Activation of
Carbon Monoxide by (Me(3)tpa)Rh and (Me(3)tpa)Ir
Dzik WI , Smits JMM , Reek JNH , de Bruin B
ORGANOMETALLICS Volume: 28 Issue:
6 Pages: 1631-1643
Abstract:
Cationic iridium and rhodium carbonyl complexes supported with
the tetradentate N-donor ligand Me(3)tpa (Me(3)tPa =
N,N,N-tri(6-methyl-2-pyridylmethyl)amine) were synthesized. Their
structures were investigated using X-ray diffraction, NMR, and IR, and
their redox properties were probed using cyclic voltammetry and EPR
spectroscopy. Iridium forms a trigonal bipyramidal 18 VE biscarbonyl
complex, while rhodium forms a square-planar 16 VE monocarbonyl
species. In both compounds the Me3tpa ligand coordinates in a kappa(3)
rather than the expected kappa(4) mode and is fluxional on the NMR time
scale. Complex [Ir(kappa(3)-Me(3)tpa)(CO)(2)]PF6 (2(+)) reacts at room
temperature with methanol and water to form the methoxycarbonyl iridium
compound [Ir(kappa(3)-Me(3)tpa)(CO)(H)(COOMe)]PF6 (4(+)) and the
hydroxycarbonyl iridium compound
[Ir(kappa(3)-Me(3)tpa)(CO)(H)(COOH)]PF6 (5(+)), respectively. The
hydroxycarbonyl iridium complex 5(+) is not stable and decomposes to
bis-hydride iridium complex [Ir(kappa(3)-Me(3)tpa)(CO)(H)(2)]PF6
(6(+)), thus illustrating subsequent steps of the water gas shift
reaction. Complex 2(+) is converted to
[Ir(kappa(4)-Me(3)tpa)(CO)(H)](PF6)(2) (7(+)) upon one-electron
oxidation with AgPF6. Rhodium complex [Rh(kappa(3)-Me(3)tpa)(CO)]PF6
(3(+)) is selectively oxygenated by 02 in the presence of water to form
the carbonato rhodium complex [Rh(kappa(3)-Me(3)tpa)(CO3)]PF6 (8(+)).
This represents a rare example of formation of a stable rhodium
carbonate complex via oxygenation of a coordinated CO molecule.