A simple model system for the 2D self-assembly of functionalized organic molecules on surfaces was examined in a concerted experimental and theoretical effort. Monolayers of 1-halohexanes were formed through vapor deposition onto graphite surfaces in ultrahigh vacuum. Low-temperature scanning tunneling microscopy allowed the molecular conformation, orientation, and monolayer crystallographic parameters to be determined. Essentially identical noncommensurate monolayer structures were found for all 1-halohexanes, with differences in image contrast ascribed mainly to electronic factors. Energy minimizations and molecular dynamics simulations reproduced structural parameters of 1-bromohexane monolayers quantitatively. An analysis of interactions driving the self-assembly process revealed the crucial role played by small but anisotropic electrostatic forces associated with the halogen substituent. While alkyl chain dispersion interactions drive the formation of a close-packed adsorbate monolayer, electrostatic headgroup forces are found to compete successfully in the control of both the angle between lamella and backbone axes and the angle between surface and backbone planes. This competition is consistent with energetic tradeoffs apparent in adsorption energies measured in earlier temperature-programmed desorption studies. In accordance with the higher degree of disorder observed in scanning tunneling microscopy images of 1-fluorohexane, theoretical simulations show that electrostatic forces associated with the fluorine substituent are sufficiently strong to upset the delicate balance of interactions required for the formation of an ordered monolayer. The detailed dissection of the driving forces for selfassembly of these simple model systems is expected to aid in the understanding of the more complex self-assembly processes taking place in the presence of solvent.haloalkanes ͉ conformation ͉ simulations F uture advances in nanoscale science and engineering are expected to rely increasingly on the controlled bottom-up assembly of molecular arrays. The successful creation of targeted molecular device structures demands a fundamental understanding of the interactions governing 2D self-organization. Simple functionalized hydrocarbon molecules are known to form self-ordered structures at a variety of surfaces and interfaces (1-32) and can serve as ideal model systems to study the underlying forces driving the selfassembly process.Numerous experimental (1-10, 13, 14, 16-19, 21, 22, 24, 27, 28, 30-41) and theoretical (39, 42, 43) studies have investigated the self-assembled monolayers formed when a melt or solution containing alkanes or their derivatives is brought in contact with the basal plane of a graphite substrate. Scanning tunneling microscopy (STM) (2-6, 8-10, 13, 14, 16-19, 24, 27, 28, 31-38, 40, 41) and diffraction-based probes (7,39,44,45) have been used to characterize the crystallographic monolayer parameters as well as the orientation and conformation of the constituent molecular species. For many alkane...