Iridium-Fluoride Complexes

Ruthenium complexes mediate the hydroamination of ethylene with pyridine.589 The reaction, however, is not catalytic, because of strong complexation of the amine to metal sites. Iridium complexes with chiral diphosphine ligands and a small amount of fluoride cocatalyst are effective in inducing asymmetric alkene hydroamination reaction of norbomene with aniline [the best enantiomeric excess (ee) values exceed 90%].590 Strained methylenecyclopropanes react with ring opening to yield isomeric allylic enamines 591... 

Intermolecular asymmetric aminations are at an early stage of development, and consequently much lower turnover frequencies and catalytic yields have been observed at this stage. In the example shown, a key aspect is the activation of the iridium complex catalyst by fluoride ion [111] (Scheme 38). 

Although a number of complex fluorides of quinquevalent iridium, (e.g. KIrF,) are known, previous attempts to establish the simple fluoride have failed. The absence of a pentafluoride of iridium has become increasingly anomalous as the pentafluorides of the neighbouring elements, rhenium, osmium, and platinum have been prepared. Previous work - indicated that reactions which might have yielded the pentafluoride gave the tetrafluoride instead. The physical properties of this tetrafluoride. (m.p. 106—107 b.p. > 300 ), however, resembled those of a pentafluoride or oxide tetrafluoride. This indicated that iridium tetrafluoride differed structurally from its neighbouring tetrafluorides. 

The intermolecialar hydroamination has also received some attention and studies in this area have focussed on the use of iridium and nickel catalysts. Enan-tioselectivities for the intermolecular process are also generally moderate with ees observed between 60 and 70%. The highest enantioselectivities for this reaction have been obtained during the hydroamination of norbornene (2.145) with aniline in the presence of the iridium complex (2.184) and the fluoride ion source... 

There is also clear evidence of a change from predominantly class-a to class-b metal charactristics (p. 909) in passing down this group. Whereas cobalt(III) forms few complexes with the heavier donor atoms of Groups 15 and 16, rhodium(III), and more especially iridium (III), coordinate readily with P-, As- and S-donor ligands. Compounds with Se- and even Te- are also known. Thus infrared. X-ray and nmr studies show that, in complexes such as [Co(NH3)4(NCS)2]" ", the NCS acts as an A -donor ligand, whereas in [M(SCN)6] (M = Rh, Ir) it is an 5-donor. Likewise in the hexahalogeno complex anions, [MX ] ", cobalt forms only that with fluoride, whereas rhodium forms them with all the halides except iodide, and iridium forms them with all except fluoride. 

The pattern of iridium halides resembles rhodium, with the higher oxidation states only represented by fluorides. The instability of iridium(IV) halides, compared with stable complexes IrCl4L2 and the ions IrX (X = Cl, Br, I), though unexpected, finds parallels with other metals, such as plutonium. Preparations of the halides include [19]... 

Direct fluorination of metallic iridium at 543 K has produced the rather unstable, yellow di complex [IrFJ, which is isomorphous with its osmium(VI) analogue. [IrF6] tends toward dissociation, yielding fluorine and lower iridium fluorides. The octahedral [IrF6] species decomposes in water this is accompanied by ozone liberation. The magnetic moment of [IrF6] is jue r = 3.3 BM at... 

The displacement of cyclooctene or C2H4 from an iridium(I) centre by a variety of chiral phosphines (L) leads to the formation of [ (L)IrCl 2] which, in conjunction with a source of F (phosphazenium fluoride), has been used for catalytic hydroamination of olefins. This combination leads to a 6.5 fold increase in the activity of the system and a total reversal in the enantioselectivity compared to that of the chloride analogue. There is no direct evidence of formation of a metal fluoride complex, but it is proposed that it may well form in situ and that this might explain these interesting results [75]. 

Zhao, Q., Liu, S.J., Li, F.Y., et al. (2008) Highly selective phosphorescent chemosensor for fluoride based on an iridium(lll) complex containing arylborane units. Inorganic Chemistry, 47, 9256-9264. 

Parameters for a range of fluoro-olefin complexes of rhodium and iridium are given in Tables XI (97) and XII. The vinyl fluoride complex... 

The iridium(V) fluoro complex [IrFj] has been prepared via reduction of [IrF ] with silicon or dihydrogen, In the gas phase, [IrFj] possesses D h symmetrywhile in the solid state, a fluoride-bridged polymeric structure with bridges mutually cis is indicated on the basis of and F NMR... 

Iridium(V) complexes, 1158 fluorides, 1158 Iridium(VI) complexes, 1158 Iron complexes acetonitrile, 1210 analysis, 1180, biological systems, 1180 coordination geometries, 1183 coordination numbers, 1182-1187 dinitrosyldicarbonyl, 1188 Mdssbauer spectroscopy, 1181 nitric oxide, 1187-1195 nitrosyls binary, 1188 bis(dithiolene), 1193 carbonyl, 1188 dithiocarbamates, 1192 halides, 1193 iodide, 1193... 

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