Isolation and structural characterization of anionic and neutral compounds resulting from the oxidative addition of HI or CH3I to [IrI2(CO)2](-).

Abstract

The active iridium species in the methanol carbonylation reaction has been crystallized as the [PPN][IrI(2)(CO)(2)] complex and the X-ray structure solved, showing a cis-geometry and a square planar environment. Hydriodic acid reacts very quickly with this compound to provide [PPN][IrHI(3)(CO)(2)], the X-ray crystal structure of which has been determined. The two CO ligands remain in mutual cis-position in a pseudooctahedral environment. The same cis-arrangement has been observed from the X-ray structure for [PPN][IrI(3)(CH(3))(CO)(2)] resulting from the slower oxidative addition of CH(3)I to [PPN][IrI(2)(CO)(2)]. By iodide abstraction with InI(3), the anionic methyl complex gave rise to the dimeric neutral complex [Ir(2)(mu-I)(2)I(2)(CH(3))(2)(CO)(4)]. An X-ray structure showed that the methyl ligands are in the equatorial positions of the two octahedrons sharing an edge, formed by the two bridging iodide ligands. All these four complexes have been fully characterized by mass spectrometry, (1)H and (13)C NMR, and infrared both in solution and in the solid state. When necessary, the (13)CO- or (13)CH(3)-enriched complexes have been prepared and analyzed.