in this work, supported transition metals catalysts modified by tetra n-but
yltin in the presence of hydrogen are studied. It is demonstrated that this
methodology derived from the Surface Organometallic Chemistry on Metals, a
llows to control the nature of the active phase specifically formed This ac
tive phase is dependent of the temperature at which it is activated in hydr
ogen: below 423 K, organobimetallic supported phases can be obtained, havin
g a good selectivity to cinnamyl alcohol in the hydrogenation of cinnamalde
hyde. For higher activation temperatures (773 Ki, the organic fragments are
totally eliminated obtaining bimetallic systems with particular properties
in the isobutane dehydrogenation to isobutene and in the CO2 reforming of
methane to synthesis gas.