Advances in techniques for the nanoscale manipulation of matter are importa
nt for the realization of molecule-based miniature devices(1-8) with new or
advanced functions. A particularly promising approach involves the constru
ction of hybrid organic-molecule/silicon devices(9-14). But challenges rema
in-both in the formation of nanostructures that will constitute the active
parts of future devices, and in the construction of commensurately small co
nnecting wires. Atom-by-atom crafting of structures with scanning tunnellin
g microscopes(15-17), although essential to fundamental advances, is too sl
ow for any practical fabrication process; self-assembly approaches may perm
it rapid fabrication(18), but lack the ability to control growth location a
nd shape. Furthermore, molecular diffusion on silicon is greatly inhibited(
19), thereby presenting a problem for self-assembly techniques. Here we rep
ort an approach for fabricating nanoscale organic structures on silicon sur
faces, employing minimal intervention by the tip of a scanning tunnelling m
icroscope and a spontaneous self-directed chemical growth process. We demon
strate growth of straight molecular styrene lines-each composed of many org
anic molecules-and the crystalline silicon substrate determines both the or
ientation of the lines and the molecular spacing within these lines. This p
rocess should, in principle, allow parallel fabrication of identical comple
x functional structures.