15682-62-9

Upstream product

• 603-32-7 triphenyl-arsane 
• 201230-82-2 carbon monoxide 
• 73191-02-3 (tetrabutylammonium)[IrCl₂(CO)2] 

Downstream Products

• 80062-95-9 IrH((C₆H₅)2AsC₆H₄CO)Cl(CO)(As(C₆H₅)3) 
• 82345-87-7 carbonylchloro[perfluoro-NN'-dimethylethane-1,2-bis(amino-oxy)]bis(triphenylarsine)iridium(III) 
• 81599-69-1 [IrCl(O₂C(CH₃)2C₆H₅)2(CO)(As(C₆H₅)3)2] 
• 82532-07-8 chlorobis(3-chlorobenzoato)bis(triphenylarsine)iridium(III) 
• 80062-94-8 IrH((C₆H₅)2PC₆H₄CO)Cl(CO)(As(C₆H₅)3) 
• 246252-99-3 (IrH₂(As(C₆H₅)3)2(CO)Cl) 
• 246252-99-3 IrCl(CO)[As(C₆H₅)3]2H₂ 
• 60977-01-7 bis{bis(trifluoromethyl)amino-oxy}carbonylchlorobis(triphenylarsine)iridium(III) 

Relevant academic research and scientific papers

Activation of H2 by halocarbonyl bis-phosphine and bis-arsine iridium(I) complexes. The use of parahydrogen induced polarisation to detect species present at low concentration and investigate their reactivity

The iridium phosphine complexes Ir(CO)Cl(L)2 [L = PPh3, PMe3, AsPh3 and PPh2Cl, and L2 = (PPh2Cl)(PPh3)] add H2 to form the corresponding dihydrides IrH2(CO)Cl(L)2. These products are detected at enhanced levels of sensitivity through the 1H NMR signatures of their hydride resonances via para-hydrogen (p-H2) based spin state synthesis. Products corresponding to addition across both the Cl-Ir-CO and L-Ir-L axes are detected. For L = PPh3, there is a 100 fold preference for the former pathway at 295 K, while for L = AsPh3 the second product is favoured by a factor of 2.85. At elevated temperatures a third product corresponding to addition over the Cl-Ir-L axis is detected for L = AsPh3 and PPh2Cl. Under these conditions, the CO and HCl transfer products Ir(H)3(CO)2(AsPh3), and IrH(CO)Cl2(AsPh3)2 are also formed in a thermal reaction. When IrH2(CO)Cl(L)2 is warmed or photolysed with H2 and CO, the corresponding products are produced for L = PPh3 and PMe3. However after photolysis with H2 alone Ir(H)3(CO)(L)2 is the favoured product. Additional products detected during the photochemical studies include Ir(H)2(PPh)3(PPh2C5H4 CO), an unusual orthometallation product containing an η2-acyl ligand, and the binuclear products H(Cl)Ir(PMe3)2(μ-H)(μ-Cl)Ir(PMe3)(CO) and (H)2Ir(PMe3)2(μ-Cl)2Ir(PMe) 3(CO).

A high-yield synthetic approach to trans-[Ir(ER3)2(CO)X] (ER3=PMe3, PEt3, PPhMe2, PPh2Me, P(OMe)3, AsMe3, AsEt3, AsPh3, SbPh3; X=Cl, Br)

The complex [Ir(CO)2X2][NBu4] (X=Cl, Br) forms Vaska-type complexes, trans-[Ir(ER3)2(CO)X], when treated with two equivalents of aryl- or alkyl-phosphines, arsines, or stibines under a CO atmosphere. The synthesis is general for a wide range of phosphines, arsines, or stibines irrespective of the cone angle. For small cone-angle ligands, the initial addition of ligand to [Ir(CO)2X2][NBu4] is performed at low temperature. The synthesis and characterisation of three new Vaska-type complexes trans-[Ir(P(OMe)3)2(CO)Cl], trans-[Ir(AsMe3)2(CO)Cl], and trans-[Ir(AsEt3)2(CO)Cl] is also reported. Elsevier Science Ltd.

Chelate-assistftd oxidative addition of functlonallzed phosphlnes to irldlum(I)

This paper is concerned with an evaluation of the factors which influence the facility of the oxidative addition of chelating substrates. Spectrophotometrically we determined the for the chelating substrates ere than those for the nonchelating substrates.