Saddle-shaped deformation of planar porphyrin molecules is accomplished by
rotations of four phenyl-based substituents, which results from optimum ads
orption onto Au(111) surface. The nonplanar macrocyclic conformation is cle
arly visualized by using low-temperature scanning tunneling microscopy and
confirmed by molecular orbital calculations. Inside of the supramolecular m
olecular islands, we find that two different orientations of the nonplanar
porphyrins are randomly distributed. An orientational ordering is obtained
after short thermal excitations, which should be associated with steric int
ermolecular interactions between substituents. (C) 2001 American Institute
of Physics.