Iridium complexes carbon dioxide

In 1963 Vaska 164) discovered that the iridium complex Ir(PPh3)2C (CO) takes up molecular oxygen reversibly with 1 1 stoichiometry. This complex has since been shown to reversibly sorb (1 1) ethylene (755), carbon dioxide (765), F2C=CF2 and F3C—C=C—CF3 (767), as well as various other ligands (765). Ibers md La Placa (769)... 

The reversible complexing of carbon dioxide by bis[bis(l,2-diphe-nylphosphino)ethane]iridium(I) chloride, [Ir(dpe)2]Cl, in acetonitrile [Eq. (36)] (48) appears not to involve carboxylation of a cyanomethylir-idium(III) complex or its formation by decarboxylation of the cyanoacetate... 

Iridium(III) hydride forms complexes with DIOP, BDPP (2,4-bis(diphenyl-phosphino)pentane), NORPHOS, and BINAP ligands to produce amines in 11 -80% ee.679 Similar modest results are obtained in the reduction of N-arylketimines with an iridium(HI) complex with (2S,3 S) -C HIRA PHOS as the chiral ligand.680 The indium complexes with chiral phosphinodihydrooxazoles catalyze the enantioselective hydrogenation of imines in supercritical carbon dioxide with up to 80% ee, but generally lower ee values are observed in... 

Rasmussen, S.C., Richter, M.M., Yi, E., Place, H. and Brewer, KJ. (1990) Synthesis and characterization of a series of novel rhodium and iridium complexes containing polypyridyl bridging ligands Potential uses in the development of multimetal catalysts for carbon dioxide reduction. Inorg. Chem., 29, 3926—3932. 

The other carbon dioxide complex characterized by x-ray crystallography contains two linked C02 molecules in the coordination sphere (116). This complex, [IrCl(C204)(PMe3)3], was prepared by the interaction of C02 with chloro(cyclooctene)[tris(trimethylphosphine)]iridium(I), [IrCl(C8 H j 4)-(PMe3)3], in benzene solution. The structure, (25), shows essentially octahedral coordination about the iridium center, with one metal-carbon bond and a five-membered chelate ring formed with the second C02 molecule. 

In the past, this field has been dominated by ruthenium, rhodium and iridium catalysts with extraordinary activities and furthermore superior enantioselectivities however, some investigations were carried out with iron catalysts. Early efforts were reported on the successful use of hydridocarbonyliron complexes HFcm(CO) as reducing reagent for a, P-unsaturated carbonyl compounds, dienes and C=N double bonds, albeit complexes were used in stoichiometric amounts [7]. The first catalytic approach was presented by Marko et al. on the reduction of acetone in the presence of Fe3(CO)12 or Fe(CO)5 [8]. In this reaction, the hydrogen is delivered by water under more drastic reaction conditions (100 bar, 100 °C). Addition of NEt3 as co-catalyst was necessary to obtain reasonable yields. The authors assumed a reaction of Fe(CO)5 with hydroxide ions to yield H Fe(CO)4 with liberation of carbon dioxide since basic conditions are present and exclude the formation of molecular hydrogen via the water gas shift reaction. H Fe(CO)4 is believed to be the active catalyst, which transfers the hydride to the acceptor. The catalyst presented displayed activity in the reduction of several ketones and aldehydes (Scheme 4.1) [9]. 

The procedure described here is based on the observation that amine monohydroxo complexes of cobalt(III), rhodium(IIl), and iridium(III) react directly with carbon dioxide to form the corresponding carbonato complexes,2 3 without effect on the configuration of the amine ligands.4 The amine monoaqua complex is allowed to react with lithium carbonate or carbon dioxide gas at room temperature at pH 8.0 for a few minutes, and the carbonato complex is isolated by adding alcohol. The procedure has been used to prepare salts of the following cations pentaammine(carbonato)-cobalt(III),2 ds-ammine(carbonato)bis(ethylenediamine)cobalt(III),5 trans-... 

All of the carbonato cobalt(III) complexes reported here are reddish in color and extremely soluble in water. The rhodium complex is pale-yellow, whereas the iridium salt is virtually white they are both soluble in water. Treatment with dilute acid immediately gives the corresponding aqua complex with evolution of carbon dioxide. The characterization and the mechanistic details of acid hydrolysis of these complexes have been reported.3,4,11... 

Another important example of COj-hydrogenation is the synthesis of form-amides. In 1970, Haynes c/tf/. of Shell Development Co. discovered the reaction of carbon dioxide, hydrogen and certain amines, when catalyzed under mild conditions by cobalt, rhodium, iridium and palladium complexes [ I70. ... 

A range of metal catalysts have also been studied in aqueous solution for the transformation of carbon dioxide, including rhodium, ruthenium and iridium bipyridine or phenanthroline complexes.One of the most effective systems is the iridium complex shown in Figure 3.14. The ligand design concept used in this study is very clever. The catalytic activity of the complex and its solubility in aqueous solution can be tuned by the pH of the solution.Under acidic... 

In recent years, interest has intensified in the chemistry of carbon dioxide, stimulated by the current concern about alternate petrochemical feedstocks. One area under active exploration involves C02 activation via coordination to a transition metal complex.1 Several adducts of C02 have been claimed, and two monometallic complexes, with x-ray structures which have been published, are shown below schematically (1 and 2).2,3 We report here two examples of the preparation of 1 1 C02 adducts of a series of rhodium and iridium complexes and, relatedly, methods for preparing the 2 1 C02 lr complex 2. 

Scheme 8.20 Difference in interaction of carbon dioxide and dihydrogen with rhodium and iridium pincer complexes.

The combination of hard oxophilic early transition metals and soft nucleophilic late transition metals with opposite functionalities, provided they do not inhibit one another, is a priori ideal for promoting cooperative effect. A proof of concept can be found in the stoichiometric reactivity of early—late heterobimetallic complexes featuring a metal-metal bond [76]. It has been shown that such complexes are good candidates to realize the heterolytic cleavage of a bond in polar and apolar substrates. An illustrative example by Bergman et al. is the reaction of the Zr-lr complex 20 with carbon dioxide which leads to the rupture of the metal—metal bond (Scheme 18) [77]. The CO2 insertion occurs in the expected fashion with the CO2 bridging the two metals, the carbon atom coordinated to iridium, and the oxygen atom on the zirconium center. 

The iridium compound [IrCl(C8H,4)(PMe3)3] reacts with carbon dioxide to afford the complex (13.226). " Coordinated CO2 undergoes migratory insertion to the... 

C. M. Bolinger, N. Storey, B. P. Sullivan and T. J. Meyer (1988) Electrocatalytic reduction of carbon dioxide by 2,2 -bipyridine complexes of rhodium and iridium , Inow. Chem. 27, 4582-4587. 

Weigl BH, Holobar A, Trettnak W, Klimant I, Kraus H, O Leary P, Wolfbeis OS (1994) Optical triple sensor for measuring pH oxygen and carbon dioxide. J Biotechnol 32 127-138 Borisov SM, Klimant I (2007) Ultrabright oxygen optodes based on cyclometalated iridium (111) coumarin complexes. Anal Chem 79 7501-7509... 

Rate data are reported for the acid-catalysed aquation of the [M(NH3)5COal+ ions (M = Rh or Ir ), as well as the rates of formation of these carbonato-com-plexes from [M(NH3)50H] + and carbon dioxide. At 298.1 K and p = 0.5 mol 1 , the aquation rate constants are 1.13 and 1.45 s and the formation rate constants 470 and 5901 mol S for the rhodium(m) and iridium(m) complexes respectively. The close similarity of these rate constants for both metal ions indicates carbon-oxygen bond fission for the aquation reactions. 

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