The structure and conformation of a molecule determine its chemical an
d physical properties. Molecular conformation at interfaces is of part
icular importance in organic thin films(1): in organic optoelectronic
devices(2,3) for example, charge carrier injection is influenced by in
terfacial properties(4). Here we present a real-space conformational a
nalysis of individual porphyrin molecules using scanning tunnelling mi
croscopy(5,6). Porphyrins have been used as model systems to study cha
rge transfer(7) and in vivo photoactivation of drug precursors(8), and
have also been used in organic light-emitting diodes(9). We find that
changes in the porphyrins' conformation occur predominantly by rotati
ons around the bonds to four tertiary butyl appendages, which differ o
n different metal substrates. On corrugated gold(110) surfaces, we ide
ntify two different conformations as the precursory (metastable) and f
inal states of adsorption. This kind of conformational adaptation to a
surface may be general for adsorbed organic molecules, and might have
important consequences for the technological applications of organic
thin films.