The metal carbonyls [M(CO)
6
] (M = Mo or W)
were found to be molecularly adsorbed on the surface of H-ZSM-5 zeolite
crystals. Three types of adsorbed species were detected by IR
spectroscopy: weakly physisorbed metal carbonyls and [M(CO)
6
]
molecules interacting (via a CO ligand) with OH groups or with
Lewis-acid sites (co-ordinatively unsaturated Al
3+
ions). For
physisorbed species a single C–O stretching mode (T
1u
)
was observed, around 1990 cm
-1
. The (OC)
5
MCO

·

·

·

HOSi
species gave a band at 1965 cm
-1
(anchored CO
ligand) and the corresponding E + 2A
1
modes at
higher frequency. O-Bonding between the metal hexacarbonyls and
Lewis-acid centres gives rise to a characteristic IR absorption band in
the range 1750–1850 cm
-1
, and corresponding
E + 2A
1
modes at
CO
>
2000 cm
-1
. Close inspection of these
spectroscopic features, and comparison with IR spectra of adsorbed CO,
enables characterization of the zeolite surface. For medium-pore
zeolites an important feature of this method is that [M(CO)
6
]
molecules cannot penetrate inside the zeolite channels, therefore
discrimination between internal and external surface sites can be
accomplished. Thus, it was found that both Brønsted-acid sites
[bridged Si(OH)Al groups] and silanols are located mainly inside the
zeolite channels.