Cluster-derived FeIr/MgO catalysts prepared from [Et4N]2[Fe2Ir4(CO)16]
and [Et4N]2[Fe2Ir2(CO)12] exhibit high activity in methanol synthesis
from CO + H2. The catalyst performance improves significantly upon ra
ising the Fe:Ir ratio in the precursor from 2:4 to 2:2; with the latte
r sample, at 488-523 K and 6.1 MPa, methanol productivities up to 100
mol/mol(Ir) h are obtained with selectivity around 90%. Preliminary ex
tended X-ray absorption fine structure characterization suggests that
the formation of active sites upon activation in hydrogen at 623 K, is
related to the presence of highly dispersed iridium particles stabili
zed on the surface by interfacial iron.