In the acidic solids used in this study, ethene undergoes a cationic p
olymerisation started by proton transfer. The larger the dimensions of
the micropores, the higher is the degree of branching of the polymeri
c cationic species obtained. Such saturated polymeric cationic species
evolve upon thermal treatment by loss of hydrogen to allylic carbocat
ions (linear mono-, di- and trienic species as well as penta-cyclo and
hexa-cyclo monoenic species), which are precursors to aromatics. All
species have been characterised both in the infrared (IR) and ultravio
let (UV) regions. The overall chemistry is very close to that of prope
ne on the same systems, though ethene appears less reactive.