T. Kinnunen et K. Laasonen, Reaction mechanism of the reductive elimination in the catalytic carbonylation of methanol. A density functional study, J ORGMET CH, 628(2), 2001, pp. 222-232
Reductive elimination, the final step of the Monsanto and Cativa processes,
has been studied using the density functional theory with the hybrid B3LYP
exchange and correlation functional. To our knowledge, this is the first s
ystematic computational study of the reductive elimination for which even t
he experimental studies are rare. We have studied different isomers of the
anionic dicarbonyls [Rh(CO)(2)(COCH3)I-3](-) (1) and [Ir(CO)(2)(COCH3)I-3](
-) (2) Several possible reaction routes for the elimination of CH3COI from
1 and 2 have been explored. In addition, different isomers of the neutral t
ricarbonyl [Ir(CO)(3)(COCH3)I-2] (3) and possible reaction paths connected
to 3 have been studied. Our results show mer,trans-1 to be the dominant int
ermediate in the rhodium system although its transformation to fac,cis-1 an
d the elimination from this seems to be the most likely reaction pathway. I
n the anionic iridium system, the dominating intermediate is proposed to be
fac.cis-2. In the neutral iridium system, mer,cis-3 is proposed to be the
dominant intermediate. While inspecting the iridium system as a whole, one
could propose a transformation from anionic dicarbonyl to neutral tricarbon
yl that would enhance the total rate of the reductive elimination. This obs
ervation is similar to that already verified in the I,l-insertion in the Ca
tiva process. In general, the geometrical arrangement of the different liga
nds has a large effect on the catalytic activity of the different possible
intermediates of these processes. (C) 2001 Elsevier Science B.V. All rights
reserved.