Abstract
Laser Raman spectra are
reported for cyclopropane adsorbed on cation- exchanged zeolites X. The results
have been interpreted in terms of an edge-on interaction of the cyclopropane
molecule with the zeolitic cation site. The symmetry of cyclopropane, when adsorbed
on LiX and NaX, appears to
be lowered from the free-molecule symmetry (D3h) to C2V
as evidenced by the splitting of the E' mode (v11) of cyclopropane.
In contrast to the previously reported case of the adsorption complexes, MX+C2H2
and MA+C2H2, the adsorption interaction appears to follow
a direct polarizing-power dependence on the zeolitic cation. Force- constant
calculations support an interpretation based on a cation- induced dipole
interaction.
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