Infrared spectra are reported of acetophenone and 4-methoxyacetophenon
e adsorbed on silica-alumina catalyst. The dominant modes of adsorptio
n involved ligation via carbonyl groups to Lewis acidic Al3+ sites and
H-bonding of surface silanol groups to carbonyl groups or aromatic ri
ngs. Isotopic H/D exchange between SiOH groups and CD3 groups or SiOD
and CH3 occurred for acetophenone probably via an enolisation mechanis
m, although no enolic species could be detected. There was also little
evidence for condensation reactions. Band positions for adsorbed acet
ophenones compared with the predictions of Hartree-Fock calculations s
uggested that acetophenone was not protonated, but 4-methoxyacetopheno
ne was protonated by Bronsted acidic hydroxy groups for which -6.15 le
ss than or equal to H-0 less than or equal to -4.81. (C) 1998 Elsevier
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