Selective synthesis of iridium(iii) end-capped polyynes by oxidative addition of 1-iodopolyynes to Vaska's complex.

The reaction of bis(triphenylphosphine)iridium(i) carbonyl chloride (Vaska's complex) with a series of 1-iodopolyynes (1-CI and 2-CI) gave σ-polyynyl iridium(iii) complexes with general formula R(C[triple bond, length as m-dash]C)Ir(PPh)(Cl)(I)(CO). The use of acetonitrile as a solvent appeared crucial and allowed selectively obtaining only one from a few possible isomers. The X-ray single crystal diffraction experiment for 2-C[Ir]I allowed the determination of the exact structure of this complex. Further spectroscopic measurements, especially P NMR, confirmed the formation of the same type of isomers with trans coordinated phosphines in each case. All complexes were fully characterized with the use of NMR (H, C and P), IR, UV/Vis, cyclic voltammetry and (ESI)HRMS techniques. Moreover, DFT calculations were performed for all the resulting species. The complexes with a linear carbon chain from butadiyne to decapentayne are the longest iridium end-capped polyynes known to date since only compounds with a (C[triple bond, length as m-dash]C) structural motif have been reported so far. Moreover, we confirmed that the synthetic approach, first used for palladium(ii) end-capped polyynes, may be also applied for the synthesis of other structurally new organometallic polyynes.