The reaction between gas-phase acetylene and alumina-supported palladium sa
turated with C-13-labelled vinylidene is studied using both one-pulse, C-13
magic-angle spinning, nuclear magnetic resonance (NMR) spectroscopy and by
mass spectroscopic analysis of the reaction products to probe the reaction
pathway. The presence of vinylidene on alumina-supported palladium is conf
irmed by comparing the infrared spectra of the species formed on the suppor
ted sample with those found on a Pd(111) single crystal. It is shown using
NMR that a high pressure (similar to 350 Torr) of gas-phase acetylene react
s with adsorbed vinylidene at the same rate at which benzene is formed cata
lytically on the same sample. The resulting benzene incorporates two C-13 a
toms. This indicates that benzene is formed by a slow reaction between gas-
phase (C-12-labelled) acetylene and adsorbed vinylidene ((CH2)-C-13=C-13=)
to form a C-4 intermediate which reacts rapidly with further acetylene to y
ield benzene. There are precedents for such reactions in homogeneous phase.
The proposed reaction pathway differs from that elucidated previously from
ultrahigh vacuum studies on clean Pd(111), where it was found that benzene
synthesis also proceeds via a C-4 intermediate, in this case formed from t
wo adsorbed acetylenes.