications in contemporary homogeneous catalysis it is difficult to recall that, until the late 1970s, rhodium was one of only two metals considered likely to serve as useful catalysts, at that time typically for hydrogenation or hydroformylation. Indeed, catalyst/solvent combinations such as [IrCl(PPh3)3]/MeOH, which were modeled directly on what was previously successful for rhodium, failed for iridium. Although iridium was still considered potentially to be useful, this was only for the demonstration of stoichiometric reactions related to proposed catalytic cycles. Iridium tends to form stronger metal-ligand bonds (e.g., Cp(CO)Rh-CO, 46 kcal mol-1 Cp(CO)Ir-CO, 57 kcal mol ), and consequently compounds which act as reactive intermediates for rhodium can sometimes be isolated in the case of iridium. 

The cost of the catalysts represents a major hurdle on the road to the industrial application of homogeneous catalysis, and in particular for the production of fine chemicals [1, 2], This is particularly true for chiral catalysts that are based on expensive metals, such as rhodium, iridium, ruthenium and palladium, and on chiral ligands that are prepared by lengthy total syntheses, which often makes them more expensive than the metals. In spite of this, the number of large-scale applications for these catalysts is growing. Clearly, these can only be economic if the substrate catalyst ratio (SCR) can be very high, often between 103 and 105. 

Tejel C, Ciriano MA (2007) Catalysis and Organometallic Chemistry of Rhodium and Iridium in the Oxidation of Organic Substrates. 22 97-124 Tekavec TN, Louie J (2006) Transition Metal-Catalyzed Reactions Using N-Heterocyclic Carbene Ligands (Besides Pd- and Ru-Catalyzed Reactions). 21 159-192 Tesevic V, see Gladysz JA (2008) 23 67-89... 

Aqueous organometalHc catalysis allows the use of NH3-solutions in water for the direct synthesis of amines from olefins in a combined hydroformylation/reductive amination procedure (Scheme 4.19). The hydroformylation step was catalyzed by the proven Rh/TPPTS or Rh/BINAS (44) catalysts, while the iridium complexes formed from the same phosphine ligands and [ IrCl(COD) 2] were found suitable for the hydrogenation of the intermediate imines. With sufficiently high NH3/olefin ratios (8/1) high selectivity towards the formation of primary amines (up to 90 %) could be achieved, while in an excess of olefin the corresponding... 

---