An IR and UV-VIS study of the interaction of methyl and ethyl acetylene wit
h the acidic form of zeolite ETS-10 is here presented. It is shown that, in
the first adsorption step (at room temperature) pi hydrogen-bonded adducts
are formed between the alkyl acetylene and the zeolite hydroxy groups. The
se hydrogen bonded species act as precursors in the second step, where olig
omerization takes place, leading to formation of carbocationic double bond
conjugated systems of increasing length.