The adsorption of ethylene on Si(100)2 x 1 has been investigated at room te
mperature by high-resolution synchrotron radiation photoemission in the exp
osure range: 1-1000 L. A consistent picture in favor of molecularly di-a bo
nded ethylene is obtained from the analysis of the photoemission spectral f
eatures, which shows the progressive decreasing of the surface states in th
e valence band and the Si 2p features related to the surface dimers upon ad
sorption. By careful fitting of the Si 2p complex envelope, the appearance
of a component in the Si 2p core-level spectrum is evidenced already after
1 L exposure to ethylene. This component, which grows with exposure, is ass
igned to the formation of two Si-C bonds per dimer as a result of ethylene
adsorption. The line-shape analysis by model functions permits us to follow
the symmetrization of Si-Si dimers, which are known to be asymmetric on th
e clean surface, and the growth of a Si-C related spectral component upon a
dsorption. Relative quantitative analysis of the various peak components su
ggests that the intensity increase of the new component almost completely p
arallels the progressive decrease of the surface dimer components. No evide
nce for carbide formation has been found from the C 1s spectrum.